Henriquez Ivan, Malave Barbara, Benitez-Gabella Gemma, Parada David, Canela Marta, García-Pablo Raquel, Benavides Rocio, Rius Francesc, Arenas Meritxell
Department of Radiation Oncology, Hospital Universitari Sant Joan, Reus, Spain.
Institut d'Investigació Sanitària Pere I Virgili (IISPV), Reus, Spain.
Clin Transl Oncol. 2025 Aug 11. doi: 10.1007/s12094-025-04016-7.
TMPRSS2: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).
We 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.
A 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.
ERG 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.
TMPRSS2:ERG基因融合是前列腺癌中一种常见的改变,受雄激素受体信号通路调控。我们研究了通过免疫组织化学(IHC)评估的ERG表达是否能预测接受联合雄激素阻断(CAB)和放疗(RT)的中高危局限性前列腺癌患者的临床结局。
我们回顾性分析了接受CAB(促性腺激素释放激素激动剂+抗雄激素)和常规分割放疗的患者。使用IHC评估ERG表达。采用Kaplan-Meier曲线估计总生存期(OS)。使用竞争风险模型评估前列腺癌特异性生存期(PCSS)、无生化复发生存期(bRFS)和无进展生存期(PFS)。
共纳入86例患者(中位随访173个月)。ERG表达阳性率为69%。ERG阳性组和ERG阴性组在OS(风险比1.03;p=0.92)、PCSS(风险比0.44;p=0.22)、bRFS(风险比0.51;p=0.19)或PFS(风险比0.56;p=0.30)方面未观察到显著差异。
在该人群中,通过IHC评估的ERG表达与临床结局无关。这些结果不支持其作为接受CAB和RT治疗患者的预测生物标志物的作用。需要进一步的前瞻性研究来证实这些发现。