Unlocking the Potential of Circulating miRNAs in the Breast Cancer Neoadjuvant Setting: A Systematic Review and Meta-Analysis

Author:

Tiberio Paola1ORCID,Gaudio Mariangela12,Belloni Silvia3ORCID,Pindilli Sebastiano2,Benvenuti Chiara12ORCID,Jacobs Flavia12ORCID,Saltalamacchia Giuseppe1,Zambelli Alberto12ORCID,Santoro Armando12ORCID,De Sanctis Rita12ORCID

Affiliation:

1. Medical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy

2. Department of Biomedical Sciences, Humanitas University, 20072 Pieve Emanuele, Italy

3. Educational and Research Unit, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy

Abstract

The potential role of circulating microRNAs (miRNAs) as biomarkers in breast cancer (BC) management has been widely reported. However, the numerous discrepancies between studies in this regard hinders the implementation of circulating miRNAs in routine clinical practice. In the context of BC patients undergoing neoadjuvant chemotherapy (NAC), the possibility of predicting NAC response may lead to prognostic improvements by individualizing post-neoadjuvant therapy. In this context, the present meta-analysis aims to clarify circulating miRNAs’ predictive role with respect to NAC response among BC patients. We conducted a comprehensive literature search on five medical databases until 16 February 2023. We pooled the effect sizes of each study by applying a random-effects model. Cochran’s Q test (p-level of significance set at 0.05) scores and I2 values were assessed to determine between-study heterogeneity. The PROBAST (Prediction Model Risk of Bias Assessment Tool) tool was used to evaluate the selected studies’ risk of bias. Overall, our findings support the hypothesis that circulating miRNAs, specifically miR-21-5p and miR-155-5p, may act as predictive biomarkers in the neoadjuvant setting among BC patients. However, due to the limited number of studies included in this meta-analysis and the high degrees of clinical and statistical heterogeneity, further research is required to confirm the predictive power of circulating miR-21-5p and miR-155-5p.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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