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前列腺癌。

Prostate cancer.

机构信息

Division of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia.

University College London, London, UK.

出版信息

Lancet. 2021 Sep 18;398(10305):1075-1090. doi: 10.1016/S0140-6736(21)00950-8. Epub 2021 Aug 6.


DOI:10.1016/S0140-6736(21)00950-8
PMID:34370973
Abstract

The management of prostate cancer continues to evolve rapidly, with substantial advances being made in understanding the genomic landscape and biology underpinning both primary and metastatic prostate cancer. Similarly, the emergence of more sensitive imaging methods has improved diagnostic and staging accuracy and refined surveillance strategies. These advances have introduced personalised therapeutics to clinical practice, with treatments targeting genomic alterations in DNA repair pathways now clinically validated. An important shift in the therapeutic framework for metastatic disease has taken place, with metastatic-directed therapies being evaluated for oligometastatic disease, aggressive management of the primary lesion shown to benefit patients with low-volume metastatic disease, and with several novel androgen pathway inhibitors significantly improving survival when used as a first-line therapy for metastatic disease. Research into the molecular characterisation of localised, recurrent, and progressive disease will undoubtedly have an impact on clinical management. Similarly, emerging research into novel therapeutics, such as targeted radioisotopes and immunotherapy, holds much promise for improving the lives of patients with prostate cancer.

摘要

前列腺癌的管理仍在迅速发展,在理解原发性和转移性前列腺癌的基因组景观和生物学方面取得了重大进展。同样,更敏感的成像方法的出现提高了诊断和分期的准确性,并改进了监测策略。这些进展将个性化治疗引入了临床实践,针对 DNA 修复途径中基因组改变的治疗方法现已在临床上得到验证。转移性疾病的治疗框架发生了重要转变,转移性定向治疗正在评估寡转移性疾病,对原发性病变的积极治疗已被证明有益于低容量转移性疾病患者,并且几种新型雄激素途径抑制剂在作为转移性疾病的一线治疗时显著提高了生存率。对局部、复发性和进行性疾病的分子特征的研究无疑将对临床管理产生影响。同样,针对新型治疗方法的新兴研究,如靶向放射性同位素和免疫疗法,为改善前列腺癌患者的生活带来了很大希望。

相似文献

[1]
Prostate cancer.

Lancet. 2021-9-18

[2]
Novel Insights into the Management of Oligometastatic Prostate Cancer: A Comprehensive Review.

Eur Urol Oncol. 2018-10-9

[3]
Comparative Analysis of Genomic Alterations across Castration Sensitive and Castration Resistant Prostate Cancer via Circulating Tumor DNA Sequencing.

J Urol. 2021-2

[4]
Combining immunological and androgen-directed approaches: an emerging concept in prostate cancer immunotherapy.

Curr Opin Oncol. 2012-5

[5]
Intermittent androgen deprivation therapy in advanced prostate cancer.

Curr Treat Options Oncol. 2014-3

[6]
Novel agents for the management of castration-resistant prostate cancer.

Curr Opin Urol. 2012-5

[7]
Current management of advanced and castration resistant prostate cancer.

Can J Urol. 2014-4

[8]
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Expert Rev Anticancer Ther. 2006-5

[9]
Management of Metastatic Hormone-Sensitive Prostate Cancer (mHSPC): an Evolving Treatment Paradigm.

Curr Treat Options Oncol. 2019-7-9

[10]
Androgen deprivation and immunotherapy for the treatment of prostate cancer.

Endocr Relat Cancer. 2017-8-16

引用本文的文献

[1]
The RNA helicase DDX17 enhances androgen receptor stability by interacting with the E3 ubiquitin ligase SPOP in prostate cancer.

Transl Androl Urol. 2025-7-30

[2]
Nanomedicines for the treatment of genitourinary neoplasms.

Mater Today Bio. 2025-8-3

[3]
Cuproptosis in prostate cancer: Molecular mechanisms, prognostic biomarkers and therapeutic frontiers of cuproptosis‑related genes (Review).

Int J Oncol. 2025-9

[4]
[A preoperative prediction model for pelvic lymph node metastasis in prostate cancer: Integrating clinical characteristics and multiparametric MRI].

Beijing Da Xue Xue Bao Yi Xue Ban. 2025-8-18

[5]
Applying Unbiased, Functional Criteria Allows Selection of Novel Cyclic Peptides for Effective Targeted Drug Delivery to Malignant Prostate Cancer Cells.

Pharmaceutics. 2025-7-1

[6]
Predicting pathogenic DNA damage repair gene mutations in prostate cancer patients: a multi-center magnetic resonance imaging radiomics study.

Quant Imaging Med Surg. 2025-7-1

[7]
CXCL12/CXCR4 axis governs Treg spatial dominance over CD8+ T cells via IL-2 sequestration: a dual therapeutic target in prostate cancer.

Front Immunol. 2025-7-8

[8]
Asymptomatic Bladder Stones Exacerbate Acute Genitourinary Adverse Events During Radiation Therapy for Prostate Cancer: Insights From Two Case Reports.

Adv Radiat Oncol. 2025-6-11

[9]
Genetic alterations of prostate cancer: in localized and metastatic prostate cancer.

BMC Urol. 2025-7-14

[10]
Artificial intelligence in prostate cancer.

Chin Med J (Engl). 2025-8-5

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