Trastuzumab and pertuzumab combination therapy for advanced pre-treated HER2 exon 20-mutated non-small cell lung cancer

被引:18
作者
Henegouwen, J. M. van Berge [1 ,2 ]
Jebbink, M. [3 ]
Hoes, L. R. [2 ,4 ]
van der Wijngaart, H. [2 ,5 ]
Zeverijn, L. J. [2 ,4 ]
van der Velden, D. L. [6 ]
Roepman, P. [7 ]
de Leng, W. W. J. [8 ]
Jansen, A. M. L. [8 ]
van Werkhoven, E. [9 ]
van der Noort, V [9 ]
van der Wekken, A. J. [10 ]
de Langen, A. J. [3 ]
Voest, E. E. [2 ,4 ]
Verheul, H. M. W. [11 ]
Smit, E. F. [12 ]
Gelderblom, H. [1 ]
机构
[1] Leiden Univ Med Ctr, Dept Med Oncol, Albinusdreef 2, NL-2333 ZA Leiden, Netherlands
[2] Oncode Inst, Amsterdam, Netherlands
[3] Netherlands Canc Inst, Dept Thorac Oncol, Amsterdam, Netherlands
[4] Netherlands Canc Inst, Dept Mol Oncol & Immunol, Amsterdam, Netherlands
[5] Vrije Univ Amsterdam, Amsterdam Univ Med Ctr, Canc Ctr Amsterdam, Dept Med Oncol, Amsterdam, Netherlands
[6] Amsterdam Univ Med Ctr, Dept Radiol & Nucl Med, Amsterdam, Netherlands
[7] Hartwig Med Fdn, Amsterdam, Netherlands
[8] Univ Med Ctr Utrecht, Dept Pathol, Utrecht, Netherlands
[9] Netherlands Canc Inst, Biometr Dept, Amsterdam, Netherlands
[10] Univ Groningen, Univ Med Ctr Groningen, Dept Pulm Dis, Groningen, Netherlands
[11] Radboud Univ Nijmegen Med Ctr, Dept Med Oncol, Nijmegen, Netherlands
[12] Leiden Univ Med Ctr, Dept Pulmonol, Leiden, Netherlands
关键词
Non-small lung cancer; HER2; mutation; Targeted therapies; Precision medicine; Whole genome sequencing; KINASE DOMAIN; SOLID TUMORS; OPEN-LABEL; BREAST; MUTATIONS; MULTICENTER; MUTANT;
D O I
10.1016/j.ejca.2022.05.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: In 1-3% of non-small cell lung cancer (NSCLC) human epidermal growth factor 2 (HER2) mutations are identified as a genomic driver. Nevertheless, no HER2-targeted treatment is approved for NSCLC. In the Drug Rediscovery Protocol (DRUP), patients are treated with off-label drugs based on their molecular profile. Here, we present the results of the cohort 'trastuzumab/pertuzumab for HER2 exon20 mutation positive (HER2m+) NSCLC'. Methods: Patients with treatment refractory, advanced HER2m+ NSCLC with measurable disease (RECISTv1.1) were eligible. Treatment with intravenous trastuzumab combined with pertuzumab every 3 weeks was administered. The primary end-point was clinical benefit (CB: either objective response or stable disease >= 16 weeks). Patients were enrolled using a Simonlike 2-stage design, with 8 patients in stage 1 and up to 24 patients in stage 2 if at least 1 patient had CB in stage 1. At baseline, a biopsy for biomarker analysis, including whole genome sequencing, was obtained. Results: Twenty-four evaluable patients were enrolled and treated between May 2017 and August 2020. CB was observed in 9 patients (38%); including an objective response rate of 8.3% (2 patients had a partial response) and 7 patients with stable disease >= 16 weeks. The most frequently observed HER2 mutation was p.Y772_A775dup (71%, n = 20). Median follow-up was 13 months, median progression-free survival and overall survival 4 (95% CI 3-6) and 10 months (95% CI 4 - not reached), respectively. Whole genome sequencing data (available for 67% of patients) confirmed the inclusion mutation in all cases. No unexpected toxicity was observed. Conclusion: Despite the fact that the study did meet its primary end-point, trastuzumab/pertuzumab was only marginally active in a subset of patients with heavily pre-treated HER2m+ NSCLC. (C) 2022 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:114 / 123
页数:10
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