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首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >The treatment of acute myeloid leukemia with mitoxantrone, etoposide and low-dose cytarabine in elderly patients - a report of Polish Acute Leukemia Group (PALG) phase II study.
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The treatment of acute myeloid leukemia with mitoxantrone, etoposide and low-dose cytarabine in elderly patients - a report of Polish Acute Leukemia Group (PALG) phase II study.

机译:米托蒽醌,依托泊苷和小剂量阿糖胞苷在老年患者中治疗急性骨髓性白血病-波兰急性白血病小组(PALG)II期研究的报告。

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The common dilemma in the treatment of elderly patients with acute myeloid leukemia (AML) is whether to use intensive myelosuppresive therapy with higher risk of treatment related mortality (TRM), but a chance for complete remission (CR), or to treat less intensively in order to prolong survival time with a better quality of life. The aim of this prospective, phase II study was to assess the efficacy and toxicity of low dose combination induction treatment consisted of cytarabine at a dose of 10 mg/m2 every 12 h s.c. for 7 days, VP-16 at a dose of 100 mg/day p.o. for 7 days and mitoxantrone at a dose of 6 mg/m2 i.v daily on days 1-3. Two induction courses were planned. In the group of 44 patients 12 (27%) achieved CR, 4 (9%) patients were in PR and there were 9 (20%) early deaths (ED). Age, performance status, preceding myelodysplastic syndrome, karyotype, WBC and % of blasts in bone marrow were not significant prognostic factors for CR probability. The following initial factors appeared to be related to a shorter duration of survival time from the start of treatment: age >70 (p<0.03), poor performance status (p<0.03), and % of BM blasts 50 (p<0.05). We conclude that, despite promising results in the pilot study the efficacy of this induction treatment is not better than the efficacy of other regimens. The hematological toxicity of this treatment seems to be comparable with "3+7" regimen.
机译:在老年急性髓细胞性白血病(AML)患者中,常见的难题是是否使用强化骨髓抑制疗法,其治疗相关死亡率(TRM)较高,但有机会获得完全缓解(CR),或者在患者中降低强度为了延长生存时间,提高生活质量。这项前瞻性II期研究的目的是评估每12 h s用10 mg / m2剂量的阿糖胞苷组成的低剂量联合诱导治疗的疗效和毒性。持续7天,口服VP-16剂量为每天100 mg。持续7天,并在1-3天以每天6 mg / m2的剂量静脉注射米托蒽醌。计划了两个入门课程。在44例患者中,有12例(27%)获得CR,4例(9%)处于PR,有9例(20%)早期死亡(ED)。年龄,机能状态,骨髓增生异常综合征前的症状,核型,白细胞和骨髓原始细胞的百分比不是CR发生率的重要预后因素。以下初始因素似乎与从治疗开始起生存时间较短有关:年龄> 70(p <0.03),不良表现状态(p <0.03)和BM爆炸百分比50(p <0.05) 。我们得出结论,尽管在前期研究中取得了令人鼓舞的结果,但这种诱导治疗的疗效并不比其他方案的疗效更好。该治疗的血液学毒性似乎与“ 3 + 7”方案相当。

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