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Original Research

CD3-CD8 immune score associated with a clinical score stratifies PDAC prognosis regardless of adjuvant or neoadjuvant chemotherapy

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Article: 2294563 | Received 21 Jun 2023, Accepted 08 Dec 2023, Published online: 21 Dec 2023
 

ABSTRACT

Stratification of the prognosis of pancreatic cancer (PDAC) patients treated by surgery is based solely on clinical variables, such as tumor stage and node status. The development of biomarkers of relapse is needed, especially to drive administration of adjuvant therapy in this at-risk population. Our study evaluates the prognostic performance of a CD3- and CD8-based immune score. CD3, CD8 and Foxp3 expression were evaluated on whole slides in two retrospective PDAC cohorts totaling 334 patients. For this study, we developed an immune score to estimate CD3 and CD8 infiltration in both tumor core and invasive margin using computer-guided analysis with QuPath software. Variables were combined in a dichotomous immune score. The association between immune and clinical scores, and both PFS and OS was investigated. We observed that a dichotomous immune score predicts both PFS and OS of localized PDAC. By univariate and multivariate analysis, immune score, tumor grade, adjuvant therapy, lymph node status, and adjuvant chemotherapy administration were associated with PFS and OS. We subsequently associated the PDAC immune score and clinical variables in a combined score. This combined score predicted patient outcomes independently of adjuvant or neoadjuvant treatment, and improved patient prognostic prediction compared to clinical variables or immune score alone.

Acknowledgments

We warmly thank the Pathology department of the University Hospital of Besancon. We also thank Florence Schaffner at the “Canceropole Grand-Est” and the Pathology Department of teaching hospital of Strasbourg, especially Dr. Gerlinde Averous.

We warmly thank Dr. Fiona Caulfield for her thorough English proofreading and her relevant comments.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

Date are available on reasonable request.

Supplementary material

Supplemental data for this article can be accessed online at https://doi.org/10.1080/2162402X.2023.2294563.

Additional information

Funding

The work was supported by the Canceropole Est [Cancéropôle-Est-Valentin DERANGERE’2O2O].