TY - JOUR
T1 - High-Dose Once-Daily Thoracic Radiotherapy in Limited-Stage Small-Cell Lung Cancer
T2 - CALGB 30610 (Alliance)/RTOG 0538
AU - Bogart, Jeffrey
AU - Wang, Xiaofei
AU - Masters, Gregory
AU - Gao, Junheng
AU - Komaki, Ritsuko
AU - Gaspar, Laurie E.
AU - Heymach, John
AU - Bonner, James
AU - Kuzma, Charles
AU - Waqar, Saiama
AU - Petty, William
AU - Stinchcombe, Thomas E.
AU - Bradley, Jeffrey D.
AU - Vokes, Everett
N1 - Funding Information:
Supported by the National Cancer Institute of the National Institutes of Health under Award Nos. U10CA180821 and U10CA180882 (to the Alliance for Clinical Trials in Oncology), UG1CA189824, UG1CA189819, UG1CA189858, UG1CA233253, UG1CA233324, UG1CA233327, UG1CA233329, UG1CA233339, and U10CA180868 (NRG Oncology).
Publisher Copyright:
© American Society of Clinical Oncology.
PY - 2023/5/1
Y1 - 2023/5/1
N2 - PURPOSEAlthough level 1 evidence supports 45-Gy twice-daily radiotherapy as standard for limited-stage small-cell lung cancer, most patients receive higher-dose once-daily regimens in clinical practice. Whether increasing radiotherapy dose improves outcomes remains to be prospectively demonstrated.METHODSThis phase III trial, CALGB 30610/RTOG 0538 (ClinicalTrials.gov identifier: NCT00632853), was conducted in two stages. In the first stage, patients with limited-stage disease were randomly assigned to receive 45-Gy twice-daily, 70-Gy once-daily, or 61.2-Gy concomitant-boost radiotherapy, starting with either the first or second (of four total) chemotherapy cycles. In the second stage, allocation to the 61.2-Gy arm was discontinued following planned interim toxicity analysis, and the study continued with two remaining arms. The primary end point was overall survival (OS) in the intention-to-treat population.RESULTSTrial accrual opened on March 15, 2008, and closed on December 1, 2019. All patients randomly assigned to 45-Gy twice-daily (n = 313) or 70-Gy once-daily radiotherapy (n = 325) are included in this analysis. After a median follow-up of 4.7 years, OS was not improved on the once-daily arm (hazard ratio for death, 0.94; 95% CI, 0.76 to 1.17; P =.594). Median survival is 28.5 months for twice-daily treatment, and 30.1 months for once-daily treatment, with 5-year OS of 29% and 32%, respectively. Treatment was tolerable, and the frequency of severe adverse events, including esophageal and pulmonary toxicity, was similar on both arms.CONCLUSIONAlthough 45-Gy twice-daily radiotherapy remains the standard of care, this study provides the most robust information available to help guide the choice of thoracic radiotherapy regimen for patients with limited-stage small-cell lung cancer.
AB - PURPOSEAlthough level 1 evidence supports 45-Gy twice-daily radiotherapy as standard for limited-stage small-cell lung cancer, most patients receive higher-dose once-daily regimens in clinical practice. Whether increasing radiotherapy dose improves outcomes remains to be prospectively demonstrated.METHODSThis phase III trial, CALGB 30610/RTOG 0538 (ClinicalTrials.gov identifier: NCT00632853), was conducted in two stages. In the first stage, patients with limited-stage disease were randomly assigned to receive 45-Gy twice-daily, 70-Gy once-daily, or 61.2-Gy concomitant-boost radiotherapy, starting with either the first or second (of four total) chemotherapy cycles. In the second stage, allocation to the 61.2-Gy arm was discontinued following planned interim toxicity analysis, and the study continued with two remaining arms. The primary end point was overall survival (OS) in the intention-to-treat population.RESULTSTrial accrual opened on March 15, 2008, and closed on December 1, 2019. All patients randomly assigned to 45-Gy twice-daily (n = 313) or 70-Gy once-daily radiotherapy (n = 325) are included in this analysis. After a median follow-up of 4.7 years, OS was not improved on the once-daily arm (hazard ratio for death, 0.94; 95% CI, 0.76 to 1.17; P =.594). Median survival is 28.5 months for twice-daily treatment, and 30.1 months for once-daily treatment, with 5-year OS of 29% and 32%, respectively. Treatment was tolerable, and the frequency of severe adverse events, including esophageal and pulmonary toxicity, was similar on both arms.CONCLUSIONAlthough 45-Gy twice-daily radiotherapy remains the standard of care, this study provides the most robust information available to help guide the choice of thoracic radiotherapy regimen for patients with limited-stage small-cell lung cancer.
UR - http://www.scopus.com/inward/record.url?scp=85152485546&partnerID=8YFLogxK
U2 - 10.1200/JCO.22.01359
DO - 10.1200/JCO.22.01359
M3 - Article
C2 - 36623230
AN - SCOPUS:85152485546
SN - 0732-183X
VL - 41
SP - 2394
EP - 2402
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 13
ER -