ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026
ERG expression is not predictive of outcome in patients with intermediate- and high-risk localized prostate cancer treated with combined androgen blockade and radiotherapy.
Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- Towards implementation of precision medicine biomarkers in early detection and prognostication of prostate cancer.Cancer metastasis reviews · 2026Review
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9 authors.
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Abstract
backgroundTMPRSS2:ERG gene fusion is a common alteration in prostate cancer and is regulated by androgen receptor signaling. We investigated whether ERG expression, assessed by immunohistochemistry (IHC), predicts clinical outcomes in patients with intermediate- or high-risk localized prostate cancer treated with combined androgen blockade (CAB) and radiotherapy (RT). MATERIAL AND
methodsWe retrospectively analyzed patients treated with CAB (GnRH agonists + antiandrogens) and normofractionated RT. ERG expression was evaluated using IHC. Overall survival (OS) was estimated with Kaplan-Meier curves. Prostate cancer-specific survival (PCSS), biochemical recurrence-free survival (bRFS), and progression-free survival (PFS) were assessed using competing risk models.
resultsA total of 86 patients were included (median follow-up 173 months). ERG expression was positive in 69%. No significant differences were observed in OS (HR 1.03; p = 0.92), PCSS (HR 0.44; p = 0.22), bRFS (HR 0.51; p = 0.19), or PFS (HR 0.56; p = 0.30) between ERG-positive and ERG-negative groups.
conclusionsERG expression assessed by IHC was not associated with clinical outcomes in this population. These results do not support its role as a predictive biomarker in patients treated with CAB and RT. Further prospective studies are warranted to confirm these findings.
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