Medical Oncology Department, University Hospital 12 de Octubre, Madrid, Spain.
Clin Transl Oncol. 2012 Aug;14(8):606-12. doi: 10.1007/s12094-012-0843-x. Epub 2012 Jul 19.
The aim of this study was to compare TOMOX versus FOLFOX4 as first-line treatment of advanced colorectal cancer (CRC).
191 chemotherapy-naïve patients were randomized to receive TOMOX or FOLFOX4. Patients were evaluated every 3 months and chemotherapy was continued until disease progression or unacceptable toxicity. Overall response rate was the primary endpoint.
183 patients were included in the intent-to-treat analysis (92 TOMOX and 91 FOLFOX4). Overall response rate was 45.6 and 36.3 % (p = 0.003) for TOMOX and FOLFOX4, respectively. No statistically significant differences were observed in overall survival (15.6 and 17.2 months; p = 0.475); progression-free survival (7.7 and 8.7 months; p = 0.292), and response duration (6.4 and 7.6 months; p = 0.372) for TOMOX and FOLFOX4, respectively. Grades 3 and 4 neutropenia (p < 0.0001) and leukopenia (p = 0.028) were more common with the FOLFOX4 regimen, while hepatic disorders and asthenia were higher in TOMOX group (p = ns). There were two treatment-related deaths in the FOLFOX4 arm and one in the TOMOX arm. Quality of life analysis based on the SF-36 revealed differences between the two regimens for physical and mental composite scores after 6 weeks, and for body pain and emotional role functioning after 6 and 12 weeks; all of these favored the FOLFOX4 arm (p ≤ 0.05).
TOMOX and FOLFOX4 seem to have similar efficacy and are well tolerated in the first-line treatment for advanced CRC with different profiles of toxicity. The convenient TOMOX regimen may offer an alternative to fluoropyrimidine-based regimens.
本研究旨在比较 TOMOX 与 FOLFOX4 作为晚期结直肠癌(CRC)一线治疗方案的疗效。
191 例初治化疗患者被随机分为接受 TOMOX 或 FOLFOX4 治疗。每 3 个月评估一次患者,直到疾病进展或出现不可接受的毒性。总缓解率是主要终点。
183 例患者被纳入意向治疗分析(TOMOX 组 92 例,FOLFOX4 组 91 例)。TOMOX 和 FOLFOX4 的总缓解率分别为 45.6%和 36.3%(p=0.003)。TOMOX 和 FOLFOX4 的总生存期(15.6 个月和 17.2 个月;p=0.475)、无进展生存期(7.7 个月和 8.7 个月;p=0.292)和缓解持续时间(6.4 个月和 7.6 个月;p=0.372)均无统计学差异。FOLFOX4 方案更常见 3 级和 4 级中性粒细胞减少症(p<0.0001)和白细胞减少症(p=0.028),而 TOMOX 组肝障碍和乏力发生率更高(p=ns)。FOLFOX4 组有 2 例与治疗相关的死亡,TOMOX 组有 1 例。基于 SF-36 的生活质量分析显示,在第 6 周时,两种方案在生理和心理综合评分方面存在差异,在第 6 周和第 12 周时,在身体疼痛和情感角色功能方面存在差异,所有这些都有利于 FOLFOX4 组(p≤0.05)。
TOMOX 和 FOLFOX4 似乎在晚期 CRC 的一线治疗中具有相似的疗效和良好的耐受性,且毒性谱不同。方便的 TOMOX 方案可能是氟嘧啶类方案的替代方案。