Cocconi G, Bella M, Zironi S, Algeri R, Di Costanzo F, De Lisi V, Luppi G, Mazzocchi B, Rodinò C, Soldani M
Medical Oncology Institution of Parma, Italy.
J Clin Oncol. 1994 Dec;12(12):2687-93. doi: 10.1200/JCO.1994.12.12.2687.
The combination of cisplatin, epirubicin, and leucovorin preceding fluorouracil (PELF) includes three novel agents compared with the standard combination of fluorouracil, doxorubicin, and mitomycin (FAM) in the treatment of advanced gastric carcinoma. We report the results of a prospective randomized comparison of the two combinations in previously untreated patients.
One hundred thirty assessable patients were entered onto the trial; 52 received FAM and 85 PELF. A 1:2 unbalanced randomization in favor of the experimental treatment was chosen. Approximately 90% of patients had measurable tumor masses.
The overall response rates (complete responses [CRs] and partial responses [PRs]) were 15% and 43% for the FAM and the PELF regimens, respectively, with a statistically significant advantage for the experimental treatment (P = .001). Time to progression (median, 2.6 and 4.7 months), duration of response (median, 10.7 and 10.2 months), and survival durations (median, 5.6 and 8.1 months) were not significantly different between the FAM and PELF regimens, respectively. The PELF combination was more toxic compared with FAM, but generally tolerable.
This study showed that the PELF combination is about three times more effective than the FAM combination in inducing objective responses. Due to tolerability, it is not recommended for routine clinical use. However, it should be considered, among other second-generation chemotherapy combinations, in future randomized studies aimed to improve the therapeutic outcome in gastric carcinoma.
与氟尿嘧啶、多柔比星和丝裂霉素的标准联合方案(FAM)相比,顺铂、表柔比星和亚叶酸钙在氟尿嘧啶之前应用的联合方案(PELF)在治疗晚期胃癌时包含三种新型药物。我们报告了这两种联合方案在既往未接受过治疗的患者中进行的前瞻性随机对照研究结果。
130例可评估患者进入该试验;52例接受FAM方案,85例接受PELF方案。采用了倾向于试验性治疗的1:2非平衡随机分组。约90%的患者有可测量的肿瘤肿块。
FAM方案和PELF方案的总缓解率(完全缓解[CR]和部分缓解[PR])分别为15%和43%,试验性治疗具有统计学显著优势(P = .001)。FAM方案和PELF方案的疾病进展时间(中位数分别为2.6个月和4.7个月)、缓解持续时间(中位数分别为10.7个月和10.2个月)以及生存时间(中位数分别为5.6个月和8.1个月)之间无显著差异。与FAM方案相比,PELF联合方案毒性更大,但总体可耐受。
本研究表明,PELF联合方案在诱导客观缓解方面的疗效约为FAM联合方案的三倍。鉴于其耐受性,不推荐用于常规临床应用。然而,在未来旨在改善胃癌治疗效果的随机研究中,除其他第二代化疗联合方案外,应考虑该方案。