Gastroenterology Department, CHU Saint Louis, APHP, Paris, France; University Paris 7, Sorbonne Paris Cité, Paris, France.
Department of Medical Oncology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Eur J Cancer. 2018 Jul;98:1-9. doi: 10.1016/j.ejca.2018.03.031. Epub 2018 May 26.
Previous studies showed that high and low body mass index (BMI) was associated with worse prognosis in early-stage colorectal cancer (CRC), and low BMI was associated with worse prognosis in metastatic CRC (mCRC). We aimed to assess efficacy outcomes according to BMI.
A pooled analysis of individual data from 2085 patients enrolled in eight FFCD first-line mCRC trials from 1991 to 2013 was performed. Comparisons were made according to the BMI cut-off: Obese (BMI ≥30), overweight patients (BMI ≥ 25), normal BMI patients (BMI: 18.5-24) and thin patients (BMI <18.5). Interaction tests were performed between BMI effect and sex, age and the addition of antiangiogenics to chemotherapy.
The rate of BMI ≥25 patients was 41.5%, ranging from 37.6% (1991-1999 period) to 41.5% (2000-2006 period) and 44.8% (2007-2013 period). Comparison of overweight patients versus normal BMI range patients revealed a significant improvement of median overall survival (OS) (18.5 versus 16.3 months, HR = 0.88 [0.80-0.98] p = 0.02) and objective response rate (ORR) (42% versus 36% OR = 1.23 [1.01-1.50] p = 0.04) but a comparable median progression-free survival (PFS) (7.8 versus 7.2 months, HR = 0.96 [0.87-1.05] p = 0.35). Subgroup analyses revealed that overweight was significantly associated with better OS in men. OS and PFS were significantly shorter in thin patients.
Overweight patients had a prolonged OS compared with normal weight patients with mCRC. The association of overweight with better OS was only observed in men. The pejorative prognosis of BMI <18.5 was confirmed.
既往研究表明,高和低体质指数(BMI)与早期结直肠癌(CRC)的预后较差相关,低 BMI 与转移性 CRC(mCRC)的预后较差相关。我们旨在根据 BMI 评估疗效结果。
对 1991 年至 2013 年期间在八项 FFCD 一线 mCRC 试验中入组的 2085 名患者的个体数据进行了汇总分析。根据 BMI 截止值进行比较:肥胖(BMI≥30)、超重患者(BMI≥25)、正常 BMI 患者(BMI:18.5-24)和消瘦患者(BMI<18.5)。对 BMI 效应与性别、年龄以及抗血管生成药物联合化疗之间的交互作用进行了检验。
BMI≥25 患者的比例为 41.5%,范围为 37.6%(1991-1999 年期间)至 41.5%(2000-2006 年期间)和 44.8%(2007-2013 年期间)。超重患者与正常 BMI 范围患者相比,中位总生存期(OS)(18.5 个月与 16.3 个月,HR=0.88[0.80-0.98],p=0.02)和客观缓解率(ORR)(42%与 36%,OR=1.23[1.01-1.50],p=0.04)显著改善,但中位无进展生存期(PFS)(7.8 个月与 7.2 个月,HR=0.96[0.87-1.05],p=0.35)相当。亚组分析显示,超重与男性 OS 延长显著相关。消瘦患者的 OS 和 PFS 明显缩短。
与正常体重的 mCRC 患者相比,超重患者的 OS 延长。超重与 OS 改善的关联仅在男性中观察到。BMI<18.5 的不良预后得到了证实。