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Tucatinib plus Trastuzumab Effective in HER2+ Biliary Cancer
Next generation sequencing is now essential for patients with metastatic biliary cancer given the identification of targetable pathways, including fibroblast growth factor receptor and isocitrate dehydrogenase 1, for which there are approved treatments. HER2 has emerged as a target in metastatic biliary cancer, with studies finding 5% to 15% of cancers positive for overexpression or gene amplification.
Investigators now report results of an industry-sponsored, phase 2 basket study (SGNTUC-019) testing the combination of tucatinib — a HER2 tyrosine kinase inhibitor — and trastuzumab in patients with HER2-positive advanced biliary cancer that progressed on first-line gemcitabine/cisplatin–based chemotherapy. Local testing for HER2 was permissible via immunohistochemistry, fluorescence in situ hybridization, or next generation sequencing of tissue or blood.
Of 30 patients, half were men, 77% were Asian, half had gallbladder primaries, and half had intrahepatic or extrahepatic cholangiocarcinomas. During a median follow-up of 10.8 months, the primary endpoint of antitumor response rate was 46.7%, and duration of response was 6 months. The median progression-free survival was 5.5 months; median overall survival was 15.5 months. Treatment-related grade 3 or 4 serious adverse events were uncommon and attributable to tucatinib in 10% of patients and to trastuzumab in 6.7%; grade 3 diarrhea occurred in 6.6%.
Comment
The combination of tucatinib and trastuzumab has significant activity in HER2-positive advanced biliary cancer and adds to the growing list of such agents or combinations, including pertuzumab/trastuzumab, zanidatamab, and trastuzumab deruxtecan. HER2 testing for biliary cancers should be adopted as a care standard.
Citation(s)
Author:
Nakamura Y et al.
Title:
Tucatinib and trastuzumab for previously treated human epidermal growth factor receptor 2–positive metastatic biliary tract cancer (SGNTUC-019): A phase II basket study.
Source:
J Clin Oncol
2023
Sep
26; [e-pub].
(Abstract/FREE Full Text)
Empfohlen von
David H. Ilson, MD, PhD