Gallbladder cancer

Juan C. Roa*, Patricia García, Vinay K. Kapoor, Shishir K. Maithel, Milind Javle, Jill Koshiol

*Corresponding author for this work

Research output: Contribution to journalComment/debatepeer-review

256 Scopus citations

Abstract

Gallbladder cancer (GBC) is the most common cancer of the biliary tract, characterized by a very poor prognosis when diagnosed at advanced stages owing to its aggressive behaviour and limited therapeutic options. Early detection at a curable stage remains challenging because patients rarely exhibit symptoms; indeed, most GBCs are discovered incidentally following cholecystectomy for symptomatic gallbladder stones. Long-standing chronic inflammation is an important driver of GBC, regardless of the lithiasic or non-lithiasic origin. Advances in omics technologies have provided a deeper understanding of GBC pathogenesis, uncovering mechanisms associated with inflammation-driven tumour initiation and progression. Surgical resection is the only treatment with curative intent for GBC but very few cases are suitable for resection and most adjuvant therapy has a very low response rate. Several unmet clinical needs require to be addressed to improve GBC management, including discovery and validation of reliable biomarkers for screening, therapy selection and prognosis. Standardization of preneoplastic and neoplastic lesion nomenclature, as well as surgical specimen processing and sampling, now provides reproducible and comparable research data that provide a basis for identifying and implementing early detection strategies and improving drug discovery. Advances in the understanding of next-generation sequencing, multidisciplinary care for GBC, neoadjuvant and adjuvant strategies, and novel systemic therapies including chemotherapy and immunotherapies are gradually changing the treatment paradigm and prognosis of this recalcitrant cancer.

Original languageEnglish (US)
Article number69
JournalNature Reviews Disease Primers
Volume8
Issue number1
DOIs
StatePublished - Dec 2022

Funding

M.J. receives research funding (to Institution) from Merck, EMD Serono, Novartis, Eli Lilly, AstraZeneca, Genentech, Transthera, Meclun, BMS, Incyte, QED, Taiho, Servier, Oncosil, Basilea, Nucana; and to self or as advisory board/Data and Safety Monitoring Board member from Incyte, Zymeworks, Mundi Pharma, Nucana, MORE health and Origimed. Peer grant funding is provided from Department of Defense and NIH. S.K.M. receives research funding (to Institution) from BMS, QED/HELSINN, Natera. The other authors (J.C.R., P.G., J.K. and V.K.K.) declare no competing interests. The authors thank D. Check for creating the bar chart figure of gallbladder disease prevalence and gallbladder cancer incidence. The work of J.K. is supported by general funds from the Intramural Research Program of the NIH, National Cancer Institute, Division of Cancer Epidemiology and Genetics. The work of J.C.R. and P.G. is supported by the European Union’s Horizon 2020 Research and Innovation programme under grant agreement No. 825510 (ESCALON), and from Agencia Nacional de Investigación y Desarrollo (ANID) Fondecyt 1221345 and Millennium Science Initiative Program: Millennium Institute on Immunology and Immunotherapy (ICN09_016/ICN 2021_045; former P09/016-F).

ASJC Scopus subject areas

  • General Medicine

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