A computational imaging-based signature of immune-cell infiltration in and around a tumor could predict patients’ responses to treatment with anti–programmed cell death protein 1/programmed death-ligand 1 (PD-1/PD-L1) immunotherapies, according to data from a study presented by Sun et al at the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, held October 26–30 in Philadelphia (Abstract A051).
“Immunotherapy, a recent modality of treatment in oncology, has profoundly changed the management of multiple cancers,” said Roger Sun, MD, doctoral candidate under Eric Deutsch, MD, PhD and Charles Ferté, MD, PhD, at the laboratory INSERM U1030 at Gustave Roussy in Villejuif, France. “However, most patients do not respond to this type of treatment. That is why we need to identify biomarkers that allow identification of patients who are most likely to respond to immunotherapy.”
Studies using biopsy samples of tumor tissues have shown that the extent of immune-cell infiltration into tumors correlates with patients’ treatment responses. But because cancers are heterogeneous, biopsies only reflect the local aspect of the tumor, Dr. Sun explained.
“Medical computational imaging, also known as radiomics, is a new field of research that aims to translate standard imaging like computed tomography (CT), magnetic resonance imaging (MRI), or positron emission tomography (PET), into objective data, and use them as biomarkers,” he said. “This kind of biomarker is noninvasive, cost-effective, can be applied on all tumor localizations, and can be repeated through the course of disease.”
Dr. Sun and colleagues used radiomics to estimate the abundance of immune-cell infiltration in tumors and assess their potential to predict response to anti–PD-1/PD-L1 therapies. The team developed a radiomics-based model of tumor-infiltrating effector T cells (Teff) using data from the head and neck, liver, lung, and bladder cohorts of The Cancer Imaging Archive. They extracted 80 radiomics features and built a radiomics score that could predict the abundance of tumor-infiltrating Teff estimated using RNAseq data.
To validate the radiomics score they developed, they first tested it on the CT scans of a cohort of 134 patients for whom RNAseq data were available. They found that the radiomics score of Teff correlated with the genomics-based score of Teff.
They then tested the radiomics score on the baseline CT scans of a second cohort of 137 patients enrolled in anti–PD-1/PD-L1 phase I trials for whom survival data were available. The researchers applied the radiomics score on data from the entire cohort and used the median value to separate the cohort into two groups: those whose scores were above the median, and those whose scores were below the median. They found that at any given time, patients with a high score were 1.5 times more likely to be alive compared with those who had a low score.
“We are very encouraged by our findings that a signature based on imaging features could reflect the tumor immune infiltration and could predict response to immunotherapy,” Dr. Sun said. “These results are preliminary, and we need further clinical studies to validate them. Ultimately, this score may be useful to drive immunotherapy trials allowing stratification of patients.”
Dr. Sun added, “Enhancing data sharing and facilitating patient recruitment in clinical trials arenecessary. With further improvements to this field with multi-disciplinary working groups, radiomics can become a reliable part of the decision support system in oncology.”
A limitation of the study is that the scores were validated using cohorts of limited size and medical images from different centers with heterogeneous acquisition protocols.
“We still need to validate [the study] using large cohorts of patients and standardized imaging protocols,” Dr. Sun noted.
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