TY - JOUR
T1 - Immune checkpoint inhibitor-induced interstitial lung disease with and without CTLA-4 regimen in non-small cell lung cancer patients and PD-L1 < 1 %
T2 - A multicenter, retrospective study
AU - Murata, Daiki
AU - Azuma, Koichi
AU - Murotani, Kenta
AU - Ito, Kazuhiro
AU - Nomizo, Takashi
AU - Yamada, Kazuhiko
AU - Imabayashi, Tatsuya
AU - Iwanaga, Kentaro
AU - Chibana, Kenji
AU - Ota, Takayo
AU - Nishii, Yuuya
AU - Nakao, Akira
AU - Okada, Asuka
AU - Hamai, Kosuke
AU - Tanimura, Keiko
AU - Yoshimine, Kohei
AU - Tamura, Yosuke
AU - Takaki, Ryuichiro
AU - Goto, Yasuhiro
AU - Hibino, Makoto
AU - Oba, Tomohiro
AU - Sumi, Toshiyuki
AU - Kaneda, Hiroyasu
AU - Nishioka, Naoya
AU - Yamada, Tadaaki
AU - Takayama, Koichi
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/11
Y1 - 2025/11
N2 - Background: For patients with advanced or recurrent non-small cell lung cancer (NSCLC) and PD-L1 < 1 %, a combination of an anti-CTLA-4 and anti-PD-1 antibody with and without platinum-based chemotherapy are used as a first-line treatment. Although the combined use of anti-CTLA-4 antibody has favorable therapeutic efficacy, increased incidence and severity of immune-related adverse events, including immune checkpoint inhibitor-induced interstitial lung disease (ICI-ILD), remains a challenge. Methods: A multicenter retrospective study of patients with advanced or recurrent NSCLC and PD-L1 < 1 % who received immune checkpoint inhibitors as a first-line treatment. The primary and secondary endpoints were incidence and prognostic impact, respectively, of ICI-ILD. Results: The cohort included 376 patients, with 119 and 257 receiving a CTLA-4 regimen and non-CTLA-4 regimen, respectively. The ICI-ILD incidence tended to be higher in patients treated with the CTLA-4 regimen, but the difference from the non-CTLA-4 regimen was not significant. Patients with ICI-ILD treated with the CTLA-4 regimen tended to have longer progression-free survival and overall survival than those who received non-CLTLA-4 treatment, but the difference was not significant. Conclusion: For patients with NSCLC and PD-L1 < 1 %, the incidence of ICI-ILD tended to be higher in CTLA-4 regimens, and survival of patients with ICI-ILD tended to be longer for CTLA-4 regimens than for non-CTLA-4 regimens. Although the incidence of ICI-ILD in patients given CTLA-4 regimens tended to be higher than in those given non-CTLA-4 regimens, development of ICI-ILD does not necessarily negatively impact survival.
AB - Background: For patients with advanced or recurrent non-small cell lung cancer (NSCLC) and PD-L1 < 1 %, a combination of an anti-CTLA-4 and anti-PD-1 antibody with and without platinum-based chemotherapy are used as a first-line treatment. Although the combined use of anti-CTLA-4 antibody has favorable therapeutic efficacy, increased incidence and severity of immune-related adverse events, including immune checkpoint inhibitor-induced interstitial lung disease (ICI-ILD), remains a challenge. Methods: A multicenter retrospective study of patients with advanced or recurrent NSCLC and PD-L1 < 1 % who received immune checkpoint inhibitors as a first-line treatment. The primary and secondary endpoints were incidence and prognostic impact, respectively, of ICI-ILD. Results: The cohort included 376 patients, with 119 and 257 receiving a CTLA-4 regimen and non-CTLA-4 regimen, respectively. The ICI-ILD incidence tended to be higher in patients treated with the CTLA-4 regimen, but the difference from the non-CTLA-4 regimen was not significant. Patients with ICI-ILD treated with the CTLA-4 regimen tended to have longer progression-free survival and overall survival than those who received non-CLTLA-4 treatment, but the difference was not significant. Conclusion: For patients with NSCLC and PD-L1 < 1 %, the incidence of ICI-ILD tended to be higher in CTLA-4 regimens, and survival of patients with ICI-ILD tended to be longer for CTLA-4 regimens than for non-CTLA-4 regimens. Although the incidence of ICI-ILD in patients given CTLA-4 regimens tended to be higher than in those given non-CTLA-4 regimens, development of ICI-ILD does not necessarily negatively impact survival.
KW - Chemokine
KW - Cytokine
KW - Immune checkpoint inhibitor
KW - Interstitial lung disease
KW - NSCLC
UR - https://www.scopus.com/pages/publications/105017722410
UR - https://www.scopus.com/pages/publications/105017722410#tab=citedBy
U2 - 10.1016/j.lungcan.2025.108772
DO - 10.1016/j.lungcan.2025.108772
M3 - Article
C2 - 41046781
AN - SCOPUS:105017722410
SN - 0169-5002
VL - 209
JO - Lung Cancer
JF - Lung Cancer
M1 - 108772
ER -