TY - JOUR
T1 - Real-world effectiveness and safety of nivolumab in patients with non-small cell lung cancer
T2 - A multicenter retrospective observational study in Japan
AU - Morita, Ryo
AU - Okishio, Kyoichi
AU - Shimizu, Junichi
AU - Saito, Haruhiro
AU - Sakai, Hiroshi
AU - Kim, Young Hak
AU - Hataji, Osamu
AU - Yomota, Makiko
AU - Nishio, Makoto
AU - Aoe, Keisuke
AU - Kanai, Osamu
AU - Kumagai, Toru
AU - Kibata, Kayoko
AU - Tsukamoto, Hiroaki
AU - Oizumi, Satoshi
AU - Fujimoto, Daichi
AU - Tanaka, Hiroshi
AU - Mizuno, Keiko
AU - Masuda, Takeshi
AU - Kozuki, Toshiyuki
AU - Haku, Takashi
AU - Suzuki, Hiroyuki
AU - Okamoto, Isamu
AU - Hoshiyama, Hirotoshi
AU - Ueda, Junya
AU - Ohe, Yuichiro
N1 - Funding Information:
This study (CA209-9CR) was company-initiated and funded by Bristol-Myers Squibb K.K. (Tokyo, Japan) and Ono Pharmaceutical Co., Ltd . (Osaka, Japan). The companies were involved in the study design and interpretation of the data; however, they did not participate in data collection and data analysis. The two authors of this article who were affiliated with the companies participated in writing the manuscript and decision for its publication based on the authorship. Dr. Okishio reports personal fees from Ono Pharmaceutical Co., Ltd. and MSD K.K. outside the submitted work; Dr. Shimizu reports personal fees from Bristol-Myers Squibb K.K. and Ono Pharmaceutical Co., Ltd. outside the submitted work; Dr. Saito reports grants from Chugai Pharmaceutical Co., Ltd., AstraZeneca K.K., and MSD K.K., and personal fees from Ono Pharmaceutical Co., Ltd., Nippon Boehringer Ingelheim Co., Ltd., and Novartis Pharma K.K. outside the submitted work; Dr. Sakai reports personal fees from Ono Pharmaceutical Co., Ltd. and Bristol-Myers Squibb K.K. during the conduct of the study, and personal fees from Chugai Pharmaceutical Co., Ltd. and MSD K.K. outside the submitted work; Dr. Hataji reports other from Ono Pharmaceutical Co., Ltd. during the conduct of the study, personal fees and other from Novartis Pharma K.K., Nippon Boehringer Ingelheim Co., Ltd. and AstraZeneca K.K., and other from Kyorin Pharmaceutical Co., Ltd., Bayer Health, Daiichi Sankyo Co., Ltd., GlaxoSmithKline K.K., and Ono Pharmaceutical Co., Ltd. outside the submitted work; Dr. Yomota reports personal fees from Chugai Pharmaceutical Co., Ltd., Ono Pharmaceutical Co., Ltd., and AstraZeneca K.K. outside the submitted work; Dr. Nishio reports grants and non-financial support from Ono Pharmaceutical Co., Ltd. during the conduct of the study, grants and personal fees from Ono Pharmaceutical Co., Ltd., Bristol-Myers Squibb K.K., Pfizer Japan Inc., Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Taiho Pharmaceutical Co., Ltd., AstraZeneca K.K., MSD K.K., and Novartis Pharma K.K., and personal fees from Nippon Boehringer Ingelheim Co., Ltd., Daiichi Sankyo Healthcare Co., Ltd., and Merck Serono Co., Ltd. outside the submitted work; Dr. Aoe reports grants and personal fees from Ono Pharmaceutical Co., Ltd., Bristol-Myers Squibb K.K., AstraZeneca K.K., and Eli Lilly Japan K.K., and grants from MSD (Merk) and Novartis Pharma K.K. outside the submitted work; Dr. Kumagai reports personal fees from Ono Pharmaceutical Co., Ltd., AstraZeneca K.K., Taiho Pharmaceutical Co., Ltd., MSD K.K., Teijin Pharma Ltd., Novartis Pharma K.K., Nippon Boehringer Ingelheim Co., Ltd., Eli Lilly Japan K.K., Pfizer Japan Inc., Chugai Pharmaceutical Co., Ltd., and Bristol-Myers Squibb K.K., and grants from Ono Pharmaceutical Co., Ltd., MSD K.K., Chugai Pharmaceutical Co., Ltd., AstraZeneca K.K., Takeda Pharmaceutical Co., Ltd., Regeneron Pharmaceuticals, Inc., Merck Serono Co., Ltd., Pfizer Japan Inc., Taiho Pharmaceutical Co., Ltd., Nippon Boehringer Ingelheim Co., Ltd., Eli Lilly Japan K.K., and Novartis Pharma K.K. outside the submitted work; Dr. Oizumi reports grants and personal fees from Bristol-Myers Squibb K.K. and Ono Pharmaceutical Co., Ltd. during the conduct of the study, grants and personal fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., and Taiho Pharmaceutical Co., Ltd., grants from Kyowa Hakko Kirin Co., Ltd. and Merck Serono Co., Ltd., and personal fees from MSD K.K. and Eli Lilly Japan K.K. outside the submitted work; Dr. Fujimoto reports personal fees from Ono Pharmaceutical Co., Ltd. and Bristol-Myers Squibb K.K. during the conduct of the study, and personal fees from AstraZeneca K.K., Taiho Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co., Ltd., MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., and Eli Lilly Japan K.K. outside the submitted work; Dr. Tanaka reports grants and personal fees from Bristol-Myers Squibb K.K., Eli Lilly Japan K.K., MSD K.K., Taiho Pharmaceutical Co., Ltd., Pfizer Japan Inc., Chugai Pharmaceutical Co., Ltd., Ono Pharmaceutical Co., Ltd., AstraZeneca K.K., and Nippon Boehringer Ingelheim Co., Ltd., grants from Merck Serono Co., Ltd., and personal fees from Novartis Pharma K.K. outside the submitted work; Dr. Kozuki reports grants and personal fees from Chugai Pharmaceutical Co., Ltd., AstraZeneca K.K., Eli Lilly Japan K.K., and Bristol-Myers Squibb K.K., personal fees from Taiho Pharmaceutical Co., Ltd., Ono Pharmaceutical Co., Ltd., MSD K.K., Pfizer Japan Inc., Kyowa Hakko Kirin Co., Ltd., and Nippon Boehringer Ingelheim Co., Ltd., and grants from Merck Serono Co., Ltd. outside the submitted work; Dr. Suzuki reports other from Mebix, Inc. during the conduct of the study, and personal fees from AstraZeneca K.K. outside the submitted work; Dr. Okamoto reports grants from Nippon Boehringer Ingelheim Co., Ltd. during the conduct of the study, grants and personal fees from AstraZeneca K.K., Taiho Pharmaceutical Co., Ltd., Nippon Boehringer Ingelheim Co., Ltd., Ono Pharmaceutical Co., Ltd., MSD Oncology, Eli Lilly Japan K.K., Bristol-Myers Squibb K.K., and Chugai Pharmaceutical Co., Ltd., grants from Astellas Pharma Inc., Novartis Pharma K.K., and AbbVie GK, and personal fees from Pfizer Japan Inc. outside the submitted work; Dr. Ohe reports grants and personal fees from Ono Pharmaceutical Co., Ltd. and Bristol-Myers Squibb K.K. during the conduct of the study, grants and personal fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Pfizer Japan Inc., MSD K.K., Kyorin Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Novartis Pharma K.K., Taiho Pharmaceutical Co., Ltd., and AbbVie GK, personal fees from Celltrion Healthcare Co.,Ltd., Amgen Inc., and Nippon Boehringer Ingelheim Co., Ltd., and grants from Kissei Pharmaceutical Co., Ltd., Loxo Oncology, Inc., and Janssen Pharmaceutical K.K. outside the submitted work; Mr. Hoshiyama is an employee of Bristol-Myers Squibb K.K.; Mr. Ueda is an employee of Ono Pharmaceutical Co., Ltd.; Dr. Morita, Dr. Kim, Dr. Kanai, Dr. Kibata, Dr. Tsukamoto, Dr. Mizuno, Dr. Masuda, and Dr. Haku have nothing to declare.
Funding Information:
This study (CA209-9CR) was company-initiated and funded by Bristol-Myers Squibb K.K. (Tokyo, Japan) and Ono Pharmaceutical Co., Ltd. (Osaka, Japan). The companies were involved in the study design and interpretation of the data; however, they did not participate in data collection and data analysis. The two authors of this article who were affiliated with the companies participated in writing the manuscript and decision for its publication based on the authorship.
Publisher Copyright:
© 2019 The Authors
PY - 2020/2
Y1 - 2020/2
N2 - Objectives: To describe the treatment patterns and determine the effectiveness and safety of nivolumab treatment for non-small cell lung cancer (NSCLC) in real-world setting in Japan. Materials and methods: Japanese patients with NSCLC who received nivolumab were analyzed retrospectively. Patients who had started nivolumab treatment between April 2016 and December 2016 were enrolled. Information regarding patient demographics and clinical backgrounds, treatment patterns from diagnosis to post-nivolumab treatment, effectiveness and safety of nivolumab treatment and that of treatments just before and after nivolumab treatment, and programmed death-ligand 1 (PD-L1) expression status, if available, were collected. Factors associated with nivolumab effectiveness identified by univariate and multivariate analyses were further investigated for plotting Kaplan-Meier curves of epidermal growth factor receptor (EGFR) gene mutation status, PD-L1 expression status, and Eastern Cooperative Oncology Group performance status (ECOG PS). Results: In this study, 901 NSCLC patients were enrolled. Nivolumab was used the most as a second line treatment with a median number of nivolumab doses of five. The median overall survival (OS) was 14.6 months, one-year survival rate was 54.3 %, and median progression-free survival (PFS) was 2.1 months. The objective response rate was 20.5 % and disease control rate was 57.4 %. According to multivariate analyses, better OS and PFS were associated with favorable ECOG PS and absence of liver metastasis. Better PFS was observed in patients without EGFR mutation and patients with smoking history. PFS and best overall response in PD-L1 expression subgroups were expression level-dependent. The overall incidence of irAEs was 45.8 %, and the incidence of adverse events of grade 3 or higher was 14.0 %. Conclusion: The real-world effectiveness and safety of nivolumab is consistent with that reported by previous clinical trials and other real-world data. Subgroup analysis showed that ECOG PS, EGFR mutation status, smoking status, and PD-L1 were associated with the effectiveness of nivolumab.
AB - Objectives: To describe the treatment patterns and determine the effectiveness and safety of nivolumab treatment for non-small cell lung cancer (NSCLC) in real-world setting in Japan. Materials and methods: Japanese patients with NSCLC who received nivolumab were analyzed retrospectively. Patients who had started nivolumab treatment between April 2016 and December 2016 were enrolled. Information regarding patient demographics and clinical backgrounds, treatment patterns from diagnosis to post-nivolumab treatment, effectiveness and safety of nivolumab treatment and that of treatments just before and after nivolumab treatment, and programmed death-ligand 1 (PD-L1) expression status, if available, were collected. Factors associated with nivolumab effectiveness identified by univariate and multivariate analyses were further investigated for plotting Kaplan-Meier curves of epidermal growth factor receptor (EGFR) gene mutation status, PD-L1 expression status, and Eastern Cooperative Oncology Group performance status (ECOG PS). Results: In this study, 901 NSCLC patients were enrolled. Nivolumab was used the most as a second line treatment with a median number of nivolumab doses of five. The median overall survival (OS) was 14.6 months, one-year survival rate was 54.3 %, and median progression-free survival (PFS) was 2.1 months. The objective response rate was 20.5 % and disease control rate was 57.4 %. According to multivariate analyses, better OS and PFS were associated with favorable ECOG PS and absence of liver metastasis. Better PFS was observed in patients without EGFR mutation and patients with smoking history. PFS and best overall response in PD-L1 expression subgroups were expression level-dependent. The overall incidence of irAEs was 45.8 %, and the incidence of adverse events of grade 3 or higher was 14.0 %. Conclusion: The real-world effectiveness and safety of nivolumab is consistent with that reported by previous clinical trials and other real-world data. Subgroup analysis showed that ECOG PS, EGFR mutation status, smoking status, and PD-L1 were associated with the effectiveness of nivolumab.
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U2 - 10.1016/j.lungcan.2019.11.014
DO - 10.1016/j.lungcan.2019.11.014
M3 - Article
C2 - 31838169
AN - SCOPUS:85076139582
SN - 0169-5002
VL - 140
SP - 8
EP - 18
JO - Lung Cancer
JF - Lung Cancer
ER -