Gedlicka C, Formanek M, Selzer E, Burian M, Kornfehl J, Fiebiger W, Cartellieri M, Marks B, Kornek G V
Department of Internal Medicine I, Division of Oncology, University of Vienna, Vienna, Austria.
Oncology. 2002;63(2):145-50. doi: 10.1159/000063809.
Since the combination of cisplatin and docetaxel have demonstrated activity in squamous cell carcinomas of the lung and oesophagus before, promising results in recurrent metastatic head and neck cancer were expected.
Between September 1998 and October 2000, 40 patients entered this trial, 38 of whom were evaluable. Six patients were previously untreated, 24 had surgery and/or radiotherapy and 13 had received chemoradiation and/or surgery. Therapy consisted of 75 mg/m(2) docetaxel (1-hour infusion) and 75 mg/m(2) cisplatin (90-min infusion) on day 1, repeated every three weeks for a maximum of 6 courses. All patients received corticosteroids routinely, 5-HT3-antagonists, and hydration.
The overall response rate was 52.5% (95% confidence interval, 36.1 to 68.5%) including 7 complete (17.5% complete response; CR) and 14 partial remissions (35% partial response; PR). The overall response rate in patients who had no prior treatment (n = 6) was 100%, including 3 CR and 3 PR. In patients who had prior surgery and/or radiotherapy (n = 21) an overall response rate of 42.8% was observed, including 2 CR and 7 PR; 8 patients (38.1%) had stable disease, while disease progressed in 3 (14.3%). Six of 13 patients (46.2%) who had prior chemoradiation +/- surgery responded, including 2 CR (15.4%) and 4 PR (30.8%), no change was seen in 4 patients (30.8%) and tumour progressed in 2 (15.4%). The median response duration for all patients was 10 months (range, 3-20), the median overall survival was 11 months (range, 1-30). Myelosuppression was commonly observed; WHO grade 3 or 4 neutropenia occurred in 12 patients (30%) each, and was complicated by septicaemia in 5 cases. WHO grade 3 anaemia was observed in only 3 patients (7.5%). Severe non-hematologic toxicity except for alopecia was rarely observed, and included diarrhea in 2 (5%), nausea/vomiting in 2 patients (5%) and stomatitis in 1 patient (2.5%).
Our data suggest that docetaxel and cisplatin in combination is an effective and fairly well tolerated regimen for the treatment of head and neck cancer with an excellent response rate in previously untreated patients.
鉴于顺铂和多西他赛联合用药此前已在肺鳞状细胞癌和食管鳞状细胞癌中显示出活性,因此预期其在复发性转移性头颈癌中会产生良好疗效。
1998年9月至2000年10月期间,40例患者进入本试验,其中38例可评估。6例患者此前未接受过治疗,24例接受过手术和/或放疗,13例接受过放化疗和/或手术。治疗方案为第1天静脉输注75mg/m²多西他赛(1小时输完)和75mg/m²顺铂(90分钟输完),每三周重复一次,最多进行6个疗程。所有患者常规接受皮质类固醇、5 - HT3拮抗剂治疗并进行水化。
总缓解率为52.5%(95%置信区间,36.1%至68.5%),包括7例完全缓解(完全缓解率17.5%;CR)和14例部分缓解(部分缓解率35%;PR)。未接受过治疗的患者(n = 6)总缓解率为100%,包括3例CR和3例PR。接受过手术和/或放疗的患者(n = 21)总缓解率为42.8%,包括2例CR和7例PR;8例患者(38.1%)病情稳定,3例(14.3%)病情进展。13例接受过放化疗±手术的患者中有6例(46.2%)有反应,包括2例CR(15.4%)和4例PR(30.8%),4例患者(30.8%)病情无变化,2例(15.4%)肿瘤进展。所有患者的中位缓解持续时间为10个月(范围3 - 20个月),中位总生存期为11个月(范围1 - 30个月)。骨髓抑制较为常见;WHO 3级或4级中性粒细胞减少症各发生在12例患者(30%)中,5例并发败血症。仅3例患者(7.5%)出现WHO 3级贫血。除脱发外,严重的非血液学毒性很少见,包括2例(5%)腹泻、2例患者(5%)恶心/呕吐和1例患者(2.5%)口腔炎。
我们的数据表明,多西他赛和顺铂联合用药是治疗头颈癌的一种有效且耐受性良好的方案,对未接受过治疗的患者有极佳的缓解率。