TY - JOUR
T1 - A phase II study of induction chemotherapy followed by thoracic radiotherapy and erlotinib in poor-risk stage III non-small-cell lung cancer
T2 - Results of CALGB 30605 (Alliance)/RTOG 0972 (NRG)
AU - Lilenbaum, Rogerio
AU - Samuels, Michael
AU - Wang, Xiaofei
AU - Kong, Feng Ming
AU - Jänne, Pasi A.
AU - Masters, Gregory
AU - Katragadda, Sreedhar
AU - Hodgson, Lydia
AU - Bogart, Jeffrey
AU - Bradley, Jeffrey
AU - Vokes, Everett
N1 - Funding Information:
Disclosure: Dr. Lilenbaum was supported by grant CA16359 and received compensation outside of the submitted work for consultancy with Genentech. Dr. Wang and L. Hodgson were supported by grant CA33601. Dr. Kong was supported by (to be added). Dr. Jänne was supported by grant CA32291. Dr. Masters was supported by CA45418; Dr. Katragadda was supported by grant CA45808; Dr. Bogart was supported by CA21060; Dr. Bradley was supported by grant CA77440; Dr. Vokes was supported by grant CA41287. Related to the submitted work Dr. Jänne received compensation for consultancy for drug development from Genentech and post marketing royalties from a DCFI owned patent on EGFR mutations. Outside of the submitted work Dr. Jänne received compensation for consultancy with the following entities: Boehringer-Ingelheim, Astra Zeneca, Clovis Oncology, Merrimack Pharmaceuticals, Pfizer, and Chugai Pharmaceuticals. Dr. Bradley has an institutional ViewRay clinical trial grant and a pending NIH RO-1 application. Dr. Bradley was also an invited speaker at the 2014 Brazilian National Radiotherapy Congress. Speaker travel expenses were covered by Varian Medical, Inc. Dr. Vokes received compensation outside of the submitted work for consultancy with the following entities: Amgen, AstraZeneca, Bayer, BMS, Boehringer-Ingelheim, Celgene, Clovis, Eisei, Merck, Synta, and VentiRx. All other authors declare no conflict of interest.
Funding Information:
The research for CALGB 30605 (Alliance) was supported, in part, by grants from the National Cancer Institute (CA31946) to the Alliance for Clinical Trials in Oncology (Monica M. Bertagnolli, MD, Chair), the Alliance Statistics and Data Center (Daniel J. Sargent, PhD, CA33601), the Quality Assurance Review Center (Thomas FitzGerald, MD, CA 29511), and Radiation Therapy Oncology Group (CA 21661 and CA 37422). The content of this manuscript is solely the responsibility of the authors and does not necessarily represent the official views of the National Cancer Institute. The following institutions participated in this study: Christiana Care Health Services, Inc. CCOP, Wilmington, DE, Stephen Grubbs, MD, supported by CA45418; Cancer Centers of the Carolinas, Greenville, SC, Jeffrey K. Giguere, MD, supported by CA29165; Dana-Farber Cancer Institute, Boston, MA, Harold J. Burstein, MD, PhD, supported by CA32291; Duke University Medical Center, Durham, NC, Jeffrey Crawford, MD, supported by CA47577; Kansas City Community Clinical Oncology Program CCOP, Kansas City, MO, Rakesh Gaur, MD; Missouri Valley Consortium-CCOP, Omaha, NE, Gamini S. Soori, MD; Mount Sinai Medical Center, Miami, FL, Michael A. Schwartz, MD, supported by CA45564; Nevada Cancer Research Foundation CCOP, Las Vegas, NV, John A. Ellerton, MD, supported by CA35421; New Hampshire Oncology-Hematology PA, Concord, NH, Douglas J. Weckstein, MD; Ohio State University Medical Center, Columbus, OH, Clara D. Bloomfield, MD, supported by CA77658; Roswell Park Cancer Institute, Buffalo, NY, Ellis Levine, MD, supported by CA59518; Southeast Cancer Control Consortium Inc. CCOP, Goldsboro, NC, James N. Atkins, MD, supported by CA45808; State University of New York Upstate Medical University, Syracuse, NY, Stephen L. Graziano, MD, supported by CA21060; University of Chicago, Chicago, IL, Hedy L. Kindler, MD, supported by CA41287; University of Missouri/Ellis Fischel Cancer Center, Columbia, MO, Karl E. Freter, MD, supported by CA12046; University of North Carolina at Chapel Hill, Chapel Hill, NC, Thomas C. Shea, MD, supported by CA47559; and Wake Forest University School of Medicine, Winston-Salem, NC, David D. Hurd, MD, supported by CA03927.
Publisher Copyright:
Copyright © 2014 by the International Association for the Study of Lung Cancer.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - Introduction: Patients with stage III non-small-cell lung cancer and poor performance status and/or weight loss do not seem to benefit from standard therapy. Based on the preclinical interaction between epidermal growth factor receptor inhibitors and radiation, we designed a trial of induction chemotherapy followed by thoracic radiotherapy and concurrent erlotinib. Methods: Patients with poor-risk unresectable stage III non-small-cell lung cancer received two cycles of carboplatin at an AUC of 5 and nab-paclitaxel at 100 mg/m2 on days 1 and 8 every 21 days, followed by erlotinib administered concurrently with thoracic radiotherapy. Maintenance was not permitted. Molecular analysis was performed in available specimens. Seventy-two eligible patients were required to test whether the 1-year survival rate was less than 50% or greater than or equal to 65% with approximately 90% power at a significance level of 0.10. Results: From March 2008 to October 2011, 78 patients were enrolled, three of whom were ineligible. The median age was 68 (range, 39-88) and 32% were aged greater than or equal to 75 years. Patients were evenly distributed between stages IIIA and IIIB and the majority had performance status 2. The overall response rate was 67% and the disease control rate was 93%. Treatment was well tolerated. The median PFS and OS were 11 and 17 months, respectively. The overall 12-month OS was 57%, which narrowly missed the prespecified target for significance. Conclusions: Patients with poor-risk stage III non-small-cell lung cancer had better than expected outcomes with a regimen of induction carboplatin/nab-paclitaxel followed by thoracic radiotherapy and erlotinib. However, as per the statistical design, the 12-month OS was not sufficiently high to warrant further studies.
AB - Introduction: Patients with stage III non-small-cell lung cancer and poor performance status and/or weight loss do not seem to benefit from standard therapy. Based on the preclinical interaction between epidermal growth factor receptor inhibitors and radiation, we designed a trial of induction chemotherapy followed by thoracic radiotherapy and concurrent erlotinib. Methods: Patients with poor-risk unresectable stage III non-small-cell lung cancer received two cycles of carboplatin at an AUC of 5 and nab-paclitaxel at 100 mg/m2 on days 1 and 8 every 21 days, followed by erlotinib administered concurrently with thoracic radiotherapy. Maintenance was not permitted. Molecular analysis was performed in available specimens. Seventy-two eligible patients were required to test whether the 1-year survival rate was less than 50% or greater than or equal to 65% with approximately 90% power at a significance level of 0.10. Results: From March 2008 to October 2011, 78 patients were enrolled, three of whom were ineligible. The median age was 68 (range, 39-88) and 32% were aged greater than or equal to 75 years. Patients were evenly distributed between stages IIIA and IIIB and the majority had performance status 2. The overall response rate was 67% and the disease control rate was 93%. Treatment was well tolerated. The median PFS and OS were 11 and 17 months, respectively. The overall 12-month OS was 57%, which narrowly missed the prespecified target for significance. Conclusions: Patients with poor-risk stage III non-small-cell lung cancer had better than expected outcomes with a regimen of induction carboplatin/nab-paclitaxel followed by thoracic radiotherapy and erlotinib. However, as per the statistical design, the 12-month OS was not sufficiently high to warrant further studies.
KW - NSCLC
KW - Poor risk
KW - Stage III
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U2 - 10.1097/JTO.0000000000000347
DO - 10.1097/JTO.0000000000000347
M3 - Article
C2 - 25384173
AN - SCOPUS:84926406754
SN - 1556-0864
VL - 10
SP - 143
EP - 147
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 1
ER -