Dunphy F R, Boyd J H, Kim H J, Dunphy C H, Harrison B R, Dunleavy T L, Rodriguez J J, McDonough E M, Minster J R, Hilton J G
Saint Louis University Health Sciences Center, Department of Internal Medicine, Missouri 63110-0250, USA.
Cancer. 1997 May 15;79(10):2016-23.
Standard therapy for advanced head and neck carcinoma is surgery and radiation, and the subsequent 5-year survival with this treatment has been less than 50%. New combined modality treatment strategies are being tested to improve survival. New chemotherapy combinations are being developed and administered simultaneously with, or sequenced with, radiation and surgery. This article reports the Phase I results of administering paclitaxel and carboplatin preoperatively. The authors' objective was to develop an outpatient chemotherapy that would downstage tumors and allow organ preservation with equal or improved survival as compared with standard therapy.
Thirty-six patients with untreated Stage III/IV head and neck carcinoma were treated and were evaluable for toxicity. All patients had lesions that were measurable in perpendicular planes. A nonrandomized, Phase I design was used, according to which cohorts of patients were treated every 21 days with escalating doses of paclitaxel (150-265 mg/m2) given as a 3-hour infusion immediately preceding carboplatin. Premedication was used to avoid acute hypersensitivity reactions. Carboplatin was administered intravenously over 1 hour at a constant dose calculated with the Calvert formula (area under the curve, 7.5).
The dose-limiting toxicities were neuropathy and thrombocytopenia at a paclitaxel dose of 265 mg/m2. Neutropenic fever was observed in 30% of patients at a paclitaxel dose of 250-265 mg/m2. Other observed adverse effects included pruritus, myalgia, arthralgia, alopecia, nausea, and vomiting.
Toxicity was acceptable. The maximum tolerated dose of paclitaxel was 230 mg/m2 without hematopoietic growth factor, or 250 mg/m2 with hematopoietic growth factor, the carboplatin dose held constant, calculated at area under the curve of 7.5. Phase II studies of this combination are warranted in the treatment of these carcinomas.
晚期头颈癌的标准治疗方法是手术和放疗,采用这种治疗方法后的5年生存率一直低于50%。目前正在测试新的综合治疗策略以提高生存率。正在研发新的化疗联合方案,并与放疗和手术同时或按顺序使用。本文报告了术前给予紫杉醇和卡铂的I期研究结果。作者的目标是开发一种门诊化疗方案,该方案能够使肿瘤降期,并在生存率与标准治疗相当或提高的情况下实现器官保留。
36例未经治疗的III/IV期头颈癌患者接受了治疗,并可对毒性进行评估。所有患者的病变在垂直平面上均可测量。采用非随机I期设计,根据该设计,患者队列每21天接受一次治疗,紫杉醇剂量(150 - 265 mg/m²)逐渐增加,在给予卡铂前3小时静脉滴注3小时。使用预处理药物以避免急性过敏反应。卡铂以恒定剂量根据卡尔弗特公式(曲线下面积,7.5)计算,静脉滴注1小时。
当紫杉醇剂量为265 mg/m²时,剂量限制性毒性为神经病变和血小板减少。在紫杉醇剂量为250 - 265 mg/m²的患者中,30%观察到中性粒细胞减少性发热。其他观察到的不良反应包括瘙痒、肌痛、关节痛、脱发、恶心和呕吐。
毒性是可接受的。在不使用造血生长因子的情况下,紫杉醇的最大耐受剂量为230 mg/m²,或在使用造血生长因子的情况下为250 mg/m²,卡铂剂量保持恒定,曲线下面积计算为7.5。这种联合方案的II期研究在这些癌症的治疗中是有必要的。