# CD5 Immunoreactivity Is Associated With Longer Overall Survival in Thymic Carcinoma: A Brief Report

**Authors:** Julia R. Naso, Sarah M. Jenkins, Julie A. Vrana, Justin W. Koepplin, Kenneth R. Olivier, Stephen D. Cassivi, Julian R. Molina, Anja C. Roden

PMC · DOI: 10.1016/j.jtocrr.2025.100803 · JTO Clinical and Research Reports · 2025-02-11

## TL;DR

CD5 staining in thymic carcinoma is linked to longer survival, suggesting it could be a useful prognostic marker.

## Contribution

CD5 immunoreactivity is identified as a novel prognostic marker for thymic carcinoma.

## Key findings

- CD5-positive thymic carcinoma cases had significantly longer overall survival compared to CD5-negative cases.
- CD5 staining remained a significant predictor of survival after adjusting for treatment and tumor stage.
- Other markers like CD117, EZH2, and BAP1 did not show significant prognostic value.

## Abstract

Thymic carcinomas are a heterogeneous group of potentially aggressive malignancies. We aimed to determine the prognostic significance of CD5, CD117, EZH2, POU2F3, BAP1, and MTAP immunohistochemical staining in thymic carcinomas. Immunohistochemistry was performed on 36 thymic carcinomas from patients with retrospectively collected survival data. Thirteen cases (36%) had CD5 staining in 50% or more tumor cells, considered positive staining. Positive CD5 immunohistochemical staining was significantly associated with longer overall survival (hazard ratio = 0.18, 95% confidence interval: 0.03–0.63, p = 0.005). Three-year overall survival was 48% (95% confidence interval: 27%–70%) for CD5 negative cases, and 100% for CD5 positive cases. Positive CD5 staining remained significantly associated with overall survival after adjusting for neoadjuvant treatment, M-stage, or incomplete resection (p = 0.01). The remaining immunohistochemical markers were not significantly associated with overall survival. Our study supports the notion that CD5 immunohistochemistry may have utility as a novel prognostic marker for thymic carcinoma.

## Linked entities

- **Genes:** CD5 (CD5 molecule) [NCBI Gene 921], KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815], EZH2 (enhancer of zeste 2 polycomb repressive complex 2 subunit) [NCBI Gene 2146], POU2F3 (POU class 2 homeobox 3) [NCBI Gene 25833], BAP1 (BRCA1 associated deubiquitinase 1) [NCBI Gene 8314], MTAP (methylthioadenosine phosphorylase) [NCBI Gene 4507]
- **Diseases:** thymic carcinoma (MONDO:0006451)

## Full-text entities

- **Genes:** BAP1 (BRCA1 associated deubiquitinase 1) [NCBI Gene 8314] {aka HUCEP-13, KURIS, TPDS1, UBM2, UCHL2, UVM2}, EZH2 (enhancer of zeste 2 polycomb repressive complex 2 subunit) [NCBI Gene 2146] {aka ENX-1, ENX1, EZH2b, KMT6, KMT6A, WVS}, CD5 (CD5 molecule) [NCBI Gene 921] {aka LEU1, T1}, POU2F3 (POU class 2 homeobox 3) [NCBI Gene 25833] {aka Epoc-1, OCT-11, OCT11, OTF-11, PLA-1, PLA1}, MTAP (methylthioadenosine phosphorylase) [NCBI Gene 4507] {aka BDMF, DMSFH, DMSMFH, HEL-249, LGMBF, MSAP}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}
- **Diseases:** Thymic Carcinoma (MESH:D013945), malignancies (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12000739/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12000739/full.md

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Source: https://tomesphere.com/paper/PMC12000739