Addition of ramucirumab enhances docetaxel efficacy in patients who had received anti-PD-1/PD-L1 treatment

被引:28
作者
Tozuka, Takehiro [1 ,2 ]
Kitazono, Satoru [1 ]
Sakamoto, Hiroaki [1 ]
Yoshida, Hiroshi [1 ]
Amino, Yoshiaki [1 ]
Uematsu, Shinya [1 ]
Yoshizawa, Takahiro [1 ]
Hasegawa, Tsukasa [1 ]
Ariyasu, Ryo [1 ]
Uchibori, Ken [1 ]
Yanagitani, Noriko [1 ]
Horai, Takeshi [1 ]
Seike, Masahiro [2 ]
Gemma, Akihiko [2 ]
Nishio, Makoto [1 ]
机构
[1] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Thorac Med Oncol, Koto Ku, 3-8-31 Ariake, Tokyo 1358550, Japan
[2] Nippon Med Sch, Grad Sch Med, Dept Pulm Med & Oncol, Bunkyo Ku, 1-1-5 Sendagi, Tokyo 1138603, Japan
关键词
Immune checkpoint inhibitor; Anti PD-1/PD-L1 antibody; Docetaxel; Ramucirumab; Vascular endothelial growth factor; CELL LUNG-CANCER; RESPONSE RATES; CHEMOTHERAPY; INHIBITORS;
D O I
10.1016/j.lungcan.2020.04.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: : Docetaxel (DTX) efficacy increases in patients with non-small cell lung cancer (NSCLC) who had received anti-programmed cell death-1/ligand 1 (anti-PD-1/L1) therapy. However, the effect of ramucirumab (Ram) on DTX efficacy following anti-PD-1/L1 therapy is unknown. Here, we aimed to evaluate the effect of Ram on DTX efficacy following anti-PD-1/L1 therapy. Materials and methods: This retrospective study included 99 patients with NSCLC, who were divided into those who had (pre-ICI group) or had not (no-ICI group) received anti-PD-1/L1 antibody before DTX. Both groups were then treated with DTX or DTX plus Ram (DTX/Ram). Patient characteristics were compared between the DTX and DTX/Ram groups and adjusted with inverse probability of treatment weighting using propensity scores and the following confounding variables: age, sex, performance status, smoking status, histology, driver mutation, and line of treatment. We compared DTX/Ram and DTX in terms of efficacy in both the pre-ICI and no-ICI groups. Results: In the pre-ICI group, 18 and 21 patients received DTX and DTX/Ram, respectively. In the no-ICI group, 35 and 25 patients received DTX and DTX/Ram. In the no-ICI group, progression-free survival (PFS) and overall survival (OS) were not significantly different between DTX/Ram- and DTX-treated patients (median PFS, 2.6 versus 1.6 months; p = 0.30, median OS; 8.2 versus 8.0 months; p = 0.30). In the pre-ICI group, PFS was significantly longer in DTX/Ram-treated than in DTX-treated patients (median, 5.9 versus 2.8 months; p = 0.03). Hazard ratio for disease progression or death was 0.75 (95% confidence interval, 0.20-0.96). The OS of DTX/Ram-treated patients tended to be longer than that of DTX-treated patients (median, 19.8 versus 8.6 months; p = 0.10). Conclusions: DTX efficacy following anti-PD-1/L1 therapy may be enhanced by Ram. Further studies are needed to validate the efficacy of inhibiting the vascular endothelial growth factor pathway following anti-PD-1/L1 therapy.
引用
收藏
页码:71 / 75
页数:5
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