Department of Cancer Medicine, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer. 2011 Jan 1;117(1):110-5. doi: 10.1002/cncr.25585. Epub 2010 Aug 27.
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.
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.
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).
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.
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。
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。
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)。
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。