<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>104(12)</volume><submitter>Zhang X</submitter><pubmed_abstract>Olverembatinib is a novel third-generation TKI available in mainland China. However, there are only a few published clinical reports. In this study, we aimed to investigate the efficacy and safety of an olverembatinib-venetoclax regimen before bridging to HSCT in adult Ph/BCR-ABL1 + ALL patients with refractory/relapsed disease (n = 2) or persistent minimal residual disease (MRD) (n = 15). Seventeen Ph + ALL patients who were admitted to our center between February 2022 and January 2023 were enrolled. Four patients harbored a T315I mutation. In all, 100% achieved hematologic complete remission, and 70.6% achieved complete molecular remission. With a median follow-up of 856-day post-HSCT, the 2-year overall survival and relapsed free survival rates was 88.2 ± 7.8% and 79.4 ± 10.9%, respectively. The findings of this study suggest that in Ph + ALL patients with disease recurrence and persistent MRD positivity, olverembatinib-venetoclax regimen showed a high molecular response rate and was well-tolerated in MRD clearance bridged to allo-HSCT.</pubmed_abstract><journal>Annals of hematology</journal><pagination>6463-6466</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12764584</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Targeting relapsed/refractory and MRD + Ph + ALL: olverembatinib-venetoclax bridging enhances allo-HSCT outcome​.</pubmed_title><pmcid>PMC12764584</pmcid><pubmed_authors>Ma Q</pubmed_authors><pubmed_authors>Jiang E</pubmed_authors><pubmed_authors>Pang A</pubmed_authors><pubmed_authors>Han M</pubmed_authors><pubmed_authors>Yang D</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Liang C</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Cao W</pubmed_authors><pubmed_authors>Zhai W</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Wei J</pubmed_authors><pubmed_authors>Feng S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting relapsed/refractory and MRD + Ph + ALL: olverembatinib-venetoclax bridging enhances allo-HSCT outcome​.</name><description>Olverembatinib is a novel third-generation TKI available in mainland China. However, there are only a few published clinical reports. In this study, we aimed to investigate the efficacy and safety of an olverembatinib-venetoclax regimen before bridging to HSCT in adult Ph/BCR-ABL1 + ALL patients with refractory/relapsed disease (n = 2) or persistent minimal residual disease (MRD) (n = 15). Seventeen Ph + ALL patients who were admitted to our center between February 2022 and January 2023 were enrolled. Four patients harbored a T315I mutation. In all, 100% achieved hematologic complete remission, and 70.6% achieved complete molecular remission. With a median follow-up of 856-day post-HSCT, the 2-year overall survival and relapsed free survival rates was 88.2 ± 7.8% and 79.4 ± 10.9%, respectively. The findings of this study suggest that in Ph + ALL patients with disease recurrence and persistent MRD positivity, olverembatinib-venetoclax regimen showed a high molecular response rate and was well-tolerated in MRD clearance bridged to allo-HSCT.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T10:20:43.826Z</modification><creation>2026-05-28T03:13:06.135Z</creation></dates><accession>S-EPMC12764584</accession><cross_references><pubmed>41388081</pubmed><doi>10.1007/s00277-025-06708-0</doi></cross_references></HashMap>