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维奈托克联合 FLAG-IDA 诱导和巩固治疗新诊断和复发/难治性急性髓系白血病。

Venetoclax Combined With FLAG-IDA Induction and Consolidation in Newly Diagnosed and Relapsed or Refractory Acute Myeloid Leukemia.

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

出版信息

J Clin Oncol. 2021 Sep 1;39(25):2768-2778. doi: 10.1200/JCO.20.03736. Epub 2021 May 27.

Abstract

PURPOSE

Sixty percent of newly diagnosed patients with acute myeloid leukemia (ND-AML) receiving frontline therapy attain a complete response (CR), yet 30%-40% of patients relapse. Relapsed or refractory AML (R/R-AML) remains a particularly adverse population necessitating improved therapeutic options. This phase Ib/II study evaluated the safety and efficacy of fludarabine, cytarabine, granulocyte colony-stimulating factor, and idarubicin combined with the B-cell lymphoma-2 inhibitor venetoclax in ND-AML and R/R-AML.

MATERIALS AND METHODS

The phase IB portion (PIB) enrolled patients with R/R-AML using a 3 + 3 dose escalation and de-escalation algorithm for identification of maximum tolerated dose and dose-limiting toxicities. The phase II portion enrolled patients into two arms to evaluate response and time-to-event end points: phase IIA (PIIA): ND-AML and phase IIB (PIIB): R/R-AML.

RESULTS

Sixty-eight patients have enrolled to date (PIB, 16; PIIA, 29; PIIB, 23). Median age was 46 years (range, 20-73). Grade 3 and 4 adverse events occurring in ≥ 10% of patients included febrile neutropenia (50%), bacteremia (35%), pneumonia (28%), and sepsis (12%). The overall response rate for PIB, PIIA, and PIIB was 75%, 97%, and 70% with 75%, 90%, and 61%, respectively, achieving a composite CR. Measurable residual disease-negative composite CR was attained in 96% of ND-AML and 69% of R/R-AML patients. After a median follow-up of 12 months, median overall survival (OS) for both PII cohorts was not reached. Fifty-six percent of patients proceeded to allogeneic hematopoietic stem-cell transplantation (ND-AML, 69%; R/R-AML, 46%). In R/R-AML, allogeneic hematopoietic stem-cell transplantation resulted in a significant improvement in OS (median OS, NR; 1-year OS, 87%). One-year survival post-HSCT was 94% in ND-AML and 78% in R/R-AML.

CONCLUSION

Fludarabine, cytarabine, granulocyte colony-stimulating factor, and idarubicin + venetoclax represents an effective intensive treatment regimen in ND-AML and R/R-AML patients, associated with deep remissions and a high rate of transition to successful transplantation.

摘要

目的

接受一线治疗的 60%新发急性髓系白血病(ND-AML)患者达到完全缓解(CR),但仍有 30%-40%的患者复发。复发或难治性急性髓系白血病(R/R-AML)仍然是一个特别不利的人群,需要改进治疗选择。这项 Ib/II 期研究评估了氟达拉滨、阿糖胞苷、粒细胞集落刺激因子和伊达比星联合 B 细胞淋巴瘤-2 抑制剂维奈托克在 ND-AML 和 R/R-AML 中的安全性和疗效。

材料和方法

Ib 期部分(PIB)采用 3+3 剂量递增和递减算法,对 R/R-AML 患者进行了评估,以确定最大耐受剂量和剂量限制性毒性。II 期部分将患者分为两个队列,以评估反应和时间事件终点:IIA 期(PIIA):ND-AML 和 IIB 期(PIIB):R/R-AML。

结果

迄今为止,已有 68 名患者入组(PIB:16;PIIA:29;PIIB:23)。中位年龄为 46 岁(范围:20-73)。≥10%的患者发生 3 级和 4 级不良事件包括发热性中性粒细胞减少症(50%)、菌血症(35%)、肺炎(28%)和败血症(12%)。PIB、PIIA 和 PIIB 的总缓解率分别为 75%、97%和 70%,分别有 75%、90%和 61%达到复合 CR。96%的 ND-AML 和 69%的 R/R-AML 患者达到了可测量残留疾病阴性的复合 CR。在中位随访 12 个月后,两个 PII 队列的中位总生存期(OS)均未达到。56%的患者接受了异基因造血干细胞移植(ND-AML:69%;R/R-AML:46%)。在 R/R-AML 中,异基因造血干细胞移植显著改善了 OS(中位 OS:NR;1 年 OS:87%)。ND-AML 患者移植后 1 年生存率为 94%,R/R-AML 患者为 78%。

结论

氟达拉滨、阿糖胞苷、粒细胞集落刺激因子和伊达比星+维奈托克在 ND-AML 和 R/R-AML 患者中代表了一种有效的强化治疗方案,与深度缓解和高转化率相关。

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本文引用的文献

1
Prognostic impact of complete remission with MRD negativity in patients with relapsed or refractory AML.
Blood Adv. 2020 Dec 22;4(24):6117-6126. doi: 10.1182/bloodadvances.2020002811.
4
Outcomes of older patients with NPM1-mutated AML: current treatments and the promise of venetoclax-based regimens.
Blood Adv. 2020 Apr 14;4(7):1311-1320. doi: 10.1182/bloodadvances.2019001267.
6
Impact of Conditioning Intensity of Allogeneic Transplantation for Acute Myeloid Leukemia With Genomic Evidence of Residual Disease.
J Clin Oncol. 2020 Apr 20;38(12):1273-1283. doi: 10.1200/JCO.19.03011. Epub 2019 Dec 20.
9
Venetoclax combined with decitabine or azacitidine in treatment-naive, elderly patients with acute myeloid leukemia.
Blood. 2019 Jan 3;133(1):7-17. doi: 10.1182/blood-2018-08-868752. Epub 2018 Oct 25.
10
Acute myeloid leukemia: 2019 update on risk-stratification and management.
Am J Hematol. 2018 Oct;93(10):1267-1291. doi: 10.1002/ajh.25214.

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