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Year : 2016  |  Volume : 26  |  Issue : 1  |  Page : 81-91
Radiofrequency ablation in primary non-small cell lung cancer: What a radiologist needs to know

1 Department of Interventional Radiology, Jackson Memorial Hospital, University of Miami Hospital, Miami, Florida, USA
2 Department of Surgery, Jackson Memorial Hospital, University of Miami Hospital, Miami, Florida, USA
3 Department of Hematology and Oncology, Veterans Affairs Medical Center, Miami, Florida, USA

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Date of Web Publication9-Mar-2016


Lung cancer continues to be one of the leading causes of death worldwide. In advanced cases of lung cancer, a multimodality approach is often applied, however with poor local control rates. In early non-small cell lung cancer (NSCLC), surgery is the standard of care. Only 15-30% of patients are eligible for surgical resection. Improvements in imaging and treatment delivery systems have provided new tools to better target these tumors. Stereotactic body radiation therapy (SBRT) has evolved as the next best option. The role of radiofrequency ablation (RFA) is also growing. Currently, it is a third-line option in stage 1 NSCLC, when SBRT cannot be performed. More recent studies have demonstrated usefulness in recurrent tumors and some authors have also suggested combination of RFA with other modalities in larger tumors. Following the National Lung Screening Trial (NLST), screening by low-dose computed tomography (CT) has demonstrated high rates of early-stage lung cancer detection in high-risk populations. Hence, even considering the current role of RFA as a third-line option, in view of increasing numbers of occurrences detected, the number of potential RFA candidates may see a steep uptrend. In view of all this, it is imperative that interventional radiologists be familiar with the techniques of lung ablation. The aim of this article is to discuss the procedural technique of RFA in the lung and review the current evidence regarding RFA for NSCLC.

Keywords: Non-small cell lung cancer; radiofrequency ablation; stereotactic body radiation therapy

How to cite this article:
Bhatia S, Pereira K, Mohan P, Narayanan G, Wangpaichitr M, Savaraj N. Radiofrequency ablation in primary non-small cell lung cancer: What a radiologist needs to know. Indian J Radiol Imaging 2016;26:81-91

How to cite this URL:
Bhatia S, Pereira K, Mohan P, Narayanan G, Wangpaichitr M, Savaraj N. Radiofrequency ablation in primary non-small cell lung cancer: What a radiologist needs to know. Indian J Radiol Imaging [serial online] 2016 [cited 2020 Jul 7];26:81-91. Available from:

   Introduction Top

Overview of lung cancer


Lung cancer is the leading cause of cancer deaths worldwide in men and the second most common cancer in women. In the United States, lung cancer occurs in approximately 225,000 patients and causes over 160,000 deaths annually. [1] Worldwide, lung cancer occurred in approximately 1.8 million patients in 2012 and caused an estimated 1.6 million deaths.

Classification and treatment guidelines based on tumor node metastasis

Lung cancer is classified into two major categories: Small cell carcinoma (SLC) and non-small cell carcinoma (NSCLC). [1],[2] Knowledge of the current (seventh) edition of the Tumor Node Metastasis (TNM) staging system is crucial for treatment planning and prognostic purposes in patients with NSCLC. [3] In patients with stage I and II NSCLC and a favorable risk, surgical resection with lobectomy is recommended. However, only 15-30% of patients presenting with localized lung cancer are eligible for surgical resection due to various factors such as advanced age, co-morbidities, and poor cardiopulmonary reserve, [4],[5] necessitating the development of alternative treatments. Although standard fractionation radiation therapy is a useful tool, [4],[6],[7] for patients with a poor pulmonary reserve, stereotactic body radiation therapy (SBRT) is needed. Radiofrequency ablation (RFA) may be considered for peripheral tumors of less than 3 cm in inoperable patients. [8] In more advanced stage III and IV NSCLC, a multimodality therapy, which includes combined chemo-radiotherapy with after-look surgery is suggested. [9]

Role of RFA in lung tumors

RFA and its clinical use

RFA has been widely utilized in the management of tumors in many other solid organs - primarily the liver - for over two decades, with a high safety and efficacy profile. [10] RFA is a thermal ablative modality that causes tissue death by coagulative necrosis. [11] RFA has been shown to be safe and reasonably efficacious in the management of primary and secondary lung neoplasms. [6],[7],[12],[13],[14],[15],[16] Presently, the primary indication for lung RFA in NSCLC is stage Ia tumors less than 3 cm. [17],[18]

Rationale for use of RFA in lung tumors

Local efficacy of RFA in destroying lung tumors has been demonstrated in animal lung VX2 tumor models that show the feasibility of complete ablation. [18] More recently, a single session of percutaneous RFA in nine patients was performed before surgical resection of lung metastases. There was histologic proof of complete tumor destruction. [19] The lungs provide a unique environment for RFA under computed tomographic (CT) guidance. First, there is an excellent contrast ratio between the tissue of the targeted tumor, the aerated lung, and the metal of the needle. Second, a given quantity of RF current produces a larger volume of ablation in the lung than in other solid organs like the liver or kidney. This is because the energy deposition is greater in the lung tissue due to heat insulation and low electric conductivity. [20]

   The Lung RFA Procedure: A Practical Approach Top

Pre-procedure evaluation

Patient selection

Pre-procedure workup includes cross-sectional imaging within 4 weeks of the planned ablative therapy. Various parameters are evaluated including the size and location of the tumor (i.e., central vs. peripheral, close to vessels). [11] At present, there are no set lower parameter limits like forced expiratory volume in 1 s (FEV1) to determine candidacy for the ablation procedure. The presence of pulmonary fibrosis serves as a relative contraindication. [21],[22]

The procedure

Anesthesia versus sedation

Most thermal ablations are performed under general anesthesia. Even in the lung, authors have reported lower feasibility rates and higher peri-procedural pain after conscious sedation compared with general anesthesia. [23],[24] The feasibility of the technique under general anesthesia is reported to be as high as 97%. [13] However, most of the patients who present for RFA have medical co-morbidities, which presents a high anesthesiology risk. Hoffmann et al. reported similar results in terms of feasibility, complication rate, hospitalization, and local tumor control after general anesthesia or conscious sedation, and concluded that conscious sedation should be preferred, reserving general anesthesia for non-compliant patients. [25]

Imaging guidance

CT is the only accurate image guidance modality for lung RFA. Accurate planning of the needle track is a key factor for technical success. The path should be the shortest possible, and should avoid interlobar fissures and vital structures.

Multiplanar reconstruction and real-time CT with foot-pedal control results in faster and more accurate needle placement. [17] The choice of electrode length, active tip length, and the target ablation zone is determined by the size and location of the tumor.


Parameters of temperature and impedance should be adjusted according to manufacturer specifications for the RF device used. Treatments generally range between 5 and 12 min in any given position. Multiple overlapping ablations are performed in larger tumors to ensure adequate coverage and optimal margins. [21],[26] RF protocols have to be adapted to the tumor location, which can cause variation in impedance. [17]

Post-procedure follow-up


Post-ablation follow-up regimens vary. Most authors suggest performing an immediate post-ablation chest CT, mainly to check for complications and to assess the adequacy of the ablation zone. A new baseline post-contrast CT is performed at 1 month with the next routine follow-up at 4 months. [27] Abtin et al. suggest performing bedside chest radiography at 1 and 3 h. Initial CT is performed, usually at 1-2 months after RFA, and is followed by positron emission tomography PET/CT at 3 months, which thereafter is alternated with CT every 6 months for 2 years. [28]

Immediate post-procedure imaging

After the probe removal, a CT is required to exclude immediate complications, such as pneumothorax (PTX), and to estimate the area of ablation. An area of ground-glass opacity around the tumor margins is expected. [29] Most pneumothoraces are small and asymptomatic. For larger ones, a pleural catheter attached to wall suction can be used to treat the air leak. Again, chest radiographs are obtained to ensure resolution of the air leak prior to discharge.

Tumor response

CT and PET/CT have been used to follow-up ablated tumors.

Normal "expected" findings

An immediate post-treatment CT showing a halo of ground-glass opacification (GGO) encompassing the lesion with a satisfactory margin is a good indicator of successful treatment. [24],[29],[30],[31],[32] At 3 months, the ablated lesion is usually slightly larger than baseline owing to residual edema, but by 6 months, the ablation zone usually starts to decrease in size. [33] Early, uniform, non-nodular arterial enhancement is common early after ablation, reflecting reactive hyperemia in the tissues at the margin of the treatment zone and may persist for up to 6 months [Figure 1]. [32]
Figure 1 (A-E): A 55-year-old male with NSCLC. (A) CT scan (Siemens Healthcare, Knoxville, Tennessee, USA) of the chest shows a nodule measuring 1.4 × 1.4 cm in the left lower lobe (black arrow) (B) CT-guided RFA performed (Boston Scientific, Natick, MA, USA). A small area of GGO is seen developing around the nodule (C) CT 1 month later shows increase in size of the nodule as compared to pre-RFA, measuring 2.1 × 2.1 cm and showing central cavitation (D) CT 3 months later shows reduction in size of nodule to 1.5 × 1.3 cm (black arrow) (E) CT at 6 months shows further reduction in size (black arrow). Meanwhile, another nodule had developed (red arrow)

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PET/CT may detect recurrence earlier than does conventional CT, but there is limited evidence to support this. [34],[35] In a study of 68 patients, standardized uptake value (SUV) <8 was found to be a predictor of improved disease-free survival [Figure 2]. [36]
Figure 2 (A-E): A 56-year-old male with NSCLC. (A) Pre-RFA PET-CT scan (Siemens Healthcare, Knoxville, Tennessee, USA) shows a lung nodule measuring 1.4 × 1.4 cm in the right lower lobe, SUV 4.9 (white arrow) (B) CT-guided RFA performed using an RF ablation system (Boston Scientific, Natick, MA, USA) (C) A large area of GGO is seen around the nodule immediately after ablation (D) PET-CT performed the next day shows GGO around the nodule. However, there is resolution to background of the fluorodeoxyglucose (FDG) activity (white arrow) (E) CT follow-up at 3 months shows residual GGO, but no obvious increase in the solid aspect of the nodule

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Signs of relapse/recurrence

CT and PET imaging features suggestive of residual or recurrent disease include: [28]

  • Change of CT morphology from ground-glass opacity to solid opacity
  • Growth of the RFA zone after 3 months (when compared to baseline) and definitely after 6 months, especially peripheral nodular growth
  • Contrast enhancement in the ablation zone (nodular > 10 mm, central > 15 HU, and enhancement greater than the baseline)
  • Regional or distant lymph node enlargement and new intrathoracic or extrathoracic disease
  • Increased metabolic activity beyond 2 months, residual activity centrally or at the ablated tumor, and development of nodular activity [Figure 3].
Figure 3 (A-E): A 65-year-old male with NSCLC. Pre-RFA PET-CT (A) and CT (B) Scans show a cavitatory lung nodule 1.6 × 1.5 cm in the right lower lobe, SUV 6.2 (C) CT-guided RFA performed (D) Large area of GGO is seen around the nodule (E) CT at 6 weeks shows a large solid nodular area now measuring 2.9 × 2.6 cm. PET-CT MIP images (F) and axial images (G) at 3 months show FDG uptake in the nodule, SUV 7.7 (red arrow in F) compared to prior SUV 6.2 and measuring 2.9 × 2.6 cm, with photopenia/necrosis in the posterior half of the lesion

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Tumor response after RFA is summarized in [Table 1].
Table 1: Tumor response after RFA

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Amended RECIST criteria have also been proposed, taking into account not only the lesion size, but also tumor geometry and contrast enhancement. In a large multicenter trial, complete response was defined as a decrease in the longest diameter of at least 30% compared with the diameter measured at the 1-month CT examination, with no evidence of peripheral tumor growth or contrast enhancement. [37]

Literature review of studies on RFA of NSCLC

A review of the English literature was conducted by searching the PubMed database using the keywords "non-small cell lung cancer" and "radiofrequency ablation." We restricted this review solely to the use of RFA for NCSLC in humans and with the number of patients >30. There were some reports of RFA in both NCSLC and metastasis. In some of these, we separated out the data only for NSCLC patients for local efficacy and survival. With regard to complications, the use of RFA in NCSLC as well as metastasis was studied, since in our opinion, the procedural details for both are similar. The search resulted in 10 relevant studies - 3 prospective and 7 retrospective. All relevant articles were subsequently evaluated.

Local efficacy

Review of recent literature of lung RFA for both primary and secondary lung tumors showed a median complete ablation rate of 90% (range 38-97%). [38] In their review of 14 studies limited to NCSLC that was conducted in 2014, Hiraki et al. reported a rate of about 31-42%. [39] In the 10 series reviewed, we too found the same number (13-41%). [Table 2] summarizes a review of 10 series of RFA ablation of lung tumors.
Table 2: Review of 10 series of RFA ablation of lung tumors

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Three factors have been described that appear to be predictive of complete ablation:

  • Size of the tumor: Tumor size is the single most important factor associated with local recurrence. According to several reports with prolonged imaging follow-up, tumors less than 2 cm in size can be successfully ablated in 78-96% of cases. A statistically significant lower success rate of ablation is reported for tumors greater than 2-3 cm [12],[40],[41],[42],[43],[44]
  • Ablation margins: Unlike most classical hepatocellular carcinomas, lung tumors are not usually encapsulated; hence, it is necessary to obtain an adequate ablative margin. [45],[46] Beland et al. [47] suggest an ablation zone "that includes the primary tumor plus at least an additional 8-10 mm of ablation beyond the visible tumor margin in all directions" as ideal. Newer studies have shown that RFA with overlapping ablations may prove useful [44] and is not followed by many complications [40],[48]
  • Location of the tumor: Proximity of the target lesion to major vasculature has been shown to increase the risk of incomplete ablation due to the "heat sink phenomenon," explained by the fact that flowing blood carries heat away from adjacent tissues, thereby cooling and protecting these tissues from lethal thermal injury. The presence of an adjacent large vessel within 3 mm of the lesion has been reported by several authors as a negative predictor for complete tumor ablation. [49],[50],[51] Percutaneous balloon occlusion of the involved pulmonary artery branch during lung RFA has been reported in animal studies to improve the shape and volume of ablation. [52]

Overall and cancer-specific survival

Survival data for RFA of NSCLC are scarce due to the relative recent application of this ablative modality in lungs with the first report published in 2000. [7]

The RAPTURE trial (a prospective multicenter trial) reported overall survival (OS) of 70% and 48% at 1 and 2 years, respectively, and cancer-specific survival (CS) of 92% and 73% at 1 and 2 years, respectively. [37] Co-morbidities explained the gap between OS and CS.

In their review of 14 studies limited to NCSLC that was conducted in 2014, Hiraki et al. reported the 1-, 2-, 3-, and 5-year OS rates after RFA of stage I NSCLC to be 78-100%, 53-86%, 36-88%, and 25-61%, respectively. The median survival time ranged from 29 to 67 months. The 1-, 2-, and 3-year CS rates after RFA of stage I NSCLC were 89-100%, 92-93%, and 59-88%, respectively. [39]

In our review of 10 studies, the 1-, 3-, and 5-year OS rates were 70-100%, 36-77%, and 19-61%, respectively. The 1-, 3-, and 5-year CS rates were 78-100%, 33-73%, and 40-74%, respectively. Median OS was between 29 and 67 months. [16],[37],[43],[53],[54],[55],[56],[57],[58]

There appear to be two factors that predict OS, which are as follows:

  • Size of tumor: Size as a prognostic factor of survival was explained by Kodama et al. In their study, they found 1-, 3-, and 5-year OS rates of 100%, 79.8%, and 60.5%, respectively, in patients with tumors measuring <3.0 cm, compared with 1-year and 3-year OS rates of 83.3% and 31.3%, respectively, in patients with tumors measuring 3.1-4.0 cm. [59] Again Palussiere et al. reported better survival in tumors ≤3 cm, with a survival rate close to 50% at 5 years in 135 patients. However, results were in the same range with the 1-, 3-, and 4-year OS rates [43]
  • Co-morbidities: Indeed, lung RFA for NSCLC is usually performed in non-surgical patients with severe co-morbidities. It is important to note that deaths reported in the literature are not typically related to cancer progression, but to co-morbidities. Both Simon et al. in 2012 [57] and Lencioni et al. [37] reported that co-morbidities explain the gap between OS and CS.

Simon et al. retrospectively reviewed 82 patients treated with RFA using the Charlson Co-morbidity Index (CCI) as the survival predictor. They explained that CCI appeared to be a strong predictor of OS in patients treated with RFA for NSCLC. A CCI score ≥5 (OS: 10.43 months; 95% CI: 7.61-19.85) was associated with significantly increased mortality compared to patients who had a CCI grade of 1-2 (OS: 55.5 months; 95% CI: 39.46-64.02) or 3-4 (OS: 36.62 months; 95% CI: 25.54-58.29). No statistically significant difference was observed between CCI grades 1-2 and 3-4. [40],[57],[60]

   Tolerance and Complications Top


Studies have shown no changes in post-ablation pulmonary function tests when evaluated prospectively at 1 and 12 months. There have been no reports of patients requiring long-term or permanent oxygen therapy as a result of RFA. [13],[37]


The largest assessment of serious complications comes from a retrospective single institution series of 420 patients with 1403 lung tumors who underwent 1000 RFA sessions. There were four deaths related to the RFA procedure (0.4%). The major complication rate was 9.8%, the most frequent of which were aseptic pleuritis, pneumonia, lung abscess, bleeding requiring transfusion, and PTX requiring pleural sclerosis. [61]

In a review of 14 series conducted in 2014, Hiraki et al. concluded that although mortality after RFA was quite rare, it occurred in isolated cases due to acute respiratory distress or pulmonary embolus. PTX was frequently associated with a maximum of 63% of the cases, 2-13% of which needed a chest tube. Other complications were less frequent. [39]

We reviewed our series of 10 studies for complications [Table 3]. There is no uniform standard for reporting complications. We labeled PTX and PTX requiring drainage as the major complications. Minor complications in our review included pleural effusions/hemothorax, parenchyma hemorrhage and hemoptysis, neuropathy, bronchopleural fistula, and needle track seeding. In our review, we found that the overall major and minor complication rates associated with lung RFA have been reported as: PTX 11-50%, PTX needing drainage 5-20%, and minor complications 4.2-20%.
Table 3: Review of complications in 10 series of RFA ablation of lung tumors

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The common complications and their management are subsequently discussed.

Peri-procedural complications

  • PTX (11-63%): Risk factors associated with PTX include: Male gender, multiple tumor ablations, tumors at the bases of the lungs, long intrapulmonary course of the electrode, pulmonary emphysema, advanced age, small tumors, and traversal of the major fissure by the electrode. [62],[63],[64],[65],[66],[67] In 2-29% of PTX cases, chest tube placement for drainage may be required. In 10% of cases, PTX can also present after a delay following RFA. Rarely, RFA is complicated by formation of a bronchopleural fistula that results in intractable PTX. The mechanism is thought to be RFA-induced necrosis of the lung tissue between the pleural space and the bronchus. This is managed by pleurodesis, endobronchial repair, or surgical repair [68]
  • Pleural effusion (6-19%): Pleural effusion is thought to result from pleuritis caused by thermal injury and is almost always treated conservatively. Associated risk factors include the use of a cluster electrode and a short distance from the lesion to the pleura [62],[66],[69]
  • Parenchyma hemorrhage and hemoptysis (6-18% and 3-9% of ablations, respectively): [66],[67],[70] Hemoptysis, in most cases, is self-limiting. More severe hemorrhage can occur in tumors in contact with the hilum. Delayed major hemorrhage due to development of false aneurysms of the pulmonary artery may need coil embolization [71]
  • Needle track seeding: This rarely occurs. Risk factors include the use of an internally cooled electrode, an electrode tip temperature of less than 60°C immediately after RFA, lack of tract ablation, biopsy prior to RFA, and poor differentiation of cancers [72]
  • Thermal neuropathy: Although rare, injury to nerves such as the brachial plexus, phrenic nerve, and the intercostal nerves has been reported from treatment of nearby tumors [73],[74]
  • Rare adverse effects include interstitial pneumonitis, bronchiolitis obliterans organizing pneumonia, and air embolism. [69],[72],[75] Asymptomatic microbubble embolism depicted by duplex ultrasound has been reported during lung RFA in humans. [76] Non-fatal major air embolism has been reported as a consequence of RF probe placement in two case reports. [75],[77] Only one case of cerebral infarction after lung RFA was found. [23]

Post-procedural complications

The expected post-ablation course includes mild-to-moderate pain, fever, and mild dyspnea during the first week. These can be managed with oral analgesics and nasal or mask administration of oxygen. Most patients can be discharged the next day. [40] Post-procedural hemoptysis is usually minor, consists of brownish blood, and lasts from 2 to 7 days without requiring treatment.

Advantages and drawbacks of RFA in the lung: A synopsis

A summary of the advantages and disadvantages of RFA for NSCLC is presented in [Table 4].
Table 4: Summary of advantage and disadvantages of RFA for NSCLC

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Comparison to other available modalities

Sublobar resection

Zemlyak et al., in their study comparing RFA and surgery, reported a longer cancer-free survival in the surgical group and a higher recurrence in the RFA group. [78] Kwan et al.[79] used the National Cancer Institute Surveillance, Epidemiology, and End Results Medicare-linked data to examine the survival of patients with early-stage NSCLC after RFA and sublobar resection. They suggested that although local recurrence after RFA presents a major problem, it does not have a significant impact on OS or CS, explained by the fact that patients who underwent RFA were older and tended to have substantial co-morbidities, so they tended to die due to causes other than cancer recurrence. [79]

Stereotactic body radiation therapy

SBRT is associated with favorable local control and survival rates in patients with stage I NSCLC. Hiraki et al. analyzed about 14 studies of SBRT for stage I NSCLC. In most studies, no mortality was found. Grade 5 toxicities were found in 7-9% of patients, and Grade 3 toxicities were found in less than 5% of patients. Local recurrence was reported in up to 20% of patients. The 1-, 3-, and 5-year OS rates were 80-95%, 43-85%, and 25-70%, respectively. The median OS was 32-62 months. The 3- and 5-year CS survival rates were 67-88% and 41-76%, respectively. [39]

Whether RFA offers better results than SBRT in patients with NSCLC who are unfit for surgery has been evaluated in two studies where a "best evidence topic" was constructed according to a structured protocol. These studies are summarized in [Table 5]. In 2013, Renaud et al. opined that the current evidence shows that SBRT is a safe and effective procedure and should be proposed first to patients suffering from primary NSCLC who are unfit for surgery as it offers lower complications, better control rates, and OS as well as CS. [80] Bilal et al. opined that in the choice between SBRT and RFA, treatment for early-stage inoperable NSCLC should be tailored to individual patients, and under certain circumstances, a combined approach may be beneficial. They reported that both treatments have a similar incidence of complications, and OS at 1 year was similar. However, the local progression was lower and the 5-year survival was higher with SBRT. [81]
Table 5: Summary of studies comparing RFA and SBRT

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Thus, SBRT appears to have evolved as the next best option for early NSCLC in inoperable patients, with the main advantage being superior local control of the tumor. However, some of the drawbacks of SBRT include patients who have tumors in central locations (near hilum, mediastinum, and vertebral body) or in the lower lobe in patients with considerable respiratory motion. Also, SBRT involves multiple fractionated doses. SBRT is a relative contraindication in severe pulmonary dysfunction and is not useful for re-treatment in recurrence following primary SBRT treatments, due to high rates of toxicity. It is in this specific subset of patients that RFA has the potential to replace SBRT. With new developments in RFA technique, interventional radiologists have started treating more centrally occurring tumors. Important advantages are its minimally invasive nature, insignificant impact on pulmonary function, [37],[46] ability to be performed regardless of any previous treatments (even in the event of SBRT failure), and multiplicity. [39] Also, another distinct advantage is the cost-effectiveness of RFA. Sher et al. showed a significantly higher cost of SBRT (about 4.5 times higher) in comparison to RFA. [82]

Current role of RFA in the management of NSCLC

In patients with no high risks, RFA falls significantly behind surgery as well as SBRT, primarily due to the higher rate of local failure, especially for larger tumors. It is, however, debatable how much of this increased local failure impacts survival outcomes in old and high-risk patients. [83] A recently completed National Cancer Institute NCI-funded multicenter pilot trial (ACOSOG Z4033) compared the selection criteria and short-term outcomes of RFA to sublobar resection and SBRT from other completed multicenter trials - SBRT (RTOG trial 0236), sublobar resection (ACOSOG trial Z4032). Despite the RFA cohorts being older and sicker, their survival was similar. The overall 90-day mortality for SBRT, surgery, and RFA was 0%, 2.4%, and 2.0%, respectively (P = 0.5). [84] Although a fallback option in medically inoperable patients who cannot receive SBRT, RFA is beginning to play an increasingly important role in this subset of patients. [8],[83]

Various other roles of RFA are being described as an alternative/adjunctive. Schoellnast et al.[85] and Kodama et al.[59] suggest that RFA may be a good treatment option for patients with metachronous lung cancer or residual/recurrent disease after surgery, chemotherapy, and/or radiation. Although RFA is mostly used as a stand-alone technique, use of combination therapies with radiation therapy or systemic therapies has already been demonstrated in animal studies. [40] Bilal et al. highlighted the advantages and drawbacks of RFA and SBRT and suggested that a combined approach may be beneficial. [81] According to Dupuy et al., this may help overcome the limited local efficacy of RFA. [86] The current role of RFA in the management of NSCLC has been summarized in [Figure 4].
Figure 4: A clinical practice algorithm in the "triage" of patient with stage 1 NSCLC. Solid lines indicate current role, dotted line indicates emerging/potential roles

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   Conclusion Top

Following the National Lung Screening Trial (NLST), screening by low-dose CT has demonstrated high rates of early-stage lung cancer detection in high-risk populations. [87] Although the current role of RFA is limited, in view of increasing numbers of occurrences detected, a fifth of which are inoperable, the number of "potential" RFA candidates may see a steep uptrend. [88] In this age of declining health care reimbursement, the significantly lower cost of RFA compared to that of other modalities [82] may help push RFA to the frontline. In view of all this, it is imperative that radiologists, with the strong support of the bigger societies, aggressively push for funding and development of research protocols to prospectively evaluate the efficacy of RFA and provide comparisons to other modalities like SBRT. We need to step up our game in order to move this attractive treatment option from a "defender position" to "center forward" in the management of lung cancer. [89]

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

   References Top

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Correspondence Address:
Dr. Keith Pereira
Jackson Memorial Hospital, University of Miami Hospital, 1611 Northwest 12th Avenue, Miami, Florida - 33136
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0971-3026.178347

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