Zacchi Francesca, Carles Joan, Gonzalez Macarena, Maldonado Xavier, Perez-Lopez Raquel, Semidey Maria Eugenia, Mateo Joaquin
Section of Innovation Biomedicine-Oncology Area, Department of Engineering for Innovation Medicine (DIMI), University of Verona and University and Hospital Trust (AOUI) of Verona, Verona, Italy.
Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
Front Oncol. 2024 Mar 8;14:1331643. doi: 10.3389/fonc.2024.1331643. eCollection 2024.
Despite the development of new therapies in the last few years, metastatic prostate cancer (PCa) is still a lethal disease. Radium-223 (Ra-223) is approved for patients with advanced castration-resistant prostate cancer (CRPC) with bone metastases and no visceral disease. However, patients' outcomes are heterogenous, and there is lack of validated predictive biomarkers of response, while biomarkers for early identification of patients who benefit from treatment are limited. This case report describes a remarkable and durable response to Ra-223 in a CRPC patient with bone metastases who had rapidly progressed to many previous therapies; this response is now lasting for 5 years even after having stopped backbone androgen deprivation therapy (ADT). Here, we present the clinical course of this exceptional response, as well as comprehensive genomic and histopathology analyses on sequential biopsies acquired before and after therapy. Additionally, we review current knowledge on predictive and response biomarkers to Ra-223 in metastatic prostate cancer.
尽管在过去几年中出现了新的治疗方法,但转移性前列腺癌(PCa)仍然是一种致命疾病。镭-223(Ra-223)已被批准用于治疗有骨转移且无内脏疾病的晚期去势抵抗性前列腺癌(CRPC)患者。然而,患者的治疗结果存在异质性,缺乏经过验证的反应预测生物标志物,而用于早期识别从治疗中获益患者的生物标志物也很有限。本病例报告描述了一名有骨转移的CRPC患者对Ra-223产生显著且持久的反应,该患者此前对多种治疗均迅速进展;即使在停止脊柱雄激素剥夺治疗(ADT)后,这种反应目前仍持续了5年。在此,我们展示了这一特殊反应的临床过程,以及对治疗前后连续活检样本进行的全面基因组和组织病理学分析。此外,我们还综述了目前关于转移性前列腺癌中Ra-223预测和反应生物标志物的知识。