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Clinical Trial
. 2018 Sep 1;4(9):1263-1266.
doi: 10.1001/jamaoncol.2018.1251.

Stereotactic Body Radiation Therapy for Operable Early-Stage Lung Cancer: Findings From the NRG Oncology RTOG 0618 Trial

Affiliations
Clinical Trial

Stereotactic Body Radiation Therapy for Operable Early-Stage Lung Cancer: Findings From the NRG Oncology RTOG 0618 Trial

Robert D Timmerman et al. JAMA Oncol. .

Abstract

Importance: Stereotactic body radiation therapy (SBRT) has become a standard treatment for patients with medically inoperable early-stage lung cancer. However, its effectiveness in patients medically suitable for surgery is unclear.

Objective: To evaluate whether noninvasive SBRT delivered on an outpatient basis can safely eradicate lung cancer and cure selected patients with operable lung cancer, obviating the need for surgical resection.

Design, setting, and participants: Single-arm phase 2 NRG Oncology Radiation Therapy Oncology Group 0618 study enrolled patients from December 2007 to May 2010 with median follow-up of 48.1 months (range, 15.4-73.7 months). The setting was a multicenter North American academic and community practice cancer center consortium. Patients had operable biopsy-proven peripheral T1 to T2, N0, M0 non-small cell tumors no more than 5 cm in diameter, forced expiratory volume in 1 second (FEV1) and diffusing capacity greater than 35% predicted, arterial oxygen tension greater than 60 mm Hg, arterial carbon dioxide tension less than 50 mm Hg, and no severe medical problems. The data analysis was performed in October 2014.

Interventions: The SBRT prescription dose was 54 Gy delivered in 3 18-Gy fractions over 1.5 to 2.0 weeks.

Main outcomes and measures: Primary end point was primary tumor control, with survival, adverse events, and the incidence and outcome of surgical salvage as secondary end points.

Results: Of 33 patients accrued, 26 were evaluable (23 T1 and 3 T2 tumors; 15 [58%] male; median age, 72.5 [range, 54-88] years). Median FEV1 and diffusing capacity of the lung for carbon monoxide at enrollment were 72.5% (range, 38%-136%) and 68% (range, 22%-96%) of predicted, respectively. Only 1 patient had a primary tumor recurrence. Involved lobe failure, the other component defining local failure, did not occur in any patient, so the estimated 4-year primary tumor control and local control rate were both 96% (95% CI, 83%-100%). As per protocol guidelines, the single patient with local recurrence underwent salvage lobectomy 1.2 years after SBRT, complicated by a grade 4 cardiac arrhythmia. The 4-year estimates of disease-free and overall survival were 57% (95% CI, 36%-74%) and 56% (95% CI, 35%-73%), respectively. Median overall survival was 55.2 months (95% CI, 37.7 months to not reached). Protocol-specified treatment-related grade 3, 4, and 5 adverse events were reported in 2 (8%; 95% CI, 0.1%-25%), 0, and 0 patients, respectively.

Conclusions and relevance: As given, SBRT appears to be associated with a high rate of primary tumor control, low treatment-related morbidity, and infrequent need for surgical salvage in patients with operable early-stage lung cancer.

Trial registration: ClinicalTrials.gov Identifier: NCT00551369.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Timmerman reports receiving a research grant for technology development from Varian Medical Systems, Accuray, Inc, and Elekta Oncology. Each of these companies manufactures equipment used in the performance of stereotactic body radiation therapy. Dr Robinson reports grants from Varian Medical Systems. Dr Loo reports grants to his institution and honoraria for educational lectures from Varian Medical Systems and grants to his institution from RaySearch Laboratories. Dr Loo is also a Board Member of TibaRay, Inc. Dr Bradley reports grants from ViewRay, Inc. No other disclosures are reported.

Figures

Figure 1.
Figure 1.. CONSORT Diagram
CT/PET indicates computed tomography/positron emission tomography; SBRT, stereotactic body radiation therapy.
Figure 2.
Figure 2.. Overall Survival (OS) and Disease-Free Survival (DFS)
Of 26 patients evaluated for OS and DFS, 12 experienced failure and 14 were censored for each outcome. Median OS was 55.2 months (95% CI, 37.7 months to not reached), and median DFS was 55.2 months (95% CI, 31.9 months to not reached). SBRT indicates stereotactic body radiation therapy.

References

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