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

被引:26
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
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
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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共 176 条
  • [11] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [12] Serum microRNAs as novel biomarkers for primary sclerosing cholangitis and cholangiocarcinoma
    Bernuzzi, F.
    Marabita, F.
    Lleo, A.
    Carbone, M.
    Mirolo, M.
    Marzioni, M.
    Alpini, G.
    Alvaro, D.
    Boberg, K. M.
    Locati, M.
    Torzilli, G.
    Rimassa, L.
    Piscaglia, F.
    He, X. -S.
    Bowlus, C. L.
    Yang, G. -X.
    Gershwin, M. E.
    Invernizzi, P.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2016, 185 (01) : 61 - 71
  • [13] Silmitasertib (CX-4945) in combination with gemcitabine and cisplatin as first-line treatment for patients with locally advanced or metastatic cholangiocarcinoma: A phase Ib/II study.
    Borad, Mitesh J.
    Bai, Li-Yuan
    Chen, Ming-Huang
    Hubbard, Joleen M.
    Mody, Kabir
    Rha, Sun Young
    Richards, Donald A.
    Davis, Lindsey S.
    Soong, John
    Huang, Chi-En C-E
    Tse, Emmett
    Ahn, Daniel H.
    Chang, Heung-Moon
    Yen, Chia-Jui
    Oh, Do-Youn
    Park, Joon Oh
    Hsu, Chiun
    Becerra, Carlos Roberto
    Chen, Jen-Shi
    Chen, Yen-Yang
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (03)
  • [14] Frequent Mutation of Isocitrate Dehydrogenase (IDH)1 and IDH2 in Cholangiocarcinoma Identified Through Broad-Based Tumor Genotyping
    Borger, Darrell R.
    Tanabe, Kenneth K.
    Fan, Kenneth C.
    Lopez, Hector U.
    Fantin, Valeria R.
    Straley, Kimberly S.
    Schenkein, David P.
    Hezel, Aram F.
    Ancukiewicz, Marek
    Liebman, Hannah M.
    Kwak, Eunice L.
    Clark, Jeffrey W.
    Ryan, David P.
    Deshpande, Vikram
    Dias-Santagata, Dora
    Ellisen, Leif W.
    Zhu, Andrew X.
    Iafrate, A. John
    [J]. ONCOLOGIST, 2012, 17 (01) : 72 - 79
  • [15] Extracellular vesicles: structure, function, and potential clinical uses in renal diseases
    Borges, F. T.
    Reis, L. A.
    Schor, N.
    [J]. BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2013, 46 (10) : 824 - 830
  • [16] Transcriptome classification of HCC is related to gene alterations and to new therapeutic targets
    Boyault, Sandrine
    Rickman, David S.
    de Reynies, Aurelien
    Balabaud, Charles
    Rebouissou, Sandra
    Jeannot, Emmanuelle
    Herault, Aurelie
    Saric, Jean
    Belghiti, Jacques
    Franco, Dominique
    Bioulac-Sage, Paulette
    Laurent-Puig, Pierre
    Zucman-Rossi, Jessica
    [J]. HEPATOLOGY, 2007, 45 (01) : 42 - 52
  • [17] Epigenome-Wide Analysis of Methylation Changes in the Sequence of Gallstone Disease, Dysplasia, and Gallbladder Cancer
    Braegelmann, Johannes
    Barahona Ponce, Carol
    Marcelain, Katherine
    Roessler, Stephanie
    Goeppert, Benjamin
    Gallegos, Ivan
    Colombo, Alicia
    Sanhueza, Veronica
    Morales, Erik
    Rivera, Maria Teresa
    de Toro, Gonzalo
    Ortega, Alejandro
    Muller, Bettina
    Gabler, Fernando
    Scherer, Dominique
    Waldenberger, Melanie
    Reischl, Eva
    Boekstegers, Felix
    Garate-Calderon, Valentina
    Umu, Sinan U.
    Rounge, Trine B.
    Popanda, Odilia
    Lorenzo Bermejo, Justo
    [J]. HEPATOLOGY, 2021, 73 (06) : 2293 - 2310
  • [18] Efficacy and safety of futibatinib in intrahepatic cholangiocarcinoma (iCCA) harboring FGFR2 fusions/other rearrangements: Subgroup analyses of a phase II study (FOENIX-CCA2)
    Bridgewater, J.
    Meric-Bernstam, F.
    Hollebecque, A.
    Valle, J. W.
    Morizane, C.
    Karasic, T.
    Abrams, T.
    Furuse, J.
    Kelley, R. K.
    Cassier, P.
    Klumpen, H-J.
    Uboha, N.
    Mahipal, A.
    Mitchell, E.
    Ahn, E. R.
    Chang, H-M.
    Masuda, K.
    He, Y.
    Benhadji, K.
    Goyal, L.
    [J]. ANNALS OF ONCOLOGY, 2020, 31 : S261 - S262
  • [19] Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers
    Chan-on, Waraporn
    Nairismaegi, Maarja-Liisa
    Ong, Choon Kiat
    Lim, Weng Khong
    Dima, Simona
    Pairojkul, Chawalit
    Lim, Kiat Hon
    McPherson, John R.
    Cutcutache, Ioana
    Heng, Hong Lee
    Ooi, London
    Chung, Alexander
    Chow, Pierce
    Cheow, Peng Chung
    Lee, Ser Yee
    Choo, Su Pin
    Tan, Iain Bee Huat
    Duda, Dan
    Nastase, Anca
    Myint, Swe Swe
    Wong, Bernice Huimin
    Gan, Anna
    Rajasegaran, Vikneswari
    Ng, Cedric Chuan Young
    Nagarajan, Sanjanaa
    Jusakul, Apinya
    Zhang, Shenli
    Vohra, Priya
    Yu, Willie
    Huang, DaChuan
    Sithithaworn, Paiboon
    Yongvanit, Puangrat
    Wongkham, Sopit
    Khuntikeo, Narong
    Bhudhisawasdi, Vajaraphongsa
    Popescu, Irinel
    Rozen, Steven G.
    Tan, Patrick
    Teh, Bin Tean
    [J]. NATURE GENETICS, 2013, 45 (12) : 1474 - U100
  • [20] Downregulation of MGMT promotes proliferation of intrahepatic cholangiocarcinoma by regulating p21
    Chen, Jun
    Li, Zequn
    Chen, Jian
    Du, Yehui
    Song, Wenfeng
    Xuan, Zefeng
    Zhao, Long
    Song, Guangyuan
    Song, Penghong
    Zheng, Shusen
    [J]. CLINICAL & TRANSLATIONAL ONCOLOGY, 2020, 22 (03) : 392 - 400