JASPER: Phase 2 trial of first-line niraparib plus pembrolizumab in patients with advanced non-small cell lung cancer

被引:52
作者
Ramalingam, Suresh S. [1 ]
Thara, Eddie [2 ]
Awad, Mark M. [3 ]
Dowlati, Afshin [4 ,5 ]
Haque, Basir [6 ]
Stinchcombe, Thomas E. [7 ]
Dy, Grace K. [8 ]
Spigel, David R. [9 ]
Lu, Sharon [10 ]
Iyer Singh, Nithya [10 ]
Tang, Yongqiang [10 ]
Teslenko, Iryna [10 ]
Iannotti, Nicholas [11 ]
机构
[1] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[2] Oncol Inst Hope & Innovat, Los Angeles, CA USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Univ Hosp, Seidman Canc Ctr, Cleveland, OH USA
[5] Case Western Reserve Univ, Cleveland, OH 44106 USA
[6] Kadlec Clin Hematol & Oncol, Kennewick, WA, Australia
[7] Duke Univ, Sch Med, Duke Canc Inst, Durham, NC USA
[8] Roswell Pk Comprehens Canc Ctr, Buffalo, NY USA
[9] Sarah Cannon Res Inst Tennessee Oncol, Nashville, TN USA
[10] GlaxoSmithKline, Waltham, MA USA
[11] Hematol Oncol Associates Treasure Coast, Port St Lucie, FL USA
关键词
clinical study; combination drug therapy; lung neoplasms; niraparib; non-small cell lung carcinoma; pembrolizumab; poly(ADP-ribose) polymerase inhibitors; PARP; RESISTANCE; INHIBITORS; THERAPY;
D O I
10.1002/cncr.33885
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Poly(ADP-ribose) polymerase (PARP) inhibitors may synergize with programmed cell death receptor-1 (PD-1) inhibitors to enhance adaptive and innate antitumor immune responses. In the phase 2 JASPER study (NCT04475939), the PARP inhibitor niraparib was evaluated in combination with the PD-1 inhibitor pembrolizumab in patients with metastatic and/or locally advanced non-small cell lung cancer (NSCLC). Methods Patients whose tumors had programmed cell death ligand 1 (PD-L1) tumor proportion scores (TPS) >= 50% (cohort 1) or 1%-49% (cohort 2) received first-line niraparib (200 mg once daily) plus pembrolizumab (200 mg every 3 weeks). The primary end point was investigator-assessed objective response rate (ORR). Secondary end points included duration of response (DoR), progression-free survival (PFS), overall survival (OS), safety, and pharmacokinetics. Results Thirty-eight patients were enrolled in cohorts 1 and 2. In cohort 1, ORR (95% confidence interval [CI]) was 56.3% (9 of 16 patients; 29.9%-80.2%); 2 of 16 patients had complete responses and 7 of 16 had partial responses (PRs). In cohort 2, ORR was 20.0% (5.7%-43.7%) with 4 of 20 PRs. In cohorts 1 and 2, the median DoR was 19.7 months (95% CI, 4.2 months to not estimable [NE]) and 9.4 months (95% CI, 4.2 months to NE), the median PFS was 8.4 months (95% CI, 3.9-22.1 months) and 4.2 months (95% CI, 2.0-6.2 months), and the median OS was NE (95% CI, 6.0 months to NE) and 7.7 months (95% CI, 4.0-12.5 months), respectively. Grade >= 3 treatment-emergent adverse events occurred in 88.2% and 85.7% of patients in cohorts 1 and 2, respectively. Safety was consistent with known profiles of single-agent niraparib and pembrolizumab. Conclusions Niraparib plus pembrolizumab showed clinical activity in patients with advanced and/or metastatic NSCLC. Lay Summary The JASPER clinical trial studied a new combination treatment for advanced or metastatic non-small cell lung cancer (NSCLC). Pembrolizumab, a drug approved for NSCLC, was given with niraparib. Previous research showed that these 2 drugs together might work better than either drug alone. This study found that more than half of patients with high levels of a tumor marker responded to the combination, and one-fifth of patients with lower levels of the marker responded. The types of side effects from the combination were similar to side effects from both drugs alone. These results support more research on this combination.
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页码:65 / 74
页数:10
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