Academic Journal

Targeting mTOR signaling for the treatment of intrahepatic cholangiocarcinoma with TSC1/ARID1A mutations: a case report with an unexpected response

التفاصيل البيبلوغرافية
العنوان: Targeting mTOR signaling for the treatment of intrahepatic cholangiocarcinoma with TSC1/ARID1A mutations: a case report with an unexpected response
المؤلفون: Clémentine Daugan, Romain Boidot, François Ghiringhelli, Christophe Borg, Angélique Vienot
المصدر: Therapeutic Advances in Medical Oncology, Vol 16 (2024)
بيانات النشر: SAGE Publishing
سنة النشر: 2024
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Biliary tract cancer incidence is increasing and the prognostic remains dismal. The development of personalized medicine is a pivotal issue in proposing therapeutic options for biliary tract cancer patients. Whole exome sequencing identifies approximately 15% of IDH1 mutations and 15% of FGFR2 fusions in intrahepatic cholangiocarcinoma. Other patients are not currently eligible for targeted therapy. Here, we present a patient treated for a metastatic cholangiocarcinoma with an unexpected response to a mammalian target of rapamycin (mTOR) targeting agent. Whole exome sequencing enabled the identification of TSC1 and ARID1A mutations. Reintroduction of mTOR inhibitors with similar results sustains the main role of these targeted agents in the control of the disease. These results suggest the existence of an mTOR oncogenic addiction in biliary tract cancer. Our results support the interest in performing exome sequencing in liver cancers and the potential to identify actionable mutations with important therapeutic issues.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1758-8359
Relation: https://doi.org/10.1177/17588359241271793; https://doaj.org/toc/1758-8359; https://doaj.org/article/51c99f82ed53476c90515933212ae6e6
DOI: 10.1177/17588359241271793
الاتاحة: https://doi.org/10.1177/17588359241271793
https://doaj.org/article/51c99f82ed53476c90515933212ae6e6
رقم الانضمام: edsbas.99CD0815
قاعدة البيانات: BASE
الوصف
تدمد:17588359
DOI:10.1177/17588359241271793