TY - JOUR
T1 - Significance of PD-L1 expression in the cytological samples of non-small cell lung cancer patients treated with immune checkpoint inhibitors
AU - Hara, Naofumi
AU - Ichihara, Eiki
AU - Harada, Daijiro
AU - Inoue, Koji
AU - Fujiwara, Keiichi
AU - Hosokawa, Shinobu
AU - Kishino, Daizo
AU - Haruyuki, Kawai
AU - Ochi, Nobuaki
AU - Oda, Naohiro
AU - Hotta, Katsuyuki
AU - Maeda, Yoshinobu
AU - Kiura, Katsuyuki
N1 - Funding Information:
EI received honoraria from Chugai Pharmaceutical. EI received additional research funding from MSD. KH received honoraria from Taiho Pharmaceutical, and Chugai Pharmaceutical. KH received additional research funding from MSD, and Chugai Pharmaceutical. TM received honoraria from Chugai Pharmaceutical, and Bristol–Myers Squibb. KK received honoraria from Chugai Pharmaceuticals. All other authors declare no conflicts of interest regarding this study.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2021/12
Y1 - 2021/12
N2 - Objectives: The programmed death-ligand 1 (PD-L1) tumor proportion score (TPS) in tumor tissue samples is an established clinical biomarker for non-small cell lung cancer (NSCLC). However, the significance of PD-L1 expression in other types of samples has not been fully investigated. Patients and methods: We conducted a multicenter retrospective cohort study of advanced NSCLC patients who received ICI treatment during the clinical course and investigated the effects of ICIs according to PD-L1 expression in cytology samples, including cell block and endobronchial ultrasound-guided (EBUS) transbronchial needle aspiration (TBNA) samples. Results: A total of 264 patients were included in this study: PD-L1 expression was determined in cell block or TBNA specimens in 55 patients, and in tissue samples in 209 patients. Among the former patients, the median progression-free survival (PFS) of those with a TPS for PD-L1 ≥ 50% was significantly longer compared to that of those with a TPS < 50% (6.5 vs. 1.9 months, respectively, p = 0.008). When the cutoff value was set at 1%, the median PFS was 4.2 months in patients with a TPS ≥ 1% and 1.5 months in patients with a TPS < 1% (p < 0.001). Conclusion: PD-L1 expression determined using cytology specimens predicts the efficacy of ICIs.
AB - Objectives: The programmed death-ligand 1 (PD-L1) tumor proportion score (TPS) in tumor tissue samples is an established clinical biomarker for non-small cell lung cancer (NSCLC). However, the significance of PD-L1 expression in other types of samples has not been fully investigated. Patients and methods: We conducted a multicenter retrospective cohort study of advanced NSCLC patients who received ICI treatment during the clinical course and investigated the effects of ICIs according to PD-L1 expression in cytology samples, including cell block and endobronchial ultrasound-guided (EBUS) transbronchial needle aspiration (TBNA) samples. Results: A total of 264 patients were included in this study: PD-L1 expression was determined in cell block or TBNA specimens in 55 patients, and in tissue samples in 209 patients. Among the former patients, the median progression-free survival (PFS) of those with a TPS for PD-L1 ≥ 50% was significantly longer compared to that of those with a TPS < 50% (6.5 vs. 1.9 months, respectively, p = 0.008). When the cutoff value was set at 1%, the median PFS was 4.2 months in patients with a TPS ≥ 1% and 1.5 months in patients with a TPS < 1% (p < 0.001). Conclusion: PD-L1 expression determined using cytology specimens predicts the efficacy of ICIs.
KW - Cytology
KW - EBUS-TBNA
KW - Immune checkpoint inhibitor
KW - Non-small cell lung cancer
KW - PD-L1 expression
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U2 - 10.1007/s00432-021-03615-5
DO - 10.1007/s00432-021-03615-5
M3 - Article
C2 - 33779840
AN - SCOPUS:85103417369
SN - 0171-5216
VL - 147
SP - 3749
EP - 3755
JO - Journal of Cancer Research and Clinical Oncology
JF - Journal of Cancer Research and Clinical Oncology
IS - 12
ER -