专家共识
ENGLISH ABSTRACT
延胡索酸水合酶缺陷型肾细胞癌临床诊治共识
中国抗癌协会泌尿男生殖系肿瘤专业委员会少见肾癌协作组
作者及单位信息
·
DOI: 10.3760/cma.j.cn112139-20220729-00328
Consensus on clinical diagnosis and treatment of fumarate hydratase-deficient renal cell carcinoma
Rare Kidney Cancer Collaborative Group, Genitourinary Cancer Committee, China Anti-Cancer Association
Wei Qiang
Xue Wei
Authors Info & Affiliations
Rare Kidney Cancer Collaborative Group, Genitourinary Cancer Committee, China Anti-Cancer Association
Wei Qiang
Department of Urology, West China Hospital, Sichuan University, Chengdu 610041, China
Xue Wei
Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China
·
DOI: 10.3760/cma.j.cn112139-20220729-00328
2638
475
0
0
11
4
PDF下载
APP内阅读
摘要

延胡索酸水合酶缺失性肾细胞癌(FH-RCC)是一种驱动基因明确的高度恶性的独立肾细胞癌病理学亚型,由 FH胚系或体系突变导致。FH-RCC发病年龄早、影像学表现不典型、病理学形态多变,临床诊断困难,且传统药物治疗效果不佳,对患者健康造成极大威胁。中国抗癌协会泌尿男生殖系肿瘤专业委员会少见肾癌协作组总结现有工作基础,汇总国内外相关研究进展,基于基础研究、临床队列和循证医学证据制定本共识,包括疾病影像学表现、病理学诊断、基因检测、手术与系统治疗选择,为该疾病的诊治提出建议和参考。

肾肿瘤;诊断;治疗;指南;延胡索酸水合酶缺陷型肾细胞癌
ABSTRACT

Fumarate hydratase-deficient renal cell carcinoma (FH-RCC) is an independent pathological subtype of renal cell carcinoma with a clear driver gene and a high degree of malignancy. Recent studies have found that patients with somatic FH mutations have similar clinico-biological behavior and poor prognosis to patients with germline FH mutations. FH-RCC has the characteristics of early age of onset, atypical imaging manifestations, variable pathological patterns, difficult clinical diagnosis and poor effect on traditional drug treatment, thus greatly endangering the life and health of patients. Under the organization of the Rare Kidney Cancer Collaborative Group, Genitourinary Cancer Committee, China Anti-Cancer Association, this guideline was developed based on basic research, clinical cohort and evidence-based medicine evidence, including imaging manifestations, pathological diagnosis, genetic testing, surgical and systemic treatment options, and provided recommendations and references for the diagnosis and treatment norms.

Kidney neoplasms;Diagnosis;Treatment;Guidebooks;Fumarate hydratase-deficient renal cell carcinoma
Wei Qiang, Department of Urology, West China Hospital, Sichuan University, Chengdu 610041, China, Email: mocdef.labiamtoh339qw
Xue Wei, Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China, Email: mocdef.iabjnerieweux
引用本文

中国抗癌协会泌尿男生殖系肿瘤专业委员会少见肾癌协作组. 延胡索酸水合酶缺陷型肾细胞癌临床诊治共识[J]. 中华外科杂志,2022,60(11):961-968.

DOI:10.3760/cma.j.cn112139-20220729-00328

PERMISSIONS

Request permissions for this article from CCC.

评价本文
*以上评分为匿名评价
一、概述
随着对肾癌发病分子特征的研究不断深入,越来越多具有明确肿瘤驱动基因的肾细胞癌逐渐被认识,成为WHO认可的独立病理学亚型。遗传性平滑肌瘤病和肾细胞癌综合征(hereditary leiomyomatosis and renal cell carcinoma syndrome,HLRCC)是一种延胡索酸水合酶(fumarate hydratase,FH)基因胚系突变导致的遗传性疾病,可表现为皮肤、子宫平滑肌瘤病及肾恶性肿瘤。因存在独特的临床病理学及分子生物学特征,在2016版WHO肾脏肿瘤分类中成为独立亚型 1FH体系突变同样可能导致肾细胞癌发生,且与 FH胚系突变导致的HLRCC具有极其相似的生物学行为。因此,2022新版WHO肾脏肿瘤分类中已将 FH胚系或体系突变导致的肾细胞癌统称为FH缺陷型肾细胞癌(fumarate hydratase-deficiency renal cell carcinoma,FH-RCC)。
FH-RCC发病年龄早,影像学表现不典型,病理学形态多变,临床诊断极其困难,缺乏标准化的诊断流程。另一方面,其侵袭性高,易早期发生淋巴结转移及骨转移等远处转移,且缺乏有效的系统治疗手段。因此,如何通过影像学手段早期发现,发现后如何通过组织病理学、分子病理学甚至基因检测准确诊断,确诊后如何制定最佳治疗策略,是泌尿肿瘤科医师面临的重大挑战。
本协作组系统梳理国内外FH-RCC的相关临床研究成果,综合多学科医师对该病的诊疗认识,由于FH-RCC临床研究缺乏高级别证据,因此通过专家讨论和投票提出下述FH-RCC临床影像学预警、病理学精准诊断和全生命周期管理的临床诊疗共识,并在临床建议后用括号标注专家赞同的比例。本共识的制定旨在优化该病的早诊早治,改善患者生存和预后。
试读结束,您可以通过登录机构账户或个人账户后获取全文阅读权限。
参考文献
[1]
Moch H , Cubilla AL , Humphrey PA ,et al. The 2016 WHO classification of tumours of the urinary system and male genital organs-part a: renal, penile, and testicular tumours[J]. Eur Urol, 2016,70(1):93-105. DOI: 10.1016/j.eururo.2016.02.029 .
返回引文位置Google Scholar
百度学术
万方数据
[2]
Nikolovski I , Carlo MI , Chen YB ,et al. Imaging features of fumarate hydratase-deficient renal cell carcinomas: a retrospective study[J]. Cancer Imaging, 2021,21(1):24. DOI: 10.1186/s40644-021-00392-9 .
返回引文位置Google Scholar
百度学术
万方数据
[3]
Yang L , Li XM , Hu YJ ,et al. Multidetector CT characteristics of fumarate hydratase-deficient renal cell carcinoma and papillary type Ⅱ renal cell carcinoma[J]. Korean J Radiol, 2021,22(12):1996-2005. DOI: 10.3348/kjr.2021.0212 .
返回引文位置Google Scholar
百度学术
万方数据
[4]
Paschall AK , Nikpanah M , Farhadi F ,et al. Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome: spectrum of imaging findings[J]. Clin Imaging, 2020,68:14-19. DOI: 10.1016/j.clinimag.2020.06.010 .
返回引文位置Google Scholar
百度学术
万方数据
[5]
Casey RT , McLean MA , Challis BG ,et al. Fumarate metabolic signature for the detection of reed syndrome in humans[J]. Clin Cancer Res, 2020,26(2):391-396. DOI: 10.1158/1078-0432.CCR-19-1729 .
返回引文位置Google Scholar
百度学术
万方数据
[6]
Trpkov K , Hes O , Agaimy A ,et al. Fumarate Hydratase-deficient renal cell carcinoma is strongly correlated with fumarate hydratase mutation and hereditary leiomyomatosis and renal cell carcinoma syndrome[J]. Am J Surg Pathol, 2016,40(7):865-875. DOI: 10.1097/PAS.0000000000000617 .
返回引文位置Google Scholar
百度学术
万方数据
[7]
Xu Y , Kong W , Cao M ,et al. Genomic Profiling and response to immune checkpoint inhibition plus tyrosine kinase inhibition in FH-deficient renal cell carcinoma[J/OL]. Eur Urol, 2022:S0302-2838(22)02406-X[2022-07-20]. https://www.sciencedirect.com/science/article/abs/pii/S030228382202406X. DOI: 10.1016/j.eururo.2022.05.029 published online ahead of print June 14, 2022. [ ].
返回引文位置Google Scholar
百度学术
万方数据
[8]
Sun G , Zhang X , Liang J ,et al. Integrated molecular characterization of fumarate hydratase-deficient renal cell carcinoma[J]. Clin Cancer Res, 2021,27(6):1734-1743. DOI: 10.1158/1078-0432.CCR-20-3788 .
返回引文位置Google Scholar
百度学术
万方数据
[9]
Pan X , Zhang M , Yao J ,et al. Fumaratehydratase-deficient renal cell carcinoma: a clinicopathological and molecular study of 13 cases[J]. J Clin Pathol, 2019,72(11):748-754. DOI: 10.1136/jclinpath-2019-205924 .
返回引文位置Google Scholar
百度学术
万方数据
[10]
Clerici S , Boletta A . Role of the KEAP1-NRF2 axis in renal cell carcinoma[J]. Cancers (Basel), 2020,12(11):3458. DOI: 10.3390/cancers12113458 .
返回引文位置Google Scholar
百度学术
万方数据
[11]
Kansanen E , Kuosmanen SM , Leinonen H ,et al. The Keap1-Nrf2 pathway: mechanisms of activation and dysregulation in cancer[J]. Redox Biol, 2013,1(1):45-49. DOI: 10.1016/j.redox.2012.10.001 .
返回引文位置Google Scholar
百度学术
万方数据
[12]
Ooi A , Wong JC , Petillo D ,et al. An antioxidant response phenotype shared between hereditary and sporadic type 2 papillary renal cell carcinoma[J]. Cancer Cell, 2011,20(4):511-523. DOI: 10.1016/j.ccr.2011.08.024 .
返回引文位置Google Scholar
百度学术
万方数据
[13]
Furuya M , Iribe Y , Nagashima Y ,et al. Clinicopathological and molecular features of hereditary leiomyomatosis and renal cell cancer-associated renal cell carcinomas[J]. J Clin Pathol, 2020,73(12):819-825. DOI: 10.1136/jclinpath-2020-206548 .
返回引文位置Google Scholar
百度学术
万方数据
[14]
Alaghehbandan R , Stehlik J , Trpkov K ,et al. Programmed death-1 (PD-1) receptor/PD-1 ligand (PD-L1) expression in fumarate hydratase-deficient renal cell carcinoma[J]. Ann Diagn Pathol, 2017,29:17-22. DOI: 10.1016/j.anndiagpath.2017.04.007 .
返回引文位置Google Scholar
百度学术
万方数据
[15]
Lau HD , Chan E , Fan AC ,et al. A clinicopathologic and molecular analysis of fumarate hydratase-deficient renal cell carcinoma in 32 patients[J]. Am J Surg Pathol, 2020,44(1):98-110. DOI: 10.1097/PAS.0000000000001372 .
返回引文位置Google Scholar
百度学术
万方数据
[16]
Choueiri TK , Tomczak P , Park SH ,et al. Adjuvant pembrolizumab after nephrectomy in renal-cell carcinoma[J]. N Engl J Med, 2021,385(8):683-694. DOI: 10.1056/NEJMoa2106391 .
返回引文位置Google Scholar
百度学术
万方数据
[17]
Srinivasan R , Su D , Stamatakis L ,et al. 5 Mechanism based targeted therapy for hereditary leiomyomatosis and renal cell cancer (HLRCC) and sporadic papillary renal cell carcinoma: interim results from a phase 2 study of bevacizumab and erlotinib[J]. Eur J Cancer, 2014,50Suppl 6:S8. DOI: 10.1016/S0959-8049(14)70131-5 .
返回引文位置Google Scholar
百度学术
万方数据
[18]
Srinivasan RS , Gurram M , Al Harthy EA ,et al. Results from a phase Ⅱ study of bevacizumab and erlotinib in subjects with advanced hereditary leiomyomatosis and renal cell cancer (HLRCC) or sporadic papillary renal cell cancer[J]. J Clin Oncol, 2020,38(15Suppl):S5004. DOI: 10.1200/JCO.2020.38.15_suppl.5004 .
返回引文位置Google Scholar
百度学术
万方数据
[19]
Carril-Ajuria L , Colomba E , Cerbone L ,et al. Response to systemic therapy in fumarate hydratase-deficient renal cell carcinoma[J]. Eur J Cancer, 2021,151:106-114. DOI: 10.1016/j.ejca.2021.04.009 .
返回引文位置Google Scholar
百度学术
万方数据
[20]
Yonese I , Ito M , Takemura K ,et al. A case of metastatic hereditary leiomyomatosis and renal cell cancer syndrome-associated renal cell carcinoma treated with a sequence of axitinib and nivolumab following cytoreductive nephrectomy[J]. J Kidney Cancer VHL, 2020,7(2):6-10. DOI: 10.15586/jkcvhl.2020.148 .
返回引文位置Google Scholar
百度学术
万方数据
[21]
Iribe Y , Furuya M , Shibata Y ,et al. Complete response of hereditary leiomyomatosis and renal cell cancer (HLRCC)-associated renal cell carcinoma to nivolumab and ipilimumab combination immunotherapy by: a case report[J]. Fam Cancer, 2021,20(1):75-80. DOI: 10.1007/s10689-020-00195-0 .
返回引文位置Google Scholar
百度学术
万方数据
[22]
Gleeson JP , Nikolovski I , Dinatale R ,et al. Comprehensive molecular characterization and response to therapy in fumarate hydratase-deficient renal cell carcinoma[J]. Clin Cancer Res, 2021,27(10):2910-2919. DOI: 10.1158/1078-0432.CCR-20-4367 .
返回引文位置Google Scholar
百度学术
万方数据
备注信息
A
魏强,四川大学华西医院泌尿外科,成都 610041,Email: mocdef.labiamtoh339qw
B
薛蔚,上海交通大学医学院附属仁济医院泌尿外科,上海 200127,Email: mocdef.iabjnerieweux
C

中国抗癌协会泌尿男生殖系肿瘤专业委员会少见肾癌协作组. 延胡索酸水合酶缺陷型肾细胞癌临床诊治共识[J]. 中华外科杂志, 2022, 60(11): 961-968. DOI: 10.3760/cma.j.cn112139-20220729-00328.

D
所有编者声明不存在利益冲突
评论 (0条)
注册
登录
时间排序
暂无评论,发表第一条评论抢沙发
MedAI助手(体验版)
文档即答
智问智答
机器翻译
回答内容由人工智能生成,我社无法保证其准确性和完整性,该生成内容不代表我们的态度或观点,仅供参考。
生成快照
文献快照

你好,我可以帮助您更好的了解本文,请向我提问您关注的问题。

0/2000

《中华医学会杂志社用户协议》 | 《隐私政策》

《SparkDesk 用户协议》 | 《SparkDesk 隐私政策》

网信算备340104764864601230055号 | 网信算备340104726288401230013号

技术支持:

历史对话
本文全部
还没有聊天记录
设置
模式
纯净模式沉浸模式
字号