P A Kosmidis, G Fountzilas, A Athanassiou, A Karabelis, N Mylonakis, N Tsavaris, N Karvounis, C Bacojiannis
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引用次数: 0
摘要
本研究的目的是评估晚期乳腺癌VAP联合化疗:prednimumstine 80mg /m2, p.o d 1-5,阿霉素40mg /m2和长春新碱1.4 mg/m2,周期为3周,第1天。21名女性参加了这项研究,其中19名是可评估的。根据Karnofsky,平均年龄为54.5岁(25-69岁),平均表现状态为60。10例激素受体未知,6例阳性,3例阴性。主要病变部位为软组织11例,骨骼1例,肝脏3例,肺部4例。14例患者接受环磷酰胺、甲氨蝶呤和5-氟尿嘧啶(CMF)治疗,2例接受他莫昔芬治疗,3例未接受治疗。10例患者(52.6%)部分缓解,平均生存期7.8+个月;5例患者(26.3%)病情稳定,平均生存期6.6+个月;4例患者(21.1%)病情进展,平均生存期3个月。毒性方面,所有患者均出现脱发,大部分患者出现恶心I级,5例患者出现轻度白细胞减少。我们认为VAP是一种有效且耐受性良好的晚期乳腺癌化疗组合,值得进一步的临床试验。
Combination chemotherapy with prednimustine, adriamycin, vincristine (VAP) in advanced breast cancer. A phase II study.
The purpose of this study was to evaluate VAP combination chemotherapy in advanced breast cancer: prednimustine 80 mg/m2 p.o. days 1-5, adriamycin 40 mg/m2 and vincristine 1.4 mg/m2 1st day in cycles of 3 weeks. Twenty-one women entered the study and 19 were evaluable. The mean age was 54.5 years (25-69) with an average performance status of 60 according to Karnofsky. Hormonal receptors were unknown in 10, positive in 6 and negative in 3. The dominant site of disease was soft tissues in 11, bones in 1, liver in 3 and lung in 4. Fourteen patients had as prior treatment cyclophosphamide, methotrexate and 5-fluorouracil (CMF), two had tamoxifen and three none. Ten patients (52.6%) had a partial response with a mean survival of 7.8+ months, 5 patients (26.3%) had stable disease with a mean survival 6.6+ months and 4 patients (21.1%) had progressive disease with a mean survival of 3 months. Regarding toxicity all patients had alopecia, most of the patients had nausea grade I, whereas 5 patients developed mild leukopenia. We conclude that VAP is an effective, well tolerated chemotherapy combination in patients with advanced breast cancer which deserves further clinical trials.