Rivière A, Abouz D, Ayela P, Berthaud P, Frenay M, Lagrange J L, Pujol J L, Robillard J, Le Chevalier T
Centre François-Baclesse, Caen, France.
Bull Cancer. 1989;76(10):1095-102.
The aim of this study was to test cisplatinum and 5-FU chemotherapy. Thirty-five patients with epidermoid or undifferentiated lung carcinoma were entered in a multicentric phase II trial, in an attempt to further define the activity and toxicity of this association. None of them had been previously treated by chemotherapy. The dosage schedule was cisplatinum 100 mg/m2 D1 and 5-FU 1 g/m2 D1 to D5 every 3 weeks for 3 courses before evaluation. There were CR: 2, PR: 10, for a total response rate of 35%. Median survival was 7 months. Tolerance was acceptable. We conclude that this association can be safely administered, but that the results are not superior to others previously reported. Further studies are required to define the activity of a cisplatinum, 5-FU and radiotherapy association.
本研究的目的是测试顺铂和5-氟尿嘧啶化疗方案。35例表皮样癌或未分化肺癌患者进入一项多中心II期试验,旨在进一步明确该联合方案的活性和毒性。他们均未曾接受过化疗。给药方案为顺铂100mg/m²第1天,5-氟尿嘧啶1g/m²第1天至第5天,每3周1次,共3个疗程,然后进行评估。结果有2例完全缓解(CR),10例部分缓解(PR),总缓解率为35%。中位生存期为7个月。耐受性可接受。我们得出结论,该联合方案可以安全给药,但结果并不优于先前报道的其他方案。需要进一步研究来明确顺铂、5-氟尿嘧啶与放疗联合方案的活性。