Le Guévelou Jennifer, Mathieu Romain, Peyrottes Arthur, Dariane Charles, Murthy Vedang, Nicosia Luca, Jacquet-Kammerer Solène-Florence, Zilli Thomas, Peyronnet Benoit, Chargari Cyrus, Anract Julien, Sargos Paul, Supiot Stéphane
Department of Research Laboratoire du Traitement de l'image et du Signal, Université de Rennes, Rennes, France.
Department of Research, Centre Eugène Marquis, Avenue de la bataille Flandres Dunkerque, Rennes, 35000, France.
World J Urol. 2025 Jun 7;43(1):361. doi: 10.1007/s00345-025-05730-1.
This narrative review aims to examine the biological mechanisms of toxicity in patients with benign prostatic hyperplasia (BPH) receiving prostate cancer (PCa) external beam radiotherapy (RT), as well as possible strategies to prevent genitourinary (GU) toxicity following PCa RT in men with BPH, through the adaptation of both medical, surgical, and irradiation strategies.
A broad literature search was performed in November 2024 in the PubMed database with the terms "prostate cancer", "prostate epithelial cells", "prostate stromal cells", "radiation therapy", "lower urinary tract symptoms", "stereotactic body radiotherapy", "transurethral resection of the prostate", "enucleation".
RT affects several pathophysiological contributors to LUTS, such as urothelial dysfunction, prostatic inflammation and bladder fibrosis. While preexisting LUTS appear to be a risk factor to develop severe GU toxicity following PCa RT, the development of strategies reducing the incidental dose delivered to urinary structures appears to be particularly relevant. Urethra-sparing strategies holds the potential to reduce the onset of severe GU toxicity following PCa RT. The relationship between the highest doses delivered to the bladder and the onset of severe GU toxicity highlight the pivotal role of image-guided radiotherapy (IGRT) for PCa RT. Aggressive margin reduction from 4 mm to 2 mm demonstrated its ability to halve the risk to develop severe GU toxicity 2 years following SBRT. De-escalation in either dose or target volume represent appealing strategies, currently assessed within prospective trials. Both assessment and optimization of urinary function through medical or surgical approaches is mandatory before RT.
Strategies designed to reduce the planned and delivered dose to functional structures hold promise for the limitation of urinary toxicity after PCa RT. Further efforts should be made to adapt surgical and irradiation techniques in men with BPH, with the development of studies dedicated to this population of patients.
本叙述性综述旨在探讨接受前列腺癌(PCa)外照射放疗(RT)的良性前列腺增生(BPH)患者的毒性生物学机制,以及通过调整医学、手术和放疗策略来预防BPH男性患者PCa放疗后泌尿生殖系统(GU)毒性的可能策略。
2024年11月在PubMed数据库中进行了广泛的文献检索,检索词为“前列腺癌”“前列腺上皮细胞”“前列腺基质细胞”“放射治疗”“下尿路症状”“立体定向体部放疗”“经尿道前列腺切除术”“剜除术”。
放疗会影响导致下尿路症状的多种病理生理因素,如尿路上皮功能障碍、前列腺炎症和膀胱纤维化。虽然既往存在的下尿路症状似乎是PCa放疗后发生严重GU毒性的危险因素,但制定减少传递至泌尿结构的附带剂量的策略似乎尤为重要。保留尿道的策略有可能降低PCa放疗后严重GU毒性的发生。传递至膀胱的最高剂量与严重GU毒性发生之间的关系凸显了图像引导放疗(IGRT)在PCa放疗中的关键作用。将切缘从4毫米积极减少至2毫米显示出其能够将立体定向体部放疗(SBRT)后2年发生严重GU毒性的风险减半。剂量或靶体积的降级是有吸引力的策略,目前正在前瞻性试验中进行评估。在放疗前必须通过医学或手术方法对泌尿功能进行评估和优化。
旨在减少对功能结构的计划和传递剂量的策略有望限制PCa放疗后的泌尿毒性。应进一步努力调整BPH男性患者的手术和放疗技术,并开展针对该患者群体的研究。