Beex L, Burghouts J, van Turnhout J, Breed W, Hillen H, Holdrinet A, Boetius G, Hoogendoorn G, Doesburg W, Verhulst M
Department of Medicine, St. Radboud Hospital, Nijmegen, The Netherlands.
Cancer Treat Rep. 1987 Dec;71(12):1151-6.
In a multicenter trial, 123 patients with advanced breast cancer who had been treated with tamoxifen and/or chemotherapy were randomized to receive medroxyprogesterone acetate (MPA) orally 300 mg X 3 daily or im 500 mg daily for 4 weeks and 500 mg X 2 weekly thereafter. All case histories were reviewed extramurally by the criteria of the International Union Against Cancer. Five and 11 patients were not eligible and evaluable for response, respectively. Pretreatment characteristics were well balanced in both treated groups. Twenty-five of all 107 (23%) evaluable patients achieved an objective remission, whereas in a further 15% the disease became stable after previous progression. Results in both treatment arms did not differ significantly. The median duration of objective remission was 12 and 14 months for orally and im treated patients, respectively (P greater than 0.10). No statistically significant differences in the survival times of orally and im treated patients were found. Pretreatment characteristics positively correlated with an objective remission during MPA therapy in both groups were age greater than 50 years (P less than 0.02) and no previous chemotherapy (P less than 0.01). Toxicity included an increase in body weight, cushingoid effects, muscle cramps, and tremors in both groups. In four patients on im therapy, local infections developed. Mean serum MPA levels reached values above 100 ng/ml in nine orally and eight im treated patients (P greater than 0.10), and neither differed significantly in the patients responding to or failing therapy. In both MPA arms, plasma cortisol levels were suppressed. The drop in plasma cortisol levels was more pronounced in patients with objective remissions than in patients who failed (P = 0.04). In conclusion, oral and im MPA in the given doses had similar activity. Im administration of MPA should be reserved for patients not able to take oral medication.
在一项多中心试验中,123例曾接受他莫昔芬和/或化疗的晚期乳腺癌患者被随机分组,分别口服醋酸甲羟孕酮(MPA)300mg,每日3次,共4周,之后每周2次,每次500mg;或肌肉注射MPA,500mg,每日1次,共4周,之后每周2次,每次500mg。所有病例记录均由国际抗癌联盟的标准进行外部审核。分别有5例和11例患者不符合纳入标准且无法评估疗效。两个治疗组的预处理特征均衡良好。在所有107例可评估患者中,有25例(23%)实现了客观缓解,另有15%的患者在先前病情进展后病情稳定。两个治疗组的结果无显著差异。口服和肌肉注射治疗患者的客观缓解中位持续时间分别为12个月和14个月(P>0.10)。口服和肌肉注射治疗患者的生存时间未发现有统计学显著差异。两个组中,MPA治疗期间与客观缓解呈正相关的预处理特征为年龄大于50岁(P<0.02)和既往未接受化疗(P<0.01)。毒性反应包括两组患者体重增加、库欣样效应、肌肉痉挛和震颤。在4例接受肌肉注射治疗的患者中发生了局部感染。9例口服治疗患者和8例肌肉注射治疗患者的平均血清MPA水平达到100ng/ml以上(P>0.10),且在缓解或未缓解的患者中均无显著差异。在两个MPA治疗组中,血浆皮质醇水平均受到抑制。客观缓解患者的血浆皮质醇水平下降比未缓解患者更明显(P=0.04)。总之,给定剂量的口服和肌肉注射MPA具有相似的活性。MPA的肌肉注射给药应仅用于不能口服药物的患者。