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高危急性早幼粒细胞白血病的高效治疗:全反式维甲酸+三氧化二砷+蒽环类药物诱导及巩固治疗,全反式维甲酸+利福平维持治疗

Highly Curative Treatment of High-Risk Acute Promyelocytic Leukemia: Induction and Consolidation with ATRA+ATO+anthracyclines and Maintenance with ATRA+RIF.

作者信息

Liu Dan, Tong Juan, Chen Erling, Wang Li, Xue Lei, Zhang Xuhan, Zhao Na, Hu Xing, Zheng Changcheng

机构信息

Department of Hematology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, People's Republic of China.

出版信息

Blood Lymphat Cancer. 2024 Jul 29;14:63-69. doi: 10.2147/BLCTT.S473984. eCollection 2024.

Abstract

BACKGROUND

The aim of the study was to evaluate the efficacy and safety of induction and consolidation with all-trans retinoic acid (ATRA) +arsenic trioxide (ATO) +anthracyclines and maintenance with ATRA +Realgar- formula (RIF) for high-risk APL.

METHODS

Twenty-one patients with high-risk APL treated with ATRA+ATO+ anthracyclines for induction and consolidation and ATRA+RIF for maintenance from 2012 to 2021 were analyzed. Endpoints include morphological complete remission (CR) and complete molecular remission (CMR), early death (ED) and relapse, survival and adverse events (AEs).

RESULTS

After induction treatment, all 21 patients (100%) achieved morphological CR and 14 people (66.7%) achieved CMR. Five of the 21 patients did not undergo immunological minimal residual disease (MRD) examination after induction; however, 14 of the remaining 16 patients were MRD negative (87.5%). The median time to achieve CR and CMR was 26 days (range: 16-44) and 40 days (range: 22-75), respectively. The cumulative probability of achieving CR and CMR in 45 days was 100% and 76.2% (95% CI: 56.9-91.3%), respectively. All patients achieved CMR and MRD negativity after the three courses of consolidation treatment. The median follow-up was 66 months (25-142), with no central nervous system relapse and bone marrow morphological or molecular relapse until now, and all patients survived with 100% overall survival and 100% event-free survival. Grade 4 adverse events (AEs) were observed in 3 patients (14.3%) during the induction period including arrhythmia (n = 1), pulmonary infection (n = 1) and respiratory failure (n = 1); and the most frequent grade 3 AEs were pulmonary infection, accounting for 62.0% and 28.6%, respectively, during induction and consolidation treatment, followed by neutropenia, accounting for 42.9% and 38.1%, respectively.

CONCLUSION

For newly diagnosed high-risk APL patients, induction and consolidation with ATRA+ATO+anthracyclines and maintenance with ATRA+RIF is a highly curative treatment approach.

摘要

背景

本研究旨在评估全反式维甲酸(ATRA)+三氧化二砷(ATO)+蒽环类药物进行诱导和巩固治疗,以及使用ATRA+雄黄配方(RIF)进行维持治疗对高危急性早幼粒细胞白血病(APL)的疗效和安全性。

方法

分析了2012年至2021年期间21例接受ATRA+ATO+蒽环类药物诱导和巩固治疗以及ATRA+RIF维持治疗的高危APL患者。观察指标包括形态学完全缓解(CR)和分子学完全缓解(CMR)、早期死亡(ED)和复发、生存率及不良事件(AE)。

结果

诱导治疗后,所有21例患者(100%)均达到形态学CR,14例(66.7%)达到CMR。21例患者中有5例诱导后未进行免疫微小残留病(MRD)检测;然而,其余16例患者中有14例MRD阴性(87.5%)。达到CR和CMR的中位时间分别为26天(范围:16 - 44天)和40天(范围:22 - 75天)。45天内达到CR和CMR的累积概率分别为100%和76.2%(95%CI:56.9 - 91.3%)。所有患者在三个疗程的巩固治疗后均达到CMR且MRD阴性。中位随访时间为66个月(25 - 142个月),截至目前无中枢神经系统复发及骨髓形态学或分子学复发,所有患者存活,总生存率和无事件生存率均为100%。诱导期有3例患者(14.3%)出现4级不良事件,包括心律失常(1例)、肺部感染(1例)和呼吸衰竭(1例);诱导期和巩固期最常见的3级不良事件均为肺部感染,分别占62.0%和28.6%,其次是中性粒细胞减少,分别占42.9%和38.1%。

结论

对于新诊断的高危APL患者,采用ATRA+ATO+蒽环类药物进行诱导和巩固治疗以及ATRA+RIF进行维持治疗是一种具有高治愈率的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d4/11296505/872de97dc0fb/BLCTT-14-63-g0001.jpg

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