TY - JOUR
T1 - Nivolumab treatment of elderly Japanese patients with non-small cell lung cancer
T2 - Subanalysis of a real-world retrospective observational study (CA209-9CR)
AU - Okishio, Kyoichi
AU - Morita, Ryo
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 - Yada, Nobumichi
AU - Ohe, Yuichiro
N1 - Funding Information:
Medical Writing), for providing medical writing support, which was funded by ONO Pharmaceutical Co, Ltd and Bristol-Myers Squibb K.K. and Hidehito Horinouchi (National Cancer Center, Tokyo, Japan) for advice on the conduct of the study. The authors also thank Mebix for conducting the research operation, construction of the electronic data capture, data management and statistical analysis in their role as the contract research organisation.
Funding Information:
This study (CA209-9CR) was company-initiated and funded by ONO Pharmaceutical Co, Ltd and Bristol-Myers Squibb K.K. 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.
Funding Information:
Funding This study (CA209-9CR) was company initiated and funded by ONO Pharmaceutical Co, Ltd and Bristol-Myers Squibb K.K. 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.
Publisher Copyright:
© Author (s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ on behalf of the European Society for Medical Oncology.
PY - 2020/7/20
Y1 - 2020/7/20
N2 - Objectives We conducted a subanalysis of data from the multicentre, retrospective observational Nivolumab Japan Real World (CA209-9CR) study to evaluate nivolumab effectiveness and safety in elderly patients (aged ≥75 years) with advanced/metastatic non-small cell lung cancer. Materials and methods Medical record data of patients initiating nivolumab treatment between April 2016 and December 2016 were collected using electronic data capture from 23 cancer hospitals in Japan between March 2017 and August 2018. Nivolumab treatment data were collected to investigate the treatment patterns by age group (<75 and ≥75 years), and the effectiveness and safety of nivolumab treatment. Results Of the 901 patients evaluated, 178 (19.8%) were aged ≥75 years. Overall, patients received a median of five nivolumab treatments regardless of age group. Comparable progression-free survival was observed, with a median of 2.1 months in patients aged <75 years and 2.1 months in patients aged ≥75 years (p=0.5441). No significant differences were found in duration of response, overall response rate or disease control rate between the two age groups. Median overall survival in patients aged <75 and ≥75 years was 14.7 months and 12.3 months, respectively. Grade ≥3 adverse events (AEs) occurred in 29.2% and 28.1% of patients aged <75 and ≥75 years, respectively. Immune-related AEs decreased slightly with increasing age; time to onset and rates of improvement were similar for patients aged <75 and ≥75 years. The most common grade 3-4 AEs were interstitial lung disease in both age groups (4.0% in patients aged <75 years and 2.8% in those aged ≥75 years). Poor performance status was associated with worse outcomes in both age groups. Conclusion Based on Japanese real-world data, the effectiveness and safety of nivolumab were confirmed regardless of age.
AB - Objectives We conducted a subanalysis of data from the multicentre, retrospective observational Nivolumab Japan Real World (CA209-9CR) study to evaluate nivolumab effectiveness and safety in elderly patients (aged ≥75 years) with advanced/metastatic non-small cell lung cancer. Materials and methods Medical record data of patients initiating nivolumab treatment between April 2016 and December 2016 were collected using electronic data capture from 23 cancer hospitals in Japan between March 2017 and August 2018. Nivolumab treatment data were collected to investigate the treatment patterns by age group (<75 and ≥75 years), and the effectiveness and safety of nivolumab treatment. Results Of the 901 patients evaluated, 178 (19.8%) were aged ≥75 years. Overall, patients received a median of five nivolumab treatments regardless of age group. Comparable progression-free survival was observed, with a median of 2.1 months in patients aged <75 years and 2.1 months in patients aged ≥75 years (p=0.5441). No significant differences were found in duration of response, overall response rate or disease control rate between the two age groups. Median overall survival in patients aged <75 and ≥75 years was 14.7 months and 12.3 months, respectively. Grade ≥3 adverse events (AEs) occurred in 29.2% and 28.1% of patients aged <75 and ≥75 years, respectively. Immune-related AEs decreased slightly with increasing age; time to onset and rates of improvement were similar for patients aged <75 and ≥75 years. The most common grade 3-4 AEs were interstitial lung disease in both age groups (4.0% in patients aged <75 years and 2.8% in those aged ≥75 years). Poor performance status was associated with worse outcomes in both age groups. Conclusion Based on Japanese real-world data, the effectiveness and safety of nivolumab were confirmed regardless of age.
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U2 - 10.1136/esmoopen-2019-000656
DO - 10.1136/esmoopen-2019-000656
M3 - Article
C2 - 32690620
AN - SCOPUS:85088351468
SN - 2059-7029
VL - 5
JO - ESMO Open
JF - ESMO Open
IS - 4
M1 - e000656
ER -