TY - JOUR
T1 - Predictive clinical parameters for the response of nivolumab in pretreated advanced non-small-cell lung cancer
AU - Oya, Yuko
AU - Yoshida, Tatsuya
AU - Kuroda, Hiroaki
AU - Mikubo, Masashi
AU - Kondo, Chiaki
AU - Shimizu, Junichi
AU - Horio, Yoshitsugu
AU - Sakao, Yukinori
AU - Hida, Toyoaki
AU - Yatabe, Yasushi
N1 - Publisher Copyright:
© Oya et al.
PY - 2017
Y1 - 2017
N2 - Background: Nivolumab offers a superior survival benefit over docetaxel in patients with advanced, previously treated non-small-cell lung cancer (NSCLC). An association between programmed cell death ligand-1 (PD-L1) expression and the efficacy of nivolumab has been reported in many studies. However, the association between the clinical parameters and efficacy of nivolumab remains unclear in advanced NSCLC patients. Results: Among 124 patients, 108 (88%) were performance status (PS) 0 to 1. PD-L1 expression was assessed in 89 patients, with 51 (57%) patients having PD-L1 positive expression. In all patients, the objective response rate (ORR) in patients with elevated CRP levels (≥ 1 mg/dl) was significantly worse than those without elevated CRP levels ( < 1 mg/dl) (8.3 vs 23.4%, p = 0.0180). The PS (≥ 2), smoking index ( < 400), CRP levels (≥ 1 mg/dl) and LDH (≥ 245 IU/L) were significantly associated with a shorter PFS and OS in patients treated with nivolumab. Multivariate analyses showed that the PS (≥ 2), smoking index ( < 400), CRP levels (≥ 1 mg/dl) and LDH (≥ 245 IU/L) and PD-L1 expression were significant factors associated with a longer PFS of nivolumab. Materials and Methods: We retrospectively analyzed 124 patients who received nivolumab as a subsequent treatment. The patient characteristics, laboratory data at baseline (C-reactive protein [CRP] and lactate dehydrogenase [LDH]), PD-L1 expression, nivolumab response, progression-free survival (PFS), and overall survival (OS) were evaluated. Conclusions: Clinical parameters, such as PS, serum CRP, serum LDH, and smoking status, were significantly associated with the response duration and survival in patients treated with nivolumab.
AB - Background: Nivolumab offers a superior survival benefit over docetaxel in patients with advanced, previously treated non-small-cell lung cancer (NSCLC). An association between programmed cell death ligand-1 (PD-L1) expression and the efficacy of nivolumab has been reported in many studies. However, the association between the clinical parameters and efficacy of nivolumab remains unclear in advanced NSCLC patients. Results: Among 124 patients, 108 (88%) were performance status (PS) 0 to 1. PD-L1 expression was assessed in 89 patients, with 51 (57%) patients having PD-L1 positive expression. In all patients, the objective response rate (ORR) in patients with elevated CRP levels (≥ 1 mg/dl) was significantly worse than those without elevated CRP levels ( < 1 mg/dl) (8.3 vs 23.4%, p = 0.0180). The PS (≥ 2), smoking index ( < 400), CRP levels (≥ 1 mg/dl) and LDH (≥ 245 IU/L) were significantly associated with a shorter PFS and OS in patients treated with nivolumab. Multivariate analyses showed that the PS (≥ 2), smoking index ( < 400), CRP levels (≥ 1 mg/dl) and LDH (≥ 245 IU/L) and PD-L1 expression were significant factors associated with a longer PFS of nivolumab. Materials and Methods: We retrospectively analyzed 124 patients who received nivolumab as a subsequent treatment. The patient characteristics, laboratory data at baseline (C-reactive protein [CRP] and lactate dehydrogenase [LDH]), PD-L1 expression, nivolumab response, progression-free survival (PFS), and overall survival (OS) were evaluated. Conclusions: Clinical parameters, such as PS, serum CRP, serum LDH, and smoking status, were significantly associated with the response duration and survival in patients treated with nivolumab.
UR - http://www.scopus.com/inward/record.url?scp=85035333088&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85035333088&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.21602
DO - 10.18632/oncotarget.21602
M3 - Article
C2 - 29262550
AN - SCOPUS:85035333088
SN - 1949-2553
VL - 8
SP - 103117
EP - 103128
JO - Oncotarget
JF - Oncotarget
IS - 61
ER -