中外健康文摘
中外健康文摘
중외건강문적
WORLD HEALTH DIGEST
2014年
15期
43-44
,共2页
肖锋%肖茂良%唐友斌%颜学军
肖鋒%肖茂良%唐友斌%顏學軍
초봉%초무량%당우빈%안학군
重组人血管内皮抑素%顺铂%恶性腹腔积液
重組人血管內皮抑素%順鉑%噁性腹腔積液
중조인혈관내피억소%순박%악성복강적액
rh-endostatin%cis-platinum maliganant%peritoneal effusion
目的:评价重组人血管内皮抑素(恩度)联合顺铂腹腔注射治疗恶性腹腔积液的疗效与安全性。方法:76例经病理确诊的晚期恶性肿瘤合并腹腔积液患者,行腹腔穿刺引流后,随机分为两组。试验组:腹腔注射重组人血管内皮抑素60毫克,顺铂40毫克 D1,4,7,三次为1周期;对照组:单用顺铂40毫克腹腔注射 D1,4,7,其余同试验组。按照WHO胸腹水疗效评价标准和NCI-CTC AE 4.0标准分别评估疗效及毒副反应。结果:试验组和对照组的客观有效率分别是65.7%和41.4%,,差异有统计学意义( p<0.05);疾病控制率分别是94.2%和58.5%,差异有统计学意义( p<0.05)。试验组与对照组相比生活质量有改善的趋势。不良反应主要是白细胞减少,血小板下降,心脏毒性,恶心呕吐,两组无统计学差异( p>0.05)。结论:重组人血管内皮抑素(恩度)联合顺铂腹腔注射治疗恶性腹腔积液疗效好,毒副反应小,值得临床推广。
目的:評價重組人血管內皮抑素(恩度)聯閤順鉑腹腔註射治療噁性腹腔積液的療效與安全性。方法:76例經病理確診的晚期噁性腫瘤閤併腹腔積液患者,行腹腔穿刺引流後,隨機分為兩組。試驗組:腹腔註射重組人血管內皮抑素60毫剋,順鉑40毫剋 D1,4,7,三次為1週期;對照組:單用順鉑40毫剋腹腔註射 D1,4,7,其餘同試驗組。按照WHO胸腹水療效評價標準和NCI-CTC AE 4.0標準分彆評估療效及毒副反應。結果:試驗組和對照組的客觀有效率分彆是65.7%和41.4%,,差異有統計學意義( p<0.05);疾病控製率分彆是94.2%和58.5%,差異有統計學意義( p<0.05)。試驗組與對照組相比生活質量有改善的趨勢。不良反應主要是白細胞減少,血小闆下降,心髒毒性,噁心嘔吐,兩組無統計學差異( p>0.05)。結論:重組人血管內皮抑素(恩度)聯閤順鉑腹腔註射治療噁性腹腔積液療效好,毒副反應小,值得臨床推廣。
목적:평개중조인혈관내피억소(은도)연합순박복강주사치료악성복강적액적료효여안전성。방법:76례경병리학진적만기악성종류합병복강적액환자,행복강천자인류후,수궤분위량조。시험조:복강주사중조인혈관내피억소60호극,순박40호극 D1,4,7,삼차위1주기;대조조:단용순박40호극복강주사 D1,4,7,기여동시험조。안조WHO흉복수료효평개표준화NCI-CTC AE 4.0표준분별평고료효급독부반응。결과:시험조화대조조적객관유효솔분별시65.7%화41.4%,,차이유통계학의의( p<0.05);질병공제솔분별시94.2%화58.5%,차이유통계학의의( p<0.05)。시험조여대조조상비생활질량유개선적추세。불량반응주요시백세포감소,혈소판하강,심장독성,악심구토,량조무통계학차이( p>0.05)。결론:중조인혈관내피억소(은도)연합순박복강주사치료악성복강적액료효호,독부반응소,치득림상추엄。
OBJECTIVE:To observe the clinical efficacy of recombinant human endostain combined with cis-platinum in the treatment of patients with maliganant peritoneal effusion.METHODS:76 patinets with maliganant peritoneal effusion,who were diagnosed by pathology,were randomly divided into two groups after abdominocentesis.Trial group were treated with endostain 60mg and cis-platinum 40mg each time on d1,d4,d7;control group were treated with monotherapy of cis-platinum 40mg with the same procedure..The efficacy was evaluated according to WHO criteria and safety according to NCI CTC AE 4.0 version criteria..RESULTS The objective response rate was 65.7% for trial group and 41.4% for control group,the difference was stastical significance(p<0.05).The disease control rate was 94.2% for trial group and 58.5% for control group, the difference was stastical significance(p<0.05). Trial group showed a tendency to improve the quality of life compared to control group..Toxicities mainly included neutropenia、 thrombocytopenia 、Cardiac toxicity and nausea/vomiting,but the difference was not significant (p>0.05). CONCLUSION :Recombinant hunan endostatin combined with cis-platinum is an effective and safety therapy for malignant peritoneal effusion,with fewer toxic reaction,which is wothy of spreading in the clinic.