Department of Hematology, Shaare Zedek Medical Center, Jerusalem, Israel.
Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Leuk Lymphoma. 2020 Sep;61(9):2221-2225. doi: 10.1080/10428194.2020.1761964. Epub 2020 May 18.
Data from 11 Israeli centers, where venetoclax was used for relapsed/refractory AML after intensive chemotherapy, were retrospectively collected. During 2016-2019, forty patients were identified. Median age was 67 years (21-82), 60% males, median of 2(1-4) prior lines of treatment and 42% relapsed after allogeneic transplant. 62.5% of the patients received the venetoclax with hypomethylating agents and 22.5% with low dose cytarabine. Median follow-up was 5.5 months. Of the 29 patients who survived for more than two cycles of therapy, 22 (76%) achieved neutrophil recovery and 59% ( = 17) recovered also their platelet count. In 15 (52% of those who survived > 2 months), CR/CRi was confirmed by bone marrow examination. The median OS from venetoclax initiation of all the patients and of those who survived more than 2 months was 5.5 and 6.5 months, respectively. In conclusion, this study demonstrates that venetoclax is safe and active also in AML patients with advanced disease.
从 11 个以色列中心收集了接受强化化疗后复发/难治性 AML 患者使用维奈托克的数据。在 2016-2019 年期间,共确定了 40 名患者。中位年龄为 67 岁(21-82 岁),男性占 60%,中位治疗线数为 2 线(1-4 线),42%的患者在异体移植后复发。62.5%的患者接受维奈托克联合低甲基化剂治疗,22.5%的患者接受低剂量阿糖胞苷治疗。中位随访时间为 5.5 个月。在 29 名存活超过两个疗程的患者中,22 名(76%)中性粒细胞恢复,59%(17 名)血小板计数也恢复。在 15 名(存活超过 2 个月的患者的 52%)中,骨髓检查证实了完全缓解/部分缓解。所有患者和存活超过 2 个月的患者的中位总生存期分别为 5.5 个月和 6.5 个月。总之,这项研究表明,维奈托克在疾病进展的 AML 患者中也是安全有效的。