Odabas H, Ozdemir N, Abali H, Oksuzoglu B, Isik M, Uncu D, Cihan S, Seker M, Zengin N
Ankara Numune Training and Research Hospital, Ankara, Turkey.
J BUON. 2011 Apr-Jun;16(2):247-52.
The aim of this study was to compare the efficacy and toxicity of modified (m) FOLFOX4 (folinic acid, 5-fluorouracil [5-FU], and oxaliplatin) vs. FOLFIRI-B (folinic acid, 5-FU, irinotecan, and bevacizumab) as first-line treatment of metastatic colorectal carcinoma (MCRC).
The medical records of 89 MCRC patients treated with either mFOLFOX4 (group 1) or FOLFIRI-B (group 2) as first-line chemotherapy were evaluated retrospectively.
Complete (CR) plus partial response (PR) were seen in 18 (36.7%) vs. 13 (32.5%) patients in the mFOLFOX4 vs. FOLFIRI-B, respectively (p=0.67). Median progression-free survival (PFS) was 9 months (95% CI 7.2- 9.5) vs. 10 months (95% CI 7.6-12.3) in group 1 vs. group 2, respectively (p=0.30). Median overall survival (OS) was 22 months (95% CI 17.6-26.3) and 19 months (95% CI 13-24.9) in group 1 and 2, respectively (p=0.32). There was no statistically significant difference in grade 3-4 hematological toxicity between the groups, but grade 3-4 grade weakness, diarrhea, nausea and vomiting was observed more frequently in the FOLFIRI-B patients (p=0.03, p=0.01, p=0.05, respectively).
Our data suggest that mFOLFOX4 and FOLFIRI-B are equally effective as first-line chemotherapy in MCRC patients. This may partially be explained by the fact that almost 50% of those receiving FOLFOX in the first-line received FOLFIRI-B in the second-gline, an observation suggesting that bevacizumab in the second line may be as effective as in the first line.
本研究旨在比较改良(m)FOLFOX4方案(亚叶酸、5-氟尿嘧啶[5-FU]和奥沙利铂)与FOLFIRI-B方案(亚叶酸、5-FU、伊立替康和贝伐单抗)作为转移性结直肠癌(MCRC)一线治疗的疗效和毒性。
回顾性评估89例接受mFOLFOX4方案(第1组)或FOLFIRI-B方案(第2组)作为一线化疗的MCRC患者的病历。
mFOLFOX4组和FOLFIRI-B组分别有18例(36.7%)和13例(32.5%)患者出现完全缓解(CR)加部分缓解(PR)(p = 0.67)。第1组和第2组的中位无进展生存期(PFS)分别为9个月(95%CI 7.2 - 9.5)和10个月(95%CI 7.6 - 12.3)(p = 0.30)。第1组和第2组的中位总生存期(OS)分别为22个月(95%CI 17.6 - 26.3)和19个月(95%CI 13 - 24.9)(p = 0.32)。两组之间3 - 4级血液学毒性无统计学显著差异,但FOLFIRI-B组患者3 - 4级虚弱、腹泻、恶心和呕吐的发生率更高(分别为p = 0.03、p = 0.01、p = 0.05)。
我们的数据表明,mFOLFOX4和FOLFIRI-B作为MCRC患者的一线化疗同样有效。这可能部分归因于以下事实:近50%一线接受FOLFOX方案治疗的患者二线接受了FOLFIRI-B方案治疗,这一观察结果表明二线使用贝伐单抗可能与一线同样有效。