培美曲赛联合IL-2治疗恶性胸腔积液的临床研究  被引量:5

Treatment of malignant pleural effusion by Pemetrexed combined with Interleukin-2

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作  者:陈良[1] 张道良[1] 张颖[1] 顾月清[1] 

机构地区:[1]上海交通大学胸科医院急诊科,上海200030

出  处:《中华肿瘤防治杂志》2012年第19期1503-1506,共4页Chinese Journal of Cancer Prevention and Treatment

摘  要:目的:观察引流胸腔积液后,培美曲赛联合白介素-2(IL-2)腔内注射治疗恶性胸腔积液的疗效及安全性。方法:将35例恶性胸腔积液患者分为联合治疗组(n=20,包括肺腺癌13例、恶性胸膜间皮瘤4例和乳腺癌3例)和单药治疗组(n=15,包括肺腺癌12例、恶性胸膜间皮瘤1例和乳腺癌2例)。先行胸腔置管引流,待积液引净、肺复张后,联合治疗组经导管注入培美曲赛200mg和IL-2 3×106 U,单药治疗组仅注入IL-2 3×106 U,去枕平卧后每10~15min转动体位,共翻身3圈,保留48h后抽净积液并拔管。结果:联合治疗组CR 14例(70.0%),PR 4例(20.0%),NC 2例(10.0%),总有效率90.0%。单药治疗组CR 3例(20.0%),PR 4例(26.7%),NC 8例(53.3%),总有效率46.7%。随访3和6个月后,联合治疗组SD为88.9%和77.8%,单药治疗组为57.1%和28.6%。两组均无骨髓抑制、过敏反应和>2cm的胸膜增厚发生。联合治疗组有3例(15.0%)出现轻度恶心和胃纳减低,甲氧氯普胺和维生素B6治疗后好转,单药治疗组无胃肠反应发生;联合治疗组有6例(30.0%)出现轻度胸痛,7例(35.0%)有低热,单药治疗组有4例(26.7%)轻度胸痛,5例(33.3%)低热,应用新癀片或吲哚美辛栓剂治疗后均得到控制。结论:培美曲赛联合IL-2治疗恶性胸腔积液安全、有效,值得临床推广应用。OBJECTIVE: To observe the clinical efficacy and safety of intrapleural injection of Pemetrexed combined with Interleukin-2 for malignant pleural effusion. METHOSDS: Thirty-five patients with malignant pleural effusion were divided into combination group(20 cases,including 13 with lung adenocarcinoma, 4 with malignant pleural mesothelioma, 3 with breast cancer) and single-drug group(15 cases,including 12 with lung adenocarcinoma, 1 with malignant pleural mes- othelioma,2 with breast cancer). All of the patients received closed drainage after percutancous thoracocentesis. And 200 mg of Pemetrexed and 3 million units of Interleukin-2 were injected through catheter into thoracic cavity in combina- tion group,and 3 million units of interleukin-2 only were done in single-drug group afer the effusion had been drained cleanly and the lung was reexpanded completely. The patients must rotate positions every 10-15 min in bed without pil- lows for total of 3 cycles. The residual effusion would be drawn out after the drugs had been reserved for 48 h,and the catheter would been pulled out finally. RESULTS.. In combination group, 14(70.0%) cases were determined for CR(com- plete response) ,4(20.0%) cases for PR(partial response) ,2(10.0%) eases for NC(no change) ,and the ORR(overall response rate) was 90.0%. In single-drug group, 3 (20.0K) cases were determined for CR, 4 (26. 7%) eases for PR, 8 (53.3 % ) cases for NC, and the ORR was 46.7 %. After 3-month and 6-month follow-up, the rate of SD(stable disease) in combination group were 88.9% and 77.8% respectively,and that in single-drug group were 57.1% and 28.6%. There were no bone marrow suppression, anaphylaxis and pleural thickening large than 2 cm occurred in two groups. Only 3 (15.0 %) cases in combination group and none in Single-drug group occurred mild nausea and slightly reduction of appetite which acquired improvement after the treatment by Metoclopramide and Vitamin B6. There were 6(30.0%) eases in corn

关 键 词:胸腔积液 恶性 药物疗法 白细胞介素2 治疗应用 治疗效果 

分 类 号:R730.5[医药卫生—肿瘤]

 

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