TY - JOUR
T1 - Stereotactic body radiation therapy for operable early-stage lung cancer findings from the NRG oncology RTOG 0618 trial
AU - Timmerman, Robert D.
AU - Paulus, Rebecca
AU - Pass, Harvey I.
AU - Gore, Elizabeth M.
AU - Edelman, Martin J.
AU - Galvin, James
AU - Straube, William L.
AU - Nedzi, Lucien A.
AU - McGarry, Ronald C.
AU - Robinson, Cliff G.
AU - Schiff, Peter B.
AU - Chang, Garrick
AU - Loo, Billy W.
AU - Bradley, Jeffrey D.
AU - Choy, Hak
N1 - Funding Information:
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.
Publisher Copyright:
© 2018 American Medical Association. All rights reserved.
PY - 2018/9
Y1 - 2018/9
N2 - 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 60mmHg, arterial carbon dioxide tension less than 50mmHg, 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 pointwas 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.
AB - 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 60mmHg, arterial carbon dioxide tension less than 50mmHg, 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 pointwas 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.
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U2 - 10.1001/jamaoncol.2018.1251
DO - 10.1001/jamaoncol.2018.1251
M3 - Article
C2 - 29852037
AN - SCOPUS:85050069518
SN - 2374-2437
VL - 4
SP - 1263
EP - 1266
JO - JAMA Oncology
JF - JAMA Oncology
IS - 9
ER -