Therapeutic Strategies after Imatinib Resistance in Gastrointestinal Stromal Tumors
DOI:
https://doi.org/10.54097/kn0q3e46Keywords:
Gastrointestinal Stromal Tumor (GIST), Imatinib (IM), Drug Resistance, Tyrosine Kinase Inhibitor (TKI)Abstract
Gastrointestinal stromal tumor (GIST) is a mesenchymal tumor commonly found in the gastrointestinal tract and its pathogenesis is mainly associated with c-KIT and PDGFRA gene mutations. Surgery is the standard treatment for limited GIST, while imatinib (IM) is the first-line treatment for patients with advanced or unresectable GIST. However, imatinib resistance (both primary and secondary resistance) remains a major challenge in the treatment of GIST. To address this challenge, the second-line drug sunitinib, the third-line drug regorafenib, and the fourth-line drug Ripretinib, as well as avapritinib targeting the PDGFRA D842V mutation, have been introduced into the clinic. In addition, therapeutic agents for wild-type GIST, such as SDH-deficient, NTRK-fusion and BRAF V600E mutant, have shown initial efficacy. Next-generation TKIs and other therapeutic strategies (e.g., heat shock protein inhibitors, mTOR inhibitors, immunotherapy) are still being explored, bringing new hope to patients with advanced drug-resistant GIST. In the future, the in-depth study of drug resistance mechanisms, the development of personalized treatment regimens, and the exploration of combination therapies will hopefully further improve the survival and quality of life of GIST patients.
Downloads
References
[1] ROBINSON T L, SIRCAR K, HEWLETT B R, et al. Gastrointestinal Stromal Tumors May Originate from a Subset of CD34-Positive Interstitial Cells of Cajal[J/OL]. The American Journal of Pathology, 2000, 156(4): 1157-1163. DOI: 10.1016/S0002-9440(10)64984-X. DOI: https://doi.org/10.1016/S0002-9440(10)64984-X
[2] SØREIDE K, SANDVIK O M, SØREIDE J A, et al. Global epidemiology of gastrointestinal stromal tumours (GIST): A systematic review of population-based cohort studies[J/OL]. Cancer Epidemiology, 2016, 40: 39-46. DOI:10. 1016/j. canep. 2015. 10.031. DOI: https://doi.org/10.1016/j.canep.2015.10.031
[3] CHAN K H. Gastrointestinal stromal tumors in a cohort of Chinese patients in Hong Kong[J/OL]. World Journal of Gastroenterology, 2006, 12(14): 2223. DOI:10. 3748/ wjg.v 12.i14.2223. DOI: https://doi.org/10.3748/wjg.v12.i14.2223
[4] LV M, WU C, ZHENG Y, et al. Incidence and Survival Analysis of Gastrointestinal Stromal Tumors in Shanghai: A Population-Based Study from 2001 to 2010[J/OL]. Gastroenterology Research and Practice, 2014, 2014: 1-6. DOI: 10. 1155/2014/834136. DOI: https://doi.org/10.1155/2014/834136
[5] CORLESS C L, FLETCHER J A, HEINRICH M C. Biology of Gastrointestinal Stromal Tumors[J/OL]. Journal of Clinical Oncology, 2004, 22(18): 3813-3825. DOI:10.1200/ JCO. 2004. 05.140. DOI: https://doi.org/10.1200/JCO.2004.05.140
[6] CORLESS C L, HEINRICH M C. Molecular Pathobiology of Gastrointestinal Stromal Sarcomas[J/OL]. Annual Review of Pathology: Mechanisms of Disease, 2008, 3(1): 557-586. DOI:10.1146/annurev.pathmechdis.3.121806.151538. DOI: https://doi.org/10.1146/annurev.pathmechdis.3.121806.151538
[7] CORLESS C L, BARNETT C M, HEINRICH M C. Gastrointestinal stromal tumours: origin and molecular oncology [J/OL]. Nature Reviews Cancer, 2011, 11(12): 865-878. DOI:10.1038/nrc3143. DOI: https://doi.org/10.1038/nrc3143
[8] CORLESS C L, SCHROEDER A, GRIFFITH D, et al. PDGFRA Mutations in Gastrointestinal Stromal Tumors: Frequency, Spectrum and In Vitro Sensitivity to Imatinib [J/OL]. Journal of Clinical Oncology, 2005, 23(23): 5357-5364. DOI: 10.1200/JCO.2005.14.068. DOI: https://doi.org/10.1200/JCO.2005.14.068
[9] SERRANO C, GEORGE S. Gastrointestinal Stromal Tumor: Challenges and Opportunities for a New Decade[J/OL]. Clinical Cancer Research, 2020, 26(19): 5078-5085. DOI:10. 1158/ 1078-0432.CCR-20-1706. DOI: https://doi.org/10.1158/1078-0432.CCR-20-1706
[10] BOIKOS S A, PAPPO A S, KILLIAN J K, et al. Molecular Subtypes ofKIT/PDGFRAWild-Type Gastrointestinal Stromal Tumors[J/OL]. JAMA Oncology, 2016, 2(7): 922. DOI: 10. 1001/ jamaoncol.2016.0256. DOI: https://doi.org/10.1001/jamaoncol.2016.0256
[11] MIETTINEN M, WANG Z F, SARLOMO-RIKALA M, et al. Succinate Dehydrogenase-Deficient GISTs[J/OL]. American Journal of Surgical Pathology, 2011, 35(11): 1712-1721. DOI: 10. 1097/PAS.0b013e3182260752. DOI: https://doi.org/10.1097/PAS.0b013e3182260752
[12] HOSTEIN I, FAUR N, PRIMOIS C, et al. BRAFMutation Status in Gastrointestinal Stromal Tumors[J/OL]. American Journal of Clinical Pathology, 2010, 133(1): 141-148. DOI:10.1309/AJCPPCKGA2QGBJ1R. DOI: https://doi.org/10.1309/AJCPPCKGA2QGBJ1R
[13] ATIQ M A, DAVIS J L, HORNICK J L, et al. Mesenchymal tumors of the gastrointestinal tract with NTRK rearrangements: a clinicopathological, immunophenotypic, and molecular study of eight cases, emphasizing their distinction from gastrointestinal stromal tumor (GIST)[J/OL]. Modern Pathology, 2021, 34(1): 95-103. DOI:10.1038/s41379-020-0623-z. DOI: https://doi.org/10.1038/s41379-020-0623-z
[14] SALVI P F, LORENZON L, CATERINO S, et al. Gastrointestinal stromal tumors associated with neurofibromatosis 1: a single centre experience and systematic review of the literature including 252 cases[J/OL]. International Journal of Surgical Oncology, 2013, 2013: 1-8. DOI:10.1155/2013/398570. DOI: https://doi.org/10.1155/2013/398570
[15] LASOTA J, FELISIAK-GOLABEK A, WASAG B, et al. Frequency and clinicopathologic profile of PIK3CA mutant GISTs: molecular genetic study of 529 cases[J/OL]. Modern Pathology, 2016, 29(3): 275-282. DOI:10.1038/ modpathol. 2015. 160. DOI: https://doi.org/10.1038/modpathol.2015.160
[16] SERRANO C, MARTÍN-BROTO J, ASENCIO-PASCUAL J M, et al. 2023 GEIS Guidelines for gastrointestinal stromal tumors[J/OL]. Therapeutic Advances in Medical Oncology, 2023, 15: 17588359231192388. DOI:10.1177/1758835923 1192388. DOI: https://doi.org/10.1177/17588359231192388
[17] JOENSUU H, ERIKSSON M, SUNDBY HALL K, et al. Survival Outcomes Associated With 3 Years vs 1 Year of Adjuvant Imatinib for Patients With High-Risk Gastrointestinal Stromal Tumors[J/OL]. JAMA Oncology, 2020, 6(8): 1241. DOI:10.1001/jamaoncol.2020.2091. DOI: https://doi.org/10.1001/jamaoncol.2020.2091
[18] BLANKE C D, DEMETRI G D, VON MEHREN M, et al. Long-Term Results From a Randomized Phase II Trial of Standard- Versus Higher-Dose Imatinib Mesylate for Patients With Unresectable or Metastatic Gastrointestinal Stromal Tumors Expressing KIT[J/OL]. Journal of Clinical Oncology, 2008, 26(4): 620-625. DOI:10.1200/JCO.2007.13.4403. DOI: https://doi.org/10.1200/JCO.2007.13.4403
[19] HUANG W K, WU C E, WANG S Y, et al. Systemic Therapy for Gastrointestinal Stromal Tumor: Current Standards and Emerging Challenges[J/OL]. Current Treatment Options in Oncology, 2022, 23(9): 1303. DOI:10.1007/s11864-022-00996-8. DOI: https://doi.org/10.1007/s11864-022-00996-8
[20] LI G Z, RAUT C P. <p>Targeted therapy and personalized medicine in gastrointestinal stromal tumors: drug resistance, mechanisms, and treatment strategies</p> [J/OL]. OncoTargets and Therapy, 2019, Volume 12: 5123-5133. DOI:10.2147/OTT.S180763. DOI: https://doi.org/10.2147/OTT.S180763
[21] GRAMZA A W, CORLESS C L, HEINRICH M C. Resistance to Tyrosine Kinase Inhibitors in Gastrointestinal Stromal Tumors [J/OL]. Clinical Cancer Research, 2009, 15(24): 7510-7518. DOI:10.1158/1078-0432.CCR-09-0190. DOI: https://doi.org/10.1158/1078-0432.CCR-09-0190
[22] GOUNDER M M, MAKI R G. Molecular basis for primary and secondary tyrosine kinase inhibitor resistance in gastrointestinal stromal tumor[J/OL]. Cancer Chemotherapy and Pharmacology, 2011, 67(S1): 25-43. DOI:10.1007/ s00280-010-1526-3.
[23] RAUT C P, ESPAT N J, MAKI R G, et al. Efficacy and Tolerability of 5-Year Adjuvant Imatinib Treatment for Patients With Resected Intermediate- or High-Risk Primary Gastrointestinal Stromal Tumor[J/OL]. JAMA Oncology, 2018, 4(12): e184060. DOI:10.1001/jamaoncol.2018.4060. DOI: https://doi.org/10.1001/jamaoncol.2018.4060
[24] GOUNDER M M, MAKI R G. Molecular basis for primary and secondary tyrosine kinase inhibitor resistance in gastrointestinal stromal tumor[J/OL]. Cancer Chemotherapy and Pharmacology, 2011, 67(S1): 25-43. DOI:10.1007/ s00280-010-1526-3. DOI: https://doi.org/10.1007/s00280-010-1526-3
[25] HUANG W K, GAO J, CHEN Z, et al. Heterogeneity of Metabolic Vulnerability in Imatinib-Resistant Gastrointestinal Stromal Tumor[J/OL]. Cells, 2020, 9(6): 1333. DOI:10.3390/ cells 9061333. DOI: https://doi.org/10.3390/cells9061333
[26] SHIMA T, TANIGUCHI K, TOKUMARU Y, et al. Glucose transporter‑1 inhibition overcomes imatinib resistance in gastrointestinal stromal tumor cells[J/OL]. Oncology Reports, 2022, 47(1): 7. DOI:10.3892/or.2021.8218. DOI: https://doi.org/10.3892/or.2021.8218
[27] SHAO Y, LIAN S, ZHENG J, et al. RP11-616M22.7 recapitulates imatinib resistance in gastrointestinal stromal tumor[J/OL]. Molecular Therapy - Nucleic Acids, 2021, 25: 264-276. DOI:10.1016/j.omtn.2021.05.017. DOI: https://doi.org/10.1016/j.omtn.2021.05.017
[28] AKÇAKAYA P, CARAMUTA S, ÅHLEN J, et al. microRNA expression signatures of gastrointestinal stromal tumours: associations with imatinib resistance and patient outcome [J/OL]. British Journal of Cancer, 2014, 111(11): 2091-2102. DOI: 10.1038/bjc.2014.548. DOI: https://doi.org/10.1038/bjc.2014.548
[29] BLANKE C D, RANKIN C, DEMETRI G D, et al. Phase III Randomized, Intergroup Trial Assessing Imatinib Mesylate At Two Dose Levels in Patients With Unresectable or Metastatic Gastrointestinal Stromal Tumors Expressing the Kit Receptor Tyrosine Kinase: S0033[J/OL]. Journal of Clinical Oncology, 2008, 26(4): 626-632. DOI:10.1200/JCO.2007.13.4452. DOI: https://doi.org/10.1200/JCO.2007.13.4452
[30] HEINRICH M C, RANKIN C, BLANKE C D, et al. Correlation of Long-term Results of Imatinib in Advanced Gastrointestinal Stromal Tumors With Next-Generation Sequencing Results[J/OL]. JAMA Oncology, 2017, 3(7): 944. DOI:10.1001/jamaoncol.2016.6728. DOI: https://doi.org/10.1001/jamaoncol.2016.6728
[31] Comparison of Two Doses of Imatinib for the Treatment of Unresectable or Metastatic Gastrointestinal Stromal Tumors: A Meta-Analysis of 1,640 Patients[J/OL]. Journal of Clinical Oncology, 2010, 28(7): 1247-1253. DOI:10.1200/ JCO. 2009. 24. 2099. DOI: https://doi.org/10.1200/JCO.2009.24.2099
[32] GOODMAN V L, ROCK E P, DAGHER R, et al. Approval Summary: Sunitinib for the Treatment of Imatinib Refractory or Intolerant Gastrointestinal Stromal Tumors and Advanced Renal Cell Carcinoma[J/OL]. Clinical Cancer Research, 2007, 13(5): 1367-1373. DOI:10.1158/1078-0432.CCR-06-2328. DOI: https://doi.org/10.1158/1078-0432.CCR-06-2328
[33] JIN J, XIE Y, ZHANG J S, et al. Sunitinib resistance in renal cell carcinoma: From molecular mechanisms to predictive biomarkers [J/OL]. Drug Resistance Updates, 2023, 67: 100929. DOI:10.1016/j.drup.2023.100929. DOI: https://doi.org/10.1016/j.drup.2023.100929
[34] DEMETRI G D, VAN OOSTEROM A T, GARRETT C R, et al. Efficacy and safety of sunitinib in patients with advanced gastrointestinal stromal tumour after failure of imatinib: a randomised controlled trial[J/OL]. The Lancet, 2006, 368(9544): 1329-1338. DOI:10.1016/S0140-6736(06) 69446-4. DOI: https://doi.org/10.1016/S0140-6736(06)69446-4
[35] REICHARDT P, KANG Y, RUTKOWSKI P, et al. Clinical outcomes of patients with advanced gastrointestinal stromal tumors: Safety and efficacy in a worldwide treatment‐use trial of sunitinib[J/OL]. Cancer, 2015, 121(9): 1405-1413. DOI: 10. 1002/cncr.29220. DOI: https://doi.org/10.1002/cncr.29220
[36] DEMETRI G D, GARRETT C R, SCHÖFFSKI P, et al. Complete Longitudinal Analyses of the Randomized, Placebo-Controlled, Phase III Trial of Sunitinib in Patients with Gastrointestinal Stromal Tumor following Imatinib Failure [J/OL]. Clinical Cancer Research, 2012, 18(11): 3170-3179. DOI: 10.1158/1078-0432.CCR-11-3005. DOI: https://doi.org/10.1158/1078-0432.CCR-11-3005
[37] HEINRICH M C, MAKI R G, CORLESS C L, et al. Primary and Secondary Kinase Genotypes Correlate With the Biological and Clinical Activity of Sunitinib in Imatinib-Resistant Gastrointestinal Stromal Tumor[J/OL]. Journal of Clinical Oncology, 2008, 26(33): 5352-5359. DOI:10. 1200/ JCO. 2007.15.7461. DOI: https://doi.org/10.1200/JCO.2007.15.7461
[38] WILHELM S M, DUMAS J, ADNANE L, et al. Regorafenib (BAY 73‐4506): A new oral multikinase inhibitor of angiogenic, stromal and oncogenic receptor tyrosine kinases with potent preclinical antitumor activity[J/OL]. International Journal of Cancer, 2011, 129(1): 245-255. DOI:10.1002/ ijc. 25864. DOI: https://doi.org/10.1002/ijc.25864
[39] DEMETRI G D, REICHARDT P, KANG Y K, et al. Efficacy and safety of regorafenib for advanced gastrointestinal stromal tumours after failure of imatinib and sunitinib (GRID): an international, multicentre, randomised, placebo-controlled, phase 3 trial [J/OL]. The Lancet, 2013, 381(9863): 295-302. DOI: 10.1016/S0140-6736(12)61857-1. DOI: https://doi.org/10.1016/S0140-6736(12)61857-1
[40] SERRANO C, MARIÑO-ENRÍQUEZ A, TAO D L, et al. Complementary activity of tyrosine kinase inhibitors against secondary kit mutations in imatinib-resistant gastrointestinal stromal tumours[J/OL]. British Journal of Cancer, 2019, 120(6): 612-620. DOI:10.1038/s41416-019-0389-6. DOI: https://doi.org/10.1038/s41416-019-0389-6
[41] KUMAR V, DOROS L, THOMPSON M, et al. FDA Approval Summary: Ripretinib for Advanced Gastrointestinal Stromal Tumor[J/OL]. Clinical Cancer Research, 2023, 29(11): 2020-2024. DOI:10.1158/1078-0432.CCR-22-2400. DOI: https://doi.org/10.1158/1078-0432.CCR-22-2400
[42] SMITH B D, KAUFMAN M D, LU W P, et al. Ripretinib (DCC-2618) Is a Switch Control Kinase Inhibitor of a Broad Spectrum of Oncogenic and Drug-Resistant KIT and PDGFRA Variants [J/OL]. Cancer Cell, 2019, 35(5): 738-751.e9. DOI: 10. 1016/j.ccell.2019.04.006. DOI: https://doi.org/10.1016/j.ccell.2019.04.006
[43] BLAY J Y, SERRANO C, HEINRICH M C, et al. Ripretinib in patients with advanced gastrointestinal stromal tumours (INVICTUS): a double-blind, randomised, placebo-controlled, phase 3 trial[J/OL]. The Lancet Oncology, 2020, 21(7): 923-934. DOI:10.1016/S1470-2045(20)30168-6. DOI: https://doi.org/10.1016/S1470-2045(20)30168-6
[44] BAUER S, JONES R L, BLAY J Y, et al. Ripretinib Versus Sunitinib in Patients With Advanced Gastrointestinal Stromal Tumor After Treatment With Imatinib (INTRIGUE): A Randomized, Open-Label, Phase III Trial[J/OL]. Journal of Clinical Oncology, 2022, 40(34): 3918-3928. DOI:10. 1200/ JCO. 22.00294. DOI: https://doi.org/10.1200/JCO.22.00294
[45] BAUER S, JONES R L, GEORGE S, et al. Mutational heterogeneity of imatinib resistance and efficacy of ripretinib vs sunitinib in patients with gastrointestinal stromal tumor: ctDNA analysis from INTRIGUE.[J/OL]. Journal of Clinical Oncology, 2023, 41(36_suppl): 397784-397784. DOI:10.1200/ JCO. 2023.41.36_suppl.397784. DOI: https://doi.org/10.1200/JCO.2023.41.36_suppl.397784
[46] RESEARCH C for D E and. FDA approves avapritinib for gastrointestinal stromal tumor with a rare mutation[J/OL]. Fda, 2020[2025-01-19]. https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-avapritinib-gastrointestinal-stromal-tumor-rare-mutation.
[47] BRENCA M, ROSSI S, POLANO M, et al. Transcriptome sequencing identifies ETV6–NTRK3 as a gene fusion involved in GIST[J/OL]. The Journal of Pathology, 2016, 238(4): 543-549. DOI:10.1002/path.4677. DOI: https://doi.org/10.1002/path.4677
[48] CASSIER P A, FUMAGALLI E, RUTKOWSKI P, et al. Outcome of Patients with Platelet-Derived Growth Factor Receptor Alpha–Mutated Gastrointestinal Stromal Tumors in the Tyrosine Kinase Inhibitor Era[J/OL]. Clinical Cancer Research, 2012, 18(16): 4458-4464. DOI:10.1158/1078-0432. CCR-11-3025. DOI: https://doi.org/10.1158/1078-0432.CCR-11-3025
[49] YOO C, RYU M H, JO J, et al. Efficacy of Imatinib in Patients with Platelet-Derived Growth Factor Receptor Alpha–Mutated Gastrointestinal Stromal Tumors[J/OL]. Cancer Research and Treatment, 2016, 48(2): 546-552. DOI:10.4143/crt.2015.015. DOI: https://doi.org/10.4143/crt.2015.015
[50] HEINRICH M C, JONES R L, VON MEHREN M, et al. Avapritinib in advanced PDGFRA D842V-mutant gastrointestinal stromal tumour (NAVIGATOR): a multicentre, open-label, phase 1 trial[J/OL]. The Lancet Oncology, 2020, 21(7): 935-946. DOI:10.1016/S1470-2045(20)30269-2. DOI: https://doi.org/10.1016/S1470-2045(20)30269-2
[51] JONES R L, SERRANO C, VON MEHREN M, et al. Avapritinib in unresectable or metastatic PDGFRA D842V-mutant gastrointestinal stromal tumours: Long-term efficacy and safety data from the NAVIGATOR phase I trial[J/OL]. European Journal of Cancer, 2021, 145: 132-142. DOI: 10. 1016/ j.ejca.2020.12.008. DOI: https://doi.org/10.1016/j.ejca.2020.12.008
[52] RIVERA V M, HUANG W S, LU M, et al. Abstract 1292: Preclinical characterization of THE-630, a next-generation inhibitor for KIT-mutant gastrointestinal stromal tumors (GIST)[J/OL]. Cancer Research, 2021, 81(13_Supplement): 1292-1292. DOI:10.1158/1538-7445.AM2021-1292. DOI: https://doi.org/10.1158/1538-7445.AM2021-1292
[53] THESEUS PHARMACEUTICALS. A phase 1/2 study of the safety, pharmacokinetics and anti-tumor activity of the oral KIT inhibitor THE-630 in patients with advanced gastrointestinal stromal tumors (GIST): NCT05160168[R/OL]. clinicaltrials.gov, 2024[2025-01-21]. https://clinicaltrials. gov/ study/NCT05160168.
[54] PILLA REDDY V, ANJUM R, GRONDINE M, et al. The Pharmacokinetic–Pharmacodynamic (PKPD) Relationships of AZD3229, a Novel and Selective Inhibitor of KIT, in a Range of Mouse Xenograft Models of GIST[J/OL]. Clinical Cancer Research, 2020, 26(14): 3751-3759. DOI:10.1158/1078-0432. CCR-19-2848. DOI: https://doi.org/10.1158/1078-0432.CCR-19-2848
[55] BANKS E, GRONDINE M, BHAVSAR D, et al. Discovery and pharmacological characterization of AZD3229, a potent KIT/PDGFRα inhibitor for treatment of gastrointestinal stromal tumors[J/OL]. Science Translational Medicine, 2020, 12(541): eaaz2481. DOI:10.1126/scitranslmed.aaz2481. DOI: https://doi.org/10.1126/scitranslmed.aaz2481
[56] NINGBO NEWBAY TECHNOLOGY DEVELOPMENT CO., LTD. A multicenter phase 1, open-label study of NB003 to assess safety, tolerability, pharmacokinetics and efficacy in patients with advanced malignancies: NCT04936178[R/OL]. clinicaltrials.gov, 2024[2025-01-21]. https://clinicaltrials. gov/ study/ NCT 04936178.
[57] GEBREYOHANNES Y K, BURTON E A, WOZNIAK A, et al. PLX9486 shows anti-tumor efficacy in patient-derived, tyrosine kinase inhibitor-resistant KIT-mutant xenograft models of gastrointestinal stromal tumors[J/OL]. Clinical and Experimental Medicine, 2019, 19(2): 201-210. DOI:10.1007/ s10238-018-0541-2. DOI: https://doi.org/10.1007/s10238-018-0541-2
[58] WAGNER A J, SEVERSON P L, SHIELDS A F, et al. Association of Combination of Conformation-Specific KIT Inhibitors With Clinical Benefit in Patients With Refractory Gastrointestinal Stromal Tumors[J/OL]. JAMA Oncology, 2021, 7(9): 1343. DOI:10.1001/jamaoncol.2021.2086. DOI: https://doi.org/10.1001/jamaoncol.2021.2086
[59] COGENT BIOSCIENCES, INC. A phase 3 randomized, open-label, multicenter clinical study of CGT9486+sunitinib vs. Sunitinib in subjects with locally advanced, unresectable, or metastatic gastrointestinal stromal tumors: NCT05208047 [R/OL]. clinicaltrials.gov, 2024[2025-01-21]. https:// clinicaltrials. gov/study/NCT05208047.
[60] ORTIZ R, PERAZZOLI G, CABEZA L, et al. Temozolomide: An Updated Overview of Resistance Mechanisms, Nanotechnology Advances and Clinical Applications[J/OL]. Current Neuropharmacology, 2021, 19(4): 513-537. DOI: 10. 2174/ 1570159X18666200626204005. DOI: https://doi.org/10.2174/1570159X18666200626204005
[61] DE SILVA M, RASTOGI S, CHAN D, et al. Succinate dehydrogenase-deficient gastrointestinal stromal tumor: from diagnostic dilemma to novel personalised therapy in 2 case reports[J/OL]. Translational Cancer Research, 2021, 0(0): 0-0. DOI:10.21037/tcr-21-131. DOI: https://doi.org/10.21037/tcr-21-131
[62] YEBRA M, BHARGAVA S, KUMAR A, et al. Establishment of Patient-Derived Succinate Dehydrogenase–Deficient Gastrointestinal Stromal Tumor Models for Predicting Therapeutic Response[J/OL]. Clinical Cancer Research, 2022, 28 (1): 187-200. DOI:10.1158/1078-0432.CCR-21-2092. DOI: https://doi.org/10.1158/1078-0432.CCR-21-2092
[63] SHI E, CHMIELECKI J, TANG C M, et al. FGFR1 and NTRK3 actionable alterations in “Wild-Type” gastrointestinal stromal tumors[J/OL]. Journal of Translational Medicine, 2016, 14 (1): 339. DOI:10.1186/s12967-016-1075-6. DOI: https://doi.org/10.1186/s12967-016-1075-6
[64] D’ALPINO PEIXOTO R, MEDEIROS B A, CRONEMBERGER E H. Resected High-Risk Rectal GIST Harboring NTRK1 Fusion: a Case Report and Review of the Literature[J/OL]. Journal of Gastrointestinal Cancer, 2021, 52(1): 316-319. DOI:10.1007/s12029-020-00423-x. DOI: https://doi.org/10.1007/s12029-020-00423-x
[65] DRILON A, LAETSCH T W, KUMMAR S, et al. Efficacy of Larotrectinib inTRKFusion–Positive Cancers in Adults and Children[J/OL]. New England Journal of Medicine, 2018, 378(8): 731-739. DOI:10.1056/NEJMoa1714448. DOI: https://doi.org/10.1056/NEJMoa1714448
[66] THEIN K Z, LEMERY S J, KUMMAR S. Tissue-Agnostic Drug Development: A New Path to Drug Approval[J/OL]. Cancer Discovery, 2021, 11(9): 2139-2144. DOI:10.1158/ 2159-8290.CD-21-0554. DOI: https://doi.org/10.1158/2159-8290.CD-21-0554
[67] DOEBELE R C, DRILON A, PAZ-ARES L, et al. Entrectinib in patients with advanced or metastatic NTRK fusion-positive solid tumours: integrated analysis of three phase 1–2 trials [J/OL]. The Lancet Oncology, 2020, 21(2): 271-282. DOI: 10. 1016/ S1470-2045(19)30691-6.
[68] FALCHOOK G S, TRENT J C, HEINRICH M C, et al. BRAF Mutant Gastrointestinal Stromal Tumor: First report of regression with BRAF inhibitor dabrafenib (GSK2118436) and whole exomic sequencing for analysis of acquired resistance [J/OL]. Oncotarget, 2013, 4(2): 310-315. DOI:10. 18632/ oncotarget. 864. DOI: https://doi.org/10.18632/oncotarget.864
[69] HANRAHAN A J, CHEN Z, ROSEN N, et al. BRAF — a tumour-agnostic drug target with lineage-specific dependencies [J/OL]. Nature Reviews Clinical Oncology, 2024, 21 (3): 224-247. DOI:10.1038/s41571-023-00852-0. DOI: https://doi.org/10.1038/s41571-023-00852-0
[70] SALAMA A K S, LI S, MACRAE E R, et al. Dabrafenib and Trametinib in Patients With Tumors With BRAFV600E Mutations: Results of the NCI-MATCH Trial Subprotocol H[J/OL]. Journal of Clinical Oncology, 2020, 38(33): 3895-3904. DOI:10.1200/JCO.20.00762. DOI: https://doi.org/10.1200/JCO.20.00762
[71] WHITESELL L, LINDQUIST S L. HSP90 and the chaperoning of cancer[J/OL]. Nature Reviews Cancer, 2005, 5(10): 761-772. DOI:10.1038/nrc1716. DOI: https://doi.org/10.1038/nrc1716
[72] KIHARA T, YUAN J, WATABE T, et al. Pimitespib is effective on cecal GIST in a mouse model of familial GISTs with KIT-Asp820Tyr mutation through KIT signaling inhibition[J/OL]. Experimental and Molecular Pathology, 2021, 123: 104692. DOI:10.1016/j.yexmp.2021.104692. DOI: https://doi.org/10.1016/j.yexmp.2021.104692
[73] SAITO Y, TAKAHASHI T, OBATA Y, et al. TAS-116 inhibits oncogenic KIT signalling on the Golgi in both imatinib-naïve and imatinib-resistant gastrointestinal stromal tumours[J/OL]. British Journal of Cancer, 2020, 122(5): 658-667. DOI:10.1038/s41416-019-0688-y. DOI: https://doi.org/10.1038/s41416-019-0688-y
[74] KUROKAWA Y, HONMA Y, SAWAKI A, et al. Pimitespib in patients with advanced gastrointestinal stromal tumor (CHAPTER-GIST-301): a randomized, double-blind, placebo-controlled phase III trial[J/OL]. Annals of Oncology, 2022, 33(9): 959-967. DOI:10.1016/j.annonc.2022.05.518. DOI: https://doi.org/10.1016/j.annonc.2022.05.518
[75] OHKUBO S, KODAMA Y, MURAOKA H, et al. TAS-116, a Highly Selective Inhibitor of Heat Shock Protein 90α and β, Demonstrates Potent Antitumor Activity and Minimal Ocular Toxicity in Preclinical Models[J/OL]. Molecular Cancer Therapeutics, 2015, 14(1): 14-22. DOI:10.1158/1535-7163. MCT-14-0219. DOI: https://doi.org/10.1158/1535-7163.MCT-14-0219
[76] SHIMOMURA A, YAMAMOTO N, KONDO S, et al. First-in-Human Phase I Study of an Oral HSP90 Inhibitor, TAS-116, in Patients with Advanced Solid Tumors[J/OL]. Molecular Cancer Therapeutics, 2019, 18(3): 531-540. DOI:10.1158/ 1535- 7163.MCT-18-0831. DOI: https://doi.org/10.1158/1535-7163.MCT-18-0831
[77] BAUER S, DUENSING A, DEMETRI G D, et al. KIT oncogenic signaling mechanisms in imatinib-resistant gastrointestinal stromal tumor: PI3-kinase/AKT is a crucial survival pathway[J/OL]. Oncogene, 2007, 26(54): 7560-7568. DOI:10.1038/sj.onc.1210558. DOI: https://doi.org/10.1038/sj.onc.1210558
[78] SCHÖFFSKI P, REICHARDT P, BLAY J Y, et al. A phase I–II study of everolimus (RAD001) in combination with imatinib in patients with imatinib-resistant gastrointestinal stromal tumors[J/OL]. Annals of Oncology, 2010, 21(10): 1990-1998. DOI:10.1093/annonc/mdq076. DOI: https://doi.org/10.1093/annonc/mdq076
[79] PANTALEO M A, TARANTINO G, AGOSTINELLI C, et al. Immune microenvironment profiling of gastrointestinal stromal tumors (GIST) shows gene expression patterns associated to immune checkpoint inhibitors response[J/OL]. OncoImmunology, 2019, 8(9): e1617588. DOI:10.1080/ 2162402X. 2019.1617588. DOI: https://doi.org/10.1080/2162402X.2019.1617588
[80] D’ANGELO S P, SHOUSHTARI A N, AGARAM N P, et al. Prevalence of tumor-infiltrating lymphocytes and PD-L1 expression in the soft tissue sarcoma microenvironment[J/OL]. Human Pathology, 2015, 46(3): 357-365. DOI:10.1016/j. humpath. 2014.11.001. DOI: https://doi.org/10.1016/j.humpath.2014.11.001
[81] BALACHANDRAN V P, CAVNAR M J, ZENG S, et al. Imatinib potentiates antitumor T cell responses in gastrointestinal stromal tumor through the inhibition of Ido [J/OL]. Nature Medicine, 2011, 17(9): 1094-1100. DOI: 10. 1038/ nm.2438. DOI: https://doi.org/10.1038/nm.2438
[82] SEIFERT A M, ZENG S, ZHANG J Q, et al. PD-1/PD-L1 Blockade Enhances T-cell Activity and Antitumor Efficacy of Imatinib in Gastrointestinal Stromal Tumors[J/OL]. Clinical Cancer Research, 2017, 23(2): 454-465. DOI:10.1158/1078-0432.CCR-16-1163. DOI: https://doi.org/10.1158/1078-0432.CCR-16-1163
[83] KANG Y K. A phase ib/II study of PDR001 plus imatinib for metastatic or unresectable GIST with prior failure of imatinib, sunitinib and regorafenib: NCT03609424[R/OL]. clinicaltrials.gov, 2022[2025-01-22]. https://clinicaltrials. gov/ study/ NCT03609424.
[84] KOZAK K, PANTALEO M A, FUMAGALLI E, et al. 1667TiP A phase II, single arm study of avelumab in combination with axitinib in patients with unresectable/ metastatic gastrointestinal stromal tumor after failure of standard therapy - AXAGIST[J/OL]. Annals of Oncology, 2020, 31: S990. DOI:10.1016/j.annonc.2020.08.1892. DOI: https://doi.org/10.1016/j.annonc.2020.08.1892
[85] INSTITUT BERGONIÉ. A phase I/II study of regorafenib plus avelumab in solid tumors: NCT03475953 [R/OL]. clinicaltrials.gov, 2023[2025-01-22]. https:// clinicaltrials. gov/study/NCT03475953.
[86] ABRAMS T, CONNOR A, FANTON C, et al. Preclinical Antitumor Activity of a Novel Anti–c-KIT Antibody–Drug Conjugate against Mutant and Wild-type c-KIT–Positive Solid Tumors[J/OL]. Clinical Cancer Research, 2018, 24(17): 4297-4308. DOI:10.1158/1078-0432.CCR-17-3795. DOI: https://doi.org/10.1158/1078-0432.CCR-17-3795
[87] KIM J, KIM K, BAEK E J, et al. A novel anti‐c‐Kit antibody–drug conjugate to treat wild‐type and activating‐mutant c‐Kit‐positive tumors[J/OL]. Molecular Oncology, 2022, 16(6): 1290-1308. DOI:10.1002/1878-0261.13084. DOI: https://doi.org/10.1002/1878-0261.13084
[88] IIDA K, ABDELHAMID AHMED A H, NAGATSUMA A K, et al. Identification and Therapeutic Targeting of GPR20, Selectively Expressed in Gastrointestinal Stromal Tumors, with DS-6157a, a First-in-Class Antibody–Drug Conjugate [J/OL]. Cancer Discovery, 2021, 11(6): 1508-1523. DOI:10. 1158/ 2159-8290.CD-20-1434. DOI: https://doi.org/10.1158/2159-8290.CD-20-1434
[89] GEORGE S, HEINRICH M C, SOMAIAH N, et al. A Phase I, Multicenter, Open-Label, First-in-Human Study of DS-6157a in Patients with Advanced Gastrointestinal Stromal Tumor [J/OL]. Clinical Cancer Research, 2023, 29(18): 3659-3667. DOI: 10.1158/1078-0432.CCR-23-0640. DOI: https://doi.org/10.1158/1078-0432.CCR-23-0640
Downloads
Published
Issue
Section
License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

