Abstract
Introduction: Pembrolizumab is a programmed death-ligand 1 inhibitor that was initially indicated for monotherapy in patients with advanced lung cancer. The Japanese Lung Cancer Society conducted an observational study on pembrolizumab using confirmative data obtained through postmarketing all-case surveillance (PMACS), which was performed by a pharmaceutical company under the Japanese law in 2017. Methods: This multicenter observational study was conducted by the Japanese Lung Cancer Society using PMACS data with the newly created central registration system regarding patients with NSCLC who received pembrolizumab monotherapy between February 1, 2017 and June 30, 2017; a new database was created by adding the clinical information regarding prognosis for 3 years after therapy to the existing data collected by PMACS. Results: A total of 300 patients from 43 facilities were enrolled in this study. The median overall survival and progression-free survival after pembrolizumab initiation were 558 and 188 days, respectively. Moreover, the 1- and 3-year survival rates were 58.9% and 33.7%, respectively. Results of multivariate analysis revealed performance status (p < 0.0001), histology (p = 0.0118), previous chemotherapy (p = 0.0007), programmed death-ligand 1 expression status (p = 0.0195), and previous steroid use (p = 0.0460) as significant factors that affected overall survival. The toxicity profile was similar to that previously reported. Conclusions: In this first attempt to use PMACS data, we successfully collected clinical information and found the real-world efficacy and safety of pembrolizumab.
Original language | English |
---|---|
Article number | 100404 |
Journal | JTO Clinical and Research Reports |
Volume | 3 |
Issue number | 11 |
DOIs | |
Publication status | Published - Nov 2022 |
Externally published | Yes |
Keywords
- Immune checkpoint inhibitor
- Immune-related adverse events
- Pembrolizumab
- Real-world data
ASJC Scopus subject areas
- Oncology
- Pulmonary and Respiratory Medicine
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In: JTO Clinical and Research Reports, Vol. 3, No. 11, 100404, 11.2022.
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}
TY - JOUR
T1 - Real-World Data Analysis of Pembrolizumab Monotherapy for NSCLC Using Japanese Postmarketing All-Case Surveillance Data
AU - Terai, Hideki
AU - Soejima, Kenzo
AU - Shimokawa, Asanao
AU - Horinouchi, Hidehito
AU - Shimizu, Junichi
AU - Hase, Tetsunari
AU - Kanemaru, Ryota
AU - Watanabe, Kana
AU - Ninomiya, Kiichiro
AU - Aragane, Naoko
AU - Yanagitani, Noriko
AU - Sakata, Yoshihiko
AU - Seike, Masahiro
AU - Fujimoto, Daichi
AU - Kasajima, Masashi
AU - Kubo, Akihito
AU - Kusumoto, Sojiro
AU - Oyamada, Yoshitaka
AU - Fujiwara, Keiichi
AU - Mori, Masahide
AU - Hashimoto, Midori
AU - Shingyoji, Masato
AU - Kodani, Masahiro
AU - Sakamoto, Jin
AU - Agatsuma, Toshihiko
AU - Kashiwabara, Kosuke
AU - Inomata, Minehiko
AU - Tachihara, Motoko
AU - Tanaka, Kazuhisa
AU - Hayashihara, Kenji
AU - Koyama, Nobuyuki
AU - Matsui, Kaoru
AU - Minato, Koichi
AU - Jingu, Daisuke
AU - Sakashita, Hiroyuki
AU - Hara, Satoshi
AU - Naito, Tomoyuki
AU - Okada, Asuka
AU - Tanahashi, Masayuki
AU - Sato, Yuki
AU - Asano, Koichiro
AU - Takeda, Takayuki
AU - Nakazawa, Kensuke
AU - Harada, Toshiyuki
AU - Shibata, Kazuhiko
AU - Kato, Tatsuo
AU - Miyaoka, Etsuo
AU - Yoshino, Ichiro
AU - Gemma, Akihiko
AU - Mitsudomi, Tetsuya
N1 - Funding Information: This work was supported by the Japan Agency for Medical Research and Development (grant number 17lk1010016h0002), the Ministry of Health, Labour and Welfare Science Research Grant (grant number 201708003B), the Japan Science and Technology Agency (grant number JPMJRC1503), and the Japan Lung Cancer Society. This research is neither intended for the benefit of any particular private company nor conducted under any restrictions from these sources. The authors thank Dr. Arata Takahashi, Department of Health Policy and Management, Faculty of Medicine, Keio University, for his effort of data management. We thank Dr. Tomohiro Takehara, Department of Respiratory Medicine, Tokyo Saiseikai Central Hospital, for his effort in project administration. The authors thank Editage ( http://www.editage.com ) for editing and reviewing this manuscript for English language. Funding Information: This work was supported by the Japan Agency for Medical Research and Development (grant number 17lk1010016h0002), the Ministry of Health, Labour and Welfare Science Research Grant (grant number 201708003B), the Japan Science and Technology Agency (grant number JPMJRC1503), and the Japan Lung Cancer Society. This research is neither intended for the benefit of any particular private company nor conducted under any restrictions from these sources. The authors thank Dr. Arata Takahashi, Department of Health Policy and Management, Faculty of Medicine, Keio University, for his effort of data management. We thank Dr. Tomohiro Takehara, Department of Respiratory Medicine, Tokyo Saiseikai Central Hospital, for his effort in project administration. The authors thank Editage (http://www.editage.com) for editing and reviewing this manuscript for English language. Disclosure: Sojiro Kusumoto reports receiving personal fees from AstraZeneca KK, Taiho Pharmaceutical Co. Ltd., Chugai Pharmaceutical Co. Ltd., Kracie Pharmaceutical Co. Ltd. and Novartis Pharma KK outside of the submitted work. Noriko Yanagitani reports receiving personal fees from Chugai Pharmaceutical Co. Ltd., Pfizer Inc., Ono Pharmaceutical Co. Ltd., Bristol-Myers Squibb Co. Ltd., Takeda Pharmaceutical Co., Ltd., Eli Lilly Japan KK, AstraZeneca KK, Bayer Yakuhin, Ltd. outside of the submitted work. Yoshihiko Sakata reports receiving personal fees from Chugai Pharmaceutical Co. Ltd., AstraZeneca KK, Boehringer Ingelheim Japan Inc., Bristol-Myers Squibb Co. Ltd., Eli Lilly Japan KK, Merck Sharp & Dohme KK, Taiho Pharmaceutical Co. Ltd., Takeda Pharmaceutical Co., Ltd., Akihiko Gemma reports receiving personal fees from Merck Sharp & Dohme KK, Chugai Pharmaceutical Co. Ltd., Ono Pharmaceutical Co. Ltd. outside of the submitted work. Motoko Tachihara reports receiving grants and personal fees from AstraZeneca KK and personal fees from Chugai Pharmaceutical Co. Ltd., Eli Lilly Japan KK, Merck Sharp & Dohme KK, Nippon Kayaku Co. Ltd., Takeda Pharmaceutical Co., Ltd., Ono Pharmaceutical Co. Ltd., Bristol-Myers Squibb Co. Ltd., Taiho Pharmaceutical Co. Ltd., Pfizer Inc. outside of the submitted work. Daichi Fujimoto reports receiving grants and personal fees from AstraZeneca KK and Boehringer Ingelheim Japan Inc. and personal fees from Ono Pharmaceutical Co. Ltd., Bristol-Myers Squibb Co. Ltd., Taiho Pharmaceutical Co. Ltd., Chugai Pharmaceutical Co. Ltd., Merck Sharp & Dohme KK, Eli Lilly Japan KK, Novartis Pharma KK and Takeda Pharmaceutical Co., Ltd., outside of the submitted work. Junichi Shimizu personal fees from Ono Pharmaceutical Co. Ltd., Bristol-Myers Squibb Co. Ltd., Taiho Pharmaceutical Co. Ltd., Chugai Pharmaceutical Co. Ltd., Merck Sharp & Dohme KK, Novartis Pharma KK, Takeda Pharmaceutical Co. MSD K.K., Amgen Co. Ltd., Novartis Pharma K.K. and Pfizer Japan Inc. outside of the submitted work. Kiichiro Ninomiya personal fees from AstraZeneca KK, Boehringer Ingelheim Japan Inc., Kyowa Kirin Co. Ltd., Eli Lilly Japan KK, Chugai Pharmaceutical Co. Ltd., Nippon Kayaku Co. Ltd., Taiho Pharmaceutical Co. Ltd., Merck Sharp & Dohme KK, Ono Pharmaceutical Co. Ltd., Novartis Pharma KK, Takeda Pharmaceutical Co., Pfizer Japan Inc. and Bristol-Myers Squibb Co. Ltd. outside of the submitted work. Koichi Minato reports receiving grants from Taiho Pharmaceutical Co. Ltd., Ono Pharmaceutical Co. Ltd. and Parexel International outside of the submitted work. Hiroyuki Sakashita reports receiving grants from Ono Pharmaceutical Co. Ltd., Chugai Pharmaceutical Co. Ltd., AstraZeneca KK, Taiho Pharmaceutical Co. Ltd., Boehringer Ingelheim Japan Inc., Novartis Pharma KK, Merck & Co. Inc. and SBI Pharmaceuticals outside of the submitted work. Masahiro Seike reports receiving grants and personal fees from Merck Sharp & Dohme KK, Taiho Pharmaceutical Co. Ltd., Chugai Pharmaceutical Co. Ltd., Eli Lilly Japan KK and Nippon Kayaku Co. Ltd. and personal fees from AstraZeneca KK, Ono Pharmaceutical Co. Ltd., Bristol-Myers Squibb Co. Ltd., Eli Lilly Japan KK, Nippon Kayaku Co. Ltd., Daiichi Sankyo Co. Ltd., Kyowa Kirin Co. Ltd. and Takeda Pharmaceutical Co., Ltd. outside of submitted work. Tetsuya Mitsudomi reports receiving grants and personal fees from AstraZeneca KK, Ono Pharmaceutical Co. Ltd., Chugai Pharmaceutical Co. Ltd., receiving grants from Merck Sharp & Dohme KK, and personal fees from Bristol-Myers Squibb Co. Ltd outside of submitted work. Masahide Mori reports receiving grants and personal fees from Ono Pharmaceutical Co. Ltd., Bristol-Myers Squibb Co. Ltd., Chugai Pharmaceutical Co. Ltd., grant from Delta-fly Pharma Inc., and personal fees from AstraZeneca KK, Eli Lilly Japan KK, Nippon Kayaku Co. Ltd., Novartis Pharma KK, Takeda Pharmaceutical Co., Pfizer Japan Inc., Boehringer Ingelheim Japan Inc., Kyowa Kirin Co. Ltd., Daiichi Sankyo Co. Ltd., Taiho Pharmaceutical Co. Ltd., Shionogi Pharmaceutical Co. Ltd. outside of the submitted work. Yuki Sato reports receiving personal fees from AstraZeneca KK, Ono Pharmaceutical Co. Ltd., Chugai Pharmaceutical Co. Ltd., Eli Lilly Japan KK, Nippon Kayaku Co. Ltd., Novartis Pharma KK, Takeda Pharmaceutical Co., Pfizer Japan Inc., Kyowa Kirin Co. Ltd., Bristol-Myers Squibb Co. Ltd., Merck Sharp & Dohme KK, Taiho Pharmaceutical Co. Ltd., Takeda Pharmaceutical Co. outside of the submitted work. Keiichi Fujiwara reports receiving personal fees from Merck Sharp & Dohme KK, AstraZeneca KK, Ono Pharmaceutical Co. Ltd., Sanofi KK and Eli Lilly Japan KK outside of the submitted work. Tetsunari Hase reports grant and personal fees from Chugai Pharmaceutical Co. Ltd., AstraZeneca KK, Taiho Pharmaceutical Co. Ltd., grant from Novartis Pharma KK, personal fees from Merck Sharp & Dohme KK, Bristol-Myers Squibb Co. Ltd., Eli Lilly Japan KK, Ono Pharmaceutical Co. Ltd., Kyowa Kirin Co. Ltd., Nippon Kayaku Co. Ltd., Boehringer Ingelheim Japan Inc., Pfizer Japan Inc. and Takeda Pharmaceutical Co. Hidehito Horinouchi reports grant and personal fees from Chugai Pharmaceutical Co. Ltd., AstraZeneca KK, Novartis Pharma KK, Ono Pharmaceutical Co. Ltd., Bristol-Myers Squibb Co. Ltd., Merck Sharp & Dohme KK, Daiichi Sankyo Co. Ltd., Roche, receiving grant from Merck Biopharma Co. Ltd., AbbVie Inc., and Genomic Health Inc., receiving personal fee from Eli Lilly Japan KK, Ono Pharmaceutical Co. Ltd., Kyowa Kirin Co. Ltd. outside of submitted work. Kazuhiko Shibata reports receiving personal fees from AstraZeneca KK, Chugai Pharmaceutical Co. Ltd. and Bristol-Myers Squibb Co. Ltd. outside of the submitted work. The remaining authors declare no conflict of interest. Publisher Copyright: © 2022 The Authors
PY - 2022/11
Y1 - 2022/11
N2 - Introduction: Pembrolizumab is a programmed death-ligand 1 inhibitor that was initially indicated for monotherapy in patients with advanced lung cancer. The Japanese Lung Cancer Society conducted an observational study on pembrolizumab using confirmative data obtained through postmarketing all-case surveillance (PMACS), which was performed by a pharmaceutical company under the Japanese law in 2017. Methods: This multicenter observational study was conducted by the Japanese Lung Cancer Society using PMACS data with the newly created central registration system regarding patients with NSCLC who received pembrolizumab monotherapy between February 1, 2017 and June 30, 2017; a new database was created by adding the clinical information regarding prognosis for 3 years after therapy to the existing data collected by PMACS. Results: A total of 300 patients from 43 facilities were enrolled in this study. The median overall survival and progression-free survival after pembrolizumab initiation were 558 and 188 days, respectively. Moreover, the 1- and 3-year survival rates were 58.9% and 33.7%, respectively. Results of multivariate analysis revealed performance status (p < 0.0001), histology (p = 0.0118), previous chemotherapy (p = 0.0007), programmed death-ligand 1 expression status (p = 0.0195), and previous steroid use (p = 0.0460) as significant factors that affected overall survival. The toxicity profile was similar to that previously reported. Conclusions: In this first attempt to use PMACS data, we successfully collected clinical information and found the real-world efficacy and safety of pembrolizumab.
AB - Introduction: Pembrolizumab is a programmed death-ligand 1 inhibitor that was initially indicated for monotherapy in patients with advanced lung cancer. The Japanese Lung Cancer Society conducted an observational study on pembrolizumab using confirmative data obtained through postmarketing all-case surveillance (PMACS), which was performed by a pharmaceutical company under the Japanese law in 2017. Methods: This multicenter observational study was conducted by the Japanese Lung Cancer Society using PMACS data with the newly created central registration system regarding patients with NSCLC who received pembrolizumab monotherapy between February 1, 2017 and June 30, 2017; a new database was created by adding the clinical information regarding prognosis for 3 years after therapy to the existing data collected by PMACS. Results: A total of 300 patients from 43 facilities were enrolled in this study. The median overall survival and progression-free survival after pembrolizumab initiation were 558 and 188 days, respectively. Moreover, the 1- and 3-year survival rates were 58.9% and 33.7%, respectively. Results of multivariate analysis revealed performance status (p < 0.0001), histology (p = 0.0118), previous chemotherapy (p = 0.0007), programmed death-ligand 1 expression status (p = 0.0195), and previous steroid use (p = 0.0460) as significant factors that affected overall survival. The toxicity profile was similar to that previously reported. Conclusions: In this first attempt to use PMACS data, we successfully collected clinical information and found the real-world efficacy and safety of pembrolizumab.
KW - Immune checkpoint inhibitor
KW - Immune-related adverse events
KW - Pembrolizumab
KW - Real-world data
UR - http://www.scopus.com/inward/record.url?scp=85139825498&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85139825498&partnerID=8YFLogxK
U2 - 10.1016/j.jtocrr.2022.100404
DO - 10.1016/j.jtocrr.2022.100404
M3 - Article
AN - SCOPUS:85139825498
SN - 2666-3643
VL - 3
JO - JTO Clinical and Research Reports
JF - JTO Clinical and Research Reports
IS - 11
M1 - 100404
ER -