Suppr超能文献

维奈托克在复发或难治性急性髓系白血病患者中的应用:PETHEMA注册研究经验

Use of Venetoclax in Patients with Relapsed or Refractory Acute Myeloid Leukemia: The PETHEMA Registry Experience.

作者信息

Labrador Jorge, Saiz-Rodríguez Miriam, de Miguel Dunia, de Laiglesia Almudena, Rodríguez-Medina Carlos, Vidriales María Belén, Pérez-Encinas Manuel, Sánchez-Sánchez María José, Cuello Rebeca, Roldán-Pérez Alicia, Vives Susana, Benzo-Callejo Gonzalo, Colorado Mercedes, García-Fortes María, Sayas María José, Olivier Carmen, Recio Isabel, Conde-Royo Diego, Bienert-García Álvaro, Vahi María, Muñoz-García Carmen, Seri-Merino Cristina, Tormo Mar, Vall-Llovera Ferran, Foncillas María-Ángeles, Martínez-Cuadrón David, Sanz Miguel Ángel, Montesinos Pau

机构信息

Hematology Deparment, Hospital Universitario de Burgos, 09006 Burgos, Spain.

Research Unit, Fundación Burgos por la Investigación de la Salud (FBIS), Hospital Universitario de Burgos, 09006 Burgos, Spain.

出版信息

Cancers (Basel). 2022 Mar 29;14(7):1734. doi: 10.3390/cancers14071734.

Abstract

The effectiveness of venetoclax (VEN) in relapsed or refractory acute myeloid leukemia (RR-AML) has not been well established. This retrospective, multicenter, observational database studied the effectiveness of VEN in a cohort of 51 RR-AML patients and evaluated for predictors of response and overall survival (OS). The median age was 68 years, most were at high risk, 61% received ≥2 therapies for AML, 49% had received hypomethylating agents, and ECOG was ≥2 in 52%. Complete remission (CR) rate, including CR with incomplete hematological recovery (CRi), was 12.4%. Additionally, 10.4% experienced partial response (PR). The CR/CRi was higher in combination with azacitidine (AZA; 17.9%) than with decitabine (DEC; 6.7%) and low-dose cytarabine (LDAC; 0%). Mutated NPM1 was associated with increased CR/CRi. Median OS was 104 days (95% CI: 56-151). For the combination with AZA, DEC, and LDAC, median OS was 120 days, 104 days, and 69 days, respectively; = 0.875. Treatment response and ECOG 0 influenced OS in a multivariate model. A total of 28% of patients required interruption of VEN because of toxicity. Our real-life series describes a marginal probability of CR/CRi and poor OS after VEN-based salvage. Patients included had very poor-risk features and were heavily pretreated. The small percentage of responders did not reach the median OS.

摘要

维奈克拉(VEN)在复发或难治性急性髓系白血病(RR-AML)中的有效性尚未得到充分证实。这项回顾性、多中心、观察性数据库研究了VEN在51例RR-AML患者队列中的有效性,并评估了反应和总生存期(OS)的预测因素。中位年龄为68岁,大多数患者处于高风险,61%的患者接受了≥2种AML治疗,49%的患者接受过去甲基化药物治疗,52%的患者东部肿瘤协作组(ECOG)体能状态评分≥2。完全缓解(CR)率,包括伴有血液学不完全恢复的CR(CRi),为12.4%。此外,10.4%的患者出现部分缓解(PR)。与阿扎胞苷(AZA;17.9%)联合使用时的CR/CRi高于与地西他滨(DEC;6.7%)和小剂量阿糖胞苷(LDAC;0%)联合使用时。NPM1突变与CR/CRi增加相关。中位OS为104天(95%置信区间:56-151)。与AZA、DEC和LDAC联合使用时,中位OS分别为120天、104天和69天;P=0.875。在多变量模型中,治疗反应和ECOG 0体能状态评分影响OS。共有28%的患者因毒性需要中断VEN治疗。我们的真实病例系列描述了基于VEN的挽救治疗后CR/CRi的可能性很小且OS较差。纳入的患者具有非常差的风险特征且接受过大量预处理。反应者比例小,未达到中位OS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e8/8997036/2514f34aefd5/cancers-14-01734-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验