Radiosensitivity and immune cell infiltration signature for breast cancer
Byung-Hee Kang,
Korea Republic of
OC-0264
Abstract
Radiosensitivity and immune cell infiltration signature for breast cancer
Authors: Byung-Hee Kang1, Bum Sup Jang1, In Ah Kim1
1Seoul National University, College of Medicine, Radiation Oncology, Seoul, Korea Republic of
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Purpose or Objective
There
are growing evidences that tumor radiosensitivity is associated with immune
activation in solid tumors. However, previous studies have not examined the relationship
between patterns of immune infiltration and radiation response according to
diverse molecular subtypes of breast cancer. This study evaluated radiosensitivity
and immune infiltration signature to define a group of patients would benefit
most from radiation therapy.
Material and Methods
We
performed integrative analyses of the clinical, genomic, transcriptomic, and
immunogenomic data to characterize the molecular features associated with
radiosensitivity. We analyzed 1,903 data sets of METABRIC Study cohort using the
radiosensitivity index (RSI), CIBERSORT and xCell, gene expression
deconvolution algorithm which estimates the immune composition of tumor samples.
According to RSI cut-point (0.3745), the patients were grouped into radiosensitive
(RS, RSI-low tumors, n=1,082) versus radioresistant (RR, RSI-high tumors, n=821).
Next, patients were divided into two groups according to immune and stromal
scores, immune infiltrated (IF, n= 650) and immune excluded (IE, n=1253)
subgroups.
Results
RS group showed
improved prognosis compared to RR group, and IF group had better survival than
IE group, however, these tendencies were only significant in ER-negative patients.
Radiosensitivity was significantly associated with the activation of antitumor
immunity. In contrast, radio-resistance was associated with metastatic
properties, such as epithelial-mesenchymal transition and angiogenesis. Differentially
expressed gene analysis revealed that ER signaling pathway is correlated with
suppression of antitumor immunity. Higher ER was associated with a higher
fraction of M2 macrophage and lower PD-1 expression. Integration of immune
signature and radiosensitivity index further stratified patients into four subgroups.
In ER-negative disease, IF and RS groups were associated with the best
prognosis, whereas in ER-positive disease, immune signature and radiation response
have no prognostic significance.
On multivariable Cox regression, both integrated immune infiltration and radiosensitivity
signature was independent predictors of relapse-free survival (HR 1.12, 95% CI 1.06-1.19,
p < 0.001) and overall survival (HR 1.06, 95% CI 1.01-1.11, p = 0.028).
Conclusion
Taken together,
this results suggested that tumor radiosensitivity was associated with
activation of antitumor immunity and led to better prognosis particularly in ER
negative group.