Zhao Wen-ying, Chen Dong-yun, Chen Jing-hua, Ji Zhao-ning
Department of Medical Oncology, Yijishan Hospital Wannan Medical College, No. 2 Zheshan West Road, Wuhu, 241000, Anhui, China.
Cell Biochem Biophys. 2014 Sep;70(1):623-8. doi: 10.1007/s12013-014-9965-9.
This study evaluated the efficacy and safety of intracavitary administration of recombinant human endostatin (Endostar) combined with cisplatin chemotherapy in treating malignant pleural effusion and ascites. Forty-five patients with malignant pleural effusion and ascites were divided into the EP group (n = 23), who received Endostar and cisplatin intracavitarily, and P group (n = 22), who were intracavitarily treated with cisplatin only. Pleural effusion and ascites were completely drained before treatments. The treatment was administered once a week; two treatments were considered as one course. The outcome quality of life as well as toxicity were evaluated. The objective overall response and disease control rates were, respectively, 78.3 % (18/23) and 87.0 % (20/23) in EP group. In contrast, these parameters were significantly (p < 0.05) lower in P groups: 40.9 % (9/22) and 59.1 % (13/22), respectively. The improvement rate of Karnofsky Performance Status was 87.0 % (20/23) in EP group versus 59.1 % (13/22) in P group (p < 0.05). All patients tolerated the combined treatment well, and no severe adverse effects were observed. Intracavitary injection of Endostar combined with cisplatin is effective and safe to treat malignant pleural effusion and ascites.
本研究评估了腔内注射重组人血管内皮抑素(恩度)联合顺铂化疗治疗恶性胸腔积液和腹水的疗效及安全性。45例恶性胸腔积液和腹水患者被分为EP组(n = 23),接受腔内注射恩度和顺铂;P组(n = 22),仅接受腔内注射顺铂。治疗前将胸腔积液和腹水完全引流。治疗每周进行1次;2次治疗为1个疗程。评估生活质量结局及毒性。EP组的客观总缓解率和疾病控制率分别为78.3%(18/23)和87.0%(20/23)。相比之下,P组这些参数显著较低(p < 0.05):分别为40.9%(9/22)和59.1%(13/22)。EP组卡氏功能状态改善率为87.0%(20/23),P组为59.1%(13/22)(p < 0.05)。所有患者对联合治疗耐受性良好,未观察到严重不良反应。腔内注射恩度联合顺铂治疗恶性胸腔积液和腹水有效且安全。