<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shah MV</submitter><funding>Paul Calabresi Program in Clinical/Translational Research at Mayo Clinic</funding><pagination>1013-1022</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9541522</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>97(8)</volume><pubmed_abstract>Therapy-related myeloid neoplasms (t-MN) are aggressive malignancies in need of effective therapies. The BCL-2 inhibitor venetoclax represents a paradigm shift in the treatment of acute myeloid leukemia. However, the effectiveness of venetoclax has not been studied in a large cohort of t-MN. We retrospectively analyzed 378 t-MN patients, of which 96 (25.4%, 47 therapy-related acute myeloid leukemia, 1 therapy-related chronic myelomonocytic leukemia, 48 therapy-related myelodysplastic syndrome) received venetoclax. Median interval from t-MN to venetoclax initiation was 2.9 (Interquartile range [IQR] 0.7-12) months, and patients received a median of 3 (IQR 1-4) cycles. The composite complete remission (CRc) rate, median progression-free survival (PFS), and overall survival (OS) were 39.1%, 4</pubmed_abstract><journal>American journal of hematology</journal><pubmed_title>Outcomes following venetoclax-based treatment in therapy-related myeloid neoplasms.</pubmed_title><pmcid>PMC9541522</pmcid><funding_grant_id>K12CA090628</funding_grant_id><pubmed_authors>Hiwase D</pubmed_authors><pubmed_authors>Alkhateeb HB</pubmed_authors><pubmed_authors>Begna KH</pubmed_authors><pubmed_authors>Chhetri R</pubmed_authors><pubmed_authors>Gangat N</pubmed_authors><pubmed_authors>Al-Kali A</pubmed_authors><pubmed_authors>Baranwal A</pubmed_authors><pubmed_authors>He R</pubmed_authors><pubmed_authors>Shah MV</pubmed_authors><pubmed_authors>Tiong IS</pubmed_authors><pubmed_authors>Greipp PT</pubmed_authors><pubmed_authors>Kok CH</pubmed_authors><pubmed_authors>Dholakia R</pubmed_authors><pubmed_authors>Wei AH</pubmed_authors><pubmed_authors>Patnaik MM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcomes following venetoclax-based treatment in therapy-related myeloid neoplasms.</name><description>Therapy-related myeloid neoplasms (t-MN) are aggressive malignancies in need of effective therapies. The BCL-2 inhibitor venetoclax represents a paradigm shift in the treatment of acute myeloid leukemia. However, the effectiveness of venetoclax has not been studied in a large cohort of t-MN. We retrospectively analyzed 378 t-MN patients, of which 96 (25.4%, 47 therapy-related acute myeloid leukemia, 1 therapy-related chronic myelomonocytic leukemia, 48 therapy-related myelodysplastic syndrome) received venetoclax. Median interval from t-MN to venetoclax initiation was 2.9 (Interquartile range [IQR] 0.7-12) months, and patients received a median of 3 (IQR 1-4) cycles. The composite complete remission (CRc) rate, median progression-free survival (PFS), and overall survival (OS) were 39.1%, 4</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-22T01:53:30.151Z</modification><creation>2025-04-05T20:12:10.476Z</creation></dates><accession>S-EPMC9541522</accession><cross_references><pubmed>35560061</pubmed><doi>10.1002/ajh.26589</doi></cross_references></HashMap>