Hudis C A, Seidman A D, Crown J P, Balmaceda C, Freilich R, Gilewski T A, Hakes T B, Currie V, Lebwohl D E, Baselga J, Raptis G, Gollub M, Robles M, Bruno R, Norton L
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
J Clin Oncol. 1996 Jan;14(1):58-65. doi: 10.1200/JCO.1996.14.1.58.
Because docetaxel (Taxotere, RP 56976; Rhone-Poulenc Rorer, Antony, France) appeared to be active against breast cancer in phase I trials, we performed this phase II study.
Thirty-seven patients with measurable disease were enrolled. Only prior hormone therapy was allowed, as was adjuvant chemotherapy completed > or = 12 months earlier. Docetaxel 100 mg/m2 was administered over 1 hour every 21 days. Diphenhydramine hydrochloride and/or corticosteroid premedication was added after hypersensitivity-like reactions (HSRs) were seen in two of the first six patients. Pharmacokinetic studies were performed during cycle 1 for correlation with toxicity.
Thirty-seven patients were assessable. Nineteen (51%) required dose reductions, usually for neutropenic fever. The median nadir WBC count was 1.4 x 10(3)/microL. HSRs were noted in 20 patients (54%). At a median cumulative dose of 297 mg/m2 (range, 99.6 to 424.5 mg/m2), 30 patients (81%) developed fluid retention, for which 11 (30%) subsequently stopped treatment. The first-cycle plasma area under the concentration-time curve (AUC) did not correlate with toxicity, although an ineligible patient with hepatic metastases (pretreatment bilirubin level 1.8 mg/dL) had an elevated AUC and died of toxicity. Responses were seen at all sites. On an intent-to-treat basis, there were two (5%) complete responses (CRs) and 18 (49%) partial responses (PRs). The overall response proportion (CRs plus PRs) was 54% (95% confidence interval, 37% to 71%). The median time to response was 12 weeks (range, 3 to 15) and the median duration was 26 weeks (range, 10 to 58+).
Docetaxel is active for metastatic breast cancer. Neutropenia and fluid retention are dose-limiting. The AUC did not predict toxicity, but caution is warranted when treating patients with liver dysfunction. An understanding of the pathophysiology of the fluid retention may facilitate prevention. Frequent HSR may warrant prophylactic premedication.
由于多西他赛(泰索帝,RP 56976;法国罗纳普朗克·乐安公司,安东尼)在I期试验中显示出对乳腺癌有效,我们开展了这项II期研究。
纳入37例有可测量病灶的患者。仅允许既往进行过激素治疗,辅助化疗需在≥12个月前完成。多西他赛100mg/m²每21天静脉滴注1小时。在前6例患者中有2例出现类过敏反应(HSR)后,加用盐酸苯海拉明和/或糖皮质激素进行预处理。在第1周期进行药代动力学研究以与毒性进行相关性分析。
37例患者可进行评估。19例(51%)需要降低剂量,通常是因为中性粒细胞减少性发热。中性粒细胞计数最低点的中位数为1.4×10³/μL。20例患者(54%)出现HSR。在累积剂量中位数为297mg/m²(范围99.6至424.5mg/m²)时,30例患者(81%)出现液体潴留,其中11例(30%)随后停止治疗。尽管1例不符合入组标准的肝转移患者(治疗前胆红素水平1.8mg/dL)的药时曲线下面积(AUC)升高且死于毒性,但第1周期的血浆AUC与毒性无相关性。所有部位均可见反应。在意向性分析中,有2例(5%)完全缓解(CR),18例(49%)部分缓解(PR)。总缓解率(CR加PR)为54%(95%置信区间,37%至71%)。缓解的中位时间为12周(范围3至15周),中位持续时间为26周(范围10至58 +周)。
多西他赛对转移性乳腺癌有效。中性粒细胞减少和液体潴留是剂量限制性毒性。AUC不能预测毒性,但在治疗肝功能不全患者时需谨慎。了解液体潴留的病理生理学可能有助于预防。频繁出现HSR可能需要预防性预处理。