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新诊断的伴有或不伴有维奈托克治疗的 TP53 突变急性髓系白血病患者的结局。

Outcomes in patients with newly diagnosed TP53-mutated acute myeloid leukemia with or without venetoclax-based therapy.

机构信息

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

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

出版信息

Cancer. 2021 Oct 1;127(19):3541-3551. doi: 10.1002/cncr.33675. Epub 2021 Jun 28.

DOI:10.1002/cncr.33675
PMID:34182597
Abstract

BACKGROUND

Venetoclax (VEN) in combination with a hypomethylating agent (HMA) has become the standard of care for patients aged >75 years and for those not eligible for intensive chemotherapy who have newly diagnosed acute myeloid leukemia (AML). The benefit of VEN-based therapy in patients who have newly diagnosed AML with mutations in the TP53 gene (TP53 ) over standard therapy is undefined.

METHODS

In this single-institutional, retrospective analysis, the authors assessed the clinical outcomes of 238 patients with newly diagnosed TP53 AML and compared the clinical characteristics, response to different therapies, and outcomes of those who received VEN-based (n = 58) and non-VEN-based (n = 180) regimens.

RESULTS

Patients who received VEN-based regimens were older (aged >65 years: 81% vs 65%; P = .02) and had higher response rates (complete remission, 43% vs 32%; P = .06) than those who received non-VEN-based regimens. Compared with patients who received non-VEN-based regimens, no difference in overall survival (median, 6.6 vs 5.7 months; P = .4) or relapse-free survival (median, 4.7 vs 3.5 months; P = .43) was observed in those who received VEN-based regimens, regardless of age or intensity of treatment.

CONCLUSIONS

The addition of VEN to standard treatment regimens did not improve outcomes in younger or older patients who had TP53 AML. These data highlight the need for novel therapies beyond VEN to improve the outcome of patients with TP53 AML.

摘要

背景

维奈托克(VEN)联合低甲基化药物(HMA)已成为年龄>75 岁的患者以及不适合强化化疗且新诊断为急性髓系白血病(AML)患者的标准治疗方法。对于新诊断为 AML 且 TP53 基因(TP53)突变的患者,VEN 为基础的治疗与标准治疗相比的益处尚不清楚。

方法

在这项单机构回顾性分析中,作者评估了 238 例新诊断为 TP53 AML 患者的临床结局,并比较了接受 VEN 为基础(n=58)和非 VEN 为基础(n=180)方案治疗的患者的临床特征、对不同治疗方法的反应和结局。

结果

接受 VEN 为基础方案治疗的患者年龄较大(>65 岁:81%比 65%;P=0.02),缓解率较高(完全缓解率:43%比 32%;P=0.06)。与接受非 VEN 为基础方案治疗的患者相比,接受 VEN 为基础方案治疗的患者无论年龄或治疗强度如何,其总生存(中位:6.6 比 5.7 个月;P=0.4)或无复发生存(中位:4.7 比 3.5 个月;P=0.43)均无差异。

结论

在年龄较小或较大的 TP53 AML 患者中,将 VEN 加入标准治疗方案并未改善结局。这些数据强调了需要除 VEN 之外的新型疗法来改善 TP53 AML 患者的结局。

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