Recondo G, Armand J P, Tellez-Bernal E, Domenge C, Belehradek M, De Vathaire F, Wibault P, Richard J M, Cvitkovic E
Department of Medicine, Institut Gustave-Roussy, Villejuif, France.
Laryngoscope. 1991 May;101(5):494-501. doi: 10.1288/00005537-199105000-00009.
One hundred two patients with recurrent and/or metastatic head and neck squamous cell cancer were entered into four consecutive phase II trials, all cisplatinum (C-DDP, 100 mg/m2/cycle)-based. The two combinations tried were C-DDP, bleomycin, and fluorouracil (CFB) on 54 patients, and cisplatinum and vindesin in 36 patients (CV). The CFB combination was given with C-DDP by continuous infusion over 96 hours (23 patients) or on day 1 (31 patients). The CV regimen was also given in two different schedules, with VDS at 3 mg/m2/g weekly (12 patients) or by a 96-hour continuous infusion (0.6 to 1.0 mg/m2/d) in 24 patients. The following variables: sex, age, performance status, previous therapy, local recurrence, length of disease-free interval (DFI), distant metastases, weight loss, primary site, histological differentiation, type of chemotherapy, previous chemotherapy, evaluable/measurable disease, erythrosedimentation rate, and their relation with response to chemotherapy (WHO) and survival were submitted to both univariate and multivariate analysis (Cox). Overall response rate (RR:CR + PR) was 25 (28%) of 90. In the CFB protocols, RR was 12 (22%) of 54 vs. 13 (38%) of 36 (P = 0.15, NS) in the CV combination group. For the four different combinations the RR was CFB C-DDPci 7 (30%) of 23, CFB C-DDP 1 hour 5 (16%) of 31, CV VDS weekly 2 (17%) of 12, CV VDSci 11 (45%) of 24. The patient populations were very different, with the latest combination consisting of metastatic patients exclusively. Univariate analysis of multiple variables showed age less than 60 years, PS:0 or 1, no previous therapy, absence of local relapse, metastatic disease, long DFI, and that measurable disease was significant for the probability of response. Median survival was 7 months for the 90 evaluated patients, 5 months for nonresponders, and 9 months for responders (P = 0.01). In the univariate analysis, significant factors for survival were PS:0 or 1, a weight loss below 10%, long DFI, response to chemotherapy, erythrosedimentation rate (ESR) of less than 30 mm/1st hr, presence of bone metastasis, and the number of metastases. Multivariate analysis shows PS, the absence of local relapse, and disease-free interval as significant prognostic factors for response. Multivariate analysis factors of significance for survival were PS, weight loss, and response to chemotherapy. The analysis of the clinical pattern showed an evolution in RR from 3 (8%) of 36 on previously irradiated local recurrent disease to 8 (73%) of 11 in previously untreated patients with metastatic disease at presentation.(ABSTRACT TRUNCATED AT 400 WORDS)
102例复发性和/或转移性头颈部鳞状细胞癌患者进入了4个连续的II期试验,所有试验均以顺铂(C-DDP,100mg/m²/周期)为基础。尝试的两种联合方案为:54例患者接受C-DDP、博来霉素和氟尿嘧啶(CFB),36例患者接受顺铂和长春地辛(CV)。CFB联合方案中,C-DDP通过96小时持续输注给药(23例患者)或在第1天给药(31例患者)。CV方案也采用两种不同的给药时间表,长春地辛(VDS)按3mg/m²/周给药(12例患者)或通过96小时持续输注(0.6至1.0mg/m²/天)给药(24例患者)。对以下变量:性别、年龄、体能状态、既往治疗、局部复发、无病间期(DFI)长度、远处转移、体重减轻、原发部位、组织学分化、化疗类型、既往化疗、可评估/可测量疾病、红细胞沉降率及其与化疗反应(WHO标准)和生存的关系进行单因素和多因素分析(Cox模型)。90例患者的总缓解率(RR:完全缓解+部分缓解)为25例(28%)。在CFB方案组中,54例患者的RR为12例(22%),而CV联合方案组36例患者的RR为13例(38%)(P=0.15,无统计学意义)。对于四种不同的联合方案,RR分别为:CFB C-DDPci组23例中的7例(30%),CFB C-DDP 1小时组31例中的5例(16%),CV VDS每周组12例中的2例(17%),CV VDSci组24例中的11例(45%)。患者群体差异很大,最后一种联合方案仅包括转移性患者。多变量单因素分析显示,年龄小于60岁、体能状态为0或1、无既往治疗、无局部复发、无转移性疾病、DFI长以及可测量疾病对缓解概率有显著影响。90例评估患者的中位生存期为7个月,无反应者为5个月,有反应者为9个月(P=0.01)。在单因素分析中,生存的显著因素为体能状态为0或1、体重减轻低于10%、DFI长、对化疗有反应、红细胞沉降率(ESR)小于30mm/第1小时、存在骨转移以及转移灶数量。多因素分析显示,体能状态、无局部复发和无病间期是缓解的显著预后因素。生存的多因素分析显著因素为体能状态、体重减轻和对化疗的反应。临床模式分析显示,RR从先前接受过放疗的局部复发性疾病患者中36例中的3例(8%),演变为初诊时未经治疗的转移性疾病患者中11例中的8例(73%)。(摘要截断于400字)