Ramanathan Ramesh K, Bjarnason Georg A, Bernard Stephen Alan, Desimone Philip, Braich Theodore, Evars Joseph P, Hrushesky William J, Jolivet Jacques
University of Pittsburgh Cancer Institute, PA, USA.
Clin Colorectal Cancer. 2008 Mar;7(2):134-9. doi: 10.3816/ccc.2008.n.018.
Oxaliplatin combined with 5-fluorouracil (5-FU), with or without leucovorin (LV), is effective and well tolerated for first-line therapy of advanced colorectal cancer (CRC). However, there is no consensus as to which oxaliplatin/5-FU-containing regimen is superior in the first-line setting. This randomized, multicenter phase II trial was designed to evaluate and compare the efficacy of 4 different oxaliplatin/5-FU regimens.
Patients with previously untreated metastatic CRC (mCRC; n = 129) were randomized to 1 of 4 treatment regimens: (1) continuous 5-FU infusion plus oxaliplatin (n = 23); (2) weekly 5-FU bolus with LV plus oxaliplatin (n = 40); (3) oxaliplatin with 2-day infusion 5-FU/LV (FOLFOX4, n = 41); and (4) chronomodulated 5-FU plus oxaliplatin (n = 25).
Overall response rates, after expert assessment, ranged from 24% to 34%, and median progression-free survival (PFS) ranged from 6 months to 8 months. Although no significant differences in efficacy were detected in pairwise comparisons of the 4 different regimens, patients randomized to FOLFOX4 had the highest response rate and longest PFS. The FOLFOX4 regimen was also associated with the lowest incidence of severe (grade 3/4) toxicity, with the exception of cumulative peripheral neurotoxicity.
This randomized phase II trial provides evidence that oxaliplatin/5-FU regimens are effective and well tolerated for first-line therapy of previously untreated mCRC. The FOLFOX regimens are now an established standard for CRC.
奥沙利铂联合5-氟尿嘧啶(5-FU),无论是否使用亚叶酸钙(LV),对于晚期结直肠癌(CRC)的一线治疗都是有效且耐受性良好的。然而,对于一线治疗中哪种含奥沙利铂/5-FU的方案更优尚无共识。这项随机、多中心II期试验旨在评估和比较4种不同奥沙利铂/5-FU方案的疗效。
既往未接受过治疗的转移性结直肠癌(mCRC;n = 129)患者被随机分为4种治疗方案中的1种:(1)持续输注5-FU联合奥沙利铂(n = 23);(2)每周5-FU推注联合LV及奥沙利铂(n = 40);(3)奥沙利铂与5-FU/LV进行2天输注(FOLFOX4,n = 41);(4)时辰调制的5-FU联合奥沙利铂(n = 25)。
经专家评估,总体缓解率在24%至34%之间,无进展生存期(PFS)中位数在6个月至8个月之间。虽然在4种不同方案的两两比较中未检测到疗效的显著差异,但随机接受FOLFOX4方案的患者缓解率最高且PFS最长。FOLFOX4方案除累积性外周神经毒性外,严重(3/4级)毒性的发生率也最低。
这项随机II期试验提供了证据,表明奥沙利铂/5-FU方案对于既往未接受过治疗的mCRC的一线治疗是有效且耐受性良好的。FOLFOX方案现已成为CRC的既定标准。