Avapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. The literature review and clinical case

We have three drugs for treatment of gastrointestinal stromal tumors (GIST): imatinib, sunitinib and regorafenib. Avapritinib (Ayvakit, BLU-285) is one more drug that was approved in January 2020. Avapritinib is a new selective tyrosine kinase inhibitor of PDGFRA and KIT mutations. Based on NAVIGATO...

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Autores principales: Daria A. Filonenko, Bela M. Medvedeva, Andrey A. Meshcheryakov
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Lenguaje:RU
Publicado: IP Habib O.N. 2021
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Acceso en línea:https://doaj.org/article/6e46ed6345224af8a1b117b56a28b0d7
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spelling oai:doaj.org-article:6e46ed6345224af8a1b117b56a28b0d72021-11-30T17:03:34ZAvapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. The literature review and clinical case1815-14341815-144210.26442/18151434.2020.4.200409https://doaj.org/article/6e46ed6345224af8a1b117b56a28b0d72021-02-01T00:00:00Zhttps://modernonco.orscience.ru/1815-1434/article/viewFile/61163/44252https://doaj.org/toc/1815-1434https://doaj.org/toc/1815-1442We have three drugs for treatment of gastrointestinal stromal tumors (GIST): imatinib, sunitinib and regorafenib. Avapritinib (Ayvakit, BLU-285) is one more drug that was approved in January 2020. Avapritinib is a new selective tyrosine kinase inhibitor of PDGFRA and KIT mutations. Based on NAVIGATOR trial avapritinib was approved by FDA for treatment of PDGFRA exon 18 mutant GIST including D842V. Avapritinib was included in NCCN guidelines in the first line therapy PDGFRA D842V mutant GIST. There are only several cases describe imatinib and regorafenib efficacy in D842V mutation in the literature. Avapritinib is the first drug with high efficacy in D842V mutant GIST. Avapritinib has high efficacy against second mutations that explain its activity in 4 lines of treatment. This article summarizes the results of NAVIGATOR trial and describes a clinical case of the patient with advanced GIST who received avapritinib in 6th line of treatment. Partial response was achieved that lasted 9 months. The earliest side effects were periorbital edema and increased lacrimation. Three months later the dose of аvapritinib was reduced because of hematological toxicity.Daria A. FilonenkoBela M. MedvedevaAndrey A. MeshcheryakovIP Habib O.N.articlegastrointestinal stromal tumorspdgfraavapritinibblu-285ayvakitNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282RUСовременная онкология, Vol 22, Iss 4, Pp 96-100 (2021)
institution DOAJ
collection DOAJ
language RU
topic gastrointestinal stromal tumors
pdgfra
avapritinib
blu-285
ayvakit
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle gastrointestinal stromal tumors
pdgfra
avapritinib
blu-285
ayvakit
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Daria A. Filonenko
Bela M. Medvedeva
Andrey A. Meshcheryakov
Avapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. The literature review and clinical case
description We have three drugs for treatment of gastrointestinal stromal tumors (GIST): imatinib, sunitinib and regorafenib. Avapritinib (Ayvakit, BLU-285) is one more drug that was approved in January 2020. Avapritinib is a new selective tyrosine kinase inhibitor of PDGFRA and KIT mutations. Based on NAVIGATOR trial avapritinib was approved by FDA for treatment of PDGFRA exon 18 mutant GIST including D842V. Avapritinib was included in NCCN guidelines in the first line therapy PDGFRA D842V mutant GIST. There are only several cases describe imatinib and regorafenib efficacy in D842V mutation in the literature. Avapritinib is the first drug with high efficacy in D842V mutant GIST. Avapritinib has high efficacy against second mutations that explain its activity in 4 lines of treatment. This article summarizes the results of NAVIGATOR trial and describes a clinical case of the patient with advanced GIST who received avapritinib in 6th line of treatment. Partial response was achieved that lasted 9 months. The earliest side effects were periorbital edema and increased lacrimation. Three months later the dose of аvapritinib was reduced because of hematological toxicity.
format article
author Daria A. Filonenko
Bela M. Medvedeva
Andrey A. Meshcheryakov
author_facet Daria A. Filonenko
Bela M. Medvedeva
Andrey A. Meshcheryakov
author_sort Daria A. Filonenko
title Avapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. The literature review and clinical case
title_short Avapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. The literature review and clinical case
title_full Avapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. The literature review and clinical case
title_fullStr Avapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. The literature review and clinical case
title_full_unstemmed Avapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. The literature review and clinical case
title_sort avapritinib: a new tyrosine kinase inhibitor for treatment of advanced gastrointestinal stromal tumors. the literature review and clinical case
publisher IP Habib O.N.
publishDate 2021
url https://doaj.org/article/6e46ed6345224af8a1b117b56a28b0d7
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AT belammedvedeva avapritinibanewtyrosinekinaseinhibitorfortreatmentofadvancedgastrointestinalstromaltumorstheliteraturereviewandclinicalcase
AT andreyameshcheryakov avapritinibanewtyrosinekinaseinhibitorfortreatmentofadvancedgastrointestinalstromaltumorstheliteraturereviewandclinicalcase
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