Leonardi V, Meli M, Palmeri S, Russo A, Rini G B, Peralta S, Rausa L
Policlinico P. Giaccone, University of Palermo, Italy.
J Chemother. 1995 Apr;7(2):160-6. doi: 10.1179/joc.1995.7.2.160.
Advanced breast cancer remains a major clinical problem. Current chemotherapy regimens are able to induce a clinical response in many patients but do not appear to influence significantly patients' survival. The use of new drugs such as mitoxantrone with a predicted lower toxicity and biochemical modulation of 5-fluorouracil with levo-folinate are extensively studied research areas that could combine good therapeutic efficacy with the maintenance of an acceptable quality of life. 34 patients with advanced breast carcinoma were included in the study. Only 4 women had received prior chemotherapy for advanced disease. Treatment plan was: 5-fluorouracil 400 mg/m2 + l-leucovorin 100 mg/m2 days 1-3, cyclophosphamide 600 mg/m2 and mitoxantrone 12-14 mg/m2 on day 3, q28. G-CSF (5 micrograms/kg/d days 7-14) was routinely delivered to the patients with the aim of maintaining dose intensity. 15 patients obtained a response for an overall response rate of 44%. Mean duration was 10.2+ and 11+ months for complete and partial responses respectively. Mean overall survival was 14.4+ months. A high complete response rate was seen in liver metastasis (44%), while lung lesions had a lower probability of response (25%). Toxicity was globally mild with 23% of grade 3 vomiting and 15% of grade 3-4 leukopenia. Two cases of cardiotoxicity were reported. No difference in response rate or toxicity was identified between patients receiving two different mitoxantrone doses (12 or 14 mg/m2). The schedule employed appears to be well tolerated and active in the treatment of advanced breast cancer.(ABSTRACT TRUNCATED AT 250 WORDS)
晚期乳腺癌仍然是一个主要的临床问题。当前的化疗方案能够使许多患者产生临床反应,但似乎并未显著影响患者的生存率。使用如米托蒽醌这类预计毒性较低的新药,以及用亚叶酸对5-氟尿嘧啶进行生化调节,都是广泛研究的领域,有望将良好的治疗效果与维持可接受的生活质量相结合。34例晚期乳腺癌患者被纳入该研究。只有4名女性曾接受过针对晚期疾病的化疗。治疗方案为:第1 - 3天,5-氟尿嘧啶400mg/m² + 亚叶酸钙100mg/m²,第3天环磷酰胺600mg/m²、米托蒽醌12 - 14mg/m²,每28天重复。常规给予患者粒细胞集落刺激因子(第7 - 14天,5μg/kg/d),以维持剂量强度。15例患者获得缓解,总缓解率为44%。完全缓解和部分缓解的平均持续时间分别为10.2 +个月和11 +个月。平均总生存期为14.4 +个月。肝转移患者的完全缓解率较高(44%),而肺部病变的缓解概率较低(25%)。总体毒性较轻,3级呕吐发生率为23%,3 - 4级白细胞减少发生率为15%。报告了2例心脏毒性病例。接受两种不同米托蒽醌剂量(12或14mg/m²)的患者在缓解率或毒性方面未发现差异。所采用的方案似乎耐受性良好,对晚期乳腺癌治疗有效。(摘要截断于250字)