Phase 2 study of first-line pembrolizumab monotherapy in elderly patients with non-small-cell lung cancer expressing high PD-L1

被引:3
|
作者
Masuda, Takeshi [1 ]
Fujitaka, Kazunori [1 ]
Suzuki, Tomoko [2 ]
Hamai, Kosuke [3 ]
Matsumoto, Naoko [4 ]
Matsumura, Mirai [1 ,3 ]
Isoyama, Shoko [1 ,3 ]
Ueno, Sayaka [3 ]
Mito, Mineyo [5 ]
Yamaguchi, Kakuhiro [1 ]
Sakamoto, Shinjiro [1 ]
Kawano, Reo [6 ]
Masuda, Ken [7 ]
Nishino, Ryohei [8 ]
Ishikawa, Nobuhisa [3 ]
Yamasaki, Masahiro [4 ]
Hattori, Noboru [1 ]
机构
[1] Hiroshima Univ Hosp, Dept Resp Med, Hiroshima, Japan
[2] JA Onomichi Gen Hosp, Dept Resp Internal Med, Hiroshima, Japan
[3] Hiroshima Prefectural Hosp, Dept Resp Med, Hiroshima, Japan
[4] Hiroshima Red Cross Hosp & Atom Bomb Survivors Ho, Dept Resp Internal Med, Hiroshima, Japan
[5] Kure Med Ctr, Dept Resp Internal Med, Hiroshima, Japan
[6] Hiroshima Univ Hosp, Dept Clin Res Ctr Hiroshima, Hiroshima, Japan
[7] Hiroshima City Hiroshima Citizens Hosp, Dept Resp Internal Med, Hiroshima, Japan
[8] Hiroshima City Asa Citizens Hosp, Dept Resp Internal Med, Hiroshima, Japan
关键词
elderly patients; non-small-cell lung cancer; pembrolizumab; programmed death ligand-1; OPEN-LABEL; CHEMOTHERAPY; EFFICACY; SAFETY; KEYNOTE-024; MULTICENTER; CARBOPLATIN; PACLITAXEL; NIVOLUMAB; DOCETAXEL;
D O I
10.1111/1759-7714.14428
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Pembrolizumab is the recommended first-line therapy for patients with advanced non-small-cell lung cancer (NSCLC) and a programmed death ligand-1 (PD-L1) tumor proportion score (TPS) of >= 50% without driver mutations. However, its efficacy and safety for patients >= 75 years have not been prospectively investigated; this was the aim of this study. Methods This multicenter and open-label single-arm phase II study was conducted at 12 institutions. Chemotherapy-naive patients with advanced NSCLC and a PD-L1 TPS of >= 50% without EGFR mutations or translocation of the ALK received pembrolizumab every 3 weeks. The primary endpoint was progression-free survival (PFS) with a threshold of 4.3 months. The secondary endpoints were overall survival (OS), objective response rate (ORR), disease control rate (DCR), safety, and quality of life. Results Twenty-six patients were enrolled between October 2017 and March 2020. The median PFS was 9.6 (95% confidence interval [CI] 2.1-20.6) months. The lower limit of the 95% CI did not exceed the target. The median OS was 21.6 months. The ORR and DCR were 41.7% and 70.8%, respectively. The proportion of patients with grade >= 3 treatment-related adverse events was 15.4%. The quality of life score did not change significantly during treatment. Conclusion While this study showed that pembrolizumab was a tolerable treatment for elderly patients, the safety requires further confirmation in a larger study. Although the primary endpoint, the median PFS (9.6 months), was slightly shorter than that (10.3 months) of the previous phase III study (KEYNOTE-024 study), the median PFS did not achieve the expected value.
引用
收藏
页码:1611 / 1618
页数:8
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