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基因组前列腺评分:评估中度风险前列腺癌预后及优化放疗范围和雄激素剥夺治疗的新工具。

Genomic Prostate Score: A New Tool to Assess Prognosis and Optimize Radiation Therapy Volumes and ADT in Intermediate-Risk Prostate Cancer.

作者信息

Belkacemi Yazid, Debbi Kamel, Coraggio Gabriele, Bendavid Jérome, Nourieh Maya, To Nhu Hanh, Cherif Mohamed Aziz, Saldana Carolina, Ingels Alexandre, De La Taille Alexandre, Loganadane Gokoulakrichenane

机构信息

Department of Radiation Oncology and Henri Mondor Breast Center, Henri Mondor Hospital, APHP, University of Paris Est Créteil (UPEC), IMRB, INSERM U 955, 94000 Créteil, France.

Department of Pathology, Henri Mondor Hospital, University of Paris Est Créteil (UPEC), IMRB, INSERM U 955, 94000 Créteil, France.

出版信息

Cancers (Basel). 2023 Feb 2;15(3):945. doi: 10.3390/cancers15030945.

Abstract

Genomic classifiers such as the Genomic Prostate Score (GPS) could help to personalize treatment for men with intermediate-risk prostate cancer (I-PCa). In this study, we aimed to evaluate the ability of the GPS to change therapeutic decision making in I-PCa. Only patients in the intermediate NCCN risk group with Gleason score 3 + 4 were considered. The primary objective was to assess the impact of the GPS on risk stratification: NCCN clinical and genomic risk versus NCCN clinical risk stratification alone. We also analyzed the predictive role of the GPS for locally advanced disease (≥pT3+) and the potential change in treatment strategy. Thirty patients were tested for their GPS between November 2018 and March 2020, with the median age being 70 (45-79). Twenty-three patients had a clinical T1 stage. Eighteen patients were classified as favorable intermediate risk (FIR) based on the NCCN criteria. The median GPS score was 39 (17-70). Among the 23 patients who underwent a radical prostatectomy, Gleason score 3 + 4 was found in 18 patients. There was a significant correlation between the GPS and the percentage of a Gleason grade 4 or higher pattern in the surgical sample: correlation coefficient r = 0.56; 95% CI = 0.2-0.8; = 0.005. In this study, the GPS combined with NCCN clinical risk factors resulted in significant changes in risk group.

摘要

基因组分类器,如基因组前列腺评分(GPS),有助于为中危前列腺癌(I-PCa)患者制定个性化治疗方案。在本研究中,我们旨在评估GPS改变I-PCa治疗决策的能力。仅纳入NCCN中危风险组且Gleason评分为3 + 4的患者。主要目的是评估GPS对风险分层的影响:NCCN临床和基因组风险与仅NCCN临床风险分层。我们还分析了GPS对局部晚期疾病(≥pT3+)的预测作用以及治疗策略的潜在变化。2018年11月至2020年3月期间对30例患者进行了GPS检测,中位年龄为70岁(45 - 79岁)。23例患者临床分期为T1期。根据NCCN标准,18例患者被归类为有利中危(FIR)。中位GPS评分为39(17 - 70)。在23例行根治性前列腺切除术的患者中,18例患者的Gleason评分为3 + 4。GPS与手术样本中Gleason 4级或更高分级模式的百分比之间存在显著相关性:相关系数r = 0.56;95%CI = 0.2 - 0.8;P = 0.005。在本研究中,GPS结合NCCN临床风险因素导致风险组发生显著变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/416b/9913491/71b80d73e1f6/cancers-15-00945-g001.jpg

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