|Year : 2008 | Volume
| Issue : 1 | Page : 17-36
|FDG-PET and PET/CT - Part II
Amol M Takalkar1, Ghassan El-Haddad2, David L Lilien1
1 PET Imaging Center, Biomedical Research Foundation of Northwest Louisiana; Department of Radiology, Nuclear Medicine Section, Louisiana State University Health Sciences Center - Shreveport, Shreveport, LA, USA
2 PET Imaging Center, Biomedical Research Foundation of Northwest Louisiana, Shreveport, LA, USA
Click here for correspondence address and email
|How to cite this article:|
Takalkar AM, El-Haddad G, Lilien DL. FDG-PET and PET/CT - Part II. Indian J Radiol Imaging 2008;18:17-36
| Introduction|| |
The high diagnostic accuracy of FDG-PET and PET/CT has been well documented for several neoplasms, with a consequent rapid increase in the utilization and acceptance of PET imaging in the clinical setting. As reported earlier,  initial work with PET that started in the 1980s had already established the value of FDG-PET in neurologic and cardiac applications.  FDG-PET became a clinical reality only when its importance in the management of several common malignancies was demonstrated and documented by many investigators in the early and late 1990s. The Warburg Effect (increased aerobic glycolysis in cancer cells) is the basic principle underlying the value of FDG-PET imaging in neoplasms.  FDG-PET is now routinely utilized in the evaluation of several neoplasms like lymphoma, melanoma, lung cancer, breast cancer, colorectal cancer, to name a few. Its value in several other neoplasms is being explored in the United States of America (US) with the establishment of a National Oncologic PET registry (NOPR). The introduction of dual modality PET/CT imaging in the late 1990s and early part of this century has added more strength to this powerful imaging modality. Today, FDG-PET or PET/CT imaging has become an integral component in the evaluation of numerous neoplasms and has been shown to have a tremendous clinical impact on the management of a significant number of cancer patients. In addition to FDG, other PET radiopharmaceuticals are also being developed for cancer imaging.
This article reviews the current clinical applications of FDG-PET and PET/CT in certain malignancies, specifically head and neck cancer, lung cancer, lymphoma and melanoma. Thyroid neoplasms are included in the head and neck cancer section and pleural malignancies are discussed in the lung cancer section.
| FDG-PET and PET/CT in oncology|| |
Anatomic imaging modalities like CT scan and MRI have superb structural resolution that is continuously improving with technological innovations. However, these imaging modalities rely significantly (although not exclusively) on size and shape of lesions, in addition to indirect findings such as edema, to differentiate benign from malignant disease. Therefore, disease manifestations that occur at the molecular and cellular level, before manifesting as structural changes, are frequently not detected with these modalities. FDG-PET has the capability to depict abnormal metabolic activity before any anatomic change occurs. This is particularly important in patients who undergo therapeutic interventions such as radiotherapy and chemotherapy, after which structural changes often lag behind metabolic changes, for a significant interval of time. In fact, some lesions may never shrink to normal size or disappear completely in spite of adequate treatment. Functional or metabolic imaging with FDG-PET complements structural imaging and helps overcome some of these major shortcomings. As discussed in the previous article in this series,  FDG accumulates at a higher rate in cancer cells and remains metabolically trapped in these cells. This phenomenon is the underlying basis for FDG-PET imaging in oncology. FDG-PET has been shown to have a high sensitivity and negative predictive value for the detection of malignancy. Hence in several neoplasms (with notable exceptions), FDG-PET imaging plays a critical role in initial diagnosis, staging, assessing response to therapy, restaging and assessing recurrence. The common neoplasms that have been approved by Centers for Medicare and Medicaid Services (CMS) in the US to be evaluated by FDG-PET include lymphoma, melanoma, head and neck cancer, lung cancer (except small cell lung cancer), breast cancer, esophageal cancer, colorectal cancer, cervical cancer and thyroid cancer (recurrence). However, FDG-PET has also been shown to be useful in several other neoplasms, such as gastric cancer, uterine and ovarian cancers, testicular cancer, soft tissue sarcomas and others. It is also known that a few cancers like prostate cancer and hepatocellular carcinoma do not show increased FDG uptake in a significant portion of patients; and other neoplasms, including pancreatic cancer, are affected by the low specificity of FDG uptake. Renal cancers are difficult to assess on FDG-PET imaging due to physiologic renal excretion of FDG. In May 2006, a National Oncologic PET Registry (NOPR) was established in collaboration with the American College of Radiology Imaging Network (ACRIN), the American College of Radiology (ACR) and the Academy of Molecular Imaging (AMI), in response to the proposal by Centers for Medicare and Medicaid Services (CMS) to expand coverage of FDG-PET studies to indications not currently eligible for Medicare reimbursement. The NOPR received inputs from and is endorsed by, the ACR, the American Society of Clinical Oncology (ASCO) and the Society of Nuclear Medicine (SNM) and will provide important data regarding the utility of FDG-PET in several neoplasms not routinely evaluated with FDG-PET imaging.
Head and neck cancer
Malignancies involving the head and neck region have generally been declining in incidence, but about 68,000 new cases are still estimated to occur in the US in 2007.  These are usually associated with alcohol and tobacco use; and other factors like poor nutrition and oral hygiene, immunity disorders, (human papilloma virus) HPV infections and occupational exposure. Head and neck cancers include malignancies of the lip and oral cavity; nasopharynx oropharynx and hypopharynx; larynx; ear, paranasal sinuses and salivary glands. Thyroid neoplasms will be discussed separately in the next section in view of their completely different behavior and consequent therapeutic implications, as compared to the rest of the cancers in the head and neck. In addition, lymphoma and other malignancies like melanoma may also involve the head and neck region, but will be discussed in their respective sections.
The majority of head and neck cancers tend to be squamous cell carcinomas (HNSCC) that show intense FDG uptake.  FDG-PET imaging plays an important role in diagnosis (especially in the setting of metastasis from an unknown primary site), staging, restaging (crucial for assessing residual/ recurrent disease) and monitoring response to therapy. The advent of combined PET/CT imaging has further strengthened the role of this imaging modality in the overall workup of head and neck cancers because of the intricate anatomy in this region.
The diagnosis of head and neck cancer is usually established on the basis of directed biopsies during an endoscopic evaluation (laryngoscopy, nasopharyngoscopy or panendoscopy). Head and neck cancers are staged as per the Tumor, Node and Metastasis (TNM) staging criteria. Along with clinical evaluation with direct visualization, contrast-enhanced CT and MRI are extremely useful for optimal assessment of the 'T' stage as they provide further structural information as regards tumor extension and involvement of adjacent structures. FDG-PET imaging lacks the spatial resolution for providing such exquisite structural details. Moreover, small lesions with low tumor volumes, superficial lesions (<4 mm deep) and very low grade tumors (including carcinoma in situ ) are not readily visualized on FDG-PET imaging.  However, FDG-PET plays an important role in the detection of locoregional metastatic lymphadenopathy and distant metastatic disease.
Only about 10-15% of head and neck cancers have distant metastases at the time of initial presentation and hence therapy is mainly determined by 'T' and 'N' status in a majority of patients. Traditional anatomical evaluation of nodal involvement in the head and neck region is suboptimal, since nodes may be enlarged as a result of infection/ inflammation (this is not uncommon in the head and neck region) and normal-sized nodes may frequently be involved with metastatic disease, leading to inaccurate upstaging or downstaging of the disease with conventional imaging methods. FDG-PET (and especially PET/ CT) imaging has had a tremendous impact in improving the nodal staging of head and neck cancers. Numerous studies have documented the high sensitivity (87%), specificity (94-95%) and accuracy of FDG-PET imaging in assessing nodal involvement in head and neck cancers. ,,,, FDG-PET imaging frequently detects metastatic disease in normal-sized lymph nodes [Figure 1 ]. However, caution is recommended in N0 disease per PET as micrometastases cannot be detected by FDG-PET imaging and hence the management of such patients should not solely be determined by FDG-PET findings  and other techniques like sentinel node mapping or surgical neck dissection should be employed for optimal 'N' staging in such patients. Also, sometimes malignant cervical nodes with large extensive central necrosis can be falsely negative on FDG-PET, with only mild FDG uptake at the periphery or no uptake at all [Figure - 2].
In addition to improved nodal staging, the most important added value of FDG-PET imaging is in the detection of unsuspected distant metastases [Figure - 3] that can lead to dramatic changes in patient management. As seen in [Figure - 4], unsuspected mediastinal nodal metastases (subsequently proven by mediastinoscopy and biopsy) detected on FDG-PET imaging in this patient with head and neck cancer altered the management options significantly and prevented futile attempts at curative treatment. Incorporation of FDG-PET imaging in the initial staging changes management in about 10% of patients suspected to have advanced HNSCC. 
Due to its high sensitivity and the ability to perform whole-body scanning, FDG-PET is used in the evaluation of patients presenting with malignant cervical lymphadenopathy without evidence of a primary neoplastic lesion on conventional investigations, including CT scan / MRI and panendoscopy with directed biopsies. In such cases, FDG-PET and PET/CT can help identify the primary malignant lesion [Figure - 5] in about 25% of cases. , At our center, a retrospective chart review revealed that using FDG-PET, we were able to identify the primary tumor in 61% of patients (14 of 23 cases) who presented with this scenario  with a very high negative predictive value (89%). Our higher rate of detection of the occult primary lesion may be attributable to several factors, including rigorous scan protocol (valium pre-treatment oral and intravenous hydration, 90-min delayed imaging), experienced readers, interpretations tuned to increase sensitivity (but not specificity) in this situation [Figure - 5] and a relatively small number of patients in this study. Since head and neck cancer patients are also prone to have synchronous neoplasms either in the head and neck region or elsewhere in the body, as well as subsequent development of second primaries (most frequently in the lung), FDG-PET imaging plays an important role in diagnosing these unexpected lesions  [Figure - 6].
FDG-PET imaging is useful in therapy planning for patients undergoing radiation therapy with a curative or palliative intent or as neoadjuvant therapy. The increasing implementation of intensity-modulated radiation therapy (IMRT) is well complemented by the additional functional/ metabolic information provided by the FDG imaging as it allows the delivery of maximal radiation dose to the most metabolically active areas of the tumor and more complete inclusion of loco-regional disease with sparing of the uninvolved areas. FDG-PET is very helpful in evaluating the cervical nodal chains in patients with advanced-stage head and neck cancer, since the presence of contralateral cervical lymphadenopathy will necessitate the inclusion of both sides of the neck in the radiation therapy field.
In addition to the above, FDG-PET imaging is very useful in assessing response to therapy and in restaging of head and neck cancers. , Following surgery or radiation therapy, it is extremely difficult to assess the neck with conventional imaging modalities like CT scan/MRI due to inflammatory changes, fibrosis, edema and alteration of normal structures. Determining whether residual neoplasm is present in the postsurgical/ post-radiated tumor bed is a daunting task. Compared to conventional radiological examination, FDG-PET has a better diagnostic accuracy in the assessment of residual or recurrent malignant disease in the post-therapeutic neck, including avoidance of unnecessary planned surgery in patients with a negative PET study.  Indeed, at our center, we have on several occasions seen intense residual disease after therapy on a post-treatment PET scan with a negative biopsy, which has then progressed to a larger recurrent lesion a few months later [Figure - 7]. A negative tissue biopsy after a strongly positive post-treatment PET scan can be caused by a sampling error and warrants a closer follow-up rather than routine surveillance. A decrease in the intensity of uptake on a follow-up scan confirms a false-positive post-treatment PET scan, usually due to inflammatory changes. However, persistence of a focally intense lesion or increase in the intensity of uptake warrants invasive evaluation. The timing of post-treatment PET scan is very crucial, especially after radiation therapy. Although there are no specific recommendations, generally a 3-month interval after completing radiation therapy is felt to be adequate to assess response to therapy. However, if surgery is needed for therapy completion, it is preferable to perform the surgical intervention much sooner than 3 months after radiation since more delay makes surgical dissection difficult due to post-radiation fibrosis. Hence at our center, we image such patients about 6-8 weeks after completion of radiation therapy. The superior assessment of response to therapy with FDG-PET imaging has facilitated a more conservative approach in management. In patients undergoing combined chemo-radiation therapy with a complete response on the post-treatment FDG-PET scan, there is a trend towards a more watchful approach rather than proceeding with a completion neck dissection in spite of large nodes (>3 cm) at initial staging.
There are several limitations of FDG-PET imaging in the evaluation of head and neck cancer. Although it may detect tumors that may be missed by anatomic imaging (especially in the setting of an unknown primary), the suboptimal spatial resolution as compared to direct visualization with endoscopy and CT scan / MRI limits the evaluation of small and superficial lesions. Also, low-grade tumors may be missed on PET if there is significant intense physiologic FDG uptake in an adjacent structure. As described in the earlier article in this series,  a number of structures in the head and neck region show physiologic FDG uptake, which can sometimes be quite intense. However, physiologic FDG activity is usually symmetric and the added information from CT images in a dedicated PET/CT scan can further help to discern this uptake as benign/ physiologic. Asymmetric FDG uptake (especially in the tonsils) can cause problems with interpretation. In patients being evaluated for cancers other than in the head and neck region, asymmetric tonsillar activity [Figure - 8] is frequently caused by tonsillar inflammation or lymphoid hyperplasia (unless it is strikingly intense, in which case it suggests an undetected second primary malignancy in the tonsil). In order to avoid physiologic muscle and brown fat activity that could potentially affect the interpretation of the study in the head and neck region, it is necessary to place the patient in a comfortable position and room temperature. In addition, benzodiazepines (diazepam is most commonly being used), help prevent brown fat activity. Chewing gum on one side in the mouth can give rise to unilateral intense FDG uptake in the muscles of mastication. Benign uptake in inflammatory/ infectious lesions, Warthin's tumor of the parotids (which can be intensely FDG-avid), radiation-induced inflammation and osteoradionecrosis need to be kept in mind. There may be variable uptake in the vocal cords caused either by talking/ snoring during the FDG uptake interval or due to unilateral vocal cord impairment or iatrogenic causes like Teflon injection.
Approximately 33,500 new thyroid cancer cases are estimated in the US in 2007, with about 1,500 deaths.  Thyroid neoplasms are predominantly of follicular or para-follicular cell origin. Thyroid neoplasms of follicular cell origin include papillary carcinomas, which represent 80% of all thyroid neoplasms; follicular carcinomas (second most common); as well as the less common but more aggressive Hurthle cell (3-10%) and anaplastic carcinomas (1-2%). The para-follicular or neuroendocrine-derived calcitonin-producing C cells give rise to medullary thyroid carcinomas (MTCs), which represent 5-10% of thyroid neoplasms, a small portion of which may be associated with multiple endocrine neoplasm (MEN) syndromes. In addition, there are rare thyroid neoplasms such as primary thyroid lymphomas and sarcomas.
Generally, thyroid neoplasms are diagnosed after workup for a painless thyroid nodule/ mass. Most malignant thyroid nodules show increased FDG uptake.  Usually, well-differentiated thyroid neoplasms tend to have lower FDG avidity (but excellent radio-iodine avidity) and poorly differentiated thyroid malignancies like Hurthle cell [Figure - 9] and anaplastic carcinomas tend to show intense FDG uptake (but poor iodine accumulation). In fact, the highest published standard uptake value SUV on a PET scan (SUV max : 125.1, SUV avg : 66.2) in the literature has been in an anaplastic thyroid cancer.  Hurthle cell thyroid cancer has generally low avidity for radio-iodine and FDG accumulation is usually very intense, revealing disease not detected by other imaging methods in about 50% of cases.  False negative FDG-PET exams can be seen in patients with iodine-avid Hurthle cell cancers. However, there is no defined role for FDG-PET imaging in the initial diagnosis and staging of thyroid malignancies. More frequently, there is incidental detection of focally intense lesions in the thyroid gland on scans performed to evaluate other malignant conditions. Such focal intense thyroid 'incidentalomas' warrant further evaluation, since about 25-30% of these turn out to be thyroid carcinomas. , Sometimes, these 'incidentalomas' may be quite subtle [as in [Figure - 10]], but still warrant evaluation since they can be well-differentiated thyroid carcinomas (as was proven in this case).
Except for anaplastic carcinomas, which are very aggressive rapidly progressing tumors, follicular thyroid neoplasms are treated with thyroidectomy followed by radio-iodine therapy with I-131. Follow-up usually consists of physical examination, serum thyroglobulin (Sr. Tg) levels and I-131 or I-123 whole-body scans to detect recurrence. Whole-body iodine imaging may be negative in 10-15% of patients with elevated Tg levels and clinical suspicion for disease recurrence, which can be a result of small volume disease or tumor dedifferentiation.  In this scenario, FDG-PET imaging is believed to be useful in detecting recurrent disease in about 70-90% of cases, especially if the Sr. Tg levels are more than 10 µg/dl.  However, the effect of TSH levels on the ability of FDG-PET to detect disease recurrence is still not clearly defined. Recent research suggests that elevated TSH levels (more from exogenous stimulation with recombinant TSH than with endogenous TSH stimulation via thyroid hormone withdrawal) may improve lesion detectability on FDG-PET imaging. ,, Such intensely FDG-avid lesions [Figure - 11] suggest dedifferentiation of the tumor (possibly causing lack of iodine avidity) and may also indicate the need for additional surgical resection or radiation therapy. FDG imaging is an independent predictor of survival in patients with recurrent thyroid cancer and its prognosis is worse in patients with positive FDG scans. 
MTCs behave differently from follicular thyroid carcinomas. Instead of secreting thyroid hormones, they secrete calcitonin as well as carcinoembryonic antigen (CEA). Primary treatment is surgical resection in the form of thyroidectomy. Radio-iodine therapy or radio-iodine scanning for detection of recurrence is of no use in these patients. MTCs are followed by assessing serum calcitonin and CEA levels. In the setting of elevated serum calcitonin and/ or CEA levels, FDG-PET imaging is probably the most accurate modality to detect recurrent disease with a sensitivity and specificity of around 80% (sensitivity ranging from 40-95% in various studies). ,, A recent paper from Memorial Sloan Kettering Center in New York  reported that in patients with Sr. calcitonin levels <500 pg/ml, FDG-PET has limited sensitivity in detecting recurrence and achieves meaningful sensitivity only when the levels are more than 1000 pg/ml.
In the United States, lung cancer remains the leading cause of cancer mortality for both men and women.  Broadly, lung cancers are classified into two major groups: small cell and non-small cell. Non-small cell lung carcinoma (NSCLC) is the more common type (75-80%) and includes several histological subtypes like squamous, adenocarcinoma, large cell, carcinoid, etc. Small cell lung carcinoma (SCLC) is less frequent (20-25%) but is frequently metastatic at the time of diagnosis and has different staging, therapeutic and prognostic implications. There is increased FDG activity in most lung cancers, but bronchoalveolar carcinomas (BAC) and lung carcinoids are traditionally considered non-FDG-avid. However, BAC and atypical lung carcinoids have been known to show increased FDG uptake on occasion [Figure - 12].
A solitary pulmonary nodule (SPN) is a frequent indication for a PET scan. Although many incidentally detected SPNs tend to be benign, in a high-risk patient (e.g, history of smoking), they are more likely to be malignant. As many as 20-30% of lung neoplasms initially present as SPNs and about 10-30% of all malignant SPNs are metastases from extrathoracic neoplasms [Figure - 13]. In view of the improved spatial resolution of CT scans, many more and smaller SPNs are routinely being detected. It is often a challenge to differentiate benign from malignant lesions. Although structural characteristics such as configuration, size, enhancement and calcification provide significant information, the majority of SPNs remain indeterminate on conventional imaging. Tissue diagnosis by biopsy or aspiration (bronchoscopic or CT-guided) or wedge resection although invasive is frequently necessary to confirm the true nature of the lesion. However, in high-risk patients with coexisting morbidities like severe chronic obstructive pulmonary disease (COPD), FDG-PET imaging plays an important role in the workup of these lesions.
In general, any SPN with intense FDG uptake is considered to be of neoplastic etiology unless proved otherwise [Figure - 14]. Although prior literature suggests an SUV cutoff of 2.5 (lesions with SUV >2.5 are considered malignant), ,, this is an oversimplification. Visual comparison of FDG uptake intensity with the mediastinal blood pool or liver activity is felt to be an equally reliable indicator of a neoplastic etiology. Another important consideration in the evaluation of SPNs with FDG-PET imaging is their size. Generally, modern PET and PET/CT scanners have a spatial resolution of about 6-8 mm and lesions less than 6 mm may not be adequately assessed; the intensity/ SUV may not be very high in such sub-centimeter lesions. Conversely, if a tiny lesion, supposedly below the spatial resolution for PET imaging, shows increased FDG activity, it is quite suspicious for a malignant etiology (even though the intensity may be mild).
Several studies have shown FDG-PET to be highly accurate in differentiating benign from malignant pulmonary lesions, with a sensitivity of greater than 95% and a specificity of 75-80%.  The sensitivity is affected by the lesion size (lower sensitivity for smaller lesions), its location (lower sensitivity for lesions located near the thoraco-abdominal interface because of respiratory motion or for those close to a 'hot' myocardium) and sometimes patient's body habitus (lower sensitivity due to high noise in large/ heavy patients). The high negative predictive value of FDG-PET scan makes it a very useful modality, except in sub-centimeter nodules, for reasons described above. Pure BAC and very low grade or very well-differentiated adenocarcinomas may demonstrate low FDG activity as well. Therefore, follow-up with CT scans is recommended for suspicious lung lesions to ascertain their stability. The specificity varies depending on the population being studied and is lower in areas where sarcoidosis, fungal granulomas (like histoplasmosis or coccidioidomycosis) and tuberculosis are more prevalent [Figure - 15]. False positive lesions may also be seen with active infectious / inflammatory lesions like necrotizing granulomas [Figure - 16].
Certain PET imaging centers practice dual-time point imaging (at 1 and 1.5-2 h) to improve the specificity for malignant pulmonary lesions. ,, The hypothesis of dual-point imaging is based on studies that show increased FDG accumulation in malignant lesions 60 to 90 min after injection, whereas uptake in infectious /inflammatory lesions tends to decrease with time. Early studies showed that dual-time point imaging improves the accuracy of FDG-PET, but considerable overlap between malignant and infectious/ inflammatory lesions is still seen.
An important caveat relates to the incidental detection of a focal intense lesion in the lung on FDG-PET imaging without a corresponding CT correlate [Figure - 17]. Since the newer CT scanners are very sensitive for the detection of small (<5 mm) lung nodules, in the absence of a true CT lesion, this is usually an artifact and may be due to a faulty injection technique. Such artifacts are typically seen if blood is withdrawn into the injection syringe before injecting FDG (to ensure correct intravenous access). Sometimes, misregistration between the PET and CT images due to respiratory motion (especially at the lung bases / liver dome) may also suggest a lesion on FDG-PET imaging, though a review of the CT scan images will immediately resolve the issue.
FDG-PET imaging is an important component of the TNM staging workup of NSCLC. Anatomical imaging modalities such as CT scan or MRI are superior to FDG-PET and PET/CT (using no intravenous or oral contrast and a low-dose CT scan for attenuation correction and anatomic localization only) for evaluation of the 'T' stage. However, FDG-PET imaging is superior to CT imaging for 'N' and 'M' staging. FDG-PET has proven to be more accurate in assessing nodal involvement and it can accurately identify metastatic disease in normal-sized nodes on CT. It can also better differentiate lymph node metastases from reactive, but enlarged nodes as seen on CT. The sensitivity and specificity of FDG-PET imaging in N3 disease (contralateral mediastinal and ipsilateral or contralateral supraclavicular nodal involvement) is greater than 90% and its overall accuracy for assessing mediastinal nodal involvement is around 85%. However, caution is recommended in N0 disease per PET since micrometastases cannot be detected by FDG-PET imaging and invasive staging of intra-thoracic lymph nodes may yield positive nodal disease.  The specificity is again affected by infectious/ inflammatory conditions like sarcoidosis, histoplasmosis and tuberculosis. FDG-PET imaging is also superior to other imaging modalities for detecting distant metastatic disease outside the brain. An unexpected distant metastatic lesion may be seen in up to 12% of patients  [Figure - 18].
FDG-PET imaging can also detect functional impairment of other structures due to lung carcinoma. Bulky metastatic mediastinal adenopathy can frequently compress/ involve the recurrent laryngeal and phrenic nerves. Elevation of the ipsilateral hemi-diaphragm or lack of FDG activity in the ipsilateral vocal cord with physiologic or compensatory increased FDG activity in the contralateral vocal cord indicates ipsilateral phrenic nerve or recurrent laryngeal nerve impairment respectively [Figure - 19].
FDG-PET imaging is presently considered the most accurate noninvasive means of staging a biopsy-proven NSCLC (excluding brain metastases). In addition to its high accuracy, FDG-PET imaging can also help make the diagnostic and staging workup of NSCLC more efficient and cost-effective. FDG-PET imaging can help to guide diagnostic biopsies and improve the yield from tissue sampling. We frequently see lung masses with intense FDG uptake but with a bronchoscopic workup negative for malignancy. These lesions are subsequently proven to be malignant on additional biopsies in a majority of such cases. Even CT-guided biopsies of lung masses may be falsely negative if a necrotic area is targeted during biopsy. [Figure - 20] shows a large right lung mass that had a bronchoscopic workup, as well as two CT-guided biopsies that were all negative for malignancy. The PET scan clearly showed a large area of central necrosis to be responsible for the negative biopsies and a third CT-guided biopsy from the peripheral portion of the lesion that was intensely FDG avid, finally confirmed a diagnosis of NSCLC. Also, if a distant metastatic lesion is identified on an FDG-PET scan for a lung mass, a biopsy from that site alone can prove a stage IV lung neoplasm, sometimes obviating the need for biopsy of the primary lesion (especially when lung biopsy may be deemed risky, as in patients with severe COPD). In general, a biopsy of the site suggesting the highest stage of the disease as identified on FDG-PET imaging is recommended.
FDG avidity of the lung lesion also provides prognostic information. Since FDG uptake correlates with tumor growth rate, doubling time and proliferation, intensely FDG-avid lesions tend to be more aggressive with poorer prognosis. SUV is considered an independent prognostic factor and tumors with SUV >10 have a median survival of less than a year. 
In patients undergoing curative, palliative or neoadjuvant radiation therapy, FDG-PET also helps in radiation therapy planning. Incorporation of the PET data in the process of determining the radiation therapy ports allows more accurate tumor localization, leading to tighter contouring and smaller biological volume calculation and sparing of uninvolved lung parenchyma.  This may potentially translate into better-tolerated radiation therapy with less pulmonary side effects and also better control of the disease by avoiding treatment misses to involved areas, as well as allowing the maximum possible radiation dose to the smallest possible target volume. In addition, PET/CT with respiratory gating (also referred to as '4D PET/CT') may allow even better targeting of the tumor by taking into consideration respiratory motion of the lesion in the therapy planning protocol. 
FDG-PET imaging is also playing an increasing role in restaging lung cancer patients to assess response to therapy (especially after radiation therapy) and to detect recurrence. It is superior to CT scan for differentiating post-therapy changes (after surgery, chemotherapy and/ or radiation therapy) from residual or recurrent malignant disease [Figure - 21] and the additional information from the CT images imparts greater specificity to the interpretation of the PET findings. The timing of assessment after radiation therapy is crucial; and frequently, if performed earlier, there is high uptake in the radiation therapy port. This may persist for a considerable amount of time (3-6 months) and may be quite intense in the presence of frank radiation pneumonitis. Although the intensity of FDG activity is expected to subside in 6 months or so, it may remain elevated for even longer [Figure - 22] and generally stable findings are considered negative for residual or recurrent malignant disease. Increasing intensity, focal intense uptake or a new intense lesion in or around the radiation treatment area are suspicious for recurrence. At our center, we are currently evaluating the changes in FDG-PET findings over a prolonged period of time after localized radiosurgery using tomotherapy for lung cancer. An 80% decrease or more in SUV predicts a high likelihood of complete response irrespective of the subtype of NSCLC, type of neoadjuvant therapy and final absolute SUV of the lesion. 
SCLC also shows intense FDG uptake. However, FDG-PET imaging is currently not approved by CMS for the workup of SCLC because it is frequently metastatic at the time of diagnosis and the addition of FDG-PET imaging is not felt to have a clinical impact on patient management and outcome. SCLC is generally staged as limited- and extensive-stage disease; and potentially, a small number of limited-stage SCLC patients (with T1-T2, N0, M0 disease) may be curable with aggressive surgical resection followed by chemotherapy. The major consideration in staging SCLC is to determine the need to add radiation with chemotherapy since limited-stage patients are considered for combined chemoradiation therapy with curative intent. FDG-PET has a potential role in SCLC to confirm limited-stage disease or upstage these patients to extensive-stage disease. However, this is all still under investigation.
FDG-PET imaging is also useful in evaluating pleural malignancies like mesothelioma [Figure - 23], which tend to show intense FDG uptake. In equivocal cases, pleural effusions may also be suggestive of malignancy if they show even mild increased FDG activity. Focally intense abnormalities within the pleural effusion/abnormality may help guide biopsy. In the evaluation of lung and pleural malignancies with FDG-PET imaging, it is important to bear in mind that talc pleurodesis shows intense FDG uptake [Figure - 24] that is usually sustained for a prolonged period of time and can sometimes wax and wane over time. Obtaining a relevant clinical history in such cases is obviously of paramount importance for avoiding mistakes in interpretation.
Lymphoma is the fifth most common cancer in the US and is one of the few malignancies whose incidence is rising.  Lymphoma is a heterogeneous group of neoplasms involving the immunological system and has several classifications. Broadly, it is classified into two major types: Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL), both of which have several subtypes. CT scan is considered the predominant modality of choice for lymphoma workup, although it is likely to be replaced by FDG-PET/CT imaging in the near future. Traditionally, gallium (Ga-67) scintigraphy has been used for staging and restaging lymphoma. However, FDG-PET offers several advantages over Ga-67 imaging in the form of better dosimetry (lower radiation dose), quicker scans (1.5-2 h vs. 2-3 days or more), higher sensitivity (due to superior spatial resolution, lesser physiologic bowel uptake and better contrast resolution), better quantification potential (and hence better prognostic information) and superior assessment of response to therapy. ,,,,, FDG-PET imaging has an important role in all aspects of lymphoma workup: initial diagnosis, staging, grading, restaging (evaluation for recurrence or residual disease), assessing response to therapy and surveillance (especially for higher-stage disease initially). Lymphoma is perhaps the most frequent oncologic condition for which FDG-PET imaging is performed.
Tissue diagnosis is the norm in lymphoma workup. Although FDG-PET does not image lymphoma cells per se (or any other cancer cells, for that matter) but rather images the intracellular accumulation of FDG-6-phosphate (intracellular glucose, for all practical purposes), the pattern of FDG-avid lesions may suggest a diagnosis of lymphoma when the scan is being performed for some other reason [Figure - 25]. In addition, when a diagnosis of lymphoma is suspected, it may suggest another more accessible site for tissue diagnosis [Figure - 26]. It is important to note that almost all lymphoma types show increased FDG uptake, , including low-grade NHL (unlike Ga imaging). Though MALT lymphomas have been traditionally considered not FDG avid,  a significant number (about 60%) have now been reported to show increased uptake. ,
The American Joint Committee on Cancer (AJCC) has based the staging of lymphoma on the Ann Arbor classification that considers the number of nodal regions involved, the extent of involvement and extranodal involvement along with modifiers according to the presence or absence of 'B' symptoms. FDG-PET imaging is crucial for staging lymphomas [Figure - 27] and is considered either as good as or better than CT scanning. It is superior for extranodal disease detection, especially splenic involvement. ,, It is complementary to bone marrow biopsy for assessing bone marrow involvement. , Although it can miss low-grade, diffuse involvement and may have limited specificity for diffuse involvement versus hematopoietic stimulation from other reasons, it can detect focal bone marrow involvement that may be missed on bone marrow biopsy and can also help provide a better site for bone marrow biopsy. It generally upstages about 20% of patients (although a wide range is reported in the literature) and affects management in a significant number of patients. ,,, FDG-PET/CT is considered better than CT alone or FDG-P ET al one for staging lymphoma and has been shown to be cost-effective and accurate when the initial scans have guided further conventional imaging. 
The intensity of FDG activity generally correlates with the grade of lymphoma on histology and provides prognostic information that may impact management decisions.  Aggressive lymphomas usually show an SUV ≥13 in the most intense lesion and indolent lymphomas usually show an SUV of ≤6 in the most intense lesion; though there is significant overlap.  Not infrequently, there is incongruence between the histologic grade reported and the intensity of FDG activity and usually FDG-PET imaging correctly predicts the nature of the lesion (especially if the FDG-PET shows an intense lesion suggesting high-grade/ aggressive disease and the histology shows low-grade lymphoma). The patient depicted in [Figure - 26] had a diagnosis of low-grade lymphoma on histology, but the PET study clearly and correctly showed the aggressive nature of the disease based on the intensity as well as the widespread disease, also involving the left orbital cavity [Figure - 28]. Lesions of two different grades are known to coexist in the same patient, as well [Figure - 29].
Ga-67 scintigraphy and CT scan have been the mainstay for assessing response to therapy in lymphoma patients; and the Chesson classification, based mainly on size criteria for scanning, has been in vogue since 1999.  Based on their response to therapy, this system classifies patients into one of several groups: Complete Response (CR), Unconfirmed CR (CRu), Partial Response (PR), Stable Disease (SD) and Progressive Disease (PD). With the advent of FDG-PET, these criteria have been shown to be clearly suboptimal [Figure - 30] and were recently revised - with more reliance on FDG-PET findings.  The revisions have increased the number of CRs, eliminated the category of CRu and helped discern differences in progression-free survival (PFS) between CR and PR patients.
FDG-PET imaging can correctly assess response to therapy as early as 7 days after the first chemotherapy cycle. Recent oncology practice management guidelines recommend an FDG-PET scan after two cycles of chemotherapy (around 3 weeks after the last treatment or just before the next cycle) to assess response and to then proceed with further therapy based on the results of this scan , [Figure - 31]. It is important to be aware of the known pitfalls and lesions causing false positives while interpreting these studies (like increased uptake in the thymus due to rebound thymic hypertrophy or inflammatory uptake and increased uptake in the bone marrow due to cytokine stimulation). Assessing response after radiation therapy is more complex than monitoring chemotherapy. The timing of the post-treatment FDG-PET scan is of paramount importance for assessing accurate response and there is still no consensus as regards the optimal timing for FDG-PET imaging after radiation therapy.  Studies and observations from other neoplasms indicate that FDG-PET imaging may be positive due to radiation-induced inflammation and this may last for a significant amount of time (many months). At our center, we recommend an interval of at least 3 months after completing radiation therapy, before advising a repeat scan. In such cases, the pattern of uptake (within the radiation therapy port, geometric configuration), the pre-therapy scan and the clinical information help to improve specificity.
FDG-PET imaging cannot assess microscopic disease and remission (generally meaning less than 1 billion tumor cells) is not equal to tumor eradication or cure.  However, a negative FDG-PET scan at the end of therapy does indicate excellent prognosis with sustained progression-free survival. Conversely, persistent increased FDG uptake during or at the end of therapy indicates a high risk of relapse. , Hence the current trend is towards assessing response to therapy with FDG-PET imaging early during chemotherapy and then again at the end of therapy.
FDG-PET also has proven value in assessing disease recurrence and residual disease after therapy.  A mass may never shrink completely but may be completely inactive based on FDG-PET imaging. Also, a mass may remain considerably large, but only a portion of the mass may be active on FDG-PET. In such cases, FDG-PET findings have been proven to be more accurate than CT scan for predicting residual disease. It should be noted that large masses that were intensely FDG avid prior to therapy might retain faint activity for a long period of time, usually a result of post-therapy inflammatory changes. In addition, FDG-PET also detects disease recurrence earlier; and in patients presenting initially with higher-stage disease (stage III or IV), surveillance with FDG-PET imaging may be cost-effective for detecting recurrences. ,
Thus, FDG-PET imaging plays a crucial role in the workup and management of lymphoma. However, it does have certain limitations.  Smaller lesions (<7-8 mm) and certain types of lymphoma lesions (very low grade lymphoma, few MALT and mantle cell lymphomas) may be missed. Certain lesions may be masked (renal lesions due to physiologic excretion of FDG by kidneys, GI tract lesions due to intense GI tract uptake in a few patients, patients with intense brown fat uptake, altered biodistribution of FDG due to hyperinsulinemia or rigorous physical activity prior to the FDG-PET imaging). FDG-PET imaging generally has limited sensitivity for detecting metastatic brain lesions. However, usually cerebral lymphoma lesions are 'hot' [Figure - 32]; and in HIV patients with brain lesions, FDG-PET imaging of the brain has become the test of choice to differentiate between toxoplasmosis (not 'hot' on FDG-PET) and lymphoma. ,, Some other conditions may mimic lymphoma, sarcoidosis being a frequent culprit in our part of the US [Figure - 33]. Nodal uptake due to radiotracer administration infiltration artifact and intense focal GI tract lesions (like benign lymphoid hyperplasia, inflammatory or adenomatous polyps) may also cause problems with interpretation.
Melanoma is the most serious of skin cancers and is much more frequent in white-skinned patients. In 2007, an estimated 60,000 new cases are expected in the US, with about 8,000 deaths.  Diagnosis requires a biopsy and thorough histopathological examination to assess lesion thickness (Breslow's Index) and depth of invasion (Clark's levels), which are important for staging. Early-stage diseases (stages I and II as per AJCC) are potentially curable, with high 5-year survival rates, but the mortality rate is quite high for advanced disease (especially stage IV).
Melanoma is considered one of the most FDG-avid tumors.  Imaging with FDG-PET is considered more accurate than standard diagnostic clinical procedures, including clinical examination, radiography, CT scan, MRI, ultrasound and hepatic enzymes. , However, FDG-PET imaging has a very limited role in early-stage disease. The 'sentinel node' technique is an established modality with high sensitivity, for assessing regional lymph nodes in such cases; and FDG-PET imaging is not an alternative due to its limited sensitivity in detecting micrometastases and low-volume disease (<78 mm 3 ).  Moreover, the incidence of regional or distant metastatic disease in early-stage asymptomatic patients after adequate treatment of the primary lesion (wide local excision with sentinel node biopsy and nodal basin dissection if necessary) is low enough that routine evaluation with FDG-PET imaging in such patients is not justified. However, in patients with advanced disease, FDG-PET imaging may serve as an important study for overall assessment of the disease (excluding brain and small pulmonary lesions). Although in a patient with confirmed widespread metastatic melanoma, additional information about extent of disease by FDG-PET imaging may not have significant impact on patient management and outcome; it does help in certain cases. When patients are being considered for surgical resection of isolated distant metastatic lesions, FDG-PET imaging is used to accurately assess disease extent. Additional lesions identified on FDG-PET imaging make surgical resection unwarranted. FDG-PET may have a clinical impact on management in 53% of patients by either upstaging (more frequently) or downstaging patients.  Frequently, unexpected nodal or distant metastases and cutaneous/ subcutaneous lesions are detected on FDG-PET imaging. Sometimes, lesions felt to be definite visceral metastases on other conventional modalities (like CT or MRI) may be shown to be benign on PET, thus downstaging these patients and making them candidates for potentially curable treatments. However, caution is recommended with pulmonary and intracranial lesions due to reasons described in earlier sections.
FDG-PET has a more established role in assessing response to therapy (especially with the newer treatment options) [Figure - 34] and in detecting recurrent disease [Figure - 35].  Thus, FDG-PET may provide a cost-effective tool in managing high-risk patients of malignant melanoma for initial staging and management planning, assessing response, detecting recurrence and guiding additional workup. The recent mainstream use of combined PET/CT imaging may further improve the sensitivity and specificity of this imaging modality.
A key issue in scanning melanoma patients with FDG-PET is whether or not to perform a head-to-toes scan (so-called 'true' whole-body imaging). Although no prospective studies have evaluated the value of including the brain and lower extremities in all patients, our current policy is to include the brain and lower extremities only if they are or have been previously, involved (clinically or on other modalities). In the absence of present or past lesions on the lower extremities, we also include them in the imaging field if the patient has proven or suspected disease in the inguino-femoral nodes. Literature review suggests that in the absence of the above factors, the likelihood of finding lesions in the lower extremities is very low (less than 1%) to warrant routine inclusion of these areas in imaging protocols. 
| References|| |
|1.||Takalkar AM, El-Haddad G, Lilien DL. FDG-PET and PET/CT - Part I. Indian J Radiol Imaging 2007;17:169-80. |
|2.||Tillisch J, Brunken R, Marshall R, Schwaiger M, Mandelkern M, Phelps M, et al . Reversibility of cardiac wall-motion abnormalities predicted by positron tomography. N Engl J Med 1986;314:884-8. |
|3.||Warburg O, Wind F, Negelein E. The metabolism of tumors in body. J Gen Physiol 1927;8:519-30. |
|4.||American Cancer Society. Cancer Facts and Figures 2007. Available from: http://www.cancer.org/docroot/stt/co...figures_2007.asp. |
|5.||Bailet JW, Abemayor E, Jabour BA, Hawkins RA, Ho C, Ward PH. Positron emission tomography: A new, precise imaging modality for detection of primary head and neck tumors and assessment of cervical adenopathy. Laryngoscope 1992;102:281-8. |
|6.||Hannah A, Scott AM, Tochon-Danguy H, Chan JG, Akhurst T, Berlangieri S, et al . Evaluation of 18 F-fluorodeoxyglucose positron emission tomography and computed tomography with histopathologic correlation in the initial staging of head and neck cancer. Ann Surg 2002;236:208-17. |
|7.||Di Martino E, Nowak B, Hassan HA, Hausmann R, Adam G, Buell U, et al . Diagnosis and staging of head and neck cancer: A comparison of modern imaging modalities (positron emission tomography, computed tomography, color-coded duplex sonography) with panendoscopic and histopathologic findings. Arch Otolaryngol Head Neck Surg 2000;126:1457-61. |
|8.||Kau RJ, Alexiou C, Laubenbacher C, Werner M, Schwaiger M, Arnold W. Lymph node detection of head and neck squamous cell carcinomas by positron emission tomography with fluorodeoxyglucose F 18 in a routine clinical setting. Arch Otolaryngol Head Neck Surg 1999;125:1322-8. |
|9.||Adams S, Baum RP, Stuckensen T, Bitter K, Hor G. Prospective comparison of 18F-FDG-PET with conventional imaging modalities (CT, MRI, US) in lymph node staging of head and neck cancer. Eur J Nucl Med 1998;25:1255-60. |
|10.||Laubenbacher C, Saumweber D, Wagner-Manslau C, Kau RJ, Herz M, Avril N, et al . Comparison of fluorine-18-fluorodeoxyglucose PET, MRI and endoscopy for staging head and neck squamous-cell carcinomas. J Nucl Med 1995;36:1747-57. |
|11.||Schoder H, Carlson DL, Kraus DH, Stambuk HE, G φnen M, Erdi YE, et al . 18F-FDG-PET/CT for detecting nodal metastases in patients with oral cancer staged N0 by clinical examination and CT/MRI. J Nucl Med 2006;47:755-62. |
|12.||Schmid DT, Stoeckli SJ, Bandhauer F, Huguenin P, Schmid S, von Schulthess GK, et al . Impact of positron emission tomography on the initial staging and therapy in locoregional advanced squamous cell carcinoma of the head and neck. Laryngoscope 2003;113:888-91. |
|13.||Johansen J, Eigtved A, Buchwald C, Theilgaard SA, Hansen HS. Implication of 18F-fluoro-2-deoxy-D-glucose positron emission tomography on management of carcinoma of unknown primary in the head and neck: A Danish cohort study. Laryngoscope 2002;112:2009-14. |
|14.||Jungehulsing M, Scheidhauer K, Damm M, Pietrzyk U, Eckel H, Schicha H, et al . 2[F]-fluoro-2-deoxy-D-glucose positron emission tomography is a sensitive tool for the detection of occult primary cancer (carcinoma of unknown primary syndrome) with head and neck lymph node manifestation. Otolaryngol Head Neck Surg 2000;123:294-301. |
|15.||Goodier MA, Takalkar A, Lilien DL, Lian TS, Kupferman TA, Nathan CO. Utility of Panendoscopy for unknown primary and negative PET. Otolaryngol Head Neck Surg 2006;135:S66. |
|16.||Leon X, Quer M, Diez S, Orús C, López-Pousa A, Burguιs J. Second neoplasm in patients with head and neck cancer. Head Neck 1999;21:204-10. |
|17.||McCollum AD, Burrell SC, Haddad RI, Norris CM, Tishler RB, Case MA, et al . Positron emission tomography with 18F-fluorodeoxyglucose to predict pathologic response after induction chemotherapy and definitive chemoradiotherapy in head and neck cancer. Head Neck 2004;26:890-6. |
|18.||Minn H, Paul R, Ahonen A. Evaluation of treatment response to radiotherapy in head and neck cancer with fluorine-18 fluorodeoxyglucose. J Nucl Med 1988;29:1521-5. |
|19.||Ware RE, Matthews JP, Hicks RJ, Porceddu S, Hogg A, Rischin D, et al . Usefulness of fluorine-18 fluorodeoxyglucose positron emission tomography in patients with a residual structural abnormality after definitive treatment for squamous cell carcinoma of the head and neck. Head Neck 2004;26:1008-17. |
|20.||Kresnik E, Gallowitsch HJ, Mikosch P, Stettner H, Igerc I, Gomez I, et al . Fluorine-18-fluorodeoxyglucose positron emission tomography in the preoperative assessment of thyroid nodules in an endemic goiter area. Surgery 2003;133:294-9. |
|21.||Hickeson M, Zhuang H, Chacko TK, Alavi A. How high can the standardized uptake value be? Clin Nucl Med 2002;27:819. |
|22.||Lowe VJ, Mullan BP, Hay ID, McIver B, Kasperbauer JL. 18F-FDG-PET of patients with Hurthle cell carcinoma. J Nucl Med 2003;44:1402-6. |
|23.||Chud QD, Connor MS, Lilien DL, Johnson LW, Turnage RH, Li BD. Positron emission tomography (PET) positive thyroid incidentaloma: The risk of malignancy observed in a tertiary referral center. Am Surg 2006;72:272-5. |
|24.||Schoder H, Yeung HW. Positron emission imaging of head and neck cancer, including thyroid carcinoma. Semin Nucl Med 2004;34:180-97. |
|25.||Shammas A, Degirmenci B, Mountz JM, McCook BM, Branstetter B, Bencherif B, et al . 18F-FDG-PET/CT in patients with suspected recurrent or metastatic well-differentiated thyroid cancer. J Nucl Med 2007;48:221-6. |
|26.||Chin BB, Patel P, Cohade C, Ewertz M, Wahl R, Ladenson P. Recombinant human thyrotropin stimulation of fluoro-D-glucose positron emission tomography uptake in well-differentiated thyroid carcinoma. J Clin Endocrinol Metab 2004;89:91-5. |
|27.||van Tol KM, Jager PL, Piers DA, Pruim J, de Vries EG, Dullaart RP, et al . Better yield of fluorodeoxyglucose-positron emission tomography in patients with metastatic differentiated thyroid carcinoma during thyrotropin stimulation. Thyroid 2002;12:381-7. |
|28.||Grunwald F, Biersack HJ. FDG-PET in thyroid cancer:thyroxine or not? J Nucl Med 2000;41:1996-8. |
|29.||Haugen BR, Lin EC. Isotope imaging for metastaic thyroid cancer. Endocrinol Metab Clin North Am 2001;30:469-92. |
|30.||Ong SC, Schoder H, Patel SG, Tabangay-Lim IM, Doddamane I, G φnen M, et al . Diagnostic accuracy of 18F-FDG-PET in restaging patients with medullary thyroid carcinoma and elevated calcitonin levels. J Nucl Med 2007;48:501-7. |
|31.||de Groot JW, Links TP, Jager PL, Kahraman T, Plukker JT. Impact of 18F-fluoro-2-deoxy-D-glucose positron emission tomography (FDG-PET) in patients with biochemical evidence of recurrent or residual medullary thyroid cancer. Ann Surg Oncol 2004;11:786-94. |
|32.||Diehl M, Risse JH, Brandt-Mainz K, Dietlein M, Bohuslavizki KH, Matheja P, et al . Fluorine-18 fluorodeoxyglucose positron emission tomography in medullary thyroid cancer: Results of a multicentre study. Eur J Nucl Med 2001;28:1671-6. |
|33.||Goldsmith SJ, Kostakoglu L. Role of nuclear medicine in the evaluation of the solitary pulmonary nodule. Semin Ultrasound CT MR 2000;21:129-38. |
|34.||Lowe VJ, Fletcher JW, Gobar L, Lawson M, Kirchner P, Valk P, et al . Prospective investigation of positron emission tomography in lung nodules. J Clin Oncol 1998;16:1075-84. |
|35.||Lowe VJ, Hoffman JM, DeLong DM, Patz EF, Coleman RE. Semiquantitative and visual analysis of FDG-PET images in pulmonary abnormalities. J Nucl Med 1994;35:1771-6. |
|36.||Gould MK, Maclean CC, Kuschner WG, Rydzak CE, Owens DK. Accuracy of positron emission tomography for diagnosis of pulmonary nodules and mass lesions: A meta-analysis. JAMA 2001;285:914-24. |
|37.||Matthies A, Hickeson M, Cuchiara A, Alavi A. Dual time point 18F-FDG-PET for the evaluation of pulmonary nodules. J Nucl Med 2002;43:871-5. |
|38.||Zhuang H, Pourdehand M, Lambright ES, Yamamoto AJ, Lanuti M, Li P, et al . Dual time point 18F-FDG-PET imaging for differentiating malignant from inflammatory processes. J Nucl Med 2001;42:1412-7. |
|39.||Gupta N, Gill H, Graeber G, Bishop H, Hurst J, Stephens T. Dynamic positron emission tomography with F-18 fluorodeoxyglucose imaging in differentiation of benign from malignant lung/mediastinal lesions. Chest 1998;114:1105-11. |
|40.||Tournoy KG, Maddens S, Gosselin R, Van Maele G, van Meerbeeck JP, Kelles A. Integrated FDG-PET/CT does not make invasive staging of the intrathoracic lymph nodes in non-small cell lung cancer redundant: A prospective study. Thorax 2007;62:696-701. |
|41.||Hellwig D, Ukena D, Paulsen F, Bamberg M, Kirsch CM; Onko-PET der Deutschen Gesellschaft fur Nuklearmedizin. Meta-analysis of the efficacy of positron emission tomography with F-18-fluorodeoxyglucose in lung tumors: Basis for discussion of the German Consensus Conference on PET in Oncology 2000. Pneumologie 2001;55:367-77. |
|42.||Ahuja V, Coleman RE, Herndon J, Patz EF Jr. The prognostic significance of fluorodeoxyglucose positron emission tomography imaging for patients with nonsmall cell lung carcinoma. Cancer 1998;83:918-24. |
|43.||Ciernik IF, Dizendorf E, Baumert BG, Reiner B, Burger C, Davis JB, et al . Radiation treatment planning with an integrated positron emission and computer tomography (PET/CT): A feasibility study. Int J Radiat Oncol Biol Phys 2003;57:853-63. |
|44.||Caggiano AJ, Vialotti C, Brunetti J. 4D PET/CT - early observations on integration and impact in radiation therapy planning for lung cancer. Int J Radiat Oncol Biol Phys 2004;60:S290. |
|45.||Cerfolio RJ, Bryant AS, Winokur TS, Ohja B, Bartolucci AA. Repeat FDG-PET after neoadjuvant therapy is a predictor of pathologic response in patients with non-small cell lung cancer. Ann Thorac Surg 2004;78:1903-9. |
|46.||Kostakoglu L, Leonard JP, Kuji I, Coleman M, Vallabhajosula S, Goldsmith SJ. Comparison of fluorine-18 fluorodeoxyglucose positron emission tomography and Ga-67 scintigraphy in the evaluation of lymphoma. Cancer 2002;94:879-88. |
|47.||Wirth A, Seymour JF, Hicks RJ, Ware R, Fisher R, Prince M, et al . Fluorine-18 fluorodeoxyglucose positron emission tomography, galluim-67 scintigraphy and conventional staging for Hodgkin's disease and non-Hodgkin's lymphoma. Am J Med 2002;112:262-8. |
|48.||Shen YY, Kao A, Yen RF. Comparison of 18F-fluoro-2-deoxyglucose positron emission tomography and galluim-67 citrate scintigraphy for detecting malignant lymphoma. Oncol Rep 2002;9:321-5. |
|49.||Bar-Shalom R, Yefremov N, Haim N, Dann EJ, Epelbaum R, Keidar Z, et al . Camera-based FDG-PET and 67Ga SPECT in evaluation of lymphoma: Comparative study. Radiology 2003;227:353-60. |
|50.||Zijlstra JM, Heokstra OS, Raijmakers PG, Comans EF, van der Hoeven JJ, Teule GJ, et al . 18 FDG positron emission tomography versus 67Ga scintigraphy as prognostic test during chemotherapy for non-Hodgkin's Lymphoma. Br J Haematol 2003;123:454-62. |
|51.||Spaepen K, Stroobants S, Verhoef G, Mortelmans L. Positron emission tomography with [(18)F]FDG for therapy response monitoring in lymphoma patients. Eur J Nucl Med Mol Imaging 2003;30:S97-105. |
|52.||Elstrom R, Guan L, Baker G, Nakhoda K, Vergilio JA, Zhuang H, et al . Utility of FDG-PET scanning in lymphoma by WHO classification. Blood 2003;101:3875-6. |
|53.||Friedberg J, Chengazi V. PET scans in the staging of lymphoma: Current status. Oncologist 2003;8:438-47. |
|54.||Hoffman M, Kletter K, Diemling M, Becherer A, Pfeffel F, Petkov V, et al . positron emission tomography with fluorine-18-2-fluoro-2-deoxy-D-glucose (F18-FDG) does not visualize extranodal B-cell lymphoma of the mucosa-associated lymphoid tissue (MALT)- type. Ann Oncol 1999;10:1185-9. |
|55.||Reske SN, Kotzerke J. FDG-PET for clinical use. Results of the 3rd German Interdisciplinary Consensus Conference, "Onko-PET III", 21 July and 19 September 2000. Eur J Nucl Med 2001;28:1707-23. |
|56.||Hueltenschmidt B, Sautter-Bihl ML, Lang O, Maul FD, Fischer J, Mergenthaler HG, et al . Whole body positron emission tomography in the treatment of Hodgkin disease. Cancer 2001;91:302-10. |
|57.||Schiepers C, Filmont JE, Czernin J. PET for staging of Hodgkin's disease and non-Hodgkin's lymphoma. Eur J Nucl Med Mol Imaging 2003;30:S82-8. |
|58.||Fuster DA, Chiang SA, Andreadis C, Guan L, Zhuang H, Schuster S, et al . Can [18F]fluorodeoxyglucose positron emission tomography imaging complement biopsy results from the iliac crest for the detection of bone marrow involvement in patients with malignant lymphoma? Nucl Med Commun 2006;27:11-5. |
|59.||Schoder H, Meta J, Yap C, Ariannejad M, Rao J, Phelps ME, et al . Effect of whole-body F-FDG-PET imaging on clinical staging and management of patients with malignant lymphoma. J Nucl Med 2001;42:1139-43. |
|60.||Dizendorf EV, Baumert BG, von Schulthess GK, Lütolf UM, Steinert HC. Impact of whole-body 18F-FDG-PET on staging and managing patients for radiation therapy. J Nucl Med 2003;44:24-9. |
|61.||Naumann R, Beuthien-Baumann B, Reiss A, Schulze J, Hδnel A, Bredow J, et al . Substantial impact of FDG-PET imaging on the therapy decision in patients with early-stage Hodgkin's lymphoma. Br J Cancer 2004;90:620-5. |
|62.||Burton C, Ell P, Linch D. The role of PET imaging in lymphoma. Br J Haematol 2004;126:772-84. |
|63.||Rodriguez M, Rehn S, Ahlstrom H, Sundstr φm C, Glimelius B. Predicting malignancy grade with PET in non-Hodgkin's lymphoma. J Nucl Med 1995;36:1790-6. |
|64.||Filmont J, Ko Yang F, Yap C. Prediction of malignancy grade using 18FDG-PET in Non Hodgkin's lymphoma patients: An urban legend? J Nucl Med 2002;43:79. |
|65.||Sch φder H, Noy A, G φnen M, Weng L, Green D, Erdi YE, et al . Intensity of 18Fluorodeoxyglucose uptake in positron emission tomography distinguishes between indolent and aggressive non-Hodgkin's Lymphoma. J Clin Oncol 2005;23:4643-51. |
|66.||Cheson BD, Horning SJ, Coiffier B, Shipp MA, Fisher RI, Connors JM, et al . Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas: NCI Sponsored International Working Group. J Clin Oncol 1999;17:1244. |
|67.||Cheson BD, Pfistner B, Juweid ME, Gascoyne RD, Specht L, Horning SJ, et al . Revised response criteria for malignant lymphoma. J Clin Oncol 2007;25:579-86. |
|68.||Hutchings M, Loft A, Hansen M, Pedersen LM, Buhl T, Jurlander J, et al . FDG-PET after two cycles of chemotherapy predicts treatment failure and progression-free survival in Hodgkin lymphoma. Blood 2006;107:52-9. |
|69.||Spaepen K, Stroobants S, Verhoef G, Mortelmans L. Positron emission tomography with [F]FDG for therapy response monitoring in lymphoma patients. Eur J Nucl Med Mol Imaging 2003;30:S97-105. |
|70.||Toal DR. Tumor cell kinetics and cancer chemotherapy. Am J Nurs 1980;80:1802-4. |
|71.||Lavely WC, Delbeke D, Greer JP, Morgan DS, Byrne DW, Price RR, et al . FDG-PET in the follow-up management of patients with newly diagnosed Hodgkin and non-Hodgkin lymphoma after first-line chemotherapy. Int J Radiat Oncol Biol Phys 2003;57:307-15. |
|72.||Guay C, Lepine M, Verreault J, Bιnard F. Prognostic value of PET using 18F-FDG in Hodgkin's disease for posttreatment evaluation. J Nucl Med 2003;44:1225-31. |
|73.||Reske SN. PET and restaging of malignant lymphoma including residual masses and relapse. Eur J Nucl Med Mol Imaging 2003;30:S89-96. |
|74.||Jerusalem G, Beguin Y, Fassotte MF, Belhocine T, Hustinx R, Rigo P, et al . Early detection of relapse by whole-body positron emission tomography in the follow-up of patients with Hodgkin's disease. Ann Oncol 2003;14:123-30. |
|75.||Freudenberg LS, Antoch G, Schutt P, Beyer T, Jentzen W, Müller SP, et al . FDG-PET/CT in re-staging of patients with lymphoma. Eur J Nucl Med Mol Imaging 2004;31:325-9. |
|76.||Barrington SF, O'Doherty MJ. Limitations of PET for imaging lymphoma. Eur J Nucl Med Mol Imaging 2003;30:S117-27. |
|77.||Hoffman JM, Waskin HA, Schifter T, Hanson MW, Gray L, Rosenfeld S, et al . FDG-PET in differentiating lymphoma from nonmalignant central nervous system lesions in patients with AIDS. J Nucl Med 1993;34:567-75. |
|78.||Pierce MA, Johnson MD, Maciunas RJ, Murray MJ, Allen GS, Harbison MA, et al . Evaluating contrast-enhancing brain lesions in patients with AIDS by using positron emission tomography. Ann Intern Med 1995;123:594-8. |
|79.||Villringer K, Jager H, Dichgans M, Ziegler S, Poppinger J, Herz M, et al . Differential diagnosis of CNS lesions in AIDS patients by FDG-PET. J Comput Assist Tomogr 1995;19:532-6. |
|80.||Wahl RL, Hutchins GD, Buchsbaum DJ, Liebert M, Grossman HB, Fisher S. 18F-2-deoxy-2 fluoro-D-glucose uptake into human xenografts. Cancer 1991;67:1544-50. |
|81.||Fuster D, Chiang S, Johnson G, Schuchter LM, Zhuang H, Alavi A. Is 18F-FDG-PET more accurate than standard diagnostic procedures in the detection of suspected recurrent melanoma. J Nucl Med 2004;45:1323-7. |
|82.||Rinne D, Baum RP, Hor G, Kaufmann R. Primary staging and follow-up of high risk melanoma patients with whole body 18F-fluorodeoxyglucose positron emission tomography: Results of a prospective study of 100 patients. Cancer 1998;82:1664-71. |
|83.||Wagner JD, Schauwecker DS, Davidson D, Wenck S, Jung SH, Hutchins G. FDG-PET sensitivity for melanoma lymph node metastases is dependent on tumor volume. J Surg Oncol 2001;77:237-42. |
|84.||Wong C, Silverman DS, Seltzer M, Schiepers C, Ariannejad M, Gambhir SS, et al . The impact of 2-deoxy-2[18F] fluoro-D-glucose whole body positron emission tomography for managing patients with melanoma: The referring physician's perspective. Mol Imaging Biol 2002;4:185-90. |
|85.||Friedman KP, Wahl RL. Clinical use of positron emission tomography in the management of cutaneous melanoma. Semin Nucl Med 2004;34:242-53. |
|86.||Loffler M, Weckesser M, Franzius CH, Nashan D, Schober O. Malignant melanoma and (18)F-FDG-PET: Should the whole body scan include the legs? Nuclearmedizin 2003;42:167-72 |
Amol M Takalkar
PET Imaging Center, Biomedical Research Foundation of Northwest Louisiana, 1505 Kings Highway, Shreveport, LA 71103
Source of Support: None, Conflict of Interest: None
[Figure - 1], [Figure - 2], [Figure - 3], [Figure - 4], [Figure - 5], [Figure - 6], [Figure - 7], [Figure - 8], [Figure - 9], [Figure - 10], [Figure - 11], [Figure - 12], [Figure - 13], [Figure - 14], [Figure - 15], [Figure - 16], [Figure - 17], [Figure - 18], [Figure - 19], [Figure - 20], [Figure - 21], [Figure - 22], [Figure - 23], [Figure - 24], [Figure - 25], [Figure - 26], [Figure - 27], [Figure - 28], [Figure - 29], [Figure - 30], [Figure - 31], [Figure - 32], [Figure - 33], [Figure - 34], [Figure - 35]
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| ||Shih-chen Wang |
| ||Chinese Medical Sciences Journal. 2009; 24(1): 3 |
|[Pubmed] | [DOI]|
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