Platelets, Chromogranin A, and C-Reactive Protein Predict Therapy Failure of Metastatic Hormone-Sensitive Prostate Cancer while miR-375 Outperforms Prostate-Specific Antigen in Stratifying Castration-Resistant Prostate Cancer
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
40139458
DOI
10.1016/j.jmoldx.2025.02.006
PII: S1525-1578(25)00063-7
Knihovny.cz E-resources
- MeSH
- Receptors, Androgen genetics MeSH
- C-Reactive Protein * metabolism MeSH
- Chromogranin A * blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Neoplasm Metastasis MeSH
- MicroRNAs * genetics blood MeSH
- Biomarkers, Tumor blood MeSH
- Prostatic Neoplasms, Castration-Resistant * blood genetics pathology drug therapy diagnosis MeSH
- Treatment Failure MeSH
- Prognosis MeSH
- Prostate-Specific Antigen * blood MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Blood Platelets * metabolism MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Receptors, Androgen MeSH
- C-Reactive Protein * MeSH
- Chromogranin A * MeSH
- MicroRNAs * MeSH
- MIRN375 microRNA, human MeSH Browser
- Biomarkers, Tumor MeSH
- Prostate-Specific Antigen * MeSH
Androgen deprivation therapy has long been the first-line treatment for hormone-sensitive prostate cancer (HSPC). After progression to castration-resistant prostate cancer (CRPC), androgen receptor pathway inhibitors (ARPIs) are commonly used. Recently, combined therapy with androgen deprivation and an ARPI has been recommended for metastatic HSPC patients. Novel markers are urgently needed for monitoring this disease and for making therapeutic decisions. Plasma samples were collected from 140 patients with either metastatic HSPC (n = 72) or CRPC (n = 68) before the start of ARPI therapy. Digital PCR was used to assess AR gene amplification, while the expression levels of miR-375 were measured by quantitative PCR. Sixteen other clinical markers were also evaluated, including prostate-specific antigen (PSA), chromogranin A (CGA), alkaline phosphatase (ALP), lactate dehydrogenase (LDH), C-reactive protein (CRP), lymphocyte-to-monocyte ratio, and platelet count. A multivariate analysis, adjusted for age and metastatic dissemination, identified miR-375 expression and lymphocyte-to-monocyte ratio to be the independent negative predictors of ARPI therapy failure in CRPC patients. Regarding the HSPC patients, this article reports the primary finding of the independent negative predictive value of platelet count, CRP, and CGA for the failure of combined androgen deprivation therapy and ARPI.
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