Department of Pharmacy, Cleveland Clinic, Cleveland, Ohio.
Am J Hematol. 2013 Oct;88(10):906-9. doi: 10.1002/ajh.23530. Epub 2013 Aug 30.
Cytotoxic chemotherapy dosages are traditionally calculated according to body surface area (BSA). No guidelines exist for chemotherapy dosing of acute myeloid leukemia (AML) patients at extremes of weight. We investigated the efficacy and safety of chemotherapy dosed according to BSA based on actual body weight (ABW) among under/normal weight, overweight, and obese AML patients. AML patients (excluding acute promyelocytic leukemia) treated with anthracycline and cytarabine-based remission induction chemotherapy from 2002 to 2009 at Cleveland Clinic were divided into three body mass index (BMI) groups: under/normal weight (BMI ≤ 24.9), overweight (BMI 25.0-29.9), and obese (BMI ≥ 30.0). Among 247 AML patients, 81 (33%) were under/normal weight, 81 (33%) were overweight, and 85 (34%) were obese. Complete remission (CR) rates were similar among these groups (69.1, 79.0, and 76.5%, respectively; P = 0.321), as was median survival (10.7, 16.7, and 14.2 months, respectively, P = 0.352) and 30-day mortality (3.7, 2.5, 7.1%, respectively, P = 0.331). There was no difference among groups in days to neutrophil or platelet recovery, hospitalization days for induction chemotherapy, and bacteremia. After adjustment for confounders (age, sex, BMI, white blood cells, cytogenetic risk, etiology, and bacteremia), overall survival was significantly shorter for normal weight compared to overweight (P = 0.006) and obese (0.038) patients. Response rates and adverse events were not significantly different among AML patients of all weight classes when induction chemotherapy was dosed according to ABW. Induction chemotherapy in these patients can be safely dosed using ABW.
细胞毒性化疗剂量传统上根据体表面积(BSA)计算。对于体重处于极端的急性髓系白血病(AML)患者,尚无化疗剂量指南。我们研究了根据实际体重(ABW)计算的 BSA 为基础的化疗剂量在体重不足/正常、超重和肥胖 AML 患者中的疗效和安全性。克利夫兰诊所 2002 年至 2009 年间接受蒽环类药物和阿糖胞苷为基础的缓解诱导化疗的 AML 患者(不包括急性早幼粒细胞白血病),根据体重指数(BMI)分为三组:体重不足/正常(BMI≤24.9)、超重(BMI 25.0-29.9)和肥胖(BMI≥30.0)。在 247 例 AML 患者中,81 例(33%)体重不足/正常,81 例(33%)超重,85 例(34%)肥胖。这些组的完全缓解(CR)率相似(分别为 69.1%、79.0%和 76.5%,P=0.321),中位生存时间(分别为 10.7、16.7 和 14.2 个月,P=0.352)和 30 天死亡率(分别为 3.7%、2.5%和 7.1%,P=0.331)也相似。中性粒细胞或血小板恢复天数、诱导化疗住院天数和菌血症在各组之间无差异。在校正混杂因素(年龄、性别、BMI、白细胞、细胞遗传学风险、病因和菌血症)后,与超重(P=0.006)和肥胖(P=0.038)患者相比,正常体重患者的总生存期明显缩短。当根据 ABW 对诱导化疗进行剂量调整时,所有体重组的 AML 患者的反应率和不良事件没有显著差异。在这些患者中,可以安全地根据 ABW 对诱导化疗进行剂量调整。