Biliary Tract Cancers: Treatment Updates and Future Directions in the Era of Precision Medicine and Immuno-Oncology

被引:29
作者
Manne, Ashish [1 ,2 ]
Woods, Edward [3 ]
Tsung, Allan [4 ,5 ,6 ]
Mittra, Arjun [1 ,2 ]
机构
[1] Ohio State Univ, Ctr Comprehens Canc, Arthur G James Canc Hosp, Dept Internal Med,Div Med Oncol, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr Comprehens Canc, Richard J Solove Res Inst, Columbus, OH 43210 USA
[3] Ohio State Univ, Coll Med, Dept Internal Med, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Surg, Wexner Med Ctr, Div Surg Oncol, Columbus, OH 43210 USA
[5] James Canc Hosp, Columbus, OH USA
[6] Solove Res Inst, Columbus, OH USA
关键词
biliary tract cancer; cholangiocarcinoma; mutation; methylation; targeted therapy; immunotherapy; biomarker; circulating DNA; MISMATCH REPAIR DEFICIENCY; CIRCULATING TUMOR DNA; CELL-FREE DNA; PHASE-II; PROMOTER METHYLATION; OPEN-LABEL; EXTRAHEPATIC CHOLANGIOCARCINOMA; DIFFERENTIAL-DIAGNOSIS; PROGNOSTIC BIOMARKER; THERAPEUTIC TARGETS;
D O I
10.3389/fonc.2021.768009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effective management of biliary tract cancers (BTCs) has been hampered by limited options for systemic therapy. In recent years, the focus on precision medicine has made technologies such as next-generation sequencing (NGS) accessible to clinicians to identify targetable mutations in BTCs in tumor tissue (primarily) as well as blood, and to treat them with targeted therapies when possible. It has also expanded our understanding of functional pathways associated with genetic alterations and opened doors for identifying novel targets for treatment. Recent advances in the precision medicine approach allowed us to identify new molecular markers in BTCs, such as epigenetic changes (methylation and histone modification) and non-DNA markers such as messenger RNA, microRNA, and long non-coding RNA. It also made detecting these markers from non-traditional sources such as blood, urine, bile, and cytology (from fine-needle aspiration and biliary brushings) possible. As these tests become more accessible, we can see the integration of different molecular markers from all available sources to aid physicians in diagnosing, assessing prognosis, predicting tumor response, and screening BTCs. Currently, there are a handful of approved targeted therapies and only one class of immunotherapy agents (immune checkpoint inhibitors or ICIs) to treat BTCs. Early success with new targets, vascular endothelial growth factor receptor (VEGFR), HER2, protein kinase receptor, and Dickkopf-1 (DKK1); new drugs for known targets, fibroblast growth factor receptors (FGFRs) such as futabatinib, derazantinib, and erdafitinib; and ICIs such as durvalumab and tremelimumab is encouraging. Novel immunotherapy agents such as bispecific antibodies (bintrafusp alfa), arginase inhibitors, vaccines, and cellular therapy (chimeric antigen receptor-T cell or CAR-T, natural killer cells, tumor-infiltrating lymphocytes) have the potential to improve outcomes of BTCs in the coming years.
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页数:15
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