Cullinan S, Moertel C G, Wieand H S, Schutt A J, Krook J E, Foley J F, Norris B D, Kardinal C G, Tschetter L K, Barlow J F
Illinois Oncology Research Association CCOP, Peoria 61603.
Cancer. 1990 May 15;65(10):2207-12. doi: 10.1002/1097-0142(19900515)65:10<2207::aid-cncr2820651007>3.0.co;2-y.
One hundred eighty-seven patients with histologically proven advanced pancreatic adenocarcinoma were randomly assigned to therapy with 5-fluorouracil (5-FU) alone, to the Mallinson regimen (combined and sequential 5-FU, cyclophosphamide, methotrexate, vincristine, and mitomycin C), or to combined 5-FU, doxorubicin, and cisplatin (FAP). Patients with both measurable and nonmeasurable disease were included and the primary study end point was survival. Among 41 patients with measurable disease, objective response rates were 7% for 5-FU alone, 21% for the Mallinson regimen, and 15% for FAP. The median interval to progression for each of the three regimens was 2.5 months. Survival curves intertwined with the median survival times for 5-FU alone and the Mallinson regimen at 4.5 months and for FAP at 3.5 months. Compared with 5-FU alone, both the Mallinson regimen and FAP produced significantly more toxicity. Neither the Mallinson regimen nor FAP can be recommended as therapy for advanced pancreatic carcinoma. Any chemotherapy for this disease should remain an experimental endeavor.
187例经组织学证实的晚期胰腺腺癌患者被随机分配接受单纯5-氟尿嘧啶(5-FU)治疗、马林森方案(联合及序贯使用5-FU、环磷酰胺、甲氨蝶呤、长春新碱和丝裂霉素C)或5-FU、阿霉素和顺铂联合方案(FAP)治疗。纳入了既有可测量病灶又有不可测量病灶的患者,主要研究终点为生存率。在41例有可测量病灶的患者中,单纯5-FU治疗的客观缓解率为7%,马林森方案为21%,FAP方案为15%。三种方案的中位进展间隔均为2.5个月。生存曲线相互交织,单纯5-FU治疗和马林森方案的中位生存时间为4.5个月,FAP方案为3.5个月。与单纯5-FU治疗相比,马林森方案和FAP方案产生的毒性均明显更大。马林森方案和FAP方案均不推荐作为晚期胰腺癌的治疗方案。针对这种疾病的任何化疗仍应是一种试验性的尝试。