Lawton F, Meanwell C, Mould J, Blackledge G
Academic Department of Obstetrics and Gynaecology, University of Birmingham, United Kingdom.
Gynecol Oncol. 1990 Jan;36(1):19-22. doi: 10.1016/0090-8258(90)90102-q.
Twenty-six patients, 22 previously untreated, with FIGO stage III/IV epithelial ovarian cancer were treated with a five-drug combination regimen consisting of cycles of cisplatinum (60 or 75 mg/m2 IV) and cyclophosphamide (600 or 750 mg/m2 IV) [CP], alternating every 3 weeks with cycles of adriamycin [50 mg/m2 IV], bleomycin [15 mg IV], and chlorambucil [6 mg/m2 orally for 7 days] [ABC]. A total of six cycles, CP x 3 and ABC x 3, were planned. There was a 67% response rate with 7 complete and 5 partial remissions in 18 patients with evaluable disease. Median progression-free interval was 13 months and median survival 24 months for the whole group. The regimen was well tolerated with WHO toxicity greater than 2 in only 5 patients and treatment delay occurring in only 18 of 128 cycles [14%] in 11 patients. The toxicity of combination cytotoxic regimens can be reduced by alternating cycles of therapy. A randomized trial comparing such a regimen with nonalternating therapy would be necessary to determine whether the response rate and duration of response are compromised when the cumulative dose of cisplatinum is reduced.
26例患者,其中22例为初治患者,患有国际妇产科联盟(FIGO)III/IV期上皮性卵巢癌,接受了一种五药联合方案治疗,该方案由顺铂(60或75mg/m²静脉注射)和环磷酰胺(600或750mg/m²静脉注射)[CP]组成周期,每3周与阿霉素[50mg/m²静脉注射]、博来霉素[15mg静脉注射]和苯丁酸氮芥[6mg/m²口服7天][ABC]组成的周期交替进行。共计划进行6个周期,即CP×3和ABC×3。在18例可评估疾病的患者中,总缓解率为67%,7例完全缓解,5例部分缓解。全组的中位无进展生存期为13个月,中位生存期为24个月。该方案耐受性良好,只有5例患者的世界卫生组织(WHO)毒性大于2级,11例患者在128个周期中仅18个周期(14%)出现治疗延迟。联合细胞毒性方案的毒性可通过交替治疗周期来降低。有必要进行一项随机试验,比较这种方案与非交替治疗方案,以确定当顺铂累积剂量降低时,缓解率和缓解持续时间是否会受到影响。