4.6 Article

The SAFFO Study: Sex-Related Prognostic Role and Cut-Off Definition of Monocyte-to-Lymphocyte Ratio (MLR) in Metastatic Colorectal Cancer

Journal

CANCERS
Volume 15, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/cancers15010175

Keywords

sex; MLR; colorectal cancer; circulating biomarkers; gender

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Recent evidence suggests the important role of immune system and cancer cells crosstalk. Gender-related immune system composition may affect immune response, chemotherapy and immunotherapy efficacy, and risk of immune-related adverse events. This study found that high monocyte-to-lymphocyte ratio (MLR) is an unfavorable independent prognostic factor in males and females with metastatic colorectal cancer.
Simple Summary In recent years, mounting evidence has recognized the key role of the crosstalk between immune system and cancer cells. Several data have suggested that gender-related immune system composition could impact on both immune response, efficacy of chemotherapy, and immunotherapy and risk of immune-related adverse events. Based on these premises, the present study aimed to evaluate the role of monocyte-to-lymphocyte ratio (MLR), representing the immune suppression cells, in the first place, and immune activating cells, in the second. The analysis, conducted on 490 patients with metastatic colorectal cancer, showed that males and females have a different profile of immune response. Of note, high MLR, both in males and females, is an unfavorable independent prognostic factor. Background: Emerging data suggest that gender-related immune system composition affects both immune response and efficacy of immunotherapy in cancer patients (pts). This study aimed to investigate the sex-related prognostic role of MLR in metastatic colorectal cancer (mCRC) pts. Methods: We analyzed a retrospective consecutive cohort of 490 mCRC patients treated from 2009 to 2018 at the Oncology Departments of Aviano and Pordenone (training set) and Udine (validation set), Italy. The prognostic impact of MLR on overall survival (OS) was evaluated with uni- and multivariable Cox regression models. The best cut-off value to predict survival was defined through ROC analyses. Results: Overall, we identified 288 males (59%) and 202 females (41%); 161 patients (33%) had a right-sided, 202 (42%) a left-sided primary, and 122 (25%) a rectal tumor. Interestingly, gender was associated with MLR (p = 0.004) and sidedness (p = 0.006). The obtained cut-off value for MLR in females and males was 0.27 and 0.49, respectively. According to univariate analysis of the training set, MLR (HR 9.07, p <= 0.001), MLR > 0.27 in females (HR 1.95, p = 0.003), and MLR > 0.49 in males (HR 2.65, p = 0.010) were associated with poorer OS, which was also confirmed in the validation set. In multivariate analysis, MLR > 0.27 in females (HR 2.77, p = 0.002), MLR > 0.49 in males (HR 5.39, p <= 0.001), BRAF mutation (HR 3.38, p <= 0.001), and peritoneal metastases (HR 2.50, p = 0.003) were still independently associated with worse OS. Conclusions: Males and females have a different immune response. Our study showed that high MLR, both in males and females, is an unfavorable Independent prognostic factor. Further prospective studies are needed to confirm these data.

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