Department of Biomedicine and Prevention, University Tor Vergata, via Montpellier,1, 00133, Rome, Italy.
Department of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.
Ann Hematol. 2018 Oct;97(10):1797-1802. doi: 10.1007/s00277-018-3400-z. Epub 2018 Jun 27.
Prolonged therapy with all-trans-retinoic acid (ATRA) and arsenic trioxide (ATO) is highly effective in newly diagnosed acute promyelocytic leukemia (APL) but there is limited data on the efficacy of this regimen in the relapse setting. We report here on 22 APL patients treated with prolonged ATRA-ATO therapy at the time of disease relapse. Twenty patients obtained molecular complete remission (CRm) after 2 cycles (90%). Of these, two patients underwent hematopoietic stem cell transplant (HSCT) while the remaining proceeded to receive additional cycles (up to a total of 5) of ATRA-ATO. With a median follow-up of 58 months from the time of relapse (range: 21-128 months), the 4-year OS probability was 0.85 (95% CI 0.61-0.94), DFS was 0.74 (95% CI 0.49-0.88), and EFS 0.68 (95% CI 0.45-0.83). Two patients were resistant to ATRA-ATO salvage and five relapsed at a median of 19 months. Of these, four died due to progressive disease while three relapsed achieved a new CRm after further salvage therapy. This experience confirms the potentially curative effect of prolonged ATRA-ATO therapy in relapsed APL, especially in patients with long first complete remission.
全反式维甲酸(ATRA)和三氧化二砷(ATO)的长期治疗对新诊断的急性早幼粒细胞白血病(APL)非常有效,但在复发情况下该方案的疗效数据有限。我们在此报告了 22 例在疾病复发时接受延长 ATRA-ATO 治疗的 APL 患者。20 例患者在 2 个周期后获得分子完全缓解(CRm)(90%)。其中,2 例患者接受了造血干细胞移植(HSCT),而其余患者继续接受额外的 ATRA-ATO 周期(最多 5 个周期)。从复发时起中位随访 58 个月(范围:21-128 个月),4 年 OS 概率为 0.85(95%CI 0.61-0.94),DFS 为 0.74(95%CI 0.49-0.88),EFS 为 0.68(95%CI 0.45-0.83)。2 例患者对 ATRA-ATO 挽救治疗耐药,5 例患者在中位时间 19 个月时复发。其中,4 例因疾病进展而死亡,而 3 例复发患者在进一步挽救治疗后获得新的 CRm。这一经验证实了延长 ATRA-ATO 治疗在复发 APL 中的潜在疗效,特别是在首次完全缓解时间较长的患者中。