AI Article Synopsis

  • Recent research highlights the connection between patients' eating habits and their impact on breast cancer management and inflammation.*
  • The study involved 82 women with breast cancer undergoing neoadjuvant chemotherapy, revealing correlations between inflammatory dietary habits and bowel FDG uptake.*
  • Results indicated that healthier diets (rich in fruits and vegetables) were associated with better treatment outcomes, suggesting that PET scans could help identify patients with poor dietary habits.*

Article Abstract

Recently, the impact of patients’ eating habits on both breast cancer (BC) management and inflammation have been proven. Here, we investigated whether inflammatory habits could correlate with baseline bowel [18]F-fluorodeoxyglucose (FDG) uptake and the latter, in turn, with pathological Complete Response (pCR) to neoadjuvant chemotherapy (NAC). We included stage I−III BC undergoing standard NAC at IRCCS Humanitas Research Hospital, Italy. Patients fulfilled a survey concerning eating/lifestyle behaviors and performed a staging [18]F-FDG positrone emission tomography/computed tomography (PET/CT). In the absence of data on the effects of individual foods, we aggregated drink and food intake for their known inflammatory properties. Data were recorded for 82 women (median age, 48). We found positive correlations between colon mean standardized uptake value (SUVmean) and pro-inflammatory drinks (alcohol and spirits; r = +0.33, p < 0.01) and foods (red and cured meats; r = +0.25, p = 0.04), and a significant negative correlation between rectum SUVmean and anti-inflammatory foods (fruits and vegetables; r = −0.23, p = 0.04). Furthermore, colon SUVmean was significantly lower in patients with pCR compared to non pCR (p = 0.02). Our study showed, for the first time, that patients’ eating habits affected bowel [18]F-FDG uptake and that colon SUVmean correlated with pCR, suggesting that PET scan could be an instrument for identifying patients presenting unhealthy behaviors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824388PMC
http://dx.doi.org/10.3390/nu15010211DOI Listing

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