Division of Hematological Malignancies and Bone Marrow Transplantation, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Leuk Lymphoma. 2023 Apr;64(4):846-855. doi: 10.1080/10428194.2023.2173523. Epub 2023 Feb 6.
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; = 0.0002) and composite CR rate (22% versus 50.0%; = 0.2444). Although mutations were associated with higher composite CR rate (80.0% versus 28.0%; = 0.0082), this was not associated with longer median OS (10.9 versus 8.0 months; = 0.2269). Future studies should include these patient subgroups.
维奈托克联合低甲基化药物(HMA/维奈托克)已成为不适合接受强化化疗的新发急性髓系白血病(AML)患者的治疗选择。在这项单中心回顾性研究中,我们评估了 35 例晚期骨髓增生性肿瘤、骨髓增生异常综合征/骨髓增生性肿瘤重叠综合征或伴髓外疾病的 AML 患者接受 HMA/维奈托克治疗后的临床结局。复合完全缓解(CR)率(包括确认/假定完全细胞遗传学缓解、急性白血病完全缓解、CR 和不完全血液学恢复的 CR)为 42.9%,中位总生存期(OS)为 9.7 个月。复杂核型与较差的中位 OS(3.7 个月与 12.2 个月; = 0.0002)和复合 CR 率(22%与 50.0%; = 0.2444)相关。虽然 突变与更高的复合 CR 率相关(80.0%与 28.0%; = 0.0082),但与较长的中位 OS 无关(10.9 个月与 8.0 个月; = 0.2269)。未来的研究应包括这些患者亚组。