This retrospective cross-sectional analysis used SEER 17 registry data from 2000 to 2022 to examine predictors of metastasis at diagnosis in small cell carcinoma of the prostate (SCCP). The study included 541 patients with microscopically confirmed SCCP. No specific intervention or comparator was reported, as the analysis focused on clinical and demographic factors associated with metastatic presentation.
The main finding was that 71.7% of patients presented with metastatic disease at diagnosis. The most common metastatic sites were bone (35.9%), liver (22.6%), lung (14.0%), and brain (3.9%). A higher percentage of positive biopsy cores was independently associated with increased odds of metastatic disease. Younger age was associated with higher odds of brain metastasis. Lower household income and residence in metropolitan counties were associated with an increased likelihood of metastatic disease, particularly bone metastases. Brain metastasis was strongly associated with concurrent liver and lung metastases.
Safety and tolerability data were not reported. Key limitations stem from the study's observational, cross-sectional design using registry data, which can only show associations, not causation. The findings may not be generalizable beyond the SEER population, and the analysis was limited to metastasis at diagnosis, not subsequent clinical outcomes. Funding and conflicts of interest were not reported. For practice, this analysis highlights the aggressive nature of SCCP and identifies patient factors associated with advanced presentation, which may inform diagnostic suspicion and staging intensity, but the evidence is associative and descriptive.
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ObjectiveTo identify clinical and demographic factors associated with the presence and distribution of metastatic disease at diagnosis in patients with small cell carcinoma of the prostate (SCCP).IntroductionSmall cell carcinoma of the prostate is a rare but highly aggressive subtype of prostate cancer, frequently presenting with distant metastases and poor survival outcomes. Despite its severity, population-level data examining predictors of metastatic disease at presentation remain limited. Understanding these factors may improve early detection and risk stratification.MethodsA retrospective, cross-sectional analysis was conducted using the SEER 17 registries (2000–2022). Patients with microscopically confirmed SCCP were identified using ICD-O-3 histology code 8041/3 and primary site code C61.9. Demographic, clinical, and metastatic variables were extracted. Univariate and multivariable logistic regression models were used to evaluate predictors of overall and site-specific metastases. Variables meeting a univariate threshold of p < 0.25 were included in multivariable models. Model assumptions were assessed using VIF, Tolerance, and Box–Tidwell tests.ResultsA total of 541 patients were identified, of whom 71.7% presented with metastatic disease. The most common metastatic sites were bone (35.9%), liver (22.6%), lung (14.0%), and brain (3.9%). On multivariate analysis, a higher percentage of positive biopsy cores was independently associated with increased odds of metastatic disease. Younger age was associated with higher odds of brain metastasis. Lower household income and residence in metropolitan counties were associated with increased likelihood of metastatic disease, particularly bone metastases. Brain metastasis was strongly associated with concurrent liver and lung metastases, suggesting a pattern of widespread systemic involvement.Conclusions/discussionPatients with SCCP frequently present with metastatic disease, and several clinical and socioeconomic factors influence metastatic risk. Higher tumor burden, lower income, metropolitan residence, and younger age were associated with a greater likelihood of metastasis at diagnosis. These findings highlight the importance of early diagnostic evaluation in high-risk groups and provide a foundation for improved prognostication and targeted care strategies in this rare and aggressive malignancy.