Meyerhardt Jeffrey A, Irwin Melinda L, Jones Lee W, Zhang Sui, Campbell Nancy, Brown Justin C, Pollak Michael, Sorrentino Alexandra, Cartmel Brenda, Harrigan Maura, Tolaney Sara M, Winer Eric, Ng Kimmie, Abrams Thomas, Fuchs Charles S, Sanft Tara, Douglas Pamela S, Hu Frank, Ligibel Jennifer A
See the Notes section for the full list of authors' affiliations.
JNCI Cancer Spectr. 2019 Nov 20;4(1):pkz096. doi: 10.1093/jncics/pkz096. eCollection 2020 Feb.
Observational data support inverse relationships between exercise or metformin use and disease outcomes in colorectal and breast cancer survivors, although the mechanisms underlying these associations are not well understood.
In a phase II trial, stage I-III colorectal and breast cancer survivors who completed standard therapy were randomly assigned to structured exercise or metformin or both or neither for 12 weeks. The primary outcome was change in fasting insulin levels; secondary outcomes included changes in other blood-based energetic biomarkers and anthropometric measurements. Analyses used linear mixed models.
In total, 139 patients were randomly assigned; 91 (65%) completed follow-up assessments. Fasting insulin levels statistically significantly decreased in all three intervention arms (-2.47 μU/mL combination arm, -0.08 μU/mL exercise only, -1.16 μU/mL metformin only, + 2.79 μU/mL control arm). Compared with the control arm, all groups experienced statistically significant weight loss between baseline and 12 weeks (-1.8% combination arm, -0.22% exercise only, -1.0% metformin only, +1.55% control). The combination arm also experienced statistically significant improvements in the homeostatic model assessment for insulin resistance (-30.6% combination arm, +61.2% control) and leptin (-42.2% combination arm, -0.8% control), compared with the control arm. The interventions did not change insulin-like growth factor-1 or insulin-like growth factor binding protein-3 measurements as compared with the control arm. Tolerance to metformin limited compliance (approximately 50% of the participants took at least 75% of the planned dosages in both treatment arms).
The combination of exercise and metformin statistically significantly improved insulin and associated metabolic markers, as compared to the control arm, with potential greater effect than either exercise or metformin alone though power limited formal synergy testing. Larger efforts are warranted to determine if such a combined modality intervention can improve outcomes in colorectal and breast cancer survivors.
观察性数据支持运动或使用二甲双胍与结直肠癌和乳腺癌幸存者的疾病转归之间存在负相关关系,尽管这些关联背后的机制尚不完全清楚。
在一项II期试验中,完成标准治疗的I - III期结直肠癌和乳腺癌幸存者被随机分配至结构化运动组、二甲双胍组、运动与二甲双胍联合组或非干预组,为期12周。主要结局为空腹胰岛素水平的变化;次要结局包括其他血液能量生物标志物和人体测量指标的变化。分析采用线性混合模型。
总共139例患者被随机分组;91例(65%)完成了随访评估。所有三个干预组的空腹胰岛素水平均有统计学显著下降(联合组-2.47 μU/mL,单纯运动组-0.08 μU/mL,单纯二甲双胍组-1.16 μU/mL,对照组+2.79 μU/mL)。与对照组相比,所有组在基线至12周期间体重均有统计学显著下降(联合组-1.8%,单纯运动组-0.22%,单纯二甲双胍组-1.0%,对照组+1.55%)。与对照组相比,联合组的胰岛素抵抗稳态模型评估(联合组-30.6%,对照组+61.2%)和瘦素(联合组-42.2%,对照组-0.8%)也有统计学显著改善。与对照组相比,干预措施未改变胰岛素样生长因子-1或胰岛素样生长因子结合蛋白-3的测量值。对二甲双胍的耐受性限制了依从性(两个治疗组中约50%的参与者服用了至少75%的计划剂量)。
与对照组相比,运动与二甲双胍联合使用在统计学上显著改善了胰岛素及相关代谢标志物,尽管由于检验效能有限无法进行正式的协同作用测试,但联合使用可能比单独运动或单独使用二甲双胍的效果更佳。有必要进一步努力确定这种联合干预方式是否能改善结直肠癌和乳腺癌幸存者的转归。