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砷剂作为一线治疗方案组成部分的治疗相关性急性早幼粒细胞白血病的疗效。

Outcome of therapy-related acute promyelocytic leukemia with or without arsenic trioxide as a component of frontline therapy.

机构信息

Department of Cancer Medicine, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Cancer. 2011 Jan 1;117(1):110-5. doi: 10.1002/cncr.25585. Epub 2010 Aug 27.

Abstract

BACKGROUND

Patients with therapy-related acute promyelocytic leukemia (t-APL) have been commonly exposed to topoisomerase inhibitors and may potentially benefit from induction regimens omitting anthracyclines.

METHODS

Retrospective analysis of the outcomes of 29 patients with t-APL who were either treated with arsenic trioxide (ATO) and all-trans-retinoic acid (ATRA) or with standard ATRA plus anthracycline-based chemotherapy was performed.

RESULTS

Prior therapy included chemotherapy alone, radiation alone, or a combination of the 2 in 19%, 33%, and 47% of patients, respectively. The combination of ATO and ATRA (n = 19) for induction resulted in a similar remission rate compared with ATRA plus chemotherapy (n = 10) (89% vs 70%; P = .35). The median overall survival for the patients treated with ATRA plus ATO was not reached compared with that for patients treated with ATRA plus chemotherapy (161 weeks; P = .79).

CONCLUSIONS

In this cohort of t-APL patients, outcomes with ATO and ATRA appeared to be comparable to anthracycline-containing induction regimens. This combination may be preferable in t-APL patients to avoid any risk of anthracycline-induced toxicities.

摘要

背景

接受过拓扑异构酶抑制剂治疗的治疗相关急性早幼粒细胞白血病(t-APL)患者可能受益于不含蒽环类药物的诱导方案。

方法

对 29 例接受三氧化二砷(ATO)和全反式维甲酸(ATRA)或标准 ATRA 联合蒽环类药物化疗治疗的 t-APL 患者的结局进行回顾性分析。

结果

分别有 19%、33%和 47%的患者既往接受单纯化疗、单纯放疗或两者联合治疗。ATO 和 ATRA 的联合诱导(n = 19)与 ATRA 联合化疗(n = 10)的缓解率相似(89%比 70%;P =.35)。接受 ATRA 加 ATO 治疗的患者的中位总生存期未达到,而接受 ATRA 加化疗治疗的患者的中位总生存期为 161 周(P =.79)。

结论

在本队列的 t-APL 患者中,ATO 和 ATRA 的疗效似乎与含蒽环类药物的诱导方案相当。对于 t-APL 患者,这种联合治疗可能更可取,以避免蒽环类药物引起的毒性风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83be/4287232/4e845ce5e7e8/nihms652588f1.jpg

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