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Mutations affecting both the rearranged and the unrearrangedPMLalleles in refractory acute promyelocytic leukaemia

机译:影响难治性急性早幼细胞白血病中重新排列和未解析的突变和未解析的突变

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摘要

Acute promyelocytic leukaemia (APL) is characterized by the PML/RARA fusion transcript. PML and RARA mutations have been shown to directly respond to arsenic trioxide (ATO) and all-trans retinoic (ATRA). We analysed the prevalence of PML mutations in 32 patients with de novo or therapy-related APL (t-APL; n = 5), treated with ATO. We identified one ATO-resistant t-APL patient, who presented a PML A216T mutation in both the rearranged and unrearranged PML alleles, and two mutations in the rearranged RARA gene. In this patient, subclones with different PML and RARA mutations acquired clonal dominance during the disease course, probably leading to treatment resistance.
机译:急性幼幼细胞白血病(APL)的特征在于PML / RARA融合转录物。已显示PML和RARA突变直接响应砷三氧化砷(ATO)和全反式视网膜(ATRA)。我们分析了32例患者PML突变的患病率,与ATO处理过的DE Novo或治疗相关APL(T-APL; n = 5)。我们鉴定了一种ATO抗性T-APL患者,其在重新排列的和不公平的PML等位基因中呈现PML A216T突变,以及重新排列的RARA基因中的两个突变。在该患者中,具有不同PML和RARA突变的亚克酮在疾病过程中获得了克隆优势,可能导致治疗抵抗。

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