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https://hdl.handle.net/11499/47419
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DC Field | Value | Language |
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dc.contributor.author | Gemici, Aliihsan | - |
dc.contributor.author | Ozkalemkas, Fahir | - |
dc.contributor.author | Dogu, Mehmet Hilmi | - |
dc.contributor.author | Tekinalp, Atakan | - |
dc.contributor.author | Alacacioglu, Inci | - |
dc.contributor.author | Guney, Tekin | - |
dc.contributor.author | Sevindik, Omur Gokmen | - |
dc.date.accessioned | 2023-01-09T21:24:30Z | - |
dc.date.available | 2023-01-09T21:24:30Z | - |
dc.date.issued | 2021 | - |
dc.identifier.issn | 2152-2650 | - |
dc.identifier.issn | 2152-2669 | - |
dc.identifier.uri | https://doi.org/10.1016/j.clml.2021.04.004 | - |
dc.description | Serin, Istemi/0000-0003-1855-774X; Pinar, Ibrahim Ethem/0000-0001-9907-1498; Dogu, Mehmet Hilmi/0000-0001-7237-2637 | en_US |
dc.description.abstract | 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). 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.iso | en | en_US |
dc.publisher | Cig Media Group, Lp | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Bcl2 | en_US |
dc.subject | Inhibitor | en_US |
dc.subject | Venetoclax | en_US |
dc.subject | Acute Myeloid Leukemia | en_US |
dc.subject | Real Life | en_US |
dc.title | A Real-Life Turkish Experience of Venetoclax Treatment in High-Risk Myelodysplastic Syndrome and Acute Myeloid Leukemia | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 21 | en_US |
dc.identifier.issue | 8 | en_US |
dc.identifier.startpage | E686 | en_US |
dc.identifier.endpage | E692 | en_US |
dc.department | Pamukkale University | en_US |
dc.authorid | Serin, Istemi/0000-0003-1855-774X | - |
dc.authorid | Pinar, Ibrahim Ethem/0000-0001-9907-1498 | - |
dc.authorid | Dogu, Mehmet Hilmi/0000-0001-7237-2637 | - |
dc.identifier.doi | 10.1016/j.clml.2021.04.004 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.authorwosid | Maral, Senem/Aah-9926-2021 | - |
dc.authorwosid | Dogu, Mehmet/W-2255-2017 | - |
dc.authorwosid | Karakuş, Volkan/A-4238-2018 | - |
dc.authorwosid | Gunes, Ahmet/Koc-4717-2024 | - |
dc.authorwosid | Eren, Rafet/G-1879-2019 | - |
dc.authorwosid | Gedük, Ayfer/Aas-1881-2020 | - |
dc.authorwosid | Pinar, Ibrahim Ethem/Jgm-6601-2023 | - |
dc.identifier.pmid | 34059487 | en_US |
dc.identifier.pmid | 34059487 | - |
dc.identifier.scopus | 2-s2.0-85107154198 | en_US |
dc.identifier.scopus | 2-s2.0-85107154198 | - |
dc.identifier.wos | WOS:000684596500017 | - |
dc.identifier.scopusquality | Q4 | - |
dc.description.woscitationindex | Science Citation Index Expanded | - |
dc.identifier.wosquality | Q3 | - |
item.cerifentitytype | Publications | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairetype | Article | - |
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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