首页> 外文期刊>Acta Haematologica >Use of all-trans retinoic acid in combination with arsenic trioxide for remission induction in patients with newly diagnosed acute promyelocytic leukemia and for consolidation/maintenance in CR patients.
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Use of all-trans retinoic acid in combination with arsenic trioxide for remission induction in patients with newly diagnosed acute promyelocytic leukemia and for consolidation/maintenance in CR patients.

机译:全反式维甲酸与三氧化二砷联用可在新诊断为急性早幼粒细胞白血病的患者中诱导缓解,并在CR患者中巩固/维持。

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摘要

In the present study, 90 patients with newly diagnosed acute promyelocytic leukemia (APL) were studied for all-trans retinoic acid (ATRA) and arsenic trioxide (As(2)O(3)) combination treatment in remission induction and postremission therapy. In addition, 20 APL patients who had achieved complete remission (CR) with an ATRA-based regimen received ATRA/As(2)O(3) combination for consolidation and maintenance were also enrolled. The results showed that ATRA/As(2)O(3) combination therapy yielded a high CR rate of 93.3% and a significantly shorter time to enter CR (median: 31 days; range: 18-59 days) compared to the ATRA-based regimen (n = 72; median: 39 days; range: 25-62 days). With the ATRA/As(2)O(3) combination for CR maintaining, regardless of the way by which CR was attained, the relapse-free survival was significantly better than with an ATRA plus cytotoxic chemotherapy regimen (92.9 +/- 3.2% vs. 72.4 +/- 7.6%, for the 3-year Kaplan-Meier estimate of relapse-free survival). The drug toxicity profile showed that with the use of As(2)O(3), the incidence of hepatotoxicity was obviously high during remission induction but decreased significantly during postremission treatment. We conclude that APL patients may benefit from the early use of the combination of ATRA and As(2)O(3), in either remission induction or consolidation/maintenance.
机译:在本研究中,对90例新诊断为急性早幼粒细胞白血病(APL)的患者进行了全反式维甲酸(ATRA)和三氧化二砷(As(2)O(3))组合治疗,以诱导缓解和缓解。此外,还纳入了20名已经采用ATRA方案实现完全缓解(CR)的APL患者,接受了ATRA / As(2)O(3)组合进行巩固和维持。结果显示,与ATRA-A相比,ATRA / As(2)O(3)联合疗法的CR率高达93.3%,进入CR的时间明显缩短(中位数:31天;范围:18-59天)。基础方案(n = 72;中位数:39天;范围:25-62天)。采用ATRA / As(2)O(3)联合治疗CR,无论获得CR的方式如何,无复发生存率均显着优于ATRA加细胞毒性化疗方案(92.9 +/- 3.2% 3年Kaplan-Meier估计的无复发生存率则为72.4 +/- 7.6%)。药物毒性特征表明,使用As(2)O(3)可以在缓解诱导期间显着提高肝毒性的发生率,而在缓解后治疗期间显着降低肝毒性的发生率。我们得出的结论是,在缓解诱导或巩固/维持中,APL患者可从ATRA和As(2)O(3)的早期使用中受益。

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