佘明金, 马祖胜, 李桂芝, 王 勤, 沈永莉. 同步放化疗联合沙利度胺治疗中晚期食管癌的临床随机对照研究[J]. 中国肿瘤临床, 2010, 37(15): 883-886. DOI: 10.3969/j.issn.1000-8179.2010.15.011
引用本文: 佘明金, 马祖胜, 李桂芝, 王 勤, 沈永莉. 同步放化疗联合沙利度胺治疗中晚期食管癌的临床随机对照研究[J]. 中国肿瘤临床, 2010, 37(15): 883-886. DOI: 10.3969/j.issn.1000-8179.2010.15.011
SHE Mingjin, MAR Zusheng, LI Guizhi, WANG Qin, SHEN Yongli. A Clinical Study on the Combination of Concurrent Chemoradiotherapy and Thalidomide for Treatment of Advanced Esophageal Cancer[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2010, 37(15): 883-886. DOI: 10.3969/j.issn.1000-8179.2010.15.011
Citation: SHE Mingjin, MAR Zusheng, LI Guizhi, WANG Qin, SHEN Yongli. A Clinical Study on the Combination of Concurrent Chemoradiotherapy and Thalidomide for Treatment of Advanced Esophageal Cancer[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2010, 37(15): 883-886. DOI: 10.3969/j.issn.1000-8179.2010.15.011

同步放化疗联合沙利度胺治疗中晚期食管癌的临床随机对照研究

A Clinical Study on the Combination of Concurrent Chemoradiotherapy and Thalidomide for Treatment of Advanced Esophageal Cancer

  • 摘要: 目的:评价同步放化疗联合沙利度胺治疗中晚期食管癌的临床疗效和患者的耐受性。方法:65例符合入组条件的局部中晚期不能手术的食管癌患者随机分为治疗组和对照组。治疗组33例采用同步放化疗联合沙利度胺(放疗总剂量60~70Gy,化疗方案为5- 氟尿嘧啶+ 顺铂;沙利度胺第1 周100mg/d ,晚睡前顿服,每日1 次,第2 周开始增加至200mg/d ,并以200mg/d 为维持剂量,口服至放疗结束),对照组32例仅接受同步放化疗。结果:治疗组和对照组的有效率分别为87.9% 和68.7% ,两组差异无统计学意义(P>0.05);局部控制率分别为93.0% 和91.0% ,两组差异无统计学意义(P>0.05);1 年的生存率分别为74.0% 和63.0% ,两组差异无统计学意义(P>0.05)。 治疗组KPS 评分的改善率为57.6% ,对照组KPS 评分的改善率为31.3% ,两组比较差异有统计学意义(P<0.05);治疗组的恶心、呕吐发生率较对照组低,差异有统计学意义(P<0.05),但治疗组的便秘、嗜睡以及乏力的发生率较对照组高,差异有统计学意义(P<0.05)。 结论:同步放化疗联合沙利度胺治疗食管癌可改善患者的生活质量,提高对放化疗的顺应性,有提高远期生存率可能,值得进一步研究。

     

    Abstract: Objective: To evaluate the response rate and tolerance in patients with advanced esophageal cancer who were treated with concurrent chemoradiotherapy plus thalidomide. Methods:Sixty-five cases of eligible patients were ran -domly assigned to either the treatment group or the control group. Thirty-three cases were treated with concurrent chemora-diotherapy plus thalidomide (radiation dosage 60~70Gy and 5-FU plus cisplatin;oral administration of thalidomide at a dose of 100 mg/day daily for the first week, 200 mg/day daily for the second week, then continuously until the end of radia -tion therapy), while 32patients who received concurrent chemoradiotherapy were monitored as matched controls. The clini-cal effects and tolerance between the two groups were compared. Results: The response rate was 87.9% in the treatment group vs.68.7% in the control group (P>0.05);the local control rate was 93% in the treatment group vs. 91% in the control group (P>0.05); the 1 year survival rate was 74.0% in the treatment group vs. 63.0% in the control group (P>0.05);The im -provement rates of KPS score in the treatment group and control group were 57.6% and 31.3% , respectively (P<0.05). More severe nausea and vomiting were present in the control group (P <0.05), while constipation, somnolence and fatigue  were more significant in the treatment group (P<0.05). Conclusion: Concurrent chemoradiotherapy combined with Thalido-mide, being effective and well tolerated, can improve the life quality of patients with advanced esophageal cancer and may have the potential to prolong the survival rate; however, further study is needed.

     

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