Department of Urology, University Hospitals Leuven, Leuven, Belgium.
Department of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.
World J Urol. 2021 Sep;39(9):3177-3185. doi: 10.1007/s00345-021-03611-x. Epub 2021 Feb 12.
There is an urgent need to develop novel treatment strategies in patients with unfavorable intermediate- and high-risk localized prostate cancer (PCa) to optimize the outcome of these patients. Androgen receptor signaling inhibitors (ARSI) have demonstrated a survival benefit in metastatic hormonesensitive and castration-resistant PCa. A similar benefit might be expected in the localized setting.
To perform a systematic review about the role of neoadjuvant ARSI in unfavorable intermediate and high-risk localized PCa.
We performed a systematic review of the following databases: MEDLINE (PubMed), EMBASE, Cochrane Library and Web of Science. Publications of ASCO were consulted to identify meeting abstract with early results of ongoing trials. This systematic review was performed and reported in accordance with the PRISMA guidelines.
Pathological complete response (pCR) following neoadjuvant ARSI treatment was observed in 4%-13% of the patients. Minimal residual disease response ranged from 36% to 73.9% when defined as residual cancer burden < 0.25 cm at final pathology and from 8% to 20% when defined as the diameter of the remaining tumor < 5 mm. Despite intense neoadjuvant ARSI treatment, residual pT3 disease was observed in 48%-76% of the patients. In contrast, positive surgical margins (PSM) were present in only 5%-22%. Only one trial reported BCR following neoadjuvant ARSI therapy (44% BCR at a median follow-up of 4 years).
Despite intense neoadjuvant ARSI therapy, pCR is rarely attained and high proportions of pT3 disease are still observed at final pathology. In contrast, promising results are obtained in terms of PSMs. Long-term survival outcomes are eagerly awaited.
目前迫切需要为预后不佳的中高危局限性前列腺癌(PCa)患者开发新的治疗策略,以优化这些患者的治疗效果。雄激素受体信号抑制剂(ARSI)已在转移性激素敏感型和去势抵抗性 PCa 中显示出生存获益。在局限性疾病中可能也会有类似的获益。
对新辅助 ARSI 在预后不佳的中高危局限性 PCa 中的作用进行系统评价。
我们对以下数据库进行了系统评价:MEDLINE(PubMed)、EMBASE、Cochrane 图书馆和 Web of Science。查阅 ASCO 会议出版物以确定正在进行的试验的早期结果的会议摘要。本系统评价按照 PRISMA 指南进行并报告。
新辅助 ARSI 治疗后观察到病理完全缓解(pCR)的患者比例为 4%-13%。当定义为最终病理学上残留的癌症负担 < 0.25 cm 时,微小残留疾病反应率为 36%-73.9%,当定义为剩余肿瘤的直径 < 5 mm 时,反应率为 8%-20%。尽管进行了强烈的新辅助 ARSI 治疗,但仍有 48%-76%的患者存在残留的 pT3 疾病。相比之下,仅 5%-22%的患者存在阳性切缘(PSM)。只有一项试验报告了新辅助 ARSI 治疗后的无生化复发生存(BCR)(中位随访 4 年后的 BCR 为 44%)。
尽管进行了强烈的新辅助 ARSI 治疗,但很少能达到 pCR,在最终的病理中仍观察到很大比例的 pT3 疾病。相比之下,PSM 的结果令人鼓舞。迫切需要等待长期生存结果。