Sustained Response on Sequential Anti-fgfr Therapy in Metastatic Gall Bladder Cancer - a Case Report and Literature Review

Author:

Sheth Hardik1,Limaye Sewanti2,Kumar Prashant3,Shreenivas Aditya4

Affiliation:

1. Kokilaben Dhirubhai Ambani Hospital and Medical Research Institute

2. Sir HN Reliance Foundation Hospital and Research Center

3. Somaiya Vidhyavihar University

4. Medical College of Wisconsin

Abstract

Abstract Advanced gall bladder cancer (aGBC) is an aggressive disease with no consensus on treatment options beyond first line chemotherapy. We report a case of an elderly male with FGFR2 altered advanced adenocarcinoma of the gallbladder who failed two prior lines of chemotherapy but had sustained response and stable disease on sequential FGFR directed targeted therapy. This treatment was based on comprehensive genomic profiling by next-generation sequencing revealed FGR2 alteration. Sequential anti-FGFR tyrosine kinase inhibitors was initiated as a treatment of choice. The patient tolerated the sequential targeted therapy very well and had a sustained response and stable disease with 5 years of survival. Our study demonstrates that aGBC with FGFR alteration can be managed on anti-FGFR therapy for prolonged periods of time, with improved survival. The study revealed a FGFR-directed therapeutic as a viable treatment option in these patients.

Publisher

Research Square Platform LLC

Reference46 articles.

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2. Howlader N, Noone AM, Krapcho M, et al., editors. SEER Cancer Statistics Review. Bethesda, MD: National Cancer Institute; 1975–2014. Available from: https://seer.cancer.gov/csr/1975_2014/. Accessed 20 December 2018.

3. Biliary cancer: intrahepatic cholangiocarcinoma vs. extrahepatic cholangiocarcinoma vs. gallbladder cancers: classification and therapeutic implications;Ahn DH;J Gastrointest Oncol,2017

4. TAS-120 Overcomes Resistance to ATP-Competitive FGFR Inhibitors in Patients with FGFR2 Fusion-Positive Intrahepatic Cholangiocarcinoma;Goyal L;Cancer Discov,2019

5. FGFR2 fusion proteins drive oncogenic transformation of mouse liver organoids towards cholangiocarcinoma;Cristinziano G;J Hepatol,2021

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