Ghielmini M, Pagani O, de Jong J, Pampallona S, Conti A, Maestroni G, Sessa C, Cavalli F
Servizio Oncologico Cantonale, Ospedale San Giovanni, Bellinzona, Switzerland.
Br J Cancer. 1999 Jun;80(7):1058-61. doi: 10.1038/sj.bjc.6690463.
A significant myeloprotective effect of melatonin in mice treated with etoposide, cyclophosphamide or carboplatin has been reported. The present study was designed to evaluate if the same effect could be observed in patients receiving chemotherapy. Twenty previously untreated patients with inoperable lung cancer received two cycles of carboplatin (given at area under the curve 5 by the Calvert formula) on day 1 and etoposide (150 mg m(-2) i.v.) on days 1-3 every 4 weeks. Melatonin 40 mg or placebo (double-blind) was given orally in the evening for 21 consecutive days, starting 2 days before chemotherapy. Patients were randomized to receive melatonin either with the first or the second cycle. Complete blood cell count with differential was done three times per week for 3 weeks. The median age of the cohort was 60 years (range 42-69), 16 patients had non-small cell and four patients small-cell lung cancer, 12 stage III and eight stage IV disease. In a multivariate analysis including age, sex, diagnosis, stage, performance status, doses of carboplatin and etoposide, and concomitant treatment with melatonin or placebo, the haematological parameters--depth and duration of toxicity for haemoglobin, platelets and neutrophils (ANC)--were not significantly different between cycles with/without melatonin. The mean ANC nadir and the mean number of days with ANC < 0.5 x 10(9) l(-1) were 0.5 x 10(9) l(-1) and 2.5 days, respectively, with/without melatonin. We concluded that, in patients with lung cancer, melatonin given orally at a dose of 40 mg per day for 21 days in the evening, does not protect against the myelotoxic effect of carboplatin and etoposide.
已有报道称褪黑素对接受依托泊苷、环磷酰胺或卡铂治疗的小鼠具有显著的骨髓保护作用。本研究旨在评估在接受化疗的患者中是否能观察到同样的效果。20例先前未接受过治疗的无法手术的肺癌患者,每4周在第1天接受两个周期的卡铂(按照卡尔弗特公式给予曲线下面积为5),并在第1 - 3天接受依托泊苷(150 mg m(-2)静脉注射)。从化疗前2天开始,连续21天每晚口服40 mg褪黑素或安慰剂(双盲)。患者被随机分为在第一个或第二个周期接受褪黑素治疗。每周进行3次全血细胞计数及分类,持续3周。该队列的中位年龄为60岁(范围42 - 69岁),16例为非小细胞肺癌,4例为小细胞肺癌,12例为Ⅲ期,8例为Ⅳ期疾病。在一项多变量分析中,纳入了年龄、性别、诊断、分期、体能状态、卡铂和依托泊苷的剂量以及褪黑素或安慰剂的联合治疗,结果显示,在接受/未接受褪黑素治疗的周期之间,血液学参数——血红蛋白、血小板和中性粒细胞(ANC)毒性的深度和持续时间——并无显著差异。接受/未接受褪黑素治疗时,ANC的平均最低点分别为0.5 x 10(9) l(-1),ANC < 0.5 x 10(9) l(-1)的平均天数分别为2.5天。我们得出结论,对于肺癌患者,每晚口服40 mg褪黑素,持续21天,不能预防卡铂和依托泊苷的骨髓毒性作用。