Department of Medicine A, Haematology and Oncology, University of Münster, Münster, Germany.
Lancet. 2010 Dec 11;376(9757):2000-8. doi: 10.1016/S0140-6736(10)62105-8. Epub 2010 Dec 3.
About 50% of patients (age ≥60 years) who have acute myeloid leukaemia and are otherwise medically healthy (ie, able to undergo intensive chemotherapy) achieve a complete remission (CR) after intensive chemotherapy, but with a substantially increased risk of early death (ED) compared with younger patients. We verified the association of standard clinical and laboratory variables with CR and ED and developed a web-based application for risk assessment of intensive chemotherapy in these patients.
Multivariate regression analysis was used to develop risk scores with or without knowledge of the cytogenetic and molecular risk profiles for a cohort of 1406 patients (aged ≥60 years) with acute myeloid leukaemia, but otherwise medically healthy, who were treated with two courses of intensive induction chemotherapy (tioguanine, standard-dose cytarabine, and daunorubicin followed by high-dose cytarabine and mitoxantrone; or with high-dose cytarabine and mitoxantrone in the first and second induction courses) in the German Acute Myeloid Leukaemia Cooperative Group 1999 study. Risk prediction was validated in an independent cohort of 801 patients (aged >60 years) with acute myeloid leukaemia who were given two courses of cytarabine and daunorubicin in the Acute Myeloid Leukaemia 1996 study.
Body temperature, age, de-novo leukaemia versus leukaemia secondary to cytotoxic treatment or an antecedent haematological disease, haemoglobin, platelet count, fibrinogen, and serum concentration of lactate dehydrogenase were significantly associated with CR or ED. The probability of CR with knowledge of cytogenetic and molecular risk (score 1) was from 12% to 91%, and without knowledge (score 2) from 21% to 80%. The predicted risk of ED was from 6% to 69% for score 1 and from 7% to 63% for score 2. The predictive power of the risk scores was confirmed in the independent patient cohort (CR score 1, from 10% to 91%; CR score 2, from 16% to 80%; ED score 1, from 6% to 69%; and ED score 2, from 7% to 61%).
The scores for acute myeloid leukaemia can be used to predict the probability of CR and the risk of ED in older patients with acute myeloid leukaemia, but otherwise medically healthy, for whom intensive induction chemotherapy is planned. This information can help physicians with difficult decisions for treatment of these patients.
Deutsche Krebshilfe and Deutsche Forschungsgemeinschaft.
大约 50%的年龄≥60 岁且在医学上健康(即能够接受强化化疗)的急性髓系白血病患者在强化化疗后达到完全缓解(CR),但与年轻患者相比,早期死亡(ED)的风险显著增加。我们验证了标准临床和实验室变量与 CR 和 ED 的相关性,并开发了一个基于网络的应用程序,用于评估这些患者接受强化化疗的风险。
使用多变量回归分析,为 1406 名年龄≥60 岁且在医学上健康但无细胞遗传学和分子风险特征的急性髓系白血病患者(接受两疗程强化诱导化疗[替鸟嘌呤、标准剂量阿糖胞苷和柔红霉素,随后高剂量阿糖胞苷和米托蒽醌;或高剂量阿糖胞苷和米托蒽醌在第一和第二诱导疗程中]治疗)的队列开发风险评分,这些患者来自德国急性髓系白血病合作组 1999 年的研究。在急性髓系白血病 1996 年研究中接受两疗程阿糖胞苷和柔红霉素治疗的 801 名年龄>60 岁的急性髓系白血病患者的独立队列中验证了风险预测。
体温、年龄、初发白血病与细胞毒性治疗继发白血病或先前血液病、血红蛋白、血小板计数、纤维蛋白原和血清乳酸脱氢酶浓度与 CR 或 ED 显著相关。在了解细胞遗传学和分子风险的情况下,CR 的概率为 12%至 91%,而不了解的情况下为 21%至 80%。对于评分 1,ED 的预测风险为 6%至 69%,对于评分 2,ED 的预测风险为 7%至 63%。风险评分的预测能力在独立患者队列中得到了证实(CR 评分 1,10%至 91%;CR 评分 2,16%至 80%;ED 评分 1,6%至 69%;ED 评分 2,7%至 61%)。
对于计划接受强化诱导化疗的年龄较大且在医学上健康的急性髓系白血病患者,急性髓系白血病评分可用于预测 CR 的概率和 ED 的风险。这些信息可以帮助医生为这些患者的治疗做出困难的决策。
德国癌症援助协会和德国研究基金会。