Department of Medical Oncology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China (mainland).
Department of Gastrointestinal Surgery, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China (mainland).
Med Sci Monit. 2020 Feb 16;26:e919031. doi: 10.12659/MSM.919031.
BACKGROUND The aim of this study was to perform an accurate exploration on the efficacy of oxaliplatin/5-fluorouracil/capecitabine-cetuximab combination therapy and its effects on K-Ras mutations in advanced colorectal cancer. MATERIAL AND METHODS Among 96 patients who suffered metastatic colorectal cancer without mutated K-Ras, 41 patients who were receiving treatment with oxaliplatin/5-fluorouracil/capecitabine and administered cetuximab as the initial treatment comprised the observation group; the remaining 55 patients receiving cetuximab as an alternative treatment comprised the control group. RESULTS The observation group experienced significantly higher objective response rates (ORRs), and disease control rates (DCRs), than the control group (P<0.05 for both). The median progression-free survival (PFS) rates of the observation group and the control groups were 11.2 months (95% confidence interval [CI]: 10.1-12.3 months) and 7.4 months (95% CI: 6.6-8.2 months). The median overall survival (OS) rates were 16.8 months (95% CI: 15.2-18.4 months) and 12.4 months (95% CI: 11.6-13.2 months), respectively. The observation group had significantly longer PFS and OS in comparison to the control group (P<0.05). The patients who underwent cetuximab treatment for ≥10 months had a slightly higher rate of K-Ras mutations than those treated with cetuximab for <10 months (9.1% versus 7.3%). CONCLUSIONS Oxaliplatin/5-fluorouracil/capecitabine plus cetuximab exhibited better efficacy as initial treatment than the alternative treatment; it was also highly safe. Unfortunately, some patients might develop K-Ras mutations after long duration of cetuximab treatment, suggesting that K-Ras mutations are correlated with tumor progression and depend on the duration or dose of cetuximab treatment.
本研究旨在对奥沙利铂/5-氟尿嘧啶/卡培他滨-西妥昔单抗联合治疗晚期结直肠癌的疗效及其对 K-Ras 突变的影响进行准确探讨。
在 96 例无 K-Ras 突变的转移性结直肠癌患者中,41 例接受奥沙利铂/5-氟尿嘧啶/卡培他滨联合治疗并作为初始治疗给予西妥昔单抗的患者为观察组;其余 55 例接受西妥昔单抗作为替代治疗的患者为对照组。
观察组的客观缓解率(ORR)和疾病控制率(DCR)均明显高于对照组(均 P<0.05)。观察组和对照组的中位无进展生存期(PFS)分别为 11.2 个月(95%置信区间[CI]:10.1-12.3 个月)和 7.4 个月(95% CI:6.6-8.2 个月)。中位总生存期(OS)分别为 16.8 个月(95% CI:15.2-18.4 个月)和 12.4 个月(95% CI:11.6-13.2 个月)。观察组的 PFS 和 OS 明显长于对照组(均 P<0.05)。接受西妥昔单抗治疗≥10 个月的患者发生 K-Ras 突变的比例略高于接受西妥昔单抗治疗<10 个月的患者(9.1%比 7.3%)。
奥沙利铂/5-氟尿嘧啶/卡培他滨联合西妥昔单抗作为初始治疗比替代治疗具有更好的疗效,且安全性高。遗憾的是,部分患者在接受长时间西妥昔单抗治疗后可能会发生 K-Ras 突变,提示 K-Ras 突变与肿瘤进展有关,且与西妥昔单抗的治疗时间或剂量有关。