Haugnes H S, Aass N, Fosså S D, Dahl O, Klepp O, Wist E A, Svartberg J, Wilsgaard T, Bremnes R M
Department of Oncology, Institute of Clinical Medicine, University of Tromsø, Norway.
Ann Oncol. 2007 Feb;18(2):241-8. doi: 10.1093/annonc/mdl372. Epub 2006 Oct 23.
A possible explanation of the excess cardiovascular risk in testicular cancer (TC) survivors is development of metabolic syndrome. The association between metabolic syndrome and TC treatment is examined in long-term survivors.
In a national follow-up study (1998-2002), 1463 TC survivors (diagnosed 1980-1994) participated. Patients >60 years were excluded in the present study, leaving 1135 patients eligible. The patients were divided in four treatment groups: surgery (n = 225); radiotherapy (n = 446) and two chemotherapy groups: cumulative cisplatin dose (Cis) <or=850 mg (n = 376) and Cis >850 mg (n = 88). A control group consisted of 1150 men from the Tromsø Population Study. Metabolic syndrome was defined according to a modified National Cholesterol Education Program definition.
Both chemotherapy groups had increased odds for metabolic syndrome compared with the surgery group, highest for the Cis >850 group [odds ratio (OR) 2.8, 95% confidence interval (CI) 1.6-4.7]. Also, the Cis >850 group had increased odds (OR 2.1, 95% CI 1.3-3.4) for metabolic syndrome compared with the control group. The association between metabolic syndrome and the Cis >850 group was strengthened after adjusting for testosterone, smoking, physical activity, education and family status.
TC survivors treated with cisplatin-based chemotherapy have an increased risk of developing metabolic syndrome compared with patients treated with other modalities or with controls.
睾丸癌(TC)幸存者心血管风险过高的一种可能解释是代谢综合征的发生。本研究在长期幸存者中探讨了代谢综合征与TC治疗之间的关联。
在一项全国性随访研究(1998 - 2002年)中,1463例TC幸存者(1980 - 1994年确诊)参与其中。本研究排除了年龄>60岁的患者,剩余1135例符合条件。患者被分为四个治疗组:手术组(n = 225);放疗组(n = 446)以及两个化疗组:累积顺铂剂量(Cis)≤850 mg组(n = 376)和顺铂剂量>850 mg组(n = 88)。对照组由来自特罗姆瑟人群研究的1150名男性组成。代谢综合征根据修改后的美国国家胆固醇教育计划定义进行界定。
与手术组相比,两个化疗组发生代谢综合征的几率均增加,顺铂剂量>850 mg组最高[比值比(OR)2.8,95%置信区间(CI)1.6 - 4.7]。此外,与对照组相比,顺铂剂量>850 mg组发生代谢综合征的几率也增加(OR 2.1,95% CI 1.3 - 3.4)。在对睾酮、吸烟、身体活动、教育程度和家庭状况进行校正后,代谢综合征与顺铂剂量>850 mg组之间的关联增强。
与接受其他治疗方式的患者或对照组相比,接受以顺铂为基础的化疗的TC幸存者发生代谢综合征的风险增加。