医学
阿法替尼
内科学
肿瘤科
癌症
来那替尼
实体瘤疗效评价标准
乳腺癌
表皮生长因子受体
临床试验
埃罗替尼
临床研究阶段
曲妥珠单抗
作者
Abdulazeez Salawu,Aaron Richard Hansen,Anna Spreafico,Esmail Mutahar Al-Ezzi,Sheila Webster,Philippe L. Bedard,Jeffrey Doi,Lisa Wang,Lillian L. Siu,Albiruni R. Abdul Razak
标识
DOI:10.1007/s11523-022-00884-z
摘要
BackgroundEpidermal growth factor receptor (EGFR)- and human epidermal growth factor receptor (HER)2-targeted therapies are approved for the treatment of breast, gastric/gastrointestinal junction (GEJ), and non-small cell lung cancer (NSCLC) with specific molecular aberrations affecting HER family members. Over 10 % of other cancers harbor genomic aberrations affecting HER family members, but their role remains undefined.ObjectiveThe MOBILITY3 trial evaluated the antitumor activity of afatinib, an oral pan-HER tyrosine kinase inhibitor (TKI) in HER-aberrant tumors outside of the licensed indications. Patients and MethodsIn this single-center basket trial, patients with advanced solid tumors that harbor mutations and/or amplifications of any of the HER family members (EGFR, ERBB2, ERBB3, ERBB4) were enrolled. The EGFR-mutated NSCLC and HER2-positive breast cancers were excluded. Participants were treated with oral afatinib 40 mg daily until disease progression or unacceptable toxicity. Objective response rate (ORR) and progression-free survival (PFS) were primary and secondary endpoints, respectively. ResultsThe study enrolled 12 patients with 6 tumor types (NSCLC, sarcoma, salivary gland, gastric/GEJ, breast and pancreatic cancer). Objective response rate was 8 % (95 % CI 0.2–38%) and median PFS was 11.4 weeks (95% CI 4.6–33.3 weeks). All 3 patients with salivary gland cancers and 1 patient with ERBB2-mutant NSCLC had clinical benefit (stable disease or partial response lasting > 24 weeks). Due to slow accrual and a lower-than-expected response rate, trial recruitment was terminated before the target of 30 patients were enrolled. ConclusionsIn the MOBILITY3 study (NCT02506517), afatinib demonstrated modest activity in tumors that possess EGFR and ERBB2 aberrations. Clinical benefit seen in all 3 salivary gland cancers supports the growing evidence for the utility of HER-targeted therapies in the treatment of this specific tumor type.
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