Literature DB >> 30274985

Robust Activity of Avapritinib, Potent and Highly Selective Inhibitor of Mutated KIT, in Patient-derived Xenograft Models of Gastrointestinal Stromal Tumors.

Yemarshet K Gebreyohannes1, Agnieszka Wozniak2, Madalina-Elena Zhai1, Jasmien Wellens1, Jasmien Cornillie1, Ulla Vanleeuw1, Erica Evans3, Alexandra K Gardino3, Christoph Lengauer3, Maria Debiec-Rychter4, Raf Sciot5, Patrick Schöffski1.   

Abstract

PURPOSE: Gastrointestinal stromal tumors (GIST) are commonly treated with tyrosine kinase inhibitors (TKI). The majority of patients with advanced GIST ultimately become resistant to TKI due to acquisition of secondary KIT mutations, whereas primary resistance is mainly caused by PDGFRA p.D842V mutation. We tested the activity of avapritinib, a potent and highly selective inhibitor of mutated KIT and PDGFRA, in three patient-derived xenograft (PDX) GIST models carrying different KIT mutations, with differential sensitivity to standard TKI.Experimental Design: NMRI nu/nu mice (n = 93) were transplanted with human GIST xenografts with KIT exon 11+17 (UZLX-GIST9 KIT 11+17 ), exon 11 (UZLX-GIST3 KIT 11 ), or exon 9 (UZLX-GIST2B KIT9 ) mutations, respectively. We compared avapritinib (10 and 30 mg/kg/once daily) versus vehicle, imatinib (50 mg/kg/bid) or regorafenib (30 mg/kg/once daily; UZLX-GIST9 KIT11+17 ); avapritinib (10, 30, 100 mg/kg/once daily) versus vehicle or imatinib [UZLX-GIST3 KIT11 ]; and avapritinib (10, 30, 60 mg/kg/once daily) versus vehicle, imatinib (50, 100 mg/kg/twice daily), or sunitinib (40 mg/kg/once daily; UZLX-GIST2B KIT9 ).
RESULTS: In all models, avapritinib resulted in reduction of tumor volume, significant inhibition of proliferation, and reduced KIT signaling. In two models, avapritinib led to remarkable histologic responses, increase in apoptosis, and inhibition of MAPK-phosphorylation. Avapritinib showed superior (UZLX-GIST9 KIT 11+17 and -GIST2B KIT 9 ) or equal (UZLX-GIST3 KIT 11 ) antitumor activity to the standard dose of imatinib. In UZLX-GIST9 KIT 11+17 , the antitumor effects of avapritinib were significantly better than with imatinib or regorafenib.
CONCLUSIONS: Avapritinib has significant antitumor activity in GIST PDX models characterized by different KIT mutations and sensitivity to established TKI. These data provide strong support for the ongoing clinical trials with avapritinib in patients with GIST (NCT02508532, NCT03465722). ©2018 American Association for Cancer Research.

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Year:  2018        PMID: 30274985     DOI: 10.1158/1078-0432.CCR-18-1858

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  17 in total

1.  Avapritinib: A Selective Inhibitor of KIT and PDGFRα that Reverses ABCB1 and ABCG2-Mediated Multidrug Resistance in Cancer Cell Lines.

Authors:  Chung-Pu Wu; Sabrina Lusvarghi; Jyun-Cheng Wang; Sung-Han Hsiao; Yang-Hui Huang; Tai-Ho Hung; Suresh V Ambudkar
Journal:  Mol Pharm       Date:  2019-06-04       Impact factor: 4.939

2.  PLX9486 shows anti-tumor efficacy in patient-derived, tyrosine kinase inhibitor-resistant KIT-mutant xenograft models of gastrointestinal stromal tumors.

Authors:  Yemarshet K Gebreyohannes; Elizabeth A Burton; Agnieszka Wozniak; Bernice Matusow; Gaston Habets; Jasmien Wellens; Jasmien Cornillie; Jack Lin; Marika Nespi; Guoxian Wu; Chao Zhang; Gideon Bollag; Maria Debiec-Rychter; Raf Sciot; Patrick Schöffski
Journal:  Clin Exp Med       Date:  2018-12-06       Impact factor: 3.984

3.  Preclinical model-based evaluation of Imatinib resistance induced by KIT mutations and its overcoming strategies in gastrointestinal stromal tumor (GIST).

Authors:  Qian Zhao; Cheng Zhang; Changsong Qi; Jing Yang; Yang Chen; Sai Ge; Lin Shen; Jing Gao; Jian Li
Journal:  Am J Transl Res       Date:  2021-12-15       Impact factor: 4.060

Review 4.  Small molecule inhibitors targeting the cancers.

Authors:  Gui-Hong Liu; Tao Chen; Xin Zhang; Xue-Lei Ma; Hua-Shan Shi
Journal:  MedComm (2020)       Date:  2022-10-13

5.  Combination of Type I and II tyrosine kinase inhibitors-avapritinib and sunitinib-in refractory gastrointestinal stromal tumor after failure to multi-line therapy: a case report.

Authors:  Xiaodan Guo; Shaoqing Huang; Yihang Shi; Zhaoming Guan; Sile Chen; Yun Feng; Yanzhe Xia; Xinhua Zhang
Journal:  Ann Transl Med       Date:  2022-09

6.  Establishment of Patient-Derived Succinate Dehydrogenase-Deficient Gastrointestinal Stromal Tumor Models for Predicting Therapeutic Response.

Authors:  Mayra Yebra; Shruti Bhargava; Avi Kumar; Adam M Burgoyne; Chih-Min Tang; Hyunho Yoon; Sudeep Banerjee; Joseph Aguilera; Thekla Cordes; Vipul Sheth; Sangkyu Noh; Rowan Ustoy; Sam Li; Sunil J Advani; Christopher L Corless; Michael C Heinrich; Razelle Kurzrock; Scott M Lippman; Paul T Fanta; Olivier Harismendy; Christian Metallo; Jason K Sicklick
Journal:  Clin Cancer Res       Date:  2021-08-23       Impact factor: 13.801

7.  Cryptotanshinone enhances the efficacy of Bcr-Abl tyrosine kinase inhibitors via inhibiting STAT3 and eIF4E signalling pathways in chronic myeloid leukaemia.

Authors:  Rubin Cheng; Yilan Huang; Yun Fang; Qirui Wang; Meixiu Yan; Yuqing Ge
Journal:  Pharm Biol       Date:  2021-12       Impact factor: 3.503

Review 8.  Early and Next-Generation KIT/PDGFRA Kinase Inhibitors and the Future of Treatment for Advanced Gastrointestinal Stromal Tumor.

Authors:  Sebastian Bauer; Suzanne George; Margaret von Mehren; Michael C Heinrich
Journal:  Front Oncol       Date:  2021-07-12       Impact factor: 6.244

Review 9.  The Emerging Role of the FGF/FGFR Pathway in Gastrointestinal Stromal Tumor.

Authors:  Annalisa Astolfi; Maria Abbondanza Pantaleo; Valentina Indio; Milena Urbini; Margherita Nannini
Journal:  Int J Mol Sci       Date:  2020-05-07       Impact factor: 5.923

10.  MRI-Based Radiomics Models for Predicting Risk Classification of Gastrointestinal Stromal Tumors.

Authors:  Haijia Mao; Bingqian Zhang; Mingyue Zou; Yanan Huang; Liming Yang; Cheng Wang; PeiPei Pang; Zhenhua Zhao
Journal:  Front Oncol       Date:  2021-05-10       Impact factor: 6.244

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