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三氧化二砷单药治疗初发急性早幼粒细胞白血病:长期随访数据。

Single-agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: long-term follow-up data.

机构信息

Department of Haematology, Christian Medical College and Hospital, Vellore 632004, India;

出版信息

J Clin Oncol. 2010 Aug 20;28(24):3866-71. doi: 10.1200/JCO.2010.28.5031. Epub 2010 Jul 19.

Abstract

PURPOSE We previously reported our results with a single-agent arsenic trioxide (ATO) -based regimen in newly diagnosed cases of acute promyelocytic leukemia (APL). The concern remained about the long-term outcome of this well-tolerated regimen. We report our long-term follow-up data on the same cohort. PATIENTS AND METHODS From January 1998 to December 2004, 72 patients with PML/RARalpha+ APL were enrolled. All patients were treated with a single-agent ATO regimen. Results Overall 62 (86.1%) achieved a hematologic remission (complete remission). After the initial report, an additional seven patients have relapsed for a total of 13 relapses. There were no additional toxicities to report on follow-up. At a median follow-up 60 months, the 5-year Kaplan-Meier estimate (+/- SE) of event-free survival, disease-free survival, and overall survival (OS) was 69% +/- 5.5%, 80% +/- 5.2%, and 74.2% +/- 5.2%, respectively. The OS in the good risk group as defined by us remains 100% over this period. CONCLUSION Single-agent ATO as used in this study in the management of newly diagnosed cases of APL is safe and is associated with durable responses. Results in the low-risk group are comparable to that reported with conventional therapy while additional interventions would probably be required in high-risk cases.

摘要

目的 我们之前报告了单药三氧化二砷(ATO)方案治疗初诊急性早幼粒细胞白血病(APL)的结果。该方案耐受性良好,但人们仍对其长期疗效存在担忧。我们报告了同一队列的长期随访数据。

患者和方法 1998 年 1 月至 2004 年 12 月,共纳入 72 例 PML/RARα+APL 患者。所有患者均接受单药 ATO 方案治疗。

结果 72 例患者中,62 例(86.1%)达到血液学缓解(完全缓解)。在最初报告后,又有 7 例患者复发,总复发率为 13%。随访期间无其他毒性反应。中位随访 60 个月后,5 年无事件生存、无病生存和总生存(OS)的 Kaplan-Meier 估计值(+/- SE)分别为 69% +/- 5.5%、80% +/- 5.2%和 74.2% +/- 5.2%。我们定义的低危组患者在这一时期的 OS 仍为 100%。

结论 在本研究中,单药 ATO 方案用于治疗初诊 APL 是安全的,且能获得持久缓解。低危组患者的结果与传统治疗相当,但高危组可能需要额外的干预措施。

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