XELOX方案联合放疗的新辅助治疗在局部进展期中低位直肠癌的不良反应及临床疗效分析

    Toxicity and Effect of Preoperative Chemoradiotherapy with XELOX on The Treatment of Advanced Mid-Low Rectal Cancer

    • 摘要: 目的 探讨XELOX方案联合放疗的新辅助治疗在局部进展期中低位直肠癌的不良反应及临床疗效。 方法 回顾性分析2014年6月至2016年12月广东省人民医院普通外科胃肠专业组收治的符合纳入排除标准的75例局部进展期中低位直肠癌患者的资料,患者接受XELOX 3周方案新辅助化疗3疗程,并联合新辅助放疗,评价患者的不良反应及临床疗效。 结果 3例患者未完成新辅助治疗,72例完成新辅助治疗;71例行根治性全直肠系膜切除术,1例因肿瘤广泛转移无法手术;总共发生不良反应173例次,Ⅲ度以上不良反应20例次。肿瘤标志物有下降趋势。病理完全缓解16例(22.2%),部分缓解49例(68.1%),疾病稳定6例(8.3%),疾病进展1例(1.4%);有效率达89.0%。 结论 XELOX方案联合放疗的新辅助治疗在局部进展期中低位直肠癌患者是安全有效的。

       

      Abstract: Objective To explore the toxicity and efficacy of neoadjuvant chemoradiotherapy with XELOX on the treatment for patients of advanced mid-low rectal cancer. Methods From June 2014 to December 2016, 75 patients with advanced mid-low rectal cancer were treated in the gastroenterology department of Guangdong General Hospital,whose data were retraspective analysed. The patients received neoadjuvant chemotherapy of XELOX every 3 weeks for 3 cycles combined with neoadjuvant radiotherapy. Results 2 cases drop-out and 1 case quited chemoradiotherapy because of serious adverse events. 72 patients received complete chemoradiotherapy, of which 71 received TME operation and 1 occured metastases. A total of 173 times of adverse reaction occured, of which 20 were ≥ grade 3. Tumor markers in these patients had a downward trend. After neoadjuvant therapy, patlogy complete response happened in 16 cases (22.2%), partial response in 49 cases (68.1%), stable disease in 6 cases (8.3%), progression in 1 cases (1.4%), the response rate was 89.0%. Conclusion Preoperative chemoradiotherapy with XELOX for patients with advanced mid-low rectal cancer is safe and effective.

       

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