Gordon J N, Trebble T M, Ellis R D, Duncan H D, Johns T, Goggin P M
Mailpoint 813, Level E, South Block, Southampton General Hospital, Southampton SO16 6YD, UK.
Gut. 2005 Apr;54(4):540-5. doi: 10.1136/gut.2004.047563.
Proinflammatory cytokines, especially tumour necrosis factor alpha (TNF-alpha), play a prominent role in the pathogenesis of cancer cachexia. Thalidomide, which is an inhibitor of TNF-alpha synthesis, may represent a novel and rational approach to the treatment of cancer cachexia.
To assess the safety and efficacy of thalidomide in attenuating weight loss in patients with cachexia secondary to advanced pancreatic cancer.
Fifty patients with advanced pancreatic cancer who had lost at least 10% of their body weight were randomised to receive thalidomide 200 mg daily or placebo for 24 weeks in a single centre, double blind, randomised controlled trial. The primary outcome was change in weight and nutritional status.
Thirty three patients (16 control, 17 thalidomide) were evaluated at four weeks, and 20 patients (eight control, 12 thalidomide) at eight weeks. At four weeks, patients who received thalidomide had gained on average 0.37 kg in weight and 1.0 cm(3) in arm muscle mass (AMA) compared with a loss of 2.21 kg (absolute difference -2.59 kg (95% confidence interval (CI) -4.3 to -0.8); p = 0.005) and 4.46 cm(3) (absolute difference -5.6 cm(3) (95% CI -8.9 to -2.2); p = 0.002) in the placebo group. At eight weeks, patients in the thalidomide group had lost 0.06 kg in weight and 0.5 cm(3) in AMA compared with a loss of 3.62 kg (absolute difference -3.57 kg (95% CI -6.8 to -0.3); p = 0.034) and 8.4 cm(3) (absolute difference -7.9 cm(3) (95% CI -14.0 to -1.8); p = 0.014) in the placebo group. Improvement in physical functioning correlated positively with weight gain (r = 0.56, p = 0.001).
Thalidomide was well tolerated and effective at attenuating loss of weight and lean body mass in patients with cachexia due to advanced pancreatic cancer.
促炎细胞因子,尤其是肿瘤坏死因子α(TNF-α),在癌症恶病质的发病机制中起重要作用。沙利度胺是一种TNF-α合成抑制剂,可能是治疗癌症恶病质的一种新的合理方法。
评估沙利度胺减轻晚期胰腺癌继发恶病质患者体重减轻的安全性和有效性。
在一项单中心、双盲、随机对照试验中,将50例体重至少减轻10%的晚期胰腺癌患者随机分为两组,分别接受每日200mg沙利度胺或安慰剂治疗24周。主要结局是体重和营养状况的变化。
4周时评估了33例患者(16例对照组,17例沙利度胺组),8周时评估了20例患者(8例对照组,12例沙利度胺组)。4周时,接受沙利度胺治疗的患者平均体重增加0.37kg,上臂肌肉量(AMA)增加1.0cm³,而安慰剂组体重减轻2.21kg(绝对差值-2.59kg(95%置信区间(CI)-4.3至-0.8);p = 0.005),AMA减少4.46cm³(绝对差值-5.6cm³(95%CI -8.9至-2.2);p = 0.002)。8周时,沙利度胺组患者体重减轻0.06kg,AMA减少0.5cm³,而安慰剂组体重减轻3.62kg(绝对差值-3.57kg(95%CI -6.8至-0.3);p = 0.034),AMA减少8.4cm³(绝对差值-7.9cm³(95%CI -14.0至-1.8);p = 0.014)。身体功能的改善与体重增加呈正相关(r = 0.56,p = 0.001)。
沙利度胺耐受性良好,可有效减轻晚期胰腺癌恶病质患者的体重和瘦体重损失。