Patel Gargi S, Ullah Shahid, Beeke Carol, Hakendorf Paul, Padbury Robert, Price Timothy J, Karapetis Christos S
Department of Medical Oncology, Flinders Medical Centre, Adelaide, South Australia, Australia.
Flinders Centre for Epidemiology and Biostatistics, School of Medicine, Flinders University, Adelaide, South Australia, Australia.
Cancer Med. 2015 Oct;4(10):1461-71. doi: 10.1002/cam4.490. Epub 2015 Jul 25.
Although a raised body mass index (BMI) is associated with increased risk of colorectal cancer (CRC) and recurrence after adjuvant treatment, data in the metastatic setting is limited. We compared overall survival (OS) across BMI groups for metastatic CRC, and specifically examined the effect of BMI within the group of patients treated with targeted therapies (TT). Retrospective data were obtained from the South Australian Registry for mCRC from February 2006 to October 2012. The BMI at first treatment was grouped as underweight <18.5 kg/m(2) , Normal = 18.5 to <25 kg/m(2) , Overweight = 25 to <30 kg/m(2) , Obese I = 30 to <35 kg/m(2) , Obese II ≥35 kg/m(2) . Of 1174 patients, 42 were underweight, 462 overweight, 175 Obese I, and 77 Obese II. The OS was shorter for patients who were underweight and overweight compared to normal (OS 13.7 and 22.3 vs. 24.1 months, respectively, hazard ratio [HR] 2.21 and 1.23). The adjusted median OS was longer for normal versus overweight or obese I patients receiving chemotherapy + targeted therapy (35.7 vs 25.1 or 22.8 months, HR 1.59 and 1.63, respectively) with no difference in OS for chemotherapy alone. On breakdown by type of targeted therapy, overweight and obese I patients had a poorer outcome with Bevacizumab. The BMI is predictive of a poorer outcome for underweight and overweight patients in the whole population. Of those receiving chemotherapy and targeted therapy, BMI is an independent predictor for OS for overweight and obese I patients, specifically for those treated with Bevacizumab. Patients who are overweight or obese (group I) may be a target group for lifestyle and nutrition advice to improve OS with TT.
尽管体重指数(BMI)升高与结直肠癌(CRC)风险增加及辅助治疗后的复发相关,但转移性结直肠癌的相关数据有限。我们比较了转移性结直肠癌患者不同BMI组的总生存期(OS),并特别研究了BMI在接受靶向治疗(TT)患者组中的影响。回顾性数据取自2006年2月至2012年10月南澳大利亚转移性结直肠癌登记处。首次治疗时的BMI分组为:体重过轻<18.5kg/m²,正常=18.5至<25kg/m²,超重=25至<30kg/m²,肥胖I级=30至<35kg/m²,肥胖II级≥35kg/m²。在1174例患者中,42例体重过轻,462例超重,175例肥胖I级,77例肥胖II级。与体重正常者相比,体重过轻和超重患者的OS较短(分别为13.7个月和22.3个月对24.1个月,风险比[HR]分别为2.21和1.23)。接受化疗+靶向治疗的正常体重患者与超重或肥胖I级患者相比,调整后的中位OS更长(分别为35.7个月对25.1个月或22.8个月,HR分别为1.59和1.63),单纯化疗的OS无差异。按靶向治疗类型细分,超重和肥胖I级患者使用贝伐单抗的预后较差。在整个人群中,BMI可预测体重过轻和超重患者的较差预后。在接受化疗和靶向治疗的患者中,BMI是超重和肥胖I级患者OS的独立预测因素,特别是对于接受贝伐单抗治疗的患者。超重或肥胖(I级)患者可能是接受生活方式和营养建议以通过TT改善OS的目标人群。