消癌平注射液联合化疗治疗中晚期食管癌的疗效和安全性
目的探讨消癌平注射液联合化疗治疗中晚期食管癌的疗效和安全性。方法选取临床确诊的中晚期食管癌、KPS评分≥60分,预计生存时间≥3个月的患者124例,采取多中心、随机、开放、平行对照试验设计,将患者分为试验组和对照组,每组62例,试验组接受消癌平注射液联合替吉奥+顺铂化疗方案,对照组单用替吉奥+顺铂化疗方案,21 d为1个治疗周期,观察两组患者的疗效和不良反应。结果试验组和对照组可评价临床疗效的患者分别为57例和55例。试验组和对照组患者的有效率分别为54.4%和34.5%,疾病控制率分别为86.0%和69.1%,试验组患者的有效率和疾病控制率均明显高于对照组,差异有统计学意义(均P〈0.05)...
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Published in | 中华肿瘤杂志 Vol. 39; no. 6; pp. 453 - 457 |
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Main Author | |
Format | Journal Article |
Language | Chinese |
Published |
450052,郑州大学第一附属医院肿瘤科%455000,安阳市肿瘤医院肿瘤 内科%吉林大学中日联谊医院放射治疗科, 长春,130033%471009,洛阳市中心医院肿瘤科%河南大学淮河医院肿瘤科, 开封,475000
2017
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Subjects | |
Online Access | Get full text |
ISSN | 0253-3766 |
DOI | 10.3760/cma.j.issn.0253-3766.2017.06.010 |
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Summary: | 目的探讨消癌平注射液联合化疗治疗中晚期食管癌的疗效和安全性。方法选取临床确诊的中晚期食管癌、KPS评分≥60分,预计生存时间≥3个月的患者124例,采取多中心、随机、开放、平行对照试验设计,将患者分为试验组和对照组,每组62例,试验组接受消癌平注射液联合替吉奥+顺铂化疗方案,对照组单用替吉奥+顺铂化疗方案,21 d为1个治疗周期,观察两组患者的疗效和不良反应。结果试验组和对照组可评价临床疗效的患者分别为57例和55例。试验组和对照组患者的有效率分别为54.4%和34.5%,疾病控制率分别为86.0%和69.1%,试验组患者的有效率和疾病控制率均明显高于对照组,差异有统计学意义(均P〈0.05)。试验组和对照组患者的中位无进展生存时间分别为7.97和6.43个月,差异有统计学意义(P=0.033);试验组和对照组患者的中位总生存时间分别为12.93和10.93个月,差异有统计学意义(P=0.023)。两组患者常见的不良反应为恶心呕吐、血小板减少、血红蛋白减少、中性粒细胞减少、白细胞减少、肝功能损害、色素沉着、口腔黏膜炎、肾功能损害和腹泻等,其中试验组患者恶心呕吐、血小板减少、白细胞减少、中性粒细胞减少和腹泻的发生率明显低于对照组,差异有统计学意义(均P〈0.05)。结论消癌平注射液联合替吉奥+顺铂化疗方案治疗中晚期食管癌患者,可明显提高近期疗效,延长患者的生存时间,降低化疗不良反应,给患者带来临床收益。 |
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Bibliography: | Wang Feng, Fan Qingxia, Wang Honghai, Han Dongmei, Song Nasha, Lu Hong (Depratement of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China ; Depratement of Medical Oncology, Anyang Tumor hospital, Anyang, 455000, China ; Department of Radiotherapy, China-Japan Union Hospital of Jilin University, Changchun, 130033, China; Department of Oncology, Luoyang Central Hospital, Luoyang, 471009, China; Department of Oncology, Huaihe Hospitalof Henan University, Kaifeng, 475000, China) 11-2152/R ObjectiveTo evaluate the efficacy and safety of Xiaoaiping combined with chemotherapy in the treatment of advanced esophageal cancer.MethodsThis is a multi-center, randomized, open label and parallel controlled study. A total of 124 advanced esophageal cancer patients with Karnofsky Performance Status (KPS) score ≥60 and expected survival time≥3 months were enrolled. We adopted design and divided the patients into study and control group. The patients in study group received Xiaoaiping combin |
ISSN: | 0253-3766 |
DOI: | 10.3760/cma.j.issn.0253-3766.2017.06.010 |