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转移性前列腺癌二十年的疾病演变及生物标志物指导下的临床决策制定

Two Decades of Disease Evolution and Biomarker-Guided Clinical Decision Making in Metastatic Prostate Cancer.

作者信息

Erazo Tatiana, Moiso Enrico, Aras Omer, Scher Howard I

机构信息

Translational Partnership Program, Memorial Sloan Kettering Cancer Center (MSK), New York, NY 10065, USA.

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

出版信息

Int J Mol Sci. 2025 Aug 6;26(15):7593. doi: 10.3390/ijms26157593.


DOI:10.3390/ijms26157593
PMID:40806723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12347661/
Abstract

Despite significant advances in prostate cancer treatment over the past two decades, metastatic castration-resistant prostate cancer (mCRPC) remains incurable. We present the case of a patient with aggressive prostate cancer diagnosed 20 years ago, underscoring the value of longitudinal genomic profiling and advanced imaging to guide clinical decisions. After multiple treatment failures, genomic analyses of tissue and liquid biopsies revealed dynamic changes in tumor biology and the emergence of resistance mechanisms, particularly AR amplification, identified with a liquid biopsy test and validated by [F]-FDHT PET scan. This finding guided treatment with bipolar androgen therapy (BAT), which achieved a dramatic clinical response, reduced AR expression, improved symptoms, and restored sensitivity to enzalutamide. This case exemplifies the utility of serial liquid biopsies in uncovering mechanisms of tumor evolution and resistance, and the crucial role of cutting-edge diagnostics in personalized cancer treatment.

摘要

尽管在过去二十年中前列腺癌治疗取得了重大进展,但转移性去势抵抗性前列腺癌(mCRPC)仍然无法治愈。我们介绍了一名20年前被诊断为侵袭性前列腺癌患者的病例,强调了纵向基因组分析和先进成像在指导临床决策中的价值。在多次治疗失败后,组织活检和液体活检的基因组分析揭示了肿瘤生物学的动态变化以及耐药机制的出现,特别是通过液体活检检测确定并经[F]-FDHT PET扫描验证的雄激素受体(AR)扩增。这一发现指导了双极雄激素疗法(BAT)的治疗,该疗法取得了显著的临床反应,降低了AR表达,改善了症状,并恢复了对恩杂鲁胺的敏感性。该病例例证了系列液体活检在揭示肿瘤演变和耐药机制方面的效用,以及前沿诊断在个性化癌症治疗中的关键作用。

相似文献

[1]
Two Decades of Disease Evolution and Biomarker-Guided Clinical Decision Making in Metastatic Prostate Cancer.

Int J Mol Sci. 2025-8-6

[2]
rechARge: a randomized phase III trial of the androgen receptor ligand-directed degrader, BMS-986365, vs investigator's choice in patients with mCRPC.

Future Oncol. 2025-6

[3]
Epigenetic profiling identifies markers of endocrine resistance and therapeutic options for metastatic castration-resistant prostate cancer.

Cell Rep Med. 2025-7-15

[4]
Loss of AR-regulated AFF3 contributes to prostate cancer progression and reduces ferroptosis sensitivity by downregulating ACSL4 based on single-cell sequencing analysis.

Apoptosis. 2024-10

[5]
Matching-adjusted indirect comparison of enzalutamide versus darolutamide doublet in mHSPC.

Future Oncol. 2025-8

[6]
Targeted Delivery of AR-V7 siRNA with Bivalent PSMA Aptamers Effectively Suppresses the Growth of Enzalutamide-Resistant Prostate Cancer.

Mol Pharm. 2024-11-4

[7]
Clinical Context Shapes the Relationship between Genomic Alterations and Response to AR Inhibitors and Chemotherapy in Metastatic Prostate Cancer.

Clin Cancer Res. 2025-7-1

[8]
Quantitative Analysis of Serial Positron Emission Tomography Imaging in Men with Metastatic Castration-resistant Prostate Cancer Treated with Enzalutamide.

Eur Urol Oncol. 2024-8

[9]
Phenotypic Plasticity and Androgen Receptor Bypass Drive Cross-Resistance to Apalutamide in Castration-Resistant Prostate Cancer Cell Models.

Int J Mol Sci. 2025-6-20

[10]
Prostate-specific Antigen Decline During Primary Androgen-deprivation Therapy for Predicting Response and Survival in Metastatic Castration-resistant Prostate Cancer Patients Receiving Enzalutamide.

In Vivo. 2025

本文引用的文献

[1]
Advances in Targeted Therapy for Metastatic Prostate Cancer.

Curr Treat Options Oncol. 2025-4-29

[2]
Lu-DOTATATE in Combination with PARP Inhibitor Olaparib Is Feasible in Patients with Somatostatin-Positive Tumors: Results from the LuPARP Phase I Trial.

J Nucl Med. 2025-5-1

[3]
Therapy-Related Myeloid Neoplasms After [Lu]Lu-PSMA Therapy in Patients with Metastatic Castration-Resistant Prostate Cancer: A Case Series.

J Nucl Med. 2025-4-1

[4]
Treatment-induced stemness and lineage plasticity in driving prostate cancer therapy resistance.

Cancer Heterog Plast. 2024

[5]
Two decades of advances in clinical oncology - lessons learned and future directions.

Nat Rev Clin Oncol. 2024-11

[6]
Challenges in the treatment of K601E-mutated lung carcinoma: a case report of rapid response and resistance to dabrafenib and trametinib.

Front Oncol. 2024-7-8

[7]
Circulating Tumor DNA Assessment for Treatment Monitoring Adds Value to PSA in Metastatic Castration-Resistant Prostate Cancer.

Clin Cancer Res. 2024-9-13

[8]
Clonal Hematopoiesis in Patients With Neuroendocrine Tumor Treated With Lutetium-177 and the Risk of Thrombocytopenia: A Prospective Study.

JCO Precis Oncol. 2024-6

[9]
Prediction of plasma ctDNA fraction and prognostic implications of liquid biopsy in advanced prostate cancer.

Nat Commun. 2024-2-28

[10]
(HER2) amplifications and co-occurring alterations in the circulating cell-free DNA of pancreatic ductal adenocarcinoma patients and response to HER2 inhibition.

Front Oncol. 2024-2-8

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