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贝伐珠单抗联合雷替曲塞或卡培他滨治疗晚期结直肠癌疗效比较

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目的 比较贝伐珠单抗联合雷替曲塞或卡培他滨治疗晚期结直肠癌的临床疗效。方法 选取沧州市中心医院 2021 年 2 月至2022 年 8 月收治的晚期结直肠癌患者 110 例,按随机数字表法分为贝伐珠单抗+卡培他滨组(简称贝+卡组)和贝伐珠单抗+雷替曲塞组(简称贝+雷组),各 55 例。两组患者均予贝伐珠单抗注射液静脉滴注,贝+卡组患者加用卡培他滨片口服,贝+雷组患者加用注射用雷替曲塞静脉滴注(另外建立一组静脉滴注通路)。两组均以 3 周为 1 个疗程,共治疗 6 个疗程,并随访 6 个月。结果 治疗后,贝+卡组患者总生存期(OS)和无进展生存期(PFS)分别为(12。26±2。94)个月和(6。17±1。74)个月,与贝+雷组的(12。57±2。15)个月和(6。62±1。80)个月相当(P>0。05)。贝+雷组的客观缓解率和疾病控制率分别为 34。55%和 65。45%,与贝+卡组的 32。73%和61。82%相当(P>0。05)。治疗后,两组患者的血管内皮生长因子、碱性成纤维细胞生长因子、血小板源性生长因子及T淋巴细胞亚群(CD3+,CD4+,CD8+)水平均显著改善(P<0。05),且贝+雷组改善幅度均显著大于贝+卡组(P<0。05)。贝+雷组Ⅰ-Ⅱ级、Ⅲ-Ⅳ级手足综合征及腹泻,Ⅰ-Ⅱ级恶心呕吐及周围神经毒性的发生率均显著低于贝+卡组(P<0。05)。结论 贝伐珠单抗联合雷替曲塞或卡培他滨治疗晚期结直肠癌的疗效相近,但前一组合在改善血清血管生长因子及T淋巴细胞亚群水平方面更具优势。
Efficacy Comparison of Bevacizumab Combined with Raltitrexed or Capecitabine in the Treatment of Advanced Colorectal Cancer
Objective To compare the clinical efficacy of bevacizumab combined with raltitrexed or capecitabine in the treatment of advanced colorectal cancer.Methods A total of 110 patients with advanced colorectal cancer admitted to the Cangzhou Central Hospital from February 2021 to August 2022 were selected and divided into the bevacizumab + capecitabine group and the bevacizumab + raltitrexed group by the random number table method,with 55 cases in each group.The patients in the two groups were given intravenous drip of Bevacizumab Injection,on this basis,the patients in the bevacizumab + capecitabine group were given Capecitabine Tablets orally,while the patients in the bevacizumab + raltitrexed group were given intravenous drip of Raltitrexed for Injection(another intravenous-drip access was established).Both groups were treated for six courses with three weeks as a course and followed up for six months.Results After treatment,the overall survival(OS)and progression-free survival(PFS)in the bevacizumab + capecitabine group were(12.26±2.94)months and(6.17±1.74)months respectively,which were similar to(12.57±2.15)months and(6.62±1.80)months in the bevacizumab + raltitrexed group(P>0.05).The objective response rate(ORR)and disease control rate(DCR)in the bevacizumab + raltitrexed group were 34.55%and 65.45%respectively,which were similar to 32.73%and 61.82%in the bevacizumab + capecitabine group(P>0.05).After treatment,the vascular endothelial growth factor(VEGF),basic fibroblast growth factor(bFGF),platelet-derived growth factor(PDGF)and T lymphocyte subsets(CD3+,CD4+,CD8+)levels in the two groups improved significantly(P<0.05),and those in the bevacizumab + raltitrexed group were significantly better than those in the bevacizumab + capecitabine group(P<0.05).The incidence of hand-foot syndrome and diarrhea with grade Ⅰ-Ⅱ and grade Ⅲ-Ⅳ,nausea,vomiting and peripheral neurotoxicity with grade Ⅰ-Ⅱ in the bevacizumab + raltitrexed group was significantly lower than that in the bevacizumab + capecitabine group(P<0.05).Conclusion Bevacizumab combined with raltitrexed or capecitabine in the treatment of advanced colorectal cancer had similar efficacy,while the former drug combination is more effective in improving the levels of serum angiogenic factors and T lymphocyte subsets.

bevacizumabraltitrexedcapecitabineadvanced colorectal cancerangiogenic factorT lymphocyte subsetsurvival status

贾楠、宋哲、陈宝胜、程进生、周文勇、刘雅刚

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河北省沧州市中心医院,河北 沧州 061001

河北省沧州市献县人民医院,河北 沧州 062250

贝伐珠单抗 雷替曲塞 卡培他滨 晚期结直肠癌 血管生长因子 T淋巴细胞亚群 生存情况

河北省医学科学研究课题计划项目

20191268

2024

中国药业
重庆市食品药品监督管理局

中国药业

CSTPCD
影响因子:1.369
ISSN:1006-4931
年,卷(期):2024.33(4)
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