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Long-term outcome of 31 cases of refractory acute promyelocytic leukemia treated with compound realgar natural indigo tablets administered alternately with chemotherapy

机译:复方雄黄天然靛蓝片交替化疗联合治疗31例难治性急性早幼粒细胞白血病的远期疗效

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The aim of the present study was to investigate the long-term survival of patients with refractory acute promyelocytic leukemia (APL) that were administered alternately with compound realgar natural indigo tablet (CRNIT) treatment and chemotherapy. In total, 31 patients with refractory APL were administered with CRNIT treatment alternately with chemotherapy. The complete remission (CR) and relapse rates were estimated by bone marrow (BM) examination. The expression of the promyelocytic leukemia-retinoic acid receptor a (PML-RAR alpha) fusion protein and the apoptosis rate in the retinoic acid (RA) -resistant NB4-R1 cell line administered with CRNIT treatment in vitro were measured by western blot analysis and flow cytometry, respectively. The patients were followed up for 12-60 months, with a median follow-up time of 43 months. The total continuous CR rate was 90.32% (28/31), and the duration of response was between 10.3 and 60 months (median, 42.4 months). The total relapse rate was 9.68% (3/31), and the median time of relapse was 13 months (range, 8-27 months). During the treatment with CRNITs, there was no evident BM depression and only limited side-effects were experienced. Additionally, in vitro cell molecular biology results revealed that CRNIT treatment resulted in a marked induction of apoptosis and degradation of the PML-RAR alpha fusion protein. The present results revealed that CRNIT treatment in combination with chemotherapy is an effective and feasible therapy for the treatment of patients with refractory APL.
机译:本研究的目的是研究难治性急性早幼粒细胞白血病(APL)患者,将其与复方雄黄天然靛蓝片剂(CRNIT)交替治疗和化疗后的长期生存期。总共有31例难治性APL患者与化疗交替接受CRNIT治疗。通过骨髓(BM)检查评估完全缓解(CR)和复发率。通过Western blot分析了体外接受CRNIT处理的视黄酸(RA)耐药NB4-R1细胞系中早幼粒细胞白血病-视黄酸受体a(PML-RARα)融合蛋白的表达和凋亡率。流式细胞仪分别。对患者进行了12-60个月的随访,中位随访时间为43个月。总持续CR率是90.32%(28/31),反应持续时间在10.3和60个月之间(中位数为42.4个月)。总复发率为9.68%(3/31),中位复发时间为13个月(范围8-27个月)。在用CRNITs治疗期间,没有明显的BM抑郁症,只有有限的副作用。此外,体外细胞分子生物学结果显示,CRNIT处理可显着诱导细胞凋亡和PML-RARα融合蛋白降解。目前的结果表明,CRNIT联合化学疗法是治疗难治性APL患者的有效方法。

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