TY - JOUR
T1 - Real-world Efficacy and Safety of Nivolumab for Advanced Non–Small-cell Lung Cancer
T2 - A Retrospective Multicenter Analysis
AU - Keio Lung Oncology Group (KLOG)
AU - Kobayashi, Keigo
AU - Nakachi, Ichiro
AU - Naoki, Katsuhiko
AU - Satomi, Ryosuke
AU - Nakamura, Morio
AU - Inoue, Takashi
AU - Tateno, Hiroki
AU - Sakamaki, Fumio
AU - Sayama, Koichi
AU - Terashima, Takeshi
AU - Koh, Hidefumi
AU - Abe, Takayuki
AU - Nishino, Makoto
AU - Arai, Daisuke
AU - Yasuda, Hiroyuki
AU - Kawada, Ichiro
AU - Soejima, Kenzo
AU - Betsuyaku, Tomoko
N1 - Funding Information:
We wish to thank Kazumi Nishio (Kawasaki City Ida Hospital, Kanagawa, Japan), Fumitake Saito (Eiju General Hospital, Tokyo, Japan), Yusuke Suzuki (Kitasato Institute Hospital, Tokyo, Japan), and Akira Umeda (International Medical Welfare College Shioya Hospital, Tochigi, Japan) for assisting in data collection, and all members of the Keio Lung Oncology Group who participated in this study. This study was funded by Ono Pharmaceutical, Co., Ltd., and Chugai Pharmaceutical, Co., Ltd.
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/5
Y1 - 2018/5
N2 - We evaluated the real-world efficacy and safety of nivolumab in 142 patients with advanced non–small-cell lung cancer in Japan and identified the clinical characteristics that influence the efficacy. Negative EGFR/ALK mutation status and previous radiotherapy were significantly associated statistically with the treatment response. These findings might aid in the efficient immunotherapeutic management of lung cancer. Background: Nivolumab, an immune checkpoint inhibitor, is now a standard treatment for previously treated advanced non–small-cell lung cancer based on the results from phase III clinical trials. We evaluated the real-world efficacy and safety of nivolumab in a nonselected population and identified the clinical characteristics that influence efficacy. Materials and Methods: A total of 142 patients with advanced non–small-cell lung cancer who were administered nivolumab at Keio University and affiliated hospitals in Japan from January to July 2016 were enrolled. The treatment efficacy and adverse events were retrospectively reviewed, and the clinical characteristics associated with the nivolumab response were evaluated using univariate and stratified analyses and the Cochran-Mantel-Haenszel test. Results: The objective response rate was 17.0% (95% confidence interval [CI], 12.0%-24.0%), the median progression-free survival (PFS) was 58 days (95% CI, 50-67 days), and the proportion of patients with adverse events of any grade was 45.0%. EGFR/ALK mutation status was inversely associated with the treatment response (P <.05), and the difference in PFS for the mutation-positive versus mutation-negative patients was statistically significant (49 vs. 63 days; hazard ratio, 1.9; 95% CI, 1.1-5.2; P =.029). Previous radiotherapy also had a positive association with the treatment response (P =.012). Conclusion: The objective response rate, PFS, and adverse event profiles were comparable to those observed in previous clinical trials. EGFR/ALK mutation-negative status and previous radiotherapy might be key clinical characteristics associated with a positive treatment response. Our findings could aid in the efficient immunotherapeutic management of lung cancer.
AB - We evaluated the real-world efficacy and safety of nivolumab in 142 patients with advanced non–small-cell lung cancer in Japan and identified the clinical characteristics that influence the efficacy. Negative EGFR/ALK mutation status and previous radiotherapy were significantly associated statistically with the treatment response. These findings might aid in the efficient immunotherapeutic management of lung cancer. Background: Nivolumab, an immune checkpoint inhibitor, is now a standard treatment for previously treated advanced non–small-cell lung cancer based on the results from phase III clinical trials. We evaluated the real-world efficacy and safety of nivolumab in a nonselected population and identified the clinical characteristics that influence efficacy. Materials and Methods: A total of 142 patients with advanced non–small-cell lung cancer who were administered nivolumab at Keio University and affiliated hospitals in Japan from January to July 2016 were enrolled. The treatment efficacy and adverse events were retrospectively reviewed, and the clinical characteristics associated with the nivolumab response were evaluated using univariate and stratified analyses and the Cochran-Mantel-Haenszel test. Results: The objective response rate was 17.0% (95% confidence interval [CI], 12.0%-24.0%), the median progression-free survival (PFS) was 58 days (95% CI, 50-67 days), and the proportion of patients with adverse events of any grade was 45.0%. EGFR/ALK mutation status was inversely associated with the treatment response (P <.05), and the difference in PFS for the mutation-positive versus mutation-negative patients was statistically significant (49 vs. 63 days; hazard ratio, 1.9; 95% CI, 1.1-5.2; P =.029). Previous radiotherapy also had a positive association with the treatment response (P =.012). Conclusion: The objective response rate, PFS, and adverse event profiles were comparable to those observed in previous clinical trials. EGFR/ALK mutation-negative status and previous radiotherapy might be key clinical characteristics associated with a positive treatment response. Our findings could aid in the efficient immunotherapeutic management of lung cancer.
KW - EGFR mutation
KW - Immunotherapy
KW - NSCLC
KW - Nivolumab
KW - Radiation
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U2 - 10.1016/j.cllc.2018.01.001
DO - 10.1016/j.cllc.2018.01.001
M3 - Article
C2 - 29398578
AN - SCOPUS:85041628347
SN - 1525-7304
VL - 19
SP - e349-e358
JO - Clinical Lung Cancer
JF - Clinical Lung Cancer
IS - 3
ER -