临床病理因素和AR-LBD突变在早期和晚期割抵抗性前列腺癌中
Monu Deswal1, Durgavati Yadav1, Vinay Kumar2
1Department of Urology, All India Institute of Medical Sciences, New Delhi, India.
Cancer management and research
|October 28, 2024
概括
了解前列腺癌的进展是关键. 高格里森得分预测早期的抵抗割的前列腺癌 (CRPC),而较低的纳迪尔PSA表明晚期的进展. 对生物标志物的进一步研究是必要的.
科学领域:
- 在瘤学瘤学.
- 泌尿器科 泌尿器科 泌尿器科 泌尿器科
- 癌症生物学 癌症生物学
背景情况:
- 前列腺癌 (PCa) 呈现出显著的生物异质性,使其进展和管理复杂化.
- 了解预测早期与晚期进展为抵抗割的前列腺癌 (CRPC) 的因素对于改善患者护理至关重要.
研究的目的:
- 确定与CRPC早期和晚期进展相关的临床和病理变量.
- 探索雄激素受体 (AR) 基因序列与CRPC发育之间的相关性.
主要方法:
- 在2018年1月至2022年1月期间诊断的98名CRPC患者的回顾性分析.
- 根据割耐药性时间 (TTCR) 将患者分为四分之一的分层.
- 基于临床,病理和AR-LBD序列数据的早期CRPC (6-12个月TTCR) 和晚期CRPC (38-120个月TTCR) 组的比较.
主要成果:
- 割抵抗的中位时间为25±26.44个月.
- 较高的格里森得分 (≥7) 与早期CRPC发育有显著的关联 (p<0.001).
- 下极点PSA水平与晚期CRPC进展有显著的相关性 (p<0.005).
- 鉴定了AR基因第7个内部区域的同卵性突变,可能会影响CRPC中的拼接变异.
结论:
- 前列腺癌向CRPC的进展是异质的,耐药性的时间范围广泛.
- 早期年龄,高初始PSA和高格里森得分与早期CRPC有关.
- 下极点PSA是晚期CRPC进展的预测指标.
- 没有发现任何显著的基因组突变,突显了对预测生物标志物的进一步研究的需要.
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