Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medical Oncology, Dana-Farber/Partners CancerCare, Boston, MA, USA.
JNCI Cancer Spectr. 2020 Aug 27;5(1). doi: 10.1093/jncics/pkaa074. eCollection 2021 Feb.
Energy balance-related biomarkers are associated with risk and prognosis of various malignancies. Their relationship to survival in metastatic colorectal cancer (mCRC) requires further study.
Baseline plasma insulin-like growth factor (IGF)-1, IGF-binding protein (IGFBP)-3, IGFBP-7, C-peptide, and adiponectin were measured at time of trial registration in a prospective cohort of patients with mCRC participating in a National Cancer Institute-sponsored trial of first-line systemic therapy. We used Cox proportional hazards regression to adjust for confounders and examine associations of each biomarker with overall survival (OS) and progression-free survival (PFS). values are 2-sided.
Median follow-up for 1086 patients was 6.2 years. Compared with patients in the lowest IGFBP-3 quintile, patients in the highest IGFBP-3 quintile experienced an adjusted hazard ratio (HR) for OS of 0.57 (95% confidence interval [CI] = 0.42 to 0.78; < .001) and for PFS of 0.61 (95% CI = 0.45 to 0.82; = .003). Compared with patients in the lowest IGFBP-7 quintile, patients in the highest IGFBP-7 quintile experienced an adjusted hazard ratio for OS of 1.60 (95% CI = 1.30 to 1.97; < .001) and for PFS of 1.38 (95% CI = 1.13 to 1.69; < .001). Plasma C-peptide and IGF-1 were not associated with patient outcomes. Adiponectin was not associated with OS; there was a nonlinear U-shaped association between adiponectin and PFS ( = .03).
Among patients with mCRC, high plasma IGFBP-3 and low IGFBP-7 were associated with longer OS and PFS. Extreme levels of adiponectin were associated with shorter PFS. These findings suggest potential avenues for prognostic and therapeutic innovation.
能量平衡相关生物标志物与各种恶性肿瘤的风险和预后相关。它们与转移性结直肠癌(mCRC)患者的生存关系需要进一步研究。
在一项由美国国立癌症研究所(NCI)资助的一线系统治疗试验中,前瞻性队列研究了 mCRC 患者在试验登记时的基线血浆胰岛素样生长因子(IGF)-1、IGF 结合蛋白(IGFBP)-3、IGFBP-7、C 肽和脂联素。我们使用 Cox 比例风险回归来调整混杂因素,并检查每种生物标志物与总生存期(OS)和无进展生存期(PFS)的相关性。 值为双侧。
1086 例患者的中位随访时间为 6.2 年。与 IGFBP-3 最低五分位数的患者相比,IGFBP-3 最高五分位数的患者 OS 的调整后的危险比(HR)为 0.57(95%置信区间[CI]为 0.42 至 0.78;.001),PFS 的 HR 为 0.61(95% CI = 0.45 至 0.82; =.003)。与 IGFBP-7 最低五分位数的患者相比,IGFBP-7 最高五分位数的患者 OS 的调整 HR 为 1.60(95% CI = 1.30 至 1.97; <.001),PFS 的 HR 为 1.38(95% CI = 1.13 至 1.69; <.001)。血浆 C 肽和 IGF-1 与患者预后无关。脂联素与 OS 无关;脂联素与 PFS 之间存在非线性 U 型关联( =.03)。
在 mCRC 患者中,高血浆 IGFBP-3 和低 IGFBP-7 与 OS 和 PFS 延长相关。脂联素的极端水平与较短的 PFS 相关。这些发现为预后和治疗创新提供了潜在途径。