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Immediate versus deferred chemotherapy after radical cystectomy in patients with pT3-pT4 or N+ M0 urothelial carcinoma of the bladder (EORTC 30994): an intergroup, open-label, randomised phase 3 trial.根治性膀胱切除术治疗 pT3-pT4 或 N+M0 膀胱尿路上皮癌患者中即刻与延迟化疗的比较(EORTC 30994):一项国际多中心、开放标签、随机 3 期临床试验。
Lancet Oncol. 2015 Jan;16(1):76-86. doi: 10.1016/S1470-2045(14)71160-X. Epub 2014 Dec 11.
2
MPDL3280A (anti-PD-L1) treatment leads to clinical activity in metastatic bladder cancer.MPDL3280A(抗 PD-L1)治疗可导致转移性膀胱癌的临床活性。
Nature. 2014 Nov 27;515(7528):558-62. doi: 10.1038/nature13904.
3
Molecular profiling of infiltrating urothelial carcinoma of bladder and nonbladder origin.膀胱浸润性尿路上皮癌及非膀胱源性浸润性尿路上皮癌的分子特征分析
Clin Genitourin Cancer. 2015 Feb;13(1):e37-49. doi: 10.1016/j.clgc.2014.07.010. Epub 2014 Aug 1.
4
Comprehensive molecular characterization of urothelial bladder carcinoma.尿路上皮膀胱癌的综合分子特征分析
Nature. 2014 Mar 20;507(7492):315-22. doi: 10.1038/nature12965. Epub 2014 Jan 29.
5
Association of T-cell co-regulatory protein expression with clinical outcomes following radical cystectomy for urothelial carcinoma of the bladder.T 细胞共调控蛋白表达与膀胱癌根治性膀胱切除术后临床结局的相关性研究。
Eur J Surg Oncol. 2014 Jan;40(1):121-7. doi: 10.1016/j.ejso.2013.08.023. Epub 2013 Sep 18.
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Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation.膀胱癌全基因组和全外显子组测序鉴定出涉及姐妹染色单体黏合和分离的基因经常发生改变。
Nat Genet. 2013 Dec;45(12):1459-63. doi: 10.1038/ng.2798. Epub 2013 Oct 13.
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Hypermethylation of the polycomb group target gene PCDH7 in bladder tumors from patients of all ages.所有年龄段膀胱肿瘤患者中多梳组靶基因 PCDH7 的高甲基化。
J Urol. 2013 Jul;190(1):311-6. doi: 10.1016/j.juro.2013.01.078. Epub 2013 Jan 28.
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Practical use of perioperative chemotherapy for muscle-invasive bladder cancer: summary of session at the Society of Urologic Oncology annual meeting.肌层浸润性膀胱癌围手术期化疗的实际应用:美国泌尿外科学会肿瘤学年会专场会议总结。
Urol Oncol. 2012 Nov-Dec;30(6):772-80. doi: 10.1016/j.urolonc.2012.01.012.
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Combinations of urinary biomarkers for surveillance of patients with incident nonmuscle invasive bladder cancer: the European FP7 UROMOL project.用于监测初发非肌肉浸润性膀胱癌患者的尿液生物标志物组合:欧洲 FP7 UROMOL 项目。
J Urol. 2013 May;189(5):1945-51. doi: 10.1016/j.juro.2012.11.115. Epub 2012 Nov 28.
10
A comprehensive immunohistochemical and molecular approach to the PI3K/AKT/mTOR (phosphoinositide 3-kinase/v-akt murine thymoma viral oncogene/mammalian target of rapamycin) pathway in bladder urothelial carcinoma.全面的免疫组化和分子方法研究膀胱尿路上皮癌中的 PI3K/AKT/mTOR(磷酸肌醇 3-激酶/v-akt 鼠胸腺瘤病毒致癌基因/雷帕霉素的哺乳动物靶标)通路。
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膀胱癌治疗中的新的且有前景的策略。

New and promising strategies in the management of bladder cancer.

作者信息

Apolo Andrea B, Vogelzang Nicholas J, Theodorescu Dan

机构信息

From the Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute at the National Institutes of Health, Bethesda, MD; US Oncology Research, Houston, TX and Comprehensive Cancer Centers of Nevada, Las Vegas, NV; University of Colorado Cancer Center, Denver, CO.

出版信息

Am Soc Clin Oncol Educ Book. 2015:105-12. doi: 10.14694/EdBook_AM.2015.35.105.

DOI:10.14694/EdBook_AM.2015.35.105
PMID:25993148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6777550/
Abstract

Bladder cancer is a complex and aggressive disease for which treatment strategies have had limited success. Improvements in detection, treatment, and outcomes in bladder cancer will require the integration of multiple new approaches, including genomic profiling, immunotherapeutics, and large randomized clinical trials. New and promising strategies are being tested in all disease states, including nonmuscle-invasive bladder cancer (NMIBC), muscle-invasive bladder cancer (MIBC), and metastatic urothelial carcinoma (UC). Efforts are underway to develop better noninvasive urine biomarkers for use in primary or secondary detection of NMIBC, exploiting our genomic knowledge of mutations in genes such as RAS, FGFR3, PIK3CA, and TP53 and methylation pathways alone or in combination. Recent data from a large, randomized phase III trial of adjuvant cisplatin-based chemotherapy add to our knowledge of the value of perioperative chemotherapy in patients with MIBC. Finally, bladder cancer is one of a growing list of tumor types that respond to immune checkpoint inhibition, opening the potential for new therapeutic strategies for treatment of this complex and aggressive disease.

摘要

膀胱癌是一种复杂且侵袭性强的疾病,其治疗策略成效有限。膀胱癌在检测、治疗和预后方面的改善需要整合多种新方法,包括基因组分析、免疫疗法以及大型随机临床试验。针对包括非肌层浸润性膀胱癌(NMIBC)、肌层浸润性膀胱癌(MIBC)和转移性尿路上皮癌(UC)在内的所有疾病状态,新的且有前景的策略正在进行测试。正在努力开发更好的非侵入性尿液生物标志物,用于NMIBC的一级或二级检测,单独或联合利用我们对RAS、FGFR3、PIK3CA和TP53等基因突变以及甲基化途径的基因组知识。一项基于顺铂的辅助化疗大型随机III期试验的最新数据增加了我们对MIBC患者围手术期化疗价值的认识。最后,膀胱癌是对免疫检查点抑制有反应的肿瘤类型之一,这为治疗这种复杂且侵袭性强的疾病开辟了新治疗策略的潜力。