Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47419
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dc.contributor.authorGemici, Aliihsan-
dc.contributor.authorOzkalemkas, Fahir-
dc.contributor.authorDogu, Mehmet Hilmi-
dc.contributor.authorTekinalp, Atakan-
dc.contributor.authorAlacacioglu, Inci-
dc.contributor.authorGuney, Tekin-
dc.contributor.authorSevindik, Omur Gokmen-
dc.date.accessioned2023-01-09T21:24:30Z-
dc.date.available2023-01-09T21:24:30Z-
dc.date.issued2021-
dc.identifier.issn2152-2650-
dc.identifier.issn2152-2669-
dc.identifier.urihttps://doi.org/10.1016/j.clml.2021.04.004-
dc.descriptionSerin, Istemi/0000-0003-1855-774X; Pinar, Ibrahim Ethem/0000-0001-9907-1498; Dogu, Mehmet Hilmi/0000-0001-7237-2637en_US
dc.description.abstractVenetoclax is a selective B-cell lymphoma 2 (BCL2) inhibitor, which is approved to treat elderly patients with newly diagnosed acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS). A total of 60 patients with a median age of 67 years from different centers were included in the final analysis. Our real-life data support the use of venetoclax in patients with both newly diagnosed and relapsed high-risk MDS and AML. Introduction: Venetoclax is a selective B-cell lymphoma 2 (BCL2) inhibitor, which is approved to treat elderly patients with newly diagnosed acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS) in combination with either low-dose cytarabine (ARA-C) or hypomethylating agents. We aimed to collect and share data among the efficacy and safety of venetoclax both as a monotherapy or in combination with other drugs used to treat high-risk MDS or AML. Materials and Methods: A total of 60 patients with a median age of 67 (30-83) years from 14 different centers were included in the final analysis. Thirty (50%) of the patients were women; 6 (10%) of the 60 patients were diagnosed with high-risk MDS and the remaining were diagnosed with AML. Results: The best objective response rate (complete remission [CR], complete remission with incomplete hematological recovery (CRi), morphological leukemia-free state [MLFS], partial response [PR]) was 35% in the entire cohort. Best responses achieved during venetoclax per patient number were as follows: 7 CR, 1 CRi, 8 MLFS, 5 PR, and stable disease. Median overall survival achieved with venetoclax was 5 months in patients who relapsed and not achieved in patients who were initially treated with venetoclax. Nearly all patients (86.7%) had experienced a grade 2 or more hematologic toxicity. Some 36.7% of these patients had received granulocyte colony stimulating factor (GCSF) support. Infection, mainly pneumonia (26.7%), was the leading nonhematologic toxicity, and fatigue, diarrhea, and skin reactions were the others reported. Conclusion: Our real-life data support the use of venetoclax in patients with both newly diagnosed and relapsed high-risk MDS and AML. (C) 2021 Elsevier Inc. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherCig Media Group, Lpen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBcl2en_US
dc.subjectInhibitoren_US
dc.subjectVenetoclaxen_US
dc.subjectAcute Myeloid Leukemiaen_US
dc.subjectReal Lifeen_US
dc.titleA Real-Life Turkish Experience of Venetoclax Treatment in High-Risk Myelodysplastic Syndrome and Acute Myeloid Leukemiaen_US
dc.typeArticleen_US
dc.identifier.volume21en_US
dc.identifier.issue8en_US
dc.identifier.startpageE686en_US
dc.identifier.endpageE692en_US
dc.departmentPamukkale Universityen_US
dc.authoridSerin, Istemi/0000-0003-1855-774X-
dc.authoridPinar, Ibrahim Ethem/0000-0001-9907-1498-
dc.authoridDogu, Mehmet Hilmi/0000-0001-7237-2637-
dc.identifier.doi10.1016/j.clml.2021.04.004-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorwosidMaral, Senem/Aah-9926-2021-
dc.authorwosidDogu, Mehmet/W-2255-2017-
dc.authorwosidKarakuş, Volkan/A-4238-2018-
dc.authorwosidGunes, Ahmet/Koc-4717-2024-
dc.authorwosidEren, Rafet/G-1879-2019-
dc.authorwosidGedük, Ayfer/Aas-1881-2020-
dc.authorwosidPinar, Ibrahim Ethem/Jgm-6601-2023-
dc.identifier.pmid34059487en_US
dc.identifier.pmid34059487-
dc.identifier.scopus2-s2.0-85107154198en_US
dc.identifier.scopus2-s2.0-85107154198-
dc.identifier.wosWOS:000684596500017-
dc.identifier.scopusqualityQ4-
dc.description.woscitationindexScience Citation Index Expanded-
dc.identifier.wosqualityQ3-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairetypeArticle-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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