» Articles » PMID: 33426464

IGF-Binding Proteins, Adiponectin, and Survival in Metastatic Colorectal Cancer: Results From CALGB (Alliance)/SWOG 80405

Abstract

Background: 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.

Methods: 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.

Results: 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).

Conclusions: 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.

Citing Articles

Adipo-oncology: adipocyte-derived factors govern engraftment, survival, and progression of metastatic cancers.

Sato S Cell Commun Signal. 2024; 22(1):52.

PMID: 38238841 PMC: 10797898. DOI: 10.1186/s12964-024-01474-4.


Serum C-peptide level and the risk of cardiovascular diseases mortality and all-cause mortality: a meta-analysis and systematic review.

Ahmadirad H, Teymoori F, Mokhtari E, Jahromi M, Norouzzadeh M, Tavakkoli S Front Cardiovasc Med. 2023; 10:1205481.

PMID: 37485272 PMC: 10360119. DOI: 10.3389/fcvm.2023.1205481.


Diabetes and Colorectal Cancer Risk: A New Look at Molecular Mechanisms and Potential Role of Novel Antidiabetic Agents.

Vekic J, Zeljkovic A, Stefanovic A, Giglio R, Ciaccio M, Rizzo M Int J Mol Sci. 2021; 22(22).

PMID: 34830295 PMC: 8622770. DOI: 10.3390/ijms222212409.


Lessons to Learn for Adequate Targeted Therapy Development in Metastatic Colorectal Cancer Patients.

Oliveres H, Pesantez D, Maurel J Int J Mol Sci. 2021; 22(9).

PMID: 34065119 PMC: 8126031. DOI: 10.3390/ijms22095019.

References
1.
Brahmkhatri V, Prasanna C, Atreya H . Insulin-like growth factor system in cancer: novel targeted therapies. Biomed Res Int. 2015; 2015():538019. PMC: 4383470. DOI: 10.1155/2015/538019. View

2.
Chong D, Mehta R, Song M, Kedrin D, Meyerhardt J, Ng K . Prediagnostic Plasma Adiponectin and Survival among Patients with Colorectal Cancer. Cancer Prev Res (Phila). 2015; 8(12):1138-45. PMC: 4670783. DOI: 10.1158/1940-6207.CAPR-15-0175. View

3.
Benassi M, Pazzaglia L, Novello C, Quattrini I, Pollino S, Magagnoli G . Tissue and serum IGFBP7 protein as biomarker in high-grade soft tissue sarcoma. Am J Cancer Res. 2016; 5(11):3446-54. PMC: 4697690. View

4.
Tomimaru Y, Eguchi H, Wada H, Kobayashi S, Marubashi S, Tanemura M . IGFBP7 downregulation is associated with tumor progression and clinical outcome in hepatocellular carcinoma. Int J Cancer. 2011; 130(2):319-27. DOI: 10.1002/ijc.25994. View

5.
Ruan W, Xu E, Xu F, Ma Y, Deng H, Huang Q . IGFBP7 plays a potential tumor suppressor role in colorectal carcinogenesis. Cancer Biol Ther. 2007; 6(3):354-9. DOI: 10.4161/cbt.6.3.3702. View