A Practical Guide for the Systemic Treatment of Biliary Tract Cancer in Canada
- PMID: 37622998
- PMCID: PMC10453186
- DOI: 10.3390/curroncol30080517
A Practical Guide for the Systemic Treatment of Biliary Tract Cancer in Canada
Abstract
Biliary tract cancers (BTC) are rare and aggressive tumors with poor prognosis. Radical surgery offers the best chance for cure; however, most patients present with unresectable disease, and among those receiving curative-intent surgery, recurrence rates remain high. While other locoregional therapies for unresectable disease may be considered, only select patients may be eligible. Consequently, systemic therapy plays a significant role in the treatment of BTC. In the adjuvant setting, capecitabine is recommended following curative-intent resection. In the neoadjuvant setting, systemic therapy has mostly been explored for downstaging in borderline resectable tumours, although evidence for its routine use is lacking. For advanced unresectable or metastatic disease, gemcitabine-cisplatin plus durvalumab has become the standard of care, while the addition of pembrolizumab to gemcitabine-cisplatin has also recently demonstrated improved survival compared to chemotherapy alone. Following progression on gemcitabine-cisplatin, several chemotherapy combinations and biomarker-driven targeted agents have been explored. However, the optimum regimen remains unclear, and access to targeted agents remains challenging in Canada. Overall, this article serves as a practical guide for the systemic treatment of BTC in Canada, providing valuable insights into the current and future treatment landscape for this challenging disease.
Keywords: adjuvant therapy; biliary tract cancer; cholangiocarcinoma; gallbladder carcinoma; immunotherapy; neoadjuvant therapy; systemic therapy; targeted therapy.
Conflict of interest statement
R.R. has received honoraria and served on advisory boards for Amgen, Eisai, AstraZeneca, Ipsen, Merck, Incyte, and Roche; has received funded grants from Amgen, Eisai, AstraZeneca, Ipsen, and Pfizer; and has participated as an investigator in clinical trials supported by Merck, AstraZeneca, Ipsen, Incyte, and Nucana. P.C. has received honoraria from Astellas Pharma, Merck, AstraZeneca, and Ipsen. V.C.T. has received honoraria and served on advisory boards for AstraZeneca, Eisai, Incyte, Ipsen, Merck, and Roche; has received institutional research funding from AstraZeneca, Eisai, Ipsen, and Roche; and has received institutional clinical trial funding from AstraZeneca, Basilea, Exelixis, Merck, and Roche. D.R. has received honoraria from Siemens Healthineers, Recordati, Roche, Accuray, Varian Medical Systems, Elekta, Novocure, and AstraZeneca, and has investments in Croton Healthcare, AFX Medical, and MisoChip. H.J.L. has received honoraria from Eisai, Taiho, Merck, Lilly, Bristol Meyers Squibb, and Amgen for consultant work and has participated as an investigator on clinical trials supported by Bayer, Bristol Meyers Squibb, Lilly, Roche, AstraZeneca, and Amgen. J.J.K. has received honoraria from AstraZeneca, Merck, Roche, Eisai, Pfizer, Ipsen, and Incyte for consultant work and has received grant or research support from AstraZeneca, Ipsen, Merck, and Roche. J.A. has no conflicts of interest to declare. S.D. has received funding from AstraZeneca Canada for medical writing services. N.C. has received funding from AstraZeneca Canada for medical writing services. R.G. has received honoraria and served on advisory boards for Amgen, AstraZeneca, Bayer, Roche, Merck, Novartis, Ipsen, AAA, Eisai, Apobiologix, Incyte, Pfizer, Mylan, and Taiho and has received grant support from Apobiologix, Ipsen, Novartis, Pfizer.
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