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CD11c and IRF8 cell densities in rectal cancer biopsies predict outcomes of neoadjuvant chemoradiotherapy. | LitMetric

AI Article Synopsis

  • About 20% of patients with locally advanced rectal cancer achieve complete tumor regression after preoperative chemoradiotherapy (CRT), but there are currently no reliable biomarkers for predicting this.
  • A study analyzing biopsies from 16 LARC patients showed that those with better tumor regression had higher levels of certain immune cells (pan-T cells and IRF8HLA-DR cells) before receiving CRT.
  • Higher densities of IRF8HLA-DR cells were linked to better survival rates (83% at 5 years), while lower levels of CD11c myeloid cells predicted longer disease-free survival, indicating these could serve as potential biomarkers for treatment outcomes.

Article Abstract

Approximately 20% of locally advanced rectal cancer (LARC) patients treated preoperatively with chemoradiotherapy (CRT) achieve pathologically confirmed complete regression. However, there are no clinically implemented biomarkers measurable in biopsies that are predictive of tumor regression. Here, we conducted multiplexed immunophenotyping of rectal cancer diagnostic biopsies from 16 LARC patients treated preoperatively with CRT. We identified that patients with greater tumor regression had higher tumor infiltration of pan-T cells and IRF8HLA-DR cells prior to CRT. High IRF8HLA-DR cell density was further associated with prolonged disease-specific survival with 83% survival at 5 y compared to 28% in patients with low infiltration. Contrastingly, low CD11c myeloid cell infiltration prior to CRT was a putative biomarker associated with longer 3- and 5-y disease-free survival. The results demonstrate the potential use of rectal cancer diagnostic biopsies to measure IRF8 HLA-DR cells as predictors of CRT-induced tumor regression and CD11c myeloid cells as predictors of LARC patient survival.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361136PMC
http://dx.doi.org/10.1080/2162402X.2023.2238506DOI Listing

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