Magnusson Marie, Höglund Peter, Johansson Karin, Jönsson Charlotta, Killander Fredrika, Malmström Per, Weddig Anna, Kjellén Elisabeth
Department of Clinical Pharmacology, Lund University Hospital, Lund SE 221 85, Sweden.
Eur J Cancer. 2009 Sep;45(14):2488-95. doi: 10.1016/j.ejca.2009.05.015. Epub 2009 Jun 17.
A previous study has shown that pentoxifylline in combination with vitamin E can reverse radiation-induced fibrosis. The aim of the present study is to investigate if the same drugs could prevent radiation-induced side-effects in women with breast cancer.
A randomised, placebo-controlled, double-blind, parallel group trial was performed. Women with breast cancer were treated for 12 months with 400 mg pentoxifylline t.i.d. or placebo, in combination with 100 mg vitamin E t.i.d., starting 1-3 months after the completion of radiotherapy. The primary end-point was passive abduction of the shoulder, and the secondary end-point was difference in arm volumes. The trial is registered on the ISRCTN.org website, number ISRCTN39143623.
83 patients were included in the study; 42 in the pentoxifylline+vitamin E group and 41 in the placebo+vitamin E group. Both treatments were generally well tolerated. Seven patients were withdrawn from the treatment due to disease progression; four in the pentoxifylline group and three in the placebo group. At inclusion, patients had impaired passive abduction of the shoulder. During treatment, both the groups improved significantly. Median improvement from baseline was 3.7 degrees (p=0.0035) on pentoxifylline and was 9.4 degrees (p=0.0041) in the placebo group, but no difference between the groups was detected (p=0.20). Arm volumes increased over time in the placebo group (1.04%), but not on pentoxifylline (0.50%), and differed significantly between the groups (p=0.0172).
The combination of pentoxifylline and vitamin E was safe and may be used for the prevention of some radiation-induced side-effects.
先前的一项研究表明,己酮可可碱联合维生素E可逆转辐射诱导的纤维化。本研究的目的是调查相同药物是否能预防乳腺癌女性的辐射诱导副作用。
进行了一项随机、安慰剂对照、双盲、平行组试验。乳腺癌女性在放疗结束后1 - 3个月开始,接受400 mg己酮可可碱每日三次或安慰剂治疗12个月,同时每日三次服用100 mg维生素E。主要终点是肩部被动外展,次要终点是手臂体积差异。该试验已在ISRCTN.org网站注册,注册号为ISRCTN39143623。
83例患者纳入研究;己酮可可碱 + 维生素E组42例,安慰剂 + 维生素E组41例。两种治疗总体耐受性良好。7例患者因疾病进展退出治疗;己酮可可碱组4例,安慰剂组3例。纳入时,患者肩部被动外展功能受损。治疗期间,两组均有显著改善。己酮可可碱组从基线的中位改善为3.7度(p = 0.0035),安慰剂组为9.4度(p = 0.0041),但两组间未检测到差异(p = 0.20)。安慰剂组手臂体积随时间增加(1.04%),己酮可可碱组未增加(0.50%),两组间差异显著(p = 0.0172)。
己酮可可碱与维生素E联合用药安全,可用于预防某些辐射诱导的副作用。