TY - JOUR
T1 - Influence of age on the efficacy of immune checkpoint inhibitors in advanced cancers
T2 - a systematic review and meta-analysis
AU - Ninomiya, Kiichiro
AU - Oze, Isao
AU - Kato, Yuka
AU - Kubo, Toshio
AU - Ichihara, Eiki
AU - Rai, Kanmei
AU - Ohashi, Kadoaki
AU - Kozuki, Toshiyuki
AU - Tabata, Masahiro
AU - Maeda, Yoshinobu
AU - Kiura, Katsuyuki
AU - Hotta, Katsuyuki
N1 - Funding Information:
The authors whose names are listed immediately below report the following details of affiliation or involvement in an organisation or entity with a financial or non-financial interest in the subject matter or materials discussed in this manuscript. KN has received honoraria outside the current work from AstraZeneca, BMS, Chugai Pharmaceutical, Ono Pharmaceutical and MSD. KH has received honoraria outside the current work from AstraZeneca, Ono Pharmaceutical, BMS, MSD, Boehringer-Ingelheim and Chugai Pharmaceutical. KH has received grants and personal fees from AstraZeneca, grants and personal fees from Eli Lilly, grants and personal fees from Bristol-Myers Squibb, personal fees from MSD, personal fees from Ono Pharmaceutical, personal fees from Nippon Kayaku, personal fees from Taiho pharmaceutical, personal fees from Novartis, personal fees from Daiichi-Sankyo, personal fees from Kyorin, personal fees from Kyowa-Kirin, personal fees from Boehringer Ingelheim, grants from Astellas, and grants and personal fees from Chugai pharmaceutical outside the submitted work. EI has recieved honoraria outside the current work from AstraZeneca, Eli Lilly Japan, Boehringer-Ingelheim and Chugai Pharmaceutical. EI also has received additional research funding outside the current work from Eli Lilly Japan and MSD. KK has received honoraria outside the current work from AstraZeneca and Chugai Pharmaceutical. All the other authors declare no conflicts of interest regarding this study.
Publisher Copyright:
© 2019, © 2019 Acta Oncologica Foundation.
PY - 2020/3/3
Y1 - 2020/3/3
N2 - Background: Immune checkpoint inhibitors (ICIs) represent a paradigm shift in the development of cancer treatment. However, it remains to be clarified whether the benefits that they confer differ according to patient age. We conducted a systematic review and meta-analysis to assess age differences in the benefits of ICI treatment. Methods: We systematically searched the PubMed database for randomised controlled trials of ICIs, including PD-1, PD-L1 and CTLA-4 inhibitors across multiple cancer types, such as melanoma, lung cancer and gastric cancer. We extracted trials including hazard ratios (HRs) for death stratified by patient age (cut-off age, 65 years). The primary objective of this study was to assess the difference in ICI efficacy between younger and older patients. We calculated pooled HRs and 95% confidence intervals (CIs) for younger and older cancer patients, and assessed data heterogeneity. Results: We identified 3999 studies in our search. Of these, 24 eligible randomised trials, including a total of 8157 (57%) younger and 6104 (43%) older cancer patients, fulfilled the criteria for our study and were thus further analysed. The pooled HRs of the younger and older patients were 0.76 (95% CI: 0.69–0.84) and 0.80 (95% CI: 0.71–0.86), respectively; the difference in ICI efficacy between younger and older cancer patients was not significant (p =.82). Regarding the PD-1 and PD-L1 inhibitors, the survival benefit was similar in both age groups (HR: 0.74; p =.96), whereas for the CTLA-4 inhibitors, there tended to be less survival benefit for older versus younger patients (HR: 0.90 and 0.77, respectively; p =.26). Conclusions: The survival benefit conferred by ICI was not age-dependent, amongst patients aged 65 years or younger. However, age-dependent benefits may vary amongst different types of ICIs.
AB - Background: Immune checkpoint inhibitors (ICIs) represent a paradigm shift in the development of cancer treatment. However, it remains to be clarified whether the benefits that they confer differ according to patient age. We conducted a systematic review and meta-analysis to assess age differences in the benefits of ICI treatment. Methods: We systematically searched the PubMed database for randomised controlled trials of ICIs, including PD-1, PD-L1 and CTLA-4 inhibitors across multiple cancer types, such as melanoma, lung cancer and gastric cancer. We extracted trials including hazard ratios (HRs) for death stratified by patient age (cut-off age, 65 years). The primary objective of this study was to assess the difference in ICI efficacy between younger and older patients. We calculated pooled HRs and 95% confidence intervals (CIs) for younger and older cancer patients, and assessed data heterogeneity. Results: We identified 3999 studies in our search. Of these, 24 eligible randomised trials, including a total of 8157 (57%) younger and 6104 (43%) older cancer patients, fulfilled the criteria for our study and were thus further analysed. The pooled HRs of the younger and older patients were 0.76 (95% CI: 0.69–0.84) and 0.80 (95% CI: 0.71–0.86), respectively; the difference in ICI efficacy between younger and older cancer patients was not significant (p =.82). Regarding the PD-1 and PD-L1 inhibitors, the survival benefit was similar in both age groups (HR: 0.74; p =.96), whereas for the CTLA-4 inhibitors, there tended to be less survival benefit for older versus younger patients (HR: 0.90 and 0.77, respectively; p =.26). Conclusions: The survival benefit conferred by ICI was not age-dependent, amongst patients aged 65 years or younger. However, age-dependent benefits may vary amongst different types of ICIs.
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U2 - 10.1080/0284186X.2019.1695062
DO - 10.1080/0284186X.2019.1695062
M3 - Review article
C2 - 31782328
AN - SCOPUS:85075715645
SN - 0284-186X
VL - 59
SP - 249
EP - 256
JO - Acta Oncologica
JF - Acta Oncologica
IS - 3
ER -