Clinicopathologic Characterization of Prostatic Cancer in Dogs.
Demitria M VasilatisParamita M GhoshPublished in: Animals : an open access journal from MDPI (2024)
Clinicopathologic data in dogs with prostate cancer (PCa) may aid in the differentiation between tumor types and subsequent treatment decisions; however, these data are often unreported. Demographic, clinicopathologic, cytologic, histologic and survival data from dogs with primary prostatic adenocarcinoma (PRAD) ( n = 56) and primary prostatic transitional cell carcinoma (P-TCC) ( n = 74) were acquired from a tertiary veterinary teaching hospital from 1992 to 2022. Red blood cell distribution width (RDW) to albumin ratio (RAR) was evaluated for diagnostic utility in differentiating between PRAD and P-TCC. Sections from PRAD tumors ( n = 50) were stained for androgen receptor (AR) expression, and laboratory data were compared between AR positive (AR+) and AR negative (AR-) groups. RDW was increased in PRAD, while albumin was decreased ( p < 0.05). P-TCC was associated with Melamed-Wolinska bodies (MWB) and necrosis on cytology ( p < 0.05). RAR had acceptable diagnostic utility in the differentiation of PCa tumors (AUC = 0.7; p < 0.05). Survival rates and metastases were equivocal. AR+ and AR- PRAD tumors did not differ in clinicopathologic data or survival ( p > 0.05). In conclusion, hypoalbuminemia was significantly associated with PRAD and decreased survival, while MWB and necrosis were significantly associated with P-TCC on cytology. These clinicopathologic data may help clinicians differentiate between these tumors ante mortem to guide appropriate treatment and intervention.
Keyphrases
- prostate cancer
- electronic health record
- big data
- radical prostatectomy
- randomized controlled trial
- squamous cell carcinoma
- poor prognosis
- magnetic resonance
- machine learning
- palliative care
- radiation therapy
- data analysis
- free survival
- benign prostatic hyperplasia
- deep learning
- combination therapy
- long non coding rna
- contrast enhanced
- childhood cancer