TY - JOUR
T1 - Programmed cell death-ligand 1 expression and efficacy of cisplatin-based chemotherapy in lung cancer
T2 - A sub-analysis of data from the two Okayama Lung Cancer Study Group prospective feasibility studies
AU - Nishii, Kazuya
AU - Hotta, Katsuyuki
AU - Ninomiya, Kiichiro
AU - Kato, Yuka
AU - Ichihara, Eiki
AU - Ohashi, Kadoaki
AU - Ninomiya, Takashi
AU - Kubo, Toshio
AU - Rai, Kanmei
AU - Tabata, Masahiro
AU - Maeda, Yoshinobu
AU - Kiura, Katsuyuki
N1 - Funding Information:
Kazuya Nishii has no conflicts of interest. Katsuyuki Hotta received honoraria from AstraZeneca and MSD, as well as research funding from Chugai Pharmaceutical, Eli Lilly Japan, Bristol-Myers Squibb, and Astellas Pharma. Katsuyuki Kiura received honoraria from AstraZeneca and Eli Lilly Japan; research funding from Boehringer Ingelheim, Ono Pharmaceutical, and Pfizer; and donations from Chugai Pharmaceutical, Taiho Pharmaceutical, Ono Pharmaceutical, Nippon Kayaku, and Boehringer Ingelheim.
Publisher Copyright:
© 2019 The Japanese Respiratory Society
PY - 2019/9
Y1 - 2019/9
N2 - Background: Cisplatin-based chemotherapy remains the mainstay treatment for advanced lung cancer; however, it remains controversial whether the efficacy of chemotherapy can be modulated by the immune-checkpoint status. In this study, we investigated the relationship between programmed cell death-ligand 1 (PD-L1) expression status and the efficacy of cisplatin-based chemotherapy by using individual patient data and pathological specimens obtained during our two previously performed prospective studies on the feasibility of short-term low-volume hydration in patients with advanced lung cancer who received cisplatin-based chemotherapy. Methods: Among 91 patients who participated in the two aforementioned trials, those with assessable tumor specimens were included in this sub-analysis. PD-L1 expression levels were determined using immunohistochemical staining, while the Response Evaluation Criteria in Solid Tumors, version 1.1, were used for determining treatment efficacy. Results: Thirty-two patients were investigated. PD-L1 expression was observed in 8 patients (25.0%; the PD-L1-positive group), with 2 exhibiting a PD-L1 expression of 50% or more. None of the patients in the PD-L1-positive group responded to treatment, while the overall response rate in the PD-L1-negative group was 20.8% (5 of 24; P = 0.296). Both the progression-free survival and overall survival rates were worse in the PD-L1-positive group than in the PD-L1-negative group (3.7 vs. 5.9 months [P = 0.018] and 5.8 vs. 37.3 months [P = 0.070], respectively). Conclusion: PD-L1 expression was negatively correlated with survival in patients receiving cisplatin-based chemotherapy.
AB - Background: Cisplatin-based chemotherapy remains the mainstay treatment for advanced lung cancer; however, it remains controversial whether the efficacy of chemotherapy can be modulated by the immune-checkpoint status. In this study, we investigated the relationship between programmed cell death-ligand 1 (PD-L1) expression status and the efficacy of cisplatin-based chemotherapy by using individual patient data and pathological specimens obtained during our two previously performed prospective studies on the feasibility of short-term low-volume hydration in patients with advanced lung cancer who received cisplatin-based chemotherapy. Methods: Among 91 patients who participated in the two aforementioned trials, those with assessable tumor specimens were included in this sub-analysis. PD-L1 expression levels were determined using immunohistochemical staining, while the Response Evaluation Criteria in Solid Tumors, version 1.1, were used for determining treatment efficacy. Results: Thirty-two patients were investigated. PD-L1 expression was observed in 8 patients (25.0%; the PD-L1-positive group), with 2 exhibiting a PD-L1 expression of 50% or more. None of the patients in the PD-L1-positive group responded to treatment, while the overall response rate in the PD-L1-negative group was 20.8% (5 of 24; P = 0.296). Both the progression-free survival and overall survival rates were worse in the PD-L1-positive group than in the PD-L1-negative group (3.7 vs. 5.9 months [P = 0.018] and 5.8 vs. 37.3 months [P = 0.070], respectively). Conclusion: PD-L1 expression was negatively correlated with survival in patients receiving cisplatin-based chemotherapy.
KW - Chemotherapy
KW - Cisplatin
KW - Lung cancer
KW - PD-L1
UR - http://www.scopus.com/inward/record.url?scp=85067045576&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85067045576&partnerID=8YFLogxK
U2 - 10.1016/j.resinv.2019.04.004
DO - 10.1016/j.resinv.2019.04.004
M3 - Article
C2 - 31186170
AN - SCOPUS:85067045576
SN - 2212-5345
VL - 57
SP - 460
EP - 465
JO - Respiratory Investigation
JF - Respiratory Investigation
IS - 5
ER -