New Insights into Macrophage Polarization and its Prognostic Role in Patients with Colorectal Cancer Liver Metastasis

Author:

Khanduri Isha1,Maki Harufumi1,Verma Anuj2,Katkhuda Riham3,Anandappa Gayathri1,Pandurengan Renganayaki1,Zhang Shanyu1,Mejia Alicia1,Tong Zhimin1,Soto Luisa M. Solis1,Jadhav Akshaya1,Wistuba Ignacio I.1,Kopetz Scott1,Parra Edwin R.1,Vauthey Jean-Nicolas1,Maru Dipen M.1

Affiliation:

1. The University of Texas MD Anderson Cancer Center

2. Yale-New Haven Hospital

3. The University of Chicago Medical Center

Abstract

Abstract Background: As liver metastasis is the most common cause of mortality in patients with colorectal cancer, studying colorectal cancer liver metastasis (CLM) microenvironment is essential for improved understanding of tumor biology and to identify novel therapeutic targets. Methods: We used multiplex immunofluorescence platform to study tumor associated macrophage (TAM) polarization and adaptive T cell subtypes in tumor samples from 105 CLM patients (49 without and 56 with preoperative chemotherapy). Results: CLM exhibited M2 macrophage polarization, and helper T cells were the prevalent adaptive T cell subtype. The density of total, M2 and TGFβ-expressing macrophages, and regulatory T cells was lower in CLM treated with preoperative chemotherapy. CLM with right-sided primary demonstrated enrichment of TGFβ-expressing macrophages, and with left-sided primary had higher densities of helper and cytotoxic T cells. In multivariate analysis, high density of M2 macrophages correlated with longer recurrence-free survival (RFS) in the entire cohort [hazard ratio (HR) 0.425, 95% CI 0.219-0.825, p=0.011) and in patients without preoperative chemotherapy (HR 0.45, 95% CI 0.221-0.932, p=0.032). High pSMAD3-expressing macrophages were associated with shorter RFS in CLM after preoperative chemotherapy. Conclusions: Our results highlight the significance of a multi-marker approach to define the macrophage subtypes and identify M2 macrophages as a predictor of favorable prognosis in CLM.

Publisher

Research Square Platform LLC

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