中国药物应用与监测
中國藥物應用與鑑測
중국약물응용여감측
CHINESE JOURNAL OF DRUG APPLICATION AND MONITORING
2015年
2期
73-75,81
,共4页
李爱洁%陶海涛%汪进良%董伟伟%李瑞新%胡毅
李愛潔%陶海濤%汪進良%董偉偉%李瑞新%鬍毅
리애길%도해도%왕진량%동위위%리서신%호의
阿瑞匹坦%顺铂%恶心%呕吐%疗效
阿瑞匹坦%順鉑%噁心%嘔吐%療效
아서필탄%순박%악심%구토%료효
Aprepitant%Cisplatin%Nausea%Vomiting%Efifcacy
目的:为明确阿瑞匹坦在预防含顺铂的化疗方案所致的化疗相关性恶心呕吐的临床疗效。方法:选取我院2014年1月1日–2014年10月1日接受含顺铂(75 mg·m-2)化疗方案的患者100例,接受阿瑞匹坦、5-HT3受体拮抗剂和地塞米松的患者为阿瑞匹坦组,同期使用5-HT3受体拮抗剂和地塞米松的患者为对照组,观察两组患者急性期(第1天)、延迟期(第2~5天)完全有效率(CR)及化疗期间(5 d)无严重恶心呕吐的发生率。结果:阿瑞匹坦组与对照组治疗急性呕吐的CR分别为70%和54%(P=0.149);而治疗迟发性呕吐两组有效率分别为78%和46%(P=0.002),阿瑞匹坦组显著优于对照组。化疗期间阿瑞匹坦组与对照组患者无严重恶心呕吐的发生率分别为86%、62%(P=0.012),阿瑞匹坦组优于对照组。两组止吐药物相关不良反应无明显差异。结论:阿瑞匹坦三联方案在预防顺铂诱发恶心和呕吐的疗效及耐受性方面表现良好,为提高患者生活质量提供了较好的选择方式。
目的:為明確阿瑞匹坦在預防含順鉑的化療方案所緻的化療相關性噁心嘔吐的臨床療效。方法:選取我院2014年1月1日–2014年10月1日接受含順鉑(75 mg·m-2)化療方案的患者100例,接受阿瑞匹坦、5-HT3受體拮抗劑和地塞米鬆的患者為阿瑞匹坦組,同期使用5-HT3受體拮抗劑和地塞米鬆的患者為對照組,觀察兩組患者急性期(第1天)、延遲期(第2~5天)完全有效率(CR)及化療期間(5 d)無嚴重噁心嘔吐的髮生率。結果:阿瑞匹坦組與對照組治療急性嘔吐的CR分彆為70%和54%(P=0.149);而治療遲髮性嘔吐兩組有效率分彆為78%和46%(P=0.002),阿瑞匹坦組顯著優于對照組。化療期間阿瑞匹坦組與對照組患者無嚴重噁心嘔吐的髮生率分彆為86%、62%(P=0.012),阿瑞匹坦組優于對照組。兩組止吐藥物相關不良反應無明顯差異。結論:阿瑞匹坦三聯方案在預防順鉑誘髮噁心和嘔吐的療效及耐受性方麵錶現良好,為提高患者生活質量提供瞭較好的選擇方式。
목적:위명학아서필탄재예방함순박적화료방안소치적화료상관성악심구토적림상료효。방법:선취아원2014년1월1일–2014년10월1일접수함순박(75 mg·m-2)화료방안적환자100례,접수아서필탄、5-HT3수체길항제화지새미송적환자위아서필탄조,동기사용5-HT3수체길항제화지새미송적환자위대조조,관찰량조환자급성기(제1천)、연지기(제2~5천)완전유효솔(CR)급화료기간(5 d)무엄중악심구토적발생솔。결과:아서필탄조여대조조치료급성구토적CR분별위70%화54%(P=0.149);이치료지발성구토량조유효솔분별위78%화46%(P=0.002),아서필탄조현저우우대조조。화료기간아서필탄조여대조조환자무엄중악심구토적발생솔분별위86%、62%(P=0.012),아서필탄조우우대조조。량조지토약물상관불량반응무명현차이。결론:아서필탄삼련방안재예방순박유발악심화구토적료효급내수성방면표현량호,위제고환자생활질량제공료교호적선택방식。
Objective:To observe the efifcacy of aprepitant in the prevention of the acute and delayed nausea and vomiting induced by cisplatin. Methods: A total of 100 cancer patients who received cisplatin (75 mg·m-2) in our hospital from January 1, 2014 to October 1, 2014 were enrolled. The antiemetic regimen for aprepitant group consisted of aprepitant, 5-HT3 receptor antagonist and dexamethasone;regimen for control group was 5-HT3 receptor antagonist and dexamethasone. The primary endpoints were the percentage of patients with a complete response (CR:no nausea and no salvage treatment) during the acute phase (day 1) and the delayed phase (days 2–5). The secondary endpoint was the percentage of patients without severe nausea during the entire study period (5 days) with chemotherapy. Results: There was no statistical differences in CR rates of acute phase between two groups (CR:70%vs 54%, P=0.149). The efifcacy of aprepitant group was better than that of control group in delayed phase (CR:78%vs 46%, P=0.002). The percentages of patients with no severe nausea during the entire study period in aprepitant group and control group were 86%and 62%(P=0.012), respectively. There were not signiifcant differences between two groups in respect of adverse reactions. Conclusion: Due to the good efifcacy and safety, the triple therapy containing aprepitant can be recommended for the prevention of cisplatin-induced nausea and vomiting.