摘要:在AR信号抑制前测量AR/增强子位点的无细胞DNA改变预示着转移性去势抵抗前列腺癌患者的总生存率较低

P. Chauhan, Steven H. Hartman, H. Dang, Jace Webster, H. Ellis, Wen-Chi Feng, P. Harris, Elisa M Ledet, E. Jaeger, P. Miller, S. Caputo, R. Pachynski, O. Sartor, C. Maher, A. Chaudhuri
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Methods: We applied EnhanceAR-Seq to plasma cell-free DNA isolated from 20 mCRPC patients from Tulane University collected between April 2015 and June 2017. Assay results were correlated with patient overall survival (OS) and progression-free survival (PFS) from the time of blood collection. Results: Median follow up time was 32 months. Seventeen patients had blood plasma analyzed before first-line ARSI treatment, while three patients had received prior ARSI treatment before blood collection. EnhanceAR-Seq revealed that the most frequent genomic events detected were AR/enhancer alterations (copy number gain, tandem duplication or missense mutations) in 9 patients (45%), of which 5 patients had both AR gene body and enhancer copy number gain. The other 4 patients each had a single genomic event detected by EnhanceAR-Seq: AR amplification, AR enhancer amplification, AR and AR enhancer tandem duplication, and AR W742C single nucleotide variation. Cell-free DNA-detected alterations in the full AR locus including the AR enhancer were highly significant for inferior OS (P = 0.0009; HR = 17.0) but not for PFS (P = 0.2; HR = 2.2) by Kaplan-Meier analysis across all 20 patients. Subset analysis of the 17 patients with plasma analyzed prior to first-line ARSI treatment revealed that AR/enhancer alterations again predicted significantly worse OS with a median survival of 16.1 months vs. not-reached (P = 0.0009; HR = 14.1). Conclusions: AR locus alterations detected by EnhanceAR-seq in plasma cell-free DNA collected prior to ARSI administration correlated with significantly worse overall survival in patients with mCRPC. If corroborated, our results suggest that AR/enhancer genomic alterations represent a potent pre-treatment prognostic biomarker in mCRPC patients. Citation Format: Pradeep Singh Chauhan, Steven H. Hartman, Ha X. Dang, Jace Webster, Haley Ellis, Wenjia Feng, Peter K. Harris, Elisa M. Ledet, Ellen B. Jaeger, Patrick J. 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引用次数: 0

摘要

背景:我们之前开发了一种液体活检法,称为雄激素受体测序增强子和邻近位点(EnhanceAR-Seq) (Dang & Chauhan等人,JCO PO, 2020)。我们将其应用于开始AR定向治疗后转移性前列腺癌患者的异质队列,并显示AR位点的改变与较差的生存率相关。在这里,我们询问在给予一线AR选择性抑制剂(ARSIs)之前在血浆无细胞DNA中检测到的AR/增强子基因组改变是否可以预测转移性去势抵抗性前列腺癌(mCRPC)患者的生存。方法:我们对2015年4月至2017年6月从杜兰大学收集的20例mCRPC患者分离的无浆细胞DNA进行了EnhanceAR-Seq检测。检测结果与患者总生存期(OS)和无进展生存期(PFS)相关。结果:中位随访时间为32个月。17例患者在一线ARSI治疗前进行血浆分析,3例患者在采血前接受过ARSI治疗。EnhanceAR-Seq显示,9例(45%)患者中最常见的基因组事件是AR/增强子改变(拷贝数增加、串联重复或错义突变),其中5例患者同时具有AR基因体和增强子拷贝数增加。另外4例患者通过EnhanceAR-Seq检测到单个基因组事件:AR扩增、AR增强子扩增、AR和AR增强子串联重复、AR W742C单核苷酸变异。包括AR增强子在内的全AR位点的无细胞dna检测改变在不良OS中高度显著(P = 0.0009;HR = 17.0),但PFS无统计学意义(P = 0.2;通过Kaplan-Meier分析,所有20例患者的HR = 2.2)。对一线ARSI治疗前血浆分析的17例患者的亚组分析显示,AR/增强子改变再次预测显着更差的OS,中位生存期为16.1个月,而未达到(P = 0.0009;Hr = 14.1)。结论:通过增强ear -seq检测到ARSI治疗前收集的血浆无细胞DNA中的AR位点改变与mCRPC患者的总生存率显著降低相关。如果得到证实,我们的研究结果表明,AR/增强子基因组改变是mCRPC患者治疗前预后的有效生物标志物。引文格式:Pradeep Singh Chauhan, Steven H. Hartman, Ha X. Dang, Jace Webster, Haley Ellis, Wenjia Feng, Peter K. Harris, Elisa M. Ledet, Ellen B. Jaeger, Patrick J. Miller, Sydney A. Caputo, Russell K. Pachynski, Oliver Sartor, Christopher A. Maher, Aadel A. Chaudhuri。在AR信号抑制前测量AR/增强子位点的无细胞DNA改变预示着转移性去势抵抗前列腺癌患者的总生存率较低[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要第550期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 550: Cell-free DNA alterations in theAR/enhancer locus measured before AR signaling inhibition portend poor overall survival in metastatic castration resistant prostate cancer patients
Background: We previously developed a liquid biopsy assay called Enhancer and neighboring loci of Androgen Receptor Sequencing (EnhanceAR-Seq) (Dang & Chauhan et al, JCO PO, 2020). We applied it to a heterogeneous cohort of metastatic prostate cancer patients after the start of AR-directed therapy, and showed that alterations in the AR locus were associated with worse survival. Here we asked if AR/enhancer genomic alterations detected in plasma cell-free DNA prior to the administration of first-line AR-selective inhibitors (ARSIs) can predict survival in metastatic castration resistant prostate cancer (mCRPC) patients. Methods: We applied EnhanceAR-Seq to plasma cell-free DNA isolated from 20 mCRPC patients from Tulane University collected between April 2015 and June 2017. Assay results were correlated with patient overall survival (OS) and progression-free survival (PFS) from the time of blood collection. Results: Median follow up time was 32 months. Seventeen patients had blood plasma analyzed before first-line ARSI treatment, while three patients had received prior ARSI treatment before blood collection. EnhanceAR-Seq revealed that the most frequent genomic events detected were AR/enhancer alterations (copy number gain, tandem duplication or missense mutations) in 9 patients (45%), of which 5 patients had both AR gene body and enhancer copy number gain. The other 4 patients each had a single genomic event detected by EnhanceAR-Seq: AR amplification, AR enhancer amplification, AR and AR enhancer tandem duplication, and AR W742C single nucleotide variation. Cell-free DNA-detected alterations in the full AR locus including the AR enhancer were highly significant for inferior OS (P = 0.0009; HR = 17.0) but not for PFS (P = 0.2; HR = 2.2) by Kaplan-Meier analysis across all 20 patients. Subset analysis of the 17 patients with plasma analyzed prior to first-line ARSI treatment revealed that AR/enhancer alterations again predicted significantly worse OS with a median survival of 16.1 months vs. not-reached (P = 0.0009; HR = 14.1). Conclusions: AR locus alterations detected by EnhanceAR-seq in plasma cell-free DNA collected prior to ARSI administration correlated with significantly worse overall survival in patients with mCRPC. If corroborated, our results suggest that AR/enhancer genomic alterations represent a potent pre-treatment prognostic biomarker in mCRPC patients. Citation Format: Pradeep Singh Chauhan, Steven H. Hartman, Ha X. Dang, Jace Webster, Haley Ellis, Wenjia Feng, Peter K. Harris, Elisa M. Ledet, Ellen B. Jaeger, Patrick J. Miller, Sydney A. Caputo, Russell K. Pachynski, Oliver Sartor, Christopher A. Maher, Aadel A. Chaudhuri. Cell-free DNA alterations in the AR/enhancer locus measured before AR signaling inhibition portend poor overall survival in metastatic castration resistant prostate cancer patients [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 550.
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