TY - JOUR
T1 - Impact of maintenance therapy following induction immunochemotherapy for untreated advanced non-small cell lung cancer patients
AU - Nakamura, Ryota
AU - Yamada, Tadaaki
AU - Morimoto, Kenji
AU - Nakao, Akira
AU - Goto, Yasuhiro
AU - Ogura, Yuri
AU - Takeda, Takayuki
AU - Takumi, Chieko
AU - Onoi, Keisuke
AU - Chihara, Yusuke
AU - Taniguchi, Ryusuke
AU - Yamada, Takahiro
AU - Hiranuma, Osamu
AU - Tanaka, Satomi
AU - Morimoto, Yoshie
AU - Iwasaku, Masahiro
AU - Tokuda, Shinsaku
AU - Kaneko, Yoshiko
AU - Uchino, Junji
AU - Takayama, Koichi
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/11
Y1 - 2022/11
N2 - Purpose: The primary objective of this study was to identify the potential predictors to assess the impact of maintenance therapy after induction immunochemotherapy in the real-world setting of patients with advanced non-small cell lung cancer (NSCLC). Methods: We retrospectively identified 152 patients with advanced NSCLC who received immunochemotherapy at 8 hospitals in Japan between January 2019 and December 2019. Patients who received at least four cycles of induction immunochemotherapy and one cycle of maintenance therapy with immune checkpoint inhibitors were included. We investigated the biomarkers for progression-free survival (PFS) for maintenance therapy after induction immunochemotherapy. Results: Out of the 92 patients with advanced NSCLC included in the study, 42 received maintenance therapy with cytotoxic agents, whereas 50 received maintenance therapy without cytotoxic agents. Among those who received maintenance therapy without cytotoxic agents, responders to prior immunochemotherapy had significantly longer PFS than non-responders (p = 0.004), except those with maintenance therapy with cytotoxic agents. In non-responders to prior immunochemotherapy, patients with maintenance therapy with cytotoxic agents had significantly longer PFS than those with maintenance therapy without cytotoxic agents (log-rank p = 0.007), whereas, among responders to prior immunochemotherapy, there was no significant difference in PFS for different maintenance regimens (log-rank p = 0.31). Conclusions: This retrospective study showed that response to prior immunochemotherapy was associated with clinical outcomes among patients with advanced NSCLC who received maintenance therapy.
AB - Purpose: The primary objective of this study was to identify the potential predictors to assess the impact of maintenance therapy after induction immunochemotherapy in the real-world setting of patients with advanced non-small cell lung cancer (NSCLC). Methods: We retrospectively identified 152 patients with advanced NSCLC who received immunochemotherapy at 8 hospitals in Japan between January 2019 and December 2019. Patients who received at least four cycles of induction immunochemotherapy and one cycle of maintenance therapy with immune checkpoint inhibitors were included. We investigated the biomarkers for progression-free survival (PFS) for maintenance therapy after induction immunochemotherapy. Results: Out of the 92 patients with advanced NSCLC included in the study, 42 received maintenance therapy with cytotoxic agents, whereas 50 received maintenance therapy without cytotoxic agents. Among those who received maintenance therapy without cytotoxic agents, responders to prior immunochemotherapy had significantly longer PFS than non-responders (p = 0.004), except those with maintenance therapy with cytotoxic agents. In non-responders to prior immunochemotherapy, patients with maintenance therapy with cytotoxic agents had significantly longer PFS than those with maintenance therapy without cytotoxic agents (log-rank p = 0.007), whereas, among responders to prior immunochemotherapy, there was no significant difference in PFS for different maintenance regimens (log-rank p = 0.31). Conclusions: This retrospective study showed that response to prior immunochemotherapy was associated with clinical outcomes among patients with advanced NSCLC who received maintenance therapy.
KW - Immune checkpoint inhibitor
KW - Immunochemotherapy
KW - Maintenance therapy
KW - Non-small cell lung cancer
KW - Pemetrexed
UR - https://www.scopus.com/pages/publications/85119987231
UR - https://www.scopus.com/pages/publications/85119987231#tab=citedBy
U2 - 10.1007/s00432-021-03866-2
DO - 10.1007/s00432-021-03866-2
M3 - Article
C2 - 34825950
AN - SCOPUS:85119987231
SN - 0171-5216
VL - 148
SP - 2985
EP - 2994
JO - Journal of Cancer Research and Clinical Oncology
JF - Journal of Cancer Research and Clinical Oncology
IS - 11
ER -