威尼斯人
医学
骨髓增生性肿瘤
髓系白血病
低甲基化剂
内科学
白血病
髓样
阿扎胞苷
胃肠病学
肿瘤科
骨髓纤维化
骨髓
慢性淋巴细胞白血病
DNA甲基化
基因
基因表达
化学
生物化学
作者
Khaled Sanber,Kevin Ye,Hua‐Ling Tsai,Matthew Newman,Jonathan Webster,Ivana Gojo,Gabriel Ghiaur,Gabrielle T. Prince,Lukasz P. Gondek,Benjamin D. Smith,Mark J. Levis,Amy E. DeZern,Alexander J. Ambinder,W. Brian Dalton,Tania Jain
标识
DOI:10.1080/10428194.2023.2173523
摘要
The combination of venetoclax and hypomethylating agent (HMA/venetoclax) has emerged as a treatment option for patients with de novo acute myeloid leukemia (AML) who are unfit to receive intensive chemotherapy. In this single-center retrospective study, we evaluated clinical outcomes following treatment with HMA/venetoclax in 35 patients with advanced myeloproliferative neoplasms, myelodysplastic syndrome/myeloproliferative neoplasm overlap syndromes or AML with extramedullary disease. The composite complete remission (CR) rate (including confirmed/presumed complete cytogenetic response, acute leukemia response-complete, CR and CR with incomplete hematologic recovery) was 42.9% with median overall survival (OS) of 9.7 months. Complex karyotype was associated with inferior median OS (3.7 versus 12.2 months; p = 0.0002) and composite CR rate (22% versus 50.0%; p = 0.2444). Although SRSF2 mutations were associated with higher composite CR rate (80.0% versus 28.0%; p = 0.0082), this was not associated with longer median OS (10.9 versus 8.0 months; p = 0.2269). Future studies should include these patient subgroups.
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