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急性早幼粒细胞白血病采用单周期定时序贯巩固化疗实现持久分子缓解。

Durable molecular remissions with a single cycle of timed sequential consolidation chemotherapy in acute promyelocytic leukemia.

作者信息

Gore Steven D, Smith B Douglas, Gojo Ivana, Grever Michael, Kaufmann Scott H, Letendre Louis, Leonard Debra G B, Marcucci Guido, Miller Carole B, Morris Lawrence, Piantadosi Steven, Prior Thomas, Stock Wendy, Karp Judith E

机构信息

The Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, Maryland 21231, USA.

出版信息

Am J Hematol. 2005 Jun;79(2):119-27. doi: 10.1002/ajh.20354.

Abstract

In a pilot study to reduce the duration of treatment and potential long-term toxicities, 39 patients with acute promyelocytic leukemia in remission received a single cycle of intensive consolidation therapy, followed by intermittent ATRA maintenance. Consolidation therapy required prolonged hospitalization and was associated with a high incidence of mucositis (43% grade II or greater) and documented infection (45%). No deaths occurred during consolidation. Seven patients have relapsed; all other patients are in molecular remission (median follow-up, 2.75 years). Kaplan-Meier estimate of 3 year disease-free survival is 73% (95% confidence interval 55-91%). The relapse rate (0.06 relapses/patient-year of follow-up) is well within the range of larger published series that administer more prolonged consolidation. One patient has developed secondary myelodysplastic syndrome. These pilot data suggest that decreasing the total duration of consolidation chemotherapy did not compromise disease-free survival for APL patients induced with ATRA/anthracycline and given intermittent ATRA maintenance. However, the toxicity of the consolidation module and the development of secondary myelodysplasia despite decreased total therapy emphasize the need to further improve and refine curative therapy for APL.

摘要

在一项旨在缩短治疗时间和降低潜在长期毒性的初步研究中,39例急性早幼粒细胞白血病缓解期患者接受了一个周期的强化巩固治疗,随后进行间歇性全反式维甲酸(ATRA)维持治疗。巩固治疗需要长时间住院,且与高发生率的粘膜炎(43%为II级或更严重)和有记录的感染(45%)相关。巩固治疗期间无死亡发生。7例患者复发;所有其他患者处于分子缓解状态(中位随访时间为2.75年)。Kaplan-Meier法估计的3年无病生存率为73%(95%置信区间为55 - 91%)。复发率(0.06次复发/患者年随访时间)完全在已发表的更长时间巩固治疗的大型系列研究范围内。1例患者发生了继发性骨髓增生异常综合征。这些初步数据表明,缩短巩固化疗的总时长并未损害接受ATRA/蒽环类药物诱导并给予间歇性ATRA维持治疗的急性早幼粒细胞白血病患者的无病生存率。然而,巩固治疗模块的毒性以及尽管总治疗时长缩短但仍出现继发性骨髓发育异常,强调了进一步改进和完善急性早幼粒细胞白血病根治性治疗的必要性。

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