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Successful Response to the Combination of Immunotherapy and Chemotherapy in Cholangiocarcinoma with High Tumour Mutational Burden and PD-L1 Expression: a Case Report

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2018 Nov 14
PMID 30419854
Citations 30
Authors
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Abstract

Background: Cholangiocarcinoma, or bile duct cancer, is a gastrointestinal cancer with limited therapeutic options and a poor outcome. Studies have revealed that some major driver genes are associated with cholangiocarcinoma, but no targeted therapies have been approved. Immune checkpoint inhibitors, which are represented by inhibitors of programmed cell death 1 (PD-1)/programmed death-ligand 1 (PD-L1), have emerged as a potential therapy for multiple types of solid cancers.

Case Presentation: A 53-year-old female presented with postoperative recurrence of PD-L1-positive intrahepatic cholangiocarcinoma with a high tumour mutational burden. This patient exhibited a marked response to the combination of anti-PD-1 immunotherapy and chemotherapy.

Conclusions: As far as we know, this is the first case report on the success of the combination of immunotherapy and chemotherapy for advanced cholangiocarcinoma with PD-L1 positivity and a high tumour mutational burden.

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References
1.
Iwai Y, Hamanishi J, Chamoto K, Honjo T . Cancer immunotherapies targeting the PD-1 signaling pathway. J Biomed Sci. 2017; 24(1):26. PMC: 5381059. DOI: 10.1186/s12929-017-0329-9. View

2.
Chalmers Z, Connelly C, Fabrizio D, Gay L, Ali S, Ennis R . Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden. Genome Med. 2017; 9(1):34. PMC: 5395719. DOI: 10.1186/s13073-017-0424-2. View

3.
Viale G, Trapani D, Curigliano G . Mismatch Repair Deficiency as a Predictive Biomarker for Immunotherapy Efficacy. Biomed Res Int. 2017; 2017:4719194. PMC: 5523547. DOI: 10.1155/2017/4719194. View

4.
Maleki Vareki S, Garrigos C, Duran I . Biomarkers of response to PD-1/PD-L1 inhibition. Crit Rev Oncol Hematol. 2017; 116:116-124. DOI: 10.1016/j.critrevonc.2017.06.001. View

5.
Dodson R, Weiss M, Cosgrove D, Herman J, Kamel I, Anders R . Intrahepatic cholangiocarcinoma: management options and emerging therapies. J Am Coll Surg. 2013; 217(4):736-750.e4. DOI: 10.1016/j.jamcollsurg.2013.05.021. View