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Plasma Protein Biomarkers in Advanced or Metastatic Colorectal Cancer Patients Receiving Chemotherapy With Bevacizumab or Cetuximab: Results from CALGB 80405 (Alliance).

Publication ,  Journal Article
Nixon, AB; Sibley, AB; Liu, Y; Hatch, AJ; Jiang, C; Mulkey, F; Starr, MD; Brady, JC; Niedzwiecki, D; Venook, AP; Baez-Diaz, L; Lenz, H-J ...
Published in: Clin Cancer Res
July 1, 2022

PURPOSE: CALGB 80405 compared the combination of first-line chemotherapy with cetuximab or bevacizumab in the treatment of advanced or metastatic colorectal cancer (mCRC). Although similar clinical outcomes were observed in the cetuximab-chemotherapy group and the bevacizumab-chemotherapy group, biomarkers could identify patients deriving more benefit from either biologic agent. PATIENTS AND METHODS: In this exploratory analysis, the Angiome, a panel of 24 soluble protein biomarkers were measured in baseline plasma samples in CALGB 80405. Prognostic biomarkers were determined using univariate Cox proportional hazards models. Predictive biomarkers were identified using multivariable Cox regression models including interaction between biomarker level and treatment. RESULTS: In the total population, high plasma levels of Ang-2, CD73, HGF, ICAM-1, IL6, OPN, TIMP-1, TSP-2, VCAM-1, and VEGF-R3 were identified as prognostic of worse progression-free survival (PFS) and overall survival (OS). PlGF was identified as predictive of lack of PFS benefit from bevacizumab [bevacizumab HR, 1.51; 95% confidence interval (CI), 1.10-2.06; cetuximab HR, 0.94; 95% CI, 0.71-1.25; Pinteraction = 0.0298] in the combined FOLFIRI/FOLFOX regimens. High levels of VEGF-D were predictive of lack of PFS benefit from bevacizumab in patients receiving FOLFOX regimen only (FOLFOX/bevacizumab HR, 1.70; 95% CI, 1.19-2.42; FOLFOX/cetuximab HR, 0.92; 95% CI, 0.68-1.24; Pinteraction = 0.0097). CONCLUSIONS: In this exploratory, hypothesis-generating analysis, the Angiome identified multiple prognostic biomarkers and two potential predictive biomarkers for patients with mCRC enrolled in CALGB 80405. PlGF and VEGF-D predicted lack of benefit from bevacizumab in a chemo-dependent manner. See related commentaries by Mishkin and Kohn, p. 2722 and George and Bertagnolli, p. 2725.

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Published In

Clin Cancer Res

DOI

EISSN

1557-3265

Publication Date

July 1, 2022

Volume

28

Issue

13

Start / End Page

2779 / 2788

Location

United States

Related Subject Headings

  • Vascular Endothelial Growth Factor D
  • Phenotype
  • Oncology & Carcinogenesis
  • Leucovorin
  • Humans
  • Genotype
  • Fluorouracil
  • Colorectal Neoplasms
  • Colonic Neoplasms
  • Cetuximab
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Nixon, A. B., Sibley, A. B., Liu, Y., Hatch, A. J., Jiang, C., Mulkey, F., … Hurwitz, H. I. (2022). Plasma Protein Biomarkers in Advanced or Metastatic Colorectal Cancer Patients Receiving Chemotherapy With Bevacizumab or Cetuximab: Results from CALGB 80405 (Alliance). Clin Cancer Res, 28(13), 2779–2788. https://doi.org/10.1158/1078-0432.CCR-21-2389
Nixon, Andrew B., Alexander B. Sibley, Yingmiao Liu, Ace J. Hatch, Chen Jiang, Flora Mulkey, Mark D. Starr, et al. “Plasma Protein Biomarkers in Advanced or Metastatic Colorectal Cancer Patients Receiving Chemotherapy With Bevacizumab or Cetuximab: Results from CALGB 80405 (Alliance).Clin Cancer Res 28, no. 13 (July 1, 2022): 2779–88. https://doi.org/10.1158/1078-0432.CCR-21-2389.
Nixon, Andrew B., et al. “Plasma Protein Biomarkers in Advanced or Metastatic Colorectal Cancer Patients Receiving Chemotherapy With Bevacizumab or Cetuximab: Results from CALGB 80405 (Alliance).Clin Cancer Res, vol. 28, no. 13, July 2022, pp. 2779–88. Pubmed, doi:10.1158/1078-0432.CCR-21-2389.
Nixon AB, Sibley AB, Liu Y, Hatch AJ, Jiang C, Mulkey F, Starr MD, Brady JC, Niedzwiecki D, Venook AP, Baez-Diaz L, Lenz H-J, O’Neil BH, Innocenti F, Meyerhardt JA, O’Reilly EM, Owzar K, Hurwitz HI. Plasma Protein Biomarkers in Advanced or Metastatic Colorectal Cancer Patients Receiving Chemotherapy With Bevacizumab or Cetuximab: Results from CALGB 80405 (Alliance). Clin Cancer Res. 2022 Jul 1;28(13):2779–2788.

Published In

Clin Cancer Res

DOI

EISSN

1557-3265

Publication Date

July 1, 2022

Volume

28

Issue

13

Start / End Page

2779 / 2788

Location

United States

Related Subject Headings

  • Vascular Endothelial Growth Factor D
  • Phenotype
  • Oncology & Carcinogenesis
  • Leucovorin
  • Humans
  • Genotype
  • Fluorouracil
  • Colorectal Neoplasms
  • Colonic Neoplasms
  • Cetuximab