Department of Breast & Endocrine Surgery, Stavanger University Hospital, Helse Stavanger HF, P.O. Box 8100, N-4068, Stavanger, Norway.
Centre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Faculty of Medicine and Dentistry, University of Bergen, Jonas Lies vei 87, N-5012, Bergen, Norway.
BMC Cancer. 2019 Nov 8;19(1):1076. doi: 10.1186/s12885-019-6275-z.
BACKGROUND: Conflicting results have been reported on the influence of carbohydrates in breast cancer. OBJECTIVE: To determine the influence of pre-operative per-oral carbohydrate load on proliferation in breast tumors. DESIGN: Randomized controlled trial. SETTING: University hospital with primary and secondary care functions in South-West Norway. PATIENTS: Sixty-one patients with operable breast cancer from a population-based cohort. INTERVENTION: Per-oral carbohydrate load (preOp™) 18 and 2-4 h before surgery (n = 26) or standard pre-operative fasting with free consumption of tap water (n = 35). MEASUREMENTS: The primary outcome was post-operative tumor proliferation measured by the mitotic activity index (MAI). The secondary outcomes were changes in the levels of serum insulin, insulin-c-peptide, glucose, IGF-1, and IGFBP3; patients' well-being, and clinical outcome over a median follow-up of 88 months (range 33-97 months). RESULTS: In the estrogen receptor (ER) positive subgroup (n = 50), high proliferation (MAI ≥ 10) occurred more often in the carbohydrate group (CH) than in the fasting group (p = 0.038). The CH group was more frequently progesterone receptor (PR) negative (p = 0.014). The CH group had a significant increase in insulin (+ 24.31 mIE/L, 95% CI 15.34 mIE/L to 33.27 mIE/L) and insulin c-peptide (+ 1.39 nM, 95% CI 1.03 nM to 1.77 nM), but reduced IGFBP3 levels (- 0.26 nM; 95% CI - 0.46 nM to - 0.051 nM) compared to the fasting group. CH-intervention ER-positive patients had poorer relapse-free survival (73%) than the fasting group (100%; p = 0.012; HR = 9.3, 95% CI, 1.1 to 77.7). In the ER-positive patients, only tumor size (p = 0.021; HR = 6.07, 95% CI 1.31 to 28.03) and the CH/fasting subgrouping (p = 0.040; HR = 9.30, 95% CI 1.11 to 77.82) had independent prognostic value. The adverse clinical outcome of carbohydrate loading occurred only in T2 patients with relapse-free survival of 100% in the fasting group vs. 33% in the CH group (p = 0.015; HR = inf). The CH group reported less pain on days 5 and 6 than the control group (p < 0.001) but otherwise exhibited no factors related to well-being. LIMITATION: Only applicable to T2 tumors in patients with ER-positive breast cancer. CONCLUSIONS: Pre-operative carbohydrate load increases proliferation and PR-negativity in ER-positive patients and worsens clinical outcome in ER-positive T2 patients. TRIAL REGISTRATION: CliniTrials.gov; NCT03886389. Retrospectively registered March 22, 2019.
背景:关于碳水化合物对乳腺癌的影响,已有相互矛盾的研究结果报告。 目的:确定术前口服碳水化合物负荷对乳腺肿瘤增殖的影响。 设计:随机对照试验。 地点:挪威西南部具有初级和二级保健功能的大学医院。 患者:来自基于人群队列的 61 名可手术乳腺癌患者。 干预措施:术前口服碳水化合物负荷(preOp™)18 小时和 2-4 小时(n=26)或标准术前禁食,自由饮用自来水(n=35)。 测量指标:主要结局是通过有丝分裂活性指数(MAI)测量的术后肿瘤增殖。次要结局是血清胰岛素、胰岛素-c 肽、葡萄糖、IGF-1 和 IGFBP3 水平的变化;患者的幸福感以及中位随访 88 个月(33-97 个月)的临床结局。 结果:在雌激素受体(ER)阳性亚组(n=50)中,碳水化合物组(CH)的高增殖(MAI≥10)比禁食组更常见(p=0.038)。CH 组孕激素受体(PR)阴性的比例更高(p=0.014)。CH 组胰岛素(+24.31 mIE/L,95%CI 15.34 mIE/L 至 33.27 mIE/L)和胰岛素 c 肽(+1.39 nM,95%CI 1.03 nM 至 1.77 nM)水平显著升高,但 IGFBP3 水平降低(-0.26 nM;95%CI-0.46 nM 至-0.051 nM)与禁食组相比。与禁食组(100%)相比,CH 干预的 ER 阳性患者无复发生存率(73%)较差(p=0.012;HR=9.3,95%CI,1.1 至 77.7)。在 ER 阳性患者中,只有肿瘤大小(p=0.021;HR=6.07,95%CI 1.31 至 28.03)和 CH/禁食亚组(p=0.040;HR=9.30,95%CI 1.11 至 77.82)具有独立的预后价值。碳水化合物负荷的不良临床结果仅发生在 T2 患者中,无复发生存率在禁食组为 100%,在 CH 组为 33%(p=0.015;HR=inf)。与对照组相比,CH 组在第 5 天和第 6 天的疼痛程度较轻(p<0.001),但在其他方面未表现出与幸福感相关的任何因素。 局限性:仅适用于 ER 阳性乳腺癌患者的 T2 肿瘤。 结论:术前口服碳水化合物负荷增加 ER 阳性患者的增殖和 PR 阴性,并使 ER 阳性 T2 患者的临床结局恶化。 试验注册:CliniTrials.gov;NCT03886389。于 2019 年 3 月 22 日进行了回顾性注册。
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