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Efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation

OBJECTIVE : To evaluate the efficacy of the B-cell lymphoma 2 (BCL2)-inhibitor venetoclax in combination therapy for relapsed acute myeloid leukemia (AML) patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS : We retrospectively analyzed 7 adults with relapsed AML w...

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Autores principales: Yang, Fan, Feng, Yueqian, Dong, Changwei, Li, Zhihui, Wu, Tong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asia-Pacific Blood and Marrow Transplantation Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847272/
https://www.ncbi.nlm.nih.gov/pubmed/36711057
http://dx.doi.org/10.31547/bct-2020-025
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author Yang, Fan
Feng, Yueqian
Dong, Changwei
Li, Zhihui
Wu, Tong
author_facet Yang, Fan
Feng, Yueqian
Dong, Changwei
Li, Zhihui
Wu, Tong
author_sort Yang, Fan
collection PubMed
description OBJECTIVE : To evaluate the efficacy of the B-cell lymphoma 2 (BCL2)-inhibitor venetoclax in combination therapy for relapsed acute myeloid leukemia (AML) patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS : We retrospectively analyzed 7 adults with relapsed AML who failed at least one prior therapy and were treated with venetoclax in combination with decitabine and/or low-dose cytarabine at the Beijing Boren hospital between March 2019 and March 2020. Four patients (57.1%) had adverse cytogenetic findings. Four patients (57.1%) had undergone a donor lymphocyte infusion (DLI) prior to venetoclax therapy, while four patients (57.1%) had leukemia and failed prior hypomethylating agent (HMA) therapy. RESULTS : The objective response rate (ORR) was 71.4% (5 patients achieved morphological complete remission with incomplete hematologic recovery, CRi). At the end of the follow-up period, 3/5 cases (60%) in the CRi group achieved minimal residual disease (MRD) negativity by flow cytometry. One patient (14.3%) successfully underwent allo-HSCT. The median follow-up time was 140 (120, 354) d. Among the seven patients, one died of relapse after remission, with an overall survival rate of 85.7% and a disease-free survival rate of 57.1% (4/7). Five of these patients (71.4%) had an identifiable infection, including septicemia (one patient), herpes zoster (two patients), and pneumonia (two patients). One patient had a tumor lysis syndrome. CONCLUSION : The venetoclax-based combinations demonstrated efficacy in treating adult patients with AML relapsing after allo-HSCT.
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spelling pubmed-98472722023-01-27 Efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation Yang, Fan Feng, Yueqian Dong, Changwei Li, Zhihui Wu, Tong Blood Cell Ther Original Article OBJECTIVE : To evaluate the efficacy of the B-cell lymphoma 2 (BCL2)-inhibitor venetoclax in combination therapy for relapsed acute myeloid leukemia (AML) patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS : We retrospectively analyzed 7 adults with relapsed AML who failed at least one prior therapy and were treated with venetoclax in combination with decitabine and/or low-dose cytarabine at the Beijing Boren hospital between March 2019 and March 2020. Four patients (57.1%) had adverse cytogenetic findings. Four patients (57.1%) had undergone a donor lymphocyte infusion (DLI) prior to venetoclax therapy, while four patients (57.1%) had leukemia and failed prior hypomethylating agent (HMA) therapy. RESULTS : The objective response rate (ORR) was 71.4% (5 patients achieved morphological complete remission with incomplete hematologic recovery, CRi). At the end of the follow-up period, 3/5 cases (60%) in the CRi group achieved minimal residual disease (MRD) negativity by flow cytometry. One patient (14.3%) successfully underwent allo-HSCT. The median follow-up time was 140 (120, 354) d. Among the seven patients, one died of relapse after remission, with an overall survival rate of 85.7% and a disease-free survival rate of 57.1% (4/7). Five of these patients (71.4%) had an identifiable infection, including septicemia (one patient), herpes zoster (two patients), and pneumonia (two patients). One patient had a tumor lysis syndrome. CONCLUSION : The venetoclax-based combinations demonstrated efficacy in treating adult patients with AML relapsing after allo-HSCT. Asia-Pacific Blood and Marrow Transplantation Group 2021-08-25 /pmc/articles/PMC9847272/ /pubmed/36711057 http://dx.doi.org/10.31547/bct-2020-025 Text en Copyright Ⓒ2021 Asia-Pacific Blood and Marrow Transplantation Group (APBMT). https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/).
spellingShingle Original Article
Yang, Fan
Feng, Yueqian
Dong, Changwei
Li, Zhihui
Wu, Tong
Efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation
title Efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation
title_full Efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation
title_fullStr Efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation
title_full_unstemmed Efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation
title_short Efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation
title_sort efficacy and safety of venetoclax in combination therapy for relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847272/
https://www.ncbi.nlm.nih.gov/pubmed/36711057
http://dx.doi.org/10.31547/bct-2020-025
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