Student Research Committee, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Gastrointestinal Cancer Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
Support Care Cancer. 2018 Jul;26(7):2479-2489. doi: 10.1007/s00520-018-4047-y. Epub 2018 Feb 13.
Previous studies reported promising efficacy for celecoxib in the treatment of cancer cachexia. We designed this study to test the hypothesis that combination therapy with megestrol acetate (MA) plus celecoxib is superior to MA alone.
Ninety eligible gastrointestinal cancer patients randomly received either MA 320 mg/day plus placebo (arm1) or MA 320 mg/day plus celecoxib 200 mg/day (arm2). Patients were evaluated at baseline, then 1 and 2 months after starting interventions. The primary outcome was body weight. Secondary outcomes were quality of life, grip strength, appetite score, performance status, plasma albumin, CRP, IL-6, and Glasgow Prognostic Score.
Patients were comparable at baseline. Sixty patients were assessable for the first month and 33 patients for the second month. After 2 months, patients in arm1 (MA + placebo) and arm2 (MA + celecoxib) experienced 4.0 ± 3.4 and 2.2 ± 3.6Kg of weight gain respectively (P = 0.163). Changes relative to baseline were statistically significant in both arms of the study (P = 0.001). Regarding secondary outcomes, comparisons between groups did not show any statistically significant difference, but within-group changes were significant in both arms of the study.
Since both MA alone and MA plus celecoxib are associated with improvement of cachexia in GI cancer patients, this study failed to show that adding celecoxib (200 mg/day) to megestrol (320 mg/day) could enhance anti-cachexic effects of megestrol.
先前的研究报告显示塞来昔布在治疗癌症恶病质方面具有良好的疗效。我们设计本研究旨在检验以下假说,即醋酸甲地孕酮(MA)联合塞来昔布治疗的疗效优于 MA 单药治疗。
90 例符合条件的胃肠道癌症患者随机接受 MA 320mg/天+安慰剂(第 1 组)或 MA 320mg/天+塞来昔布 200mg/天(第 2 组)治疗。患者在基线、干预开始后 1 个月和 2 个月进行评估。主要结局指标为体重。次要结局指标为生活质量、握力、食欲评分、体能状态、血浆白蛋白、CRP、IL-6 和格拉斯哥预后评分。
患者基线资料具有可比性。第 1 个月有 60 例患者可评估,第 2 个月有 33 例患者可评估。2 个月后,第 1 组(MA+安慰剂)和第 2 组(MA+塞来昔布)患者体重分别增加了 4.0±3.4kg 和 2.2±3.6kg(P=0.163)。两组患者体重较基线均有统计学意义的增加(P=0.001)。关于次要结局,组间比较无统计学差异,但两组内变化均有统计学意义。
由于 MA 单药和 MA 联合塞来昔布均能改善胃肠道癌症患者的恶病质,本研究未能表明加用塞来昔布(200mg/天)可增强 MA(320mg/天)的抗恶病质作用。