Real-world efficacy of atezolizumab in non-small cell lung cancer: A multicenter cohort study focused on performance status and retreatment after failure of anti-PD-1 antibody

被引:31
作者
Furuya, Naoki [1 ]
Nishino, Makoto [2 ,3 ]
Wakuda, Kazushige [4 ]
Ikeda, Satoshi [5 ]
Sato, Takashi [3 ]
Ushio, Ryota [6 ]
Tanzawa, Shigeru [7 ]
Sata, Masafumi [8 ]
Ito, Kentaro [9 ]
机构
[1] St Marianna Univ, Div Resp Med, Dept Internal Med, Sch Med, Kawasaki, Kanagawa, Japan
[2] Natl Canc Ctr, Dept Expt Therapeut, Tokyo, Japan
[3] Keiyu Hosp, Dept Med, Div Pulm Med, Yokohama, Kanagawa, Japan
[4] Shizuoka Canc Ctr, Div Thorac Oncol, Shizuoka, Japan
[5] Kanagawa Cardiovasc & Resp Ctr, Dept Resp Med, Yokohama, Kanagawa, Japan
[6] Yokohama City Univ, Resp Dis Ctr, Med Ctr, Yokohama, Kanagawa, Japan
[7] Teikyo Univ, Dept Internal Med, Div Med Oncol, Sch Med, Tokyo, Japan
[8] Jichi Med Univ, Dept Med, Div Pulm Med, Shimotsuke, Tochigi, Japan
[9] Matsusaka Municipal Hosp, Resp Ctr, Matsusaka, Japan
关键词
anti-PD-L1; atezolizumab; non-small cell lung cancer; retreatment;
D O I
10.1111/1759-7714.13824
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Atezolizumab is a programmed death-ligand 1 (PD-L1) targeted monoclonal antibody that inhibits PD-L1 interacting with its receptors PD-1 and B7-1, thereby enhancing anticancer immunity. Some real-world efficacy and safety studies of anti-PD-1 antibody have been previously reported. However, there have been no reports investigating the efficacy of atezolizumab monotherapy in clinical practice which have focused on performance status and previous anti-PD-1 antibody treatment. Methods: We retrospectively reviewed consecutive advanced NSCLC patients who received atezolizumab monotherapy between April 2018 and February 2019 at eight institutions. A total of 152 patients with NSCLC were enrolled in this study. Results: A total of 38 patients (25%) had already been treated with anti-PD-1 treatment (nivolumab or pembrolizumab) before atezolizumab. The median OS and TTF was 384 days (12.8 months) (95% confidence interval [CI]: 206-424), and 42 days (1.4 months) (95% CI: 27-56) in all patients, respectively. ECOG PS 0 had significantly longer OS (median OS; not reached, p < 0.0001) and TTF (median TTF; 63 days, p = 0.012) compared with PS 1 or 2-3. Most retreated patients were unable to continue atezolizumab for a longer period, but seven patients (18.4%) were able to continue atezolizumab over four months as an ICI retreatment. Conclusions: In previously treated advanced NSCLC patients, atezolizumab monotherapy demonstrated good efficacy and safety regardless of heavily treated patients in real-world clinical practice, and ECOG PS 0 was a favorable predictive factor. The efficacy of retreatment with atezolizumab was limited but was well tolerated in patients treated with prior anti-PD-1 antibody.
引用
收藏
页码:613 / 618
页数:6
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