A Retrospective Analysis of Biliary Tract Cancer Patients Presented to the Molecular Tumor Board at the Comprehensive Cancer Center Munich

Danmei Zhang(Deutschen Konsortium für Translationale Krebsforschung), Klara Dorman(Deutschen Konsortium für Translationale Krebsforschung), Kathrin Heinrich(Ludwig-Maximilians-Universität München), Lena Weiss(Ludwig-Maximilians-Universität München), Myrto Boukovala(Ludwig-Maximilians-Universität München), Michael Haas(Ludwig-Maximilians-Universität München), Philipp A. Greif(Deutschen Konsortium für Translationale Krebsforschung), Frank Ziemann(Ludwig-Maximilians-Universität München), Georg Beyer(LMU Klinikum), Daniel Roessler(LMU Klinikum), Elisabetta Goni(LMU Klinikum), Bernhard W. Renz(LMU Klinikum), Jan DʼHaese(LMU Klinikum), Wolfgang G. Kunz(LMU Klinikum), Max Seidensticker(LMU Klinikum), Stefanie Corradini(LMU Klinikum), Maximilian Niyazi(LMU Klinikum), Steffen Ormanns(LMU Klinikum), Jörg Kumbrink(LMU Klinikum), Andreas Jung(LMU Klinikum), Andreas Möck(LMU Klinikum), Martina Rudelius(LMU Klinikum), Frederick Klauschen(LMU Klinikum), Jens Werner(LMU Klinikum), Julia Mayerle(LMU Klinikum), Michael von Bergwelt‐Baildon(Deutschen Konsortium für Translationale Krebsforschung), Stefan Boeck(Deutschen Konsortium für Translationale Krebsforschung), Volker Heinemann(Deutschen Konsortium für Translationale Krebsforschung), C. Benedikt Westphalen(LMU Klinikum)
Targeted Oncology
August 18, 2023
Cited by 17Open Access
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Abstract

BACKGROUND AND OBJECTIVE: molecular tumor board (MTB). PATIENTS AND METHODS: In this single-center observational study, we included BTC patients with intrahepatic cholangiocarcinoma (iCCA), extrahepatic CCA (eCCA), and gallbladder cancer (GB), who had been discussed in the institutional MTB from May 29, 2017, to July 25, 2022. Patients were followed up until 31 January 2023. Data were retrospectively collected by review of medical charts, and MTB recommendation. RESULTS: In total, 153 cases were registered to the MTB with a median follow-up of 15 months. Testing was successful in 81.7% of the patients. CGP detected targetable alterations in 35.3% of our BTC patients (most commonly ARID1A/ERBB2/IDH1/PIK3CA/BRAF-mutations and FGFR2-fusions). Recommendations for molecularly guided therapy were given in 46.4%. Of those, treatment implementation of targeted therapy followed in 19.4%. In patients receiving the recommended treatment, response rate was 57% and median overall survival was 19 months (vs 8 months in the untreated cohort). The progression-free survival ratio of 1.45 suggest a clinical benefit of molecularly guided treatment. CONCLUSIONS: In line with previous work, our series demonstrates feasibility and clinical utility of comprehensive genomic profiling in BTC patients. With the growing number of targeted agents with clinical activity in BTC, CGP should become standard of care in the management of this group of patients.


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