Comparative effectiveness of mobocertinib and standard of care in patients with NSCLC with EGFR exon 20 insertion mutations: An indirect comparison

被引:2
|
作者
Ou, Sai-Hong I. [1 ]
Lin, Huamao M. [2 ]
Hong, Jin-Liern [2 ]
Yin, Yu [2 ]
Jin, Shu [2 ]
Lin, Jianchang [2 ]
Mehta, Minal [2 ]
Zhang, Pingkuan [2 ]
Nguyen, Danny [3 ]
Neal, Joel W. [4 ]
机构
[1] Univ Calif Irvine, Chao Family Comprehens Canc Ctr, Sch Med, Orange, CA USA
[2] Takeda Dev Ctr Amer Inc, Lexington, MA 02421 USA
[3] City Hope Natl Med Ctr, Duarte, CA USA
[4] Stanford Univ, Stanford Canc Inst, Stanford, CA USA
关键词
Comparative evidence; EGFR exon 20 insertion; External control; Indirect comparison; Mobocertinib; Propensity-score matching; Real-world data; CELL LUNG-CANCER; HEALTH RECORD DATA; SURVIVAL; OUTCOMES; ARMS;
D O I
10.1016/j.lungcan.2023.107186
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Mobocertinib is a novel, first-in-class, irreversible, oral epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) designed to selectively target in-frame EGFR exon 20 insertions (ex20ins). Comparative effectiveness data for mobocertinib versus real-world treatments are lacking in this rare population. This study compared data for mobocertinib reported in a Phase I/II single-arm clinical trial with an external control group consisting of patients who received available treatment in the real-world setting in the United States (US).Materials and Methods: The mobocertinib group included platinum-pretreated patients with advanced EGFR ex20ins non-small cell lung cancer (NSCLC) receiving mobocertinib 160 mg QD in an ongoing, single-arm, phase 1/2 clinical trial (NCT02716116; n = 114). The real-world data (RWD) group included platinum-pretreated patients with advanced EGFR ex20ins-mutant NSCLC from the Flatiron Health database (n = 50). Inverse probability treatment weighting based on the propensity score method controlled for potential confounding between groups. Confirmed overall response rate (cORR), progression-free survival (PFS), and overall survival (OS) were compared between groups. Results: After weighting, baseline characteristics were balanced. Patients in the RWD group received EGFR TKI (20 %), immuno-oncology therapy (40 %), or any regimens containing chemotherapy (40 %) in the second-or later-line setting. In the mobocertinib and RWD groups, respectively, cORR was 35.1 % and 11.9 % (odds ratio: 3.75 [95 % confidence interval (CI): 2.05, 6.89]); median PFS was 7.3 and 3.3 months (hazard ratio [HR]: 0.57 [95 % CI: 0.36, 0.90]); and median OS was 24.0 and 12.4 months (HR: 0.53 [95 % CI: 0.33, 0.83]) after weighting.Discussion: Mobocertinib showed substantially improved outcomes versus an external control group using available therapies in platinum-pretreated patients with EGFR ex20ins-mutant NSCLC. In the absence of comparative evidence from randomized trials, these findings help elucidate potential benefits of mobocertinib in this rare population.
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页数:8
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