阿法替尼
医学
内科学
肺癌
肿瘤科
腺癌
埃罗替尼
皮疹
癌症
无进展生存期
实体瘤疗效评价标准
临床终点
临床研究阶段
临床试验
表皮生长因子受体
化疗
作者
Scott Gettinger,Zihe Song,Karen L. Reckamp,Jeffrey A. Moscow,Robert J. Gray,Victoria Wang,Lisa M. McShane,Larry Rubinstein,David Patton,P. Mickey Williams,Stanley R. Hamilton,Xiao–Tang Kong,James V. Tricoli,Barbara A. Conley,Carlos L. Arteaga,Lyndsay N. Harris,Peter J. O’Dwyer,Alice P. Chen,Keith T. Flaherty
出处
期刊:JCO precision oncology
[American Society of Clinical Oncology]
日期:2024-07-01
卷期号: (8)
摘要
PURPOSE National Cancer Institute–Molecular Analysis for Therapy Choice (NCI-MATCH) was a multicohort phase 2 trial that assigned patients with advanced pretreated cancers to molecularly targeted therapies on the basis of tumor genomic testing. NCI-MATCH Arm A evaluated afatinib, an EGFR tyrosine kinase inhibitor (TKI) approved for advanced non–small cell lung cancer, in patients with tumors other than lung cancer harboring EGFR mutations. METHODS Patients with advanced pretreated cancers other than lung cancer found to have selected actionable EGFR mutations were offered participation in Arm A. Previous therapy with an EGFR TKI was not allowed. Patients received afatinib 40 mg once daily continuously until disease progression or unacceptable toxicity. The primary end point was objective response rate (ORR). Secondary end points included progression-free survival (PFS), 6-month PFS, and overall survival (OS). RESULTS Seventeen patients received protocol therapy. Tumor types included glioblastoma multiforme (GBM) (13), gliosarcoma (1), adenocarcinoma not otherwise specified (NOS) (2), and adenosquamous carcinoma of the breast (1). Fifty-nine percent of patients received ≥2 lines of previous therapy. The ORR was 11.8% (90% CI, 2.1 to 32.6), with one complete response lasting 16.4 months (GBM harboring a rare exon 18 EGFR-SEPT14 fusion) and one partial response lasting 12.8 months (adenocarcinoma NOS with the classic EGFR mutation, p.Glu746_Ala750del). Three patients had stable disease. The 6-month PFS was 15% (90% CI, 0 to 30.7); the median OS was 9 months (90% CI, 4.6 to 14.0). Rash and diarrhea were the most common toxicities. CONCLUSION Afatinib had modest activity in a cohort of patients with heavily pretreated cancer with advanced nonlung, EGFR-mutated tumors, but the trial's primary end point was not met. Further evaluation of afatinib in GBM with EGFR exon 18 fusions may be of interest.
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