Challenges and opportunities for treating intrahepatic cholangiocarcinoma: targeted therapy
Gahyun Gim , Nabeel Badri
Hepatoma Research ›› 2023, Vol. 9 : 51
Over the last two decades, substantial progress has been made in the scope of molecular targeted therapy, leading to transformative advancements in the treatment of various malignancies, including biliary tract cancer (BTC). BTC represents a heterogeneous group of aggressive tumors with historically poor prognoses. However, recent discoveries of novel molecular alterations in BTC have provided new avenues for targeted therapeutic interventions, exemplified by the approval of pemigatinib, specifically designed for FGFR2 gene fusions or rearrangements in advanced BTC. Furthermore, subsequent regulatory approvals and ongoing clinical trials focusing on specific gene mutations have considerably expanded the array of treatment options available, augmenting the potential for personalized treatment strategies. In light of these developments, this review aims to furnish a comprehensive and up-to-date account of the molecular characteristics and potential targeted therapies in BTC. By presenting insights into novel therapeutic approaches and outlining prospective directions for translational and clinical investigations, this review seeks to contribute to the ongoing progress and optimization of therapeutic approaches in managing BTC.
Cholangiocarcinoma / biliary tree cancer / biliary tract cancer / targeted therapy / immunotherapy / next-generation sequencing / bile duct neoplasms / hepatobiliary malignancy / intrahepatic cholangiocarcinoma
| [1] |
|
| [2] |
|
| [3] |
|
| [4] |
|
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
|
| [9] |
|
| [10] |
|
| [11] |
|
| [12] |
|
| [13] |
|
| [14] |
|
| [15] |
|
| [16] |
|
| [17] |
|
| [18] |
|
| [19] |
|
| [20] |
|
| [21] |
NCCN clinical practice guidelines in oncology (NCCN Guidelines®) biliary tract cancers, version 2.2023. Available from: https://www.nccn.org/professionals/physician_gls/pdf/btc.pdf [Last accessed on 25 Dec 2023] |
| [22] |
FDA approves ivosidenib for advanced or metastatic cholangiocarcinoma. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-ivosidenib-advanced-or-metastatic-cholangiocarcinoma [Last accessed on 25 Dec 2023] |
| [23] |
Study of LY3410738 administered to patients with advanced solid tumors with IDH1 or IDH2 mutations. Available from: https://classic.clinicaltrials.gov/ct2/show/NCT04521686 [Last accessed on 25 Dec 2023] |
| [24] |
A study of HMPL-306 in advanced solid tumors with IDH mutations. Available from: https://classic.clinicaltrials.gov/ct2/show/NCT04762602 [Last accessed on 25 Dec 2023] |
| [25] |
A study of IDH305 in patients with advanced malignancies that harbor IDH1R132 mutations. Available from: https://classic.clinicaltrials.gov/ct2/show/NCT02381886 [Last accessed on 25 Dec 2023] |
| [26] |
Gemcitabine and cisplatin with ivosidenib or pemigatinib for the treatment of unresectable or metastatic cholangiocarcinoma. Available from: https://classic.clinicaltrials.gov/ct2/show/NCT04088188 [Last accessed on 25 Dec 2023] |
| [27] |
|
| [28] |
|
| [29] |
|
| [30] |
|
| [31] |
|
| [32] |
|
| [33] |
|
| [34] |
|
| [35] |
|
| [36] |
|
| [37] |
|
| [38] |
|
| [39] |
|
| [40] |
FDA grants accelerated approval to pemigatinib for cholangiocarcinoma with an FGFR2 rearrangement or fusion. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-pemigatinib-cholangiocarcinoma-fgfr2-rearrangement-or-fusion [Last accessed on 25 Dec 2023] |
| [41] |
|
| [42] |
|
| [43] |
|
| [44] |
FDA grants accelerated approval to futibatinib for cholangiocarcinoma. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-futibatinib-cholangiocarcinoma [Last accessed on 25 Dec 2023] |
| [45] |
|
| [46] |
|
| [47] |
|
| [48] |
|
| [49] |
|
| [50] |
|
| [51] |
|
| [52] |
|
| [53] |
FDA grants accelerated approval to dabrafenib in combination with trametinib for unresectable or metastatic solid tumors with BRAF V600E mutation. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-dabrafenib-combination-trametinib-unresectable-or-metastatic-solid [Last accessed on 25 Dec 2023] |
| [54] |
|
| [55] |
|
| [56] |
|
| [57] |
|
| [58] |
|
| [59] |
|
| [60] |
|
| [61] |
|
| [62] |
|
| [63] |
|
| [64] |
|
| [65] |
|
| [66] |
|
| [67] |
|
| [68] |
|
| [69] |
|
| [70] |
|
| [71] |
|
| [72] |
|
| [73] |
|
| [74] |
|
| [75] |
|
| [76] |
|
| [77] |
|
| [78] |
|
| [79] |
U.S. Food & Drug Administration. FDA Approves larotrectinib for solid tumors with NTRK gene fusions. Available from: https://www.fda.gov/drugs/fda-approves-larotrectinib-solid-tumors-ntrk-gene-fusions [Last accessed on 25 Dec 2023] |
| [80] |
U.S. Food & Drug Administration. FDA approves entrectinib for NTRK solid tumors and ROS-1 NSCLC. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-entrectinib-ntrk-solid-tumors-and-ros-1-nsclc [Last accessed on 25 Dec 2023] |
| [81] |
|
| [82] |
|
| [83] |
|
| [84] |
|
| [85] |
|
| [86] |
|
| [87] |
|
| [88] |
|
| [89] |
|
| [90] |
|
| [91] |
FDA approves pralsetinib for lung cancer with RET gene fusions. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-pralsetinib-lung-cancer-ret-gene-fusions [Last accessed on 25 Dec 2023] |
| [92] |
FDA approves pralsetinib for RET-altered thyroid cancers. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-pralsetinib-ret-altered-thyroid-cancers#:~:text=On%20December%201%2C%202020%2C%20the,fusion%2Dpositive%20thyroid%20cancer%20who [Last accessed on 25 Dec 2023] |
| [93] |
FDA D.I.S.C.O. Burst Edition: FDA approvals of Retevmo (selpercatinib) for adult patients with locally advanced or metastatic RET fusion-positive solid tumors, and Retevmo (selpercatinib) for adult patients with locally advanced or metastatic RET fusion-positive non-small cell lung cancer. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-disco-burst-edition-fda-approvals-retevmo-selpercatinib-adult-patients-locally-advanced-or#:~:text=On%20September%2021%2C%202022%2C%20the,who%20have%20no%20satisfactory%20alternative [Last accessed on 25 Dec 2023] |
| [94] |
|
| [95] |
|
| [96] |
|
| [97] |
|
| [98] |
|
| [99] |
|
| [100] |
|
| [101] |
|
| [102] |
FDA approves pembrolizumab for adults and children with TMB-H solid tumors. Available from: https://www.fda.gov/drugs/drug-approvals-and-databases/fda-approves-pembrolizumab-adults-and-children-tmb-h-solid-tumors [Last accessed on 26 Jan 2024] |
| [103] |
|
| [104] |
|
| [105] |
|
| [106] |
FDA Converts to Full Approval Indication for KEYTRUDA® (pembrolizumab) for Certain Adult and Pediatric Patients With Advanced Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Solid Tumors. Available from: https://www.merck.com/news/fda-converts-to-full-approval-indication-for-keytruda-pembrolizumab-for-certain-adult-and-pediatric-patients-with-advanced-microsatellite-instability-high-msi-h-or-mismatch-repair-deficient/ [Last accessed on 25 Dec 2023] |
| [107] |
|
| [108] |
FDA grants accelerated approval to dostarlimab-gxly for dMMR advanced solid tumors. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-dostarlimab-gxly-dmmr-advanced-solid-tumors [Last accessed on 25 Dec 2023] |
| [109] |
|
| [110] |
|
| [111] |
|
| [112] |
|
| [113] |
|
| [114] |
|
| [115] |
|
| [116] |
|
| [117] |
|
| [118] |
|
| [119] |
|
| [120] |
|
| [121] |
|
| [122] |
|
| [123] |
Preoperative nab-paclitaxel, cisplatin, and gemcitabine chemotherapy with or without infigratinib targeted therapy for the treatment of resectable intrahepatic cholangiocarcinoma, the OPTIC trial. Available from: https://clinicaltrials.gov/study/NCT05514912?cond=targeted%20neoadjuvant%20cholangiocarcinoma&rank=1 [Last accessed on 25 Dec 2023] |
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