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Outcome of elderly patients with acute promyelocytic leukemia: results of the German Acute Myeloid Leukemia Cooperative Group

机译:老年急性早幼粒细胞白血病患者的结果:德国急性髓细胞白血病合作小组的结果

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摘要

Despite improvement of prognosis, older age remains a negative prognostic factor in acute promyelocytic leukemia (APL). Reports on disease characteristics and outcome of older patients are conflicting. We therefore analyzed 91 newly diagnosed APL patients aged 60 years or older (30 % of 305 adults with APL) registered by the German AML Cooperative Group (AMLCG) since 1994; 68 patients (75 %) were treated in studies, 23 (25 %) were non-eligible, and 31 % had high-risk APL. Fifty-six patients received induction therapy with all-trans retinoic acid and TAD (6-thioguanine, cytarabine, daunorubicin), and consolidation and maintenance therapy. Treatment intensification with a second induction cycle (high dose cytarabine, mitoxantrone; HAM) was optional (n = 14). Twelve patients were randomized to another therapy not considered in this report. The early death rate was 48 % in non-eligible and 19 % in study patients. With the AMLCG regimen, 7-year overall, event-free and relapse-free survival (RFS) and cumulative incidence of relapse were 45 %, 40 %, 48 %, and 24 %, respectively. In patients treated with TAD–HAM induction, 7-year RFS was superior (83 %; p = 0.006) compared to TAD only, and no relapse was observed. In our registered elderly patients, we see a high rate of non-eligibility for treatment in studies and of high-risk APL. In patients who can undergo a curative approach, intensified chemotherapy is highly effective, but is restricted to a selection of patients. Therefore, new less toxic treatment approaches with broader applicability are needed. Elderly patients might be a particular target group for concepts with arsenic trioxide.
机译:尽管预后得到改善,但老年仍然是急性早幼粒细胞白血病(APL)的阴性预后因素。关于老年患者的疾病特征和结局的报告相互矛盾。因此,我们分析了自1994年以来由德国反洗钱合作组织(AMLCG)注册的91名60岁以上的新诊断APL患者(占305名APL成人的30%);研究治疗了68例患者(75%),不符合条件的有23例(25%),高危APL的比例为31%。五十六名患者接受了全反式维甲酸和TAD(6-硫鸟嘌呤,阿糖胞苷,柔红霉素)的诱导治疗,以及巩固和维持治疗。第二个诱导周期(高剂量阿糖胞苷,米托蒽醌; HAM)的治疗强化是可选的(n = 14)。 12名患者被随机分配到本报告中未考虑的另一种治疗方法。不符合条件的患者的早期死亡率为48%,研究患者为19%。使用AMLCG方案时,总的7年无事件生存率和无复发生存率(RFS)以及复发的累积发生率分别为45%,40%,48%和24%。在接受TAD-HAM诱导治疗的患者中,与仅使用TAD相比,7年RFS更好(83%; p = 0.006),并且未观察到复发。在我们注册的老年患者中,我们发现研究和高风险APL的不合格率很高。在可以接受治愈的患者中,强化化疗非常有效,但仅限于部分患者。因此,需要具有更广泛适用性的新的毒性较小的治疗方法。老年患者可能是三氧化二砷概念的特定目标人群。

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