解放军医学院学报
解放軍醫學院學報
해방군의학원학보
Academic Journal of Chinese Pla Medical School
2013年
7期
671-672,692
,共3页
张欣%胡毅%汪进良%张素洁%陶海涛%孙京%吴柏寿
張訢%鬍毅%汪進良%張素潔%陶海濤%孫京%吳柏壽
장흔%호의%왕진량%장소길%도해도%손경%오백수
重组人p53腺病毒%腔内灌注%胸腔积液,恶性%腹腔积液,恶性
重組人p53腺病毒%腔內灌註%胸腔積液,噁性%腹腔積液,噁性
중조인p53선병독%강내관주%흉강적액,악성%복강적액,악성
recombinant adenovirus-p53%infusion intra-cavity%pleural effusion,malignant%peritoneal effusion,malignant
目的探讨重组人p53腺病毒在恶性胸腹腔积液治疗中的安全性和疗效。方法回顾性分析2007年10月-2012年4月我院34例接受重组人p53腺病毒胸、腹腔灌注的肿瘤患者病例资料。胸腔积液采用2×1012 VP稀释入100 ml 0.9%氯化钠注射液行胸腔灌注;腹腔积液采用4×1012 VP稀释入500 ml 0.9%氯化钠注射液行腹腔灌注。1次/5~7 d,连续使用3周。按照WHO疗效评价标准及实体瘤评价标准(RECIST)进行疗效评价,以常见不良反应评价标准(NCI CTCAE)4.0进行不良反应评价。结果34例中,5例完全缓解(4例胸腔积液和1例腹腔积液),11例部分缓解(8例胸腔积液和3例腹腔积液),客观有效率为47.06%。总体不良反应轻微,1~2级自限性发热19例,1级消化道出血1例。结论人重组p53腺病毒腔内灌注治疗胸腹腔恶性积液疗效较好,可作为晚期肿瘤患者的辅助治疗。
目的探討重組人p53腺病毒在噁性胸腹腔積液治療中的安全性和療效。方法迴顧性分析2007年10月-2012年4月我院34例接受重組人p53腺病毒胸、腹腔灌註的腫瘤患者病例資料。胸腔積液採用2×1012 VP稀釋入100 ml 0.9%氯化鈉註射液行胸腔灌註;腹腔積液採用4×1012 VP稀釋入500 ml 0.9%氯化鈉註射液行腹腔灌註。1次/5~7 d,連續使用3週。按照WHO療效評價標準及實體瘤評價標準(RECIST)進行療效評價,以常見不良反應評價標準(NCI CTCAE)4.0進行不良反應評價。結果34例中,5例完全緩解(4例胸腔積液和1例腹腔積液),11例部分緩解(8例胸腔積液和3例腹腔積液),客觀有效率為47.06%。總體不良反應輕微,1~2級自限性髮熱19例,1級消化道齣血1例。結論人重組p53腺病毒腔內灌註治療胸腹腔噁性積液療效較好,可作為晚期腫瘤患者的輔助治療。
목적탐토중조인p53선병독재악성흉복강적액치료중적안전성화료효。방법회고성분석2007년10월-2012년4월아원34례접수중조인p53선병독흉、복강관주적종류환자병례자료。흉강적액채용2×1012 VP희석입100 ml 0.9%록화납주사액행흉강관주;복강적액채용4×1012 VP희석입500 ml 0.9%록화납주사액행복강관주。1차/5~7 d,련속사용3주。안조WHO료효평개표준급실체류평개표준(RECIST)진행료효평개,이상견불량반응평개표준(NCI CTCAE)4.0진행불량반응평개。결과34례중,5례완전완해(4례흉강적액화1례복강적액),11례부분완해(8례흉강적액화3례복강적액),객관유효솔위47.06%。총체불량반응경미,1~2급자한성발열19례,1급소화도출혈1례。결론인중조p53선병독강내관주치료흉복강악성적액료효교호,가작위만기종류환자적보조치료。
Objective To study the safety and effect of rAd-p53 in patients with malignant pleuroperitoneal effusion. Methods Clinical data about 34 tumor patients treated with intra-cavity rAd-p53 infusion in our hospital from October 2007 to April 2012 were retrospectively analyzed. Pleural effusion was treated by infusion of 2×1012 VP diluted into 100 ml 0.9%NaCl while peritoneal effusion was treated by infusion of 4×1012 VP diluted into 500 ml 0.9% NaCl, once 5-7 days for 3 weeks. Their therapeutic effects were assessed according to the WHO criteria and RECIST, respectively. Adverse reactions were assessed according to the NCI CTCAE 4.0. Results Of the 34 patients, 5 (4 with pleural effusion and 1 with peritoneal effusion) were completely improved, and 11 (8 pleural effusion and 3 peritoneal effusion) were partially improved with an overall effective rate of 47.06%. The adverse reactions were mild with grade 1-2 self-limited fever occurred in 19 patients and grade 1 gastric bleeding occurred in 1 patient. Conclusion The effect of rAd-p53 infusion is rather good on pleuroperitoneal effusion and can thus be used as an accessory therapy for advanced tumor patients.