TY - JOUR
T1 - Chemoimmunotherapy Outcomes and Prognostic Factors in Patients with Advanced, Low PD-L1–Expressing Non–Small Cell Lung Cancer
AU - Hata, Tae
AU - Yamada, Tadaaki
AU - Goto, Yasuhiro
AU - Amano, Akihiko
AU - Negi, Yoshiki
AU - Watanabe, Satoshi
AU - Furuya, Naoki
AU - Oba, Tomohiro
AU - Ikoma, Tatsuki
AU - Nakao, Akira
AU - Tanimura, Keiko
AU - Taniguchi, Hirokazu
AU - Yoshimura, Akihiro
AU - Fukui, Tomoya
AU - Murata, Daiki
AU - Kaira, Kyoichi
AU - Shiotsu, Shinsuke
AU - Hibino, Makoto
AU - Okada, Asuka
AU - Chihara, Yusuke
AU - Kawachi, Hayato
AU - Kijima, Takashi
AU - Takayama, Koichi
N1 - Publisher Copyright:
©2025 The Authors.
PY - 2025/7
Y1 - 2025/7
N2 - Chemoimmunotherapy is recommended for patients with non–small cell lung cancer (NSCLC) with low PD-L1 expression, but the effect of additional immunotherapy is heterogeneous in this population. To identify patients who do not benefit from the addition of immune checkpoint inhibitors (ICI) to chemotherapy, we conducted a retrospective study at 19 institutions in Japan. We analyzed 851 patients with advanced NSCLC with a PD-L1 tumor proportion score of 1% to 49% who received chemoimmunotherapy (n = 504) or chemotherapy (n = 347) between March 2017 and June 2022. After adjustment by propensity score matching, the median overall survival (OS) was 22.3 months in the chemoimmunotherapy group and 17.0 months in the chemotherapy-alone group (P = 0.01). Multivariate analysis showed that among 12 clinical factors, liver metastases (P = 0.001) and history of antibiotic use (P = 0.02) were independently associated with shorter OS in the chemoimmunotherapy group. Patients with liver metastases (OS, P = 0.4; progression-free survival, P = 0.06) or history of antimicrobial use (OS, P = 0.24; progression-free survival, P = 0.09) did not benefit from the addition of ICI to chemotherapy. Patients with a history of antimicrobial use experienced more severe pneumonitis with chemoimmunotherapy than all patients (P = 0.04). This cohort study showed that liver metastases and prior antimicrobial therapy are the most important clinical factors that attenuate the efficacy of chemoimmunotherapy in patients with low PD-L1 expression.
AB - Chemoimmunotherapy is recommended for patients with non–small cell lung cancer (NSCLC) with low PD-L1 expression, but the effect of additional immunotherapy is heterogeneous in this population. To identify patients who do not benefit from the addition of immune checkpoint inhibitors (ICI) to chemotherapy, we conducted a retrospective study at 19 institutions in Japan. We analyzed 851 patients with advanced NSCLC with a PD-L1 tumor proportion score of 1% to 49% who received chemoimmunotherapy (n = 504) or chemotherapy (n = 347) between March 2017 and June 2022. After adjustment by propensity score matching, the median overall survival (OS) was 22.3 months in the chemoimmunotherapy group and 17.0 months in the chemotherapy-alone group (P = 0.01). Multivariate analysis showed that among 12 clinical factors, liver metastases (P = 0.001) and history of antibiotic use (P = 0.02) were independently associated with shorter OS in the chemoimmunotherapy group. Patients with liver metastases (OS, P = 0.4; progression-free survival, P = 0.06) or history of antimicrobial use (OS, P = 0.24; progression-free survival, P = 0.09) did not benefit from the addition of ICI to chemotherapy. Patients with a history of antimicrobial use experienced more severe pneumonitis with chemoimmunotherapy than all patients (P = 0.04). This cohort study showed that liver metastases and prior antimicrobial therapy are the most important clinical factors that attenuate the efficacy of chemoimmunotherapy in patients with low PD-L1 expression.
UR - https://www.scopus.com/pages/publications/105011627318
UR - https://www.scopus.com/pages/publications/105011627318#tab=citedBy
U2 - 10.1158/2767-9764.CRC-25-0157
DO - 10.1158/2767-9764.CRC-25-0157
M3 - Article
C2 - 40637162
AN - SCOPUS:105011627318
SN - 2767-9764
VL - 5
SP - 1203
EP - 1214
JO - Cancer Research Communications
JF - Cancer Research Communications
IS - 7
ER -