Conte P F, Michelotti A, Baldini E, Salvadori B, Gennari A, Da Prato M, Tibaldi C, Salzano E, Gentile A
Division of Medical Oncology, St Chiara Hospital, Pisa, Italy.
Semin Oncol. 1996 Oct;23(5 Suppl 11):28-31.
We performed a dose escalation study to evaluate the maximum tolerated dose of paclitaxel (Taxol; Bristol-Myers Squibb Company, Princeton, NJ) given over 3 hours plus bolus epirubicin 90 mg/m2. The starting dose of paclitaxel, 135 mg/m2, was escalated by 20-mg/m2 increments in cohorts of three to six patients. Courses were repeated every 3 weeks. Filgrastim (5 micrograms/kg/d) was administered to shorten the duration of grade 4 neutropenia lasting longer than 72 hours. Twenty-nine patients have been treated, 86% of whom had failed adjuvant chemotherapy (with anthracyclines in 14 cases). One hundred forty-eight courses have been administered, and the paclitaxel dose has been escalated to 225 mg/m2 without reaching the maximum tolerated dose. The most frequent dose-related toxicity has been grade 4 neutropenia, which occurred in 59% of courses. The median duration of grade 4 neutropenia was 4 days, which was shortened with filgrastim only in patients treated with paclitaxel 225 mg/m2. Eleven episodes of febrile neutropenia (7% of courses) have been observed. Nonhematologic toxicities were mild or moderate: grade 1 or 2 peripheral neuropathy was reported by 41% and 10% of patients, respectively. The cardiac toxicities of this regimen were surprisingly low: median left ventricular ejection fraction was 57% at study entry and 56% after six courses. Only two patients showed a decrease of left ventricular ejection fraction below 50% after six courses, and no signs of anthracycline-induced congestive heart failure were noted. The activity of this novel combination is encouraging: the overall response rate is 80%, with 16% complete responses. We have demonstrated that the combination of epirubicin plus paclitaxel given over 3 hours is feasible with acceptable toxicities, does not appear to be associated with clinically relevant cardiotoxicity, and is active in a population of patients who have failed adjuvant chemotherapy.
我们进行了一项剂量递增研究,以评估在3小时内给予紫杉醇(泰素;百时美施贵宝公司,新泽西州普林斯顿)加90mg/m²表柔比星推注的最大耐受剂量。紫杉醇的起始剂量为135mg/m²,在每组三至六名患者中以20mg/m²的增量递增。疗程每3周重复一次。给予非格司亭(5微克/千克/天)以缩短持续超过72小时的4级中性粒细胞减少的持续时间。29名患者接受了治疗,其中86%的患者辅助化疗失败(14例使用蒽环类药物)。已给药148个疗程,紫杉醇剂量已递增至225mg/m²,但未达到最大耐受剂量。最常见的剂量相关毒性是4级中性粒细胞减少,发生在59%的疗程中。4级中性粒细胞减少的中位持续时间为4天,仅在用225mg/m²紫杉醇治疗的患者中使用非格司亭后缩短。观察到11例发热性中性粒细胞减少(占疗程的7%)。非血液学毒性为轻度或中度:分别有41%和10%的患者报告有1级或2级周围神经病变。该方案的心脏毒性出奇地低:研究开始时左心室射血分数中位数为57%,六个疗程后为56%。只有两名患者在六个疗程后左心室射血分数下降至50%以下,未观察到蒽环类药物引起的充血性心力衰竭迹象。这种新组合的活性令人鼓舞:总缓解率为80%,完全缓解率为16%。我们已经证明,3小时内给予表柔比星加紫杉醇的组合是可行的,毒性可接受,似乎与临床相关的心脏毒性无关,并且在辅助化疗失败的患者群体中具有活性。