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米托蒽醌、依托泊苷和小剂量阿糖胞苷治疗老年急性髓系白血病——波兰急性白血病研究组(PALG)II期研究报告

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.

作者信息

Wrzesien-Kus A, Robak T, Jamroziak K, Wierzbowska A, Dmoszynska A, Adamczyk-Cioch M, Kuliczkowski K, Mazur G, Holowiecki J, Konopka L, Maj S, Marianska B, Zawilska K

机构信息

Department of Hematology, Medical University of Lodz, Poland.

出版信息

Neoplasma. 2002;49(6):405-11.

Abstract

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.

摘要

老年急性髓系白血病(AML)患者治疗中常见的两难困境是,是采用强化骨髓抑制疗法,这种疗法有较高的治疗相关死亡率(TRM),但有获得完全缓解(CR)的机会;还是采用强度较低的治疗,以延长生存时间并提高生活质量。这项前瞻性II期研究的目的是评估低剂量联合诱导治疗的疗效和毒性,该治疗方案包括:阿糖胞苷剂量为10mg/m²,每12小时皮下注射一次,共7天;依托泊苷剂量为100mg/天,口服7天;米托蒽醌剂量为6mg/m²,第1 - 3天静脉注射,每日一次。计划进行两个诱导疗程。在44例患者组中,12例(27%)达到CR,4例(9%)患者部分缓解(PR),9例(20%)早期死亡(ED)。年龄、体能状态、之前的骨髓增生异常综合征、核型、白细胞计数和骨髓中原始细胞百分比不是CR概率的显著预后因素。以下初始因素似乎与治疗开始后较短的生存时间相关:年龄>70岁(p<0.03)、体能状态差(p<0.03)以及骨髓原始细胞百分比>50%(p<0.05)。我们得出结论,尽管在前期研究中有令人鼓舞的结果,但这种诱导治疗的疗效并不优于其他方案。这种治疗的血液学毒性似乎与“3 + 7”方案相当。

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