Ravandi Farhad, Estey Eli, Jones Dan, Faderl Stefan, O'Brien Susan, Fiorentino Jackie, Pierce Sherry, Blamble Deborah, Estrov Zeev, Wierda William, Ferrajoli Alessandra, Verstovsek Srdan, Garcia-Manero Guillermo, Cortes Jorge, Kantarjian Hagop
Department of Leukemia, The University of Texas M. D. Anderson Cancer Center, Unit 428, 1515 Holcombe Blvd, Houston, TX 77030, USA.
J Clin Oncol. 2009 Feb 1;27(4):504-10. doi: 10.1200/JCO.2008.18.6130. Epub 2008 Dec 15.
We examined the outcome of patients with newly diagnosed acute promyelocytic leukemia (APL) treated with all-trans-retinoic acid (ATRA) and arsenic trioxide (ATO) with or without gemtuzumab ozogamicin (GO) but without traditional cytotoxic chemotherapy.
From February 2002 to March 2008, 82 patients with APL were treated with a combination of ATRA plus ATO. The first cohort of 65 patients received ATRA and ATO (beginning on day 10 of ATRA). High-risk patients (WBCs >or= 10 x 10(9)/L) received GO on the first day. From July 2007, the second cohort of 17 patients received ATRA and ATO concomitantly on day 1. They also received GO on day 1, if high risk, and if their WBC increased to more than 30 x 10(9)/L during induction. Monitoring for PML-RARA fusion gene was conducted after induction and throughout consolidation and follow-up.
Overall, 74 patients achieved complete remission (CR) and one achieved CR without full platelet recovery after the induction, for a response rate of 92%. Seven patients died at a median of 4 days (range, 1 to 24 days) after inclusion in the study from disease-related complications. The median follow-up is 99 weeks (range, 2 to 282 weeks). Among the responding patients, three experienced relapse at 39, 52, and 53 weeks. Three patients died after being in CR for 14, 21, and 71 weeks, all from a second malignancy. The estimated 3-year survival rate is 85%.
The combination of ATRA and ATO (with or without GO) as initial therapy for APL was effective and safe and can substitute chemotherapy-containing regimens.
我们研究了新诊断的急性早幼粒细胞白血病(APL)患者接受全反式维甲酸(ATRA)和三氧化二砷(ATO)治疗(联合或不联合吉妥单抗奥唑米星(GO))但未接受传统细胞毒性化疗的结果。
2002年2月至2008年3月,82例APL患者接受了ATRA加ATO联合治疗。首批65例患者接受ATRA和ATO治疗(从ATRA治疗第10天开始)。高危患者(白细胞计数≥10×10⁹/L)在第一天接受GO治疗。从2007年7月起,第二批17例患者在第1天同时接受ATRA和ATO治疗。如果是高危患者且诱导期白细胞计数升至超过30×10⁹/L,他们在第1天也接受GO治疗。诱导治疗后以及整个巩固治疗和随访期间均监测PML-RARA融合基因。
总体而言,74例患者实现完全缓解(CR),1例患者诱导治疗后实现CR但血小板未完全恢复,缓解率为92%。7例患者在纳入研究后中位4天(范围1至24天)死于与疾病相关并发症。中位随访时间为99周(范围2至282周)。在缓解患者中,3例分别在39、52和53周复发。3例患者在CR状态下分别于14、21和71周后死亡,均死于第二种恶性肿瘤。估计3年生存率为85%。
ATRA和ATO联合(联合或不联合GO)作为APL的初始治疗有效且安全,可替代含化疗方案。