Genomic profiling of Chinese patients with urothelial carcinoma

被引:8
作者
Yang, Bo [1 ]
Zhao, Xiao [1 ]
Wan, Chong [2 ]
Ma, Xin [3 ]
Niu, Shaoxi [3 ]
Guo, Aitao [4 ]
Wang, Jieli [1 ]
Wang, Jinliang [1 ]
Sun, Decong [1 ]
Jiao, Shunchang [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Oncol, Fuxing Rd 28, Beijing, Peoples R China
[2] Lifehealthcare Clin Labs, Hangzhou, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Urol, Beijing, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Dept Pathol, Beijing, Peoples R China
关键词
Urothelial carcinoma; Genomic alterations; ctDNA; BLADDER-CANCER; REPAIR GENES; DNA; MULTICENTER; MUTATIONS;
D O I
10.1186/s12885-021-07829-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundsUrothelial carcinoma (UC) is the most common genitourinary malignancy in China. In this study, we surveyed the genomic features in Chinese UC patients and investigated the concordance of genetic alterations between circulating tumor DNA (ctDNA) in plasma and matched tumor tissue.Materials and methodsA total of 112 UC patients were enrolled, of which 31 were upper tract UC (UTUC) and 81 were UC of bladder (UCB). Genomic alterations in 92 selected genes were analyzed by targeted next-generation sequencing.ResultsIn the study cohort, 94.64, 86.61 and 62.50% of patients were identified as having valid somatic, oncogenic and actionable somatic alterations, respectively. The most frequently altered genes included TP53, KMT2D, KDM6A, FAT4, FAT1, CREBBP and ARID1A. The higher prevalence of HRAS (22.0% vs 3.7%) and KMT2D (59.26% vs 34.57%) was identified in UTUC than in UCB. Comparisons of somatic alterations of UCB and UTUC between the study cohort and western cohorts revealed significant differences in mutant prevalence. Notably, 28.57, 17.86 and 47.32% of the cases harbored alterations in FGFRs, ERBBs and DNA damage repair genes, respectively. Furthermore, 75% of the patients carried non-benign germline variants, but only two (1.79%) were pathogenic. The overall concordance for genomic alterations in ctDNA and matched tumor tissue was 42.97% (0-100%). Notably, 47.25% of alterations detected in ctDNA were not detected in the matched tissue, and 54.14% of which were oncogenic mutations.ConclusionsWe found a unique genomic feature of Chinese UC patients. A reasonably good concordance of genomic features between ctDNA and tissue samples were identified.
引用
收藏
页数:11
相关论文
共 30 条
  • [1] Characterization of Metastatic Urothelial Carcinoma via Comprehensive Genomic Profiling of Circulating Tumor DNA
    Agarwal, Neeraj
    Pal, Sumanta K.
    Hahn, Andrew W.
    Nussenzveig, Roberto H.
    Pond, Gregory R.
    Gupta, Sumati V.
    Wang, Jue
    Bilen, Mehmet A.
    Naik, Gurudatta
    Ghatalia, Pooja
    Hoimes, Christopher J.
    Gopalakrishnan, Dharmesh
    Barata, Pedro C.
    Drakaki, Alexandra
    Faltas, Bishoy M.
    Kiedrowski, Lesli A.
    Lanman, Richard B.
    Nagy, Rebecca J.
    Vogelzang, Nicholas J.
    Boucher, Kenneth M.
    Vaishampayan, Ulka N.
    Sonpavde, Guru
    Grivas, Petros
    [J]. CANCER, 2018, 124 (10) : 2115 - 2124
  • [2] AACR Project GENIE: Powering Precision Medicine through an International Consortium
    Andre, Fabrice
    Arnedos, Monica
    Baras, Alexander S.
    Baselga, Jose
    Bedard, Philippe L.
    Berger, Michael F.
    Bierkens, Mariska
    Calvo, Fabien
    Cerami, Ethan
    Chakravarty, Debyani
    Dang, Kristen K.
    Davidson, Nancy E.
    Del Vecchio, Fitz Catherine
    Dogan, Semih
    DuBois, Raymond N.
    Ducar, Matthew D.
    Futreal, P. Andrew
    Gao Jianjiong
    Garcia, Francisco
    Gardos, Stu
    Gocke, Christopher D.
    Gross, Benjamin E.
    Guinney, Justin
    Heins, Zachary J.
    Hintzen, Stephanie
    Horlings, Hugo
    Hudecek, Jan
    Hyman, David M.
    Kamel-Reid, Suzanne
    Kandoth, Cyriac
    Kinyua, Walter
    Kumari, Priti
    Kundra, Ritika
    Ladanyi, Marc
    Lefebvre, Celine
    LeNoue-Newton, Michele L.
    Lepisto, Eva M.
    Levy, Mia A.
    Lindeman, Neal, I
    Lindsay, James
    Liu, David
    Lu Zhibin
    MacConaill, Laura E.
    Ian, Maurer
    Maxwell, David S.
    Meijer, Gerrit A.
    Meric-Bernstam, Funda
    Micheel, Christine M.
    Miller, Clinton
    Mills, Gordon
    [J]. CANCER DISCOVERY, 2017, 7 (08) : 818 - 831
  • [3] Circulating Tumor DNA Genomics Correlate with Resistance to Abiraterone and Enzalutamide in Prostate Cancer
    Annala, Matti
    Vandekerkhove, Gillian
    Khalaf, Daniel
    Taavitsainen, Sinja
    Beja, Kevin
    Warner, Evan W.
    Sunderland, Katherine
    Kollmannsberger, Christian
    Eigl, Bernhard J.
    Finch, Daygen
    Oja, Conrad D.
    Vergidis, Joanna
    Zulfiqar, Muhammad
    Azad, Arun A.
    Nykter, Matti
    Gleave, Martin E.
    Wyatt, Alexander W.
    Chi, Kim N.
    [J]. CANCER DISCOVERY, 2018, 8 (04) : 444 - 457
  • [4] European Association of Urology Guidelines on Non-muscle-invasive Bladder Cancer (TaT1 and Carcinoma In Situ)-2019 Update
    Babjuk, Marko
    Burger, Maximilian
    Comperat, Eva M.
    Gontero, Paolo
    Mostafid, A. Hugh
    Palou, Joan
    van Rhijn, Bas W. G.
    Roupret, Morgan
    Shariat, Shahrokh F.
    Sylvester, Richard
    Zigeuner, Richard
    Capoun, Otakar
    Cohen, Daniel
    Dominguez Escrig, Jose Luis
    Hernandez, Virginia
    Peyronnet, Benoit
    Seisen, Thomas
    Soukup, Viktor
    [J]. EUROPEAN UROLOGY, 2019, 76 (05) : 639 - 657
  • [5] Next-generation sequencing (NGS) of cell-free circulating tumor DNA and tumor tissue in patients with advanced urothelial cancer: a pilot assessment of concordance
    Barata, P. C.
    Koshkin, V. S.
    Funchain, P.
    Sohal, D.
    Pritchard, A.
    Klek, S.
    Adamowicz, T.
    Gopalakrishnan, D.
    Garcia, J.
    Rini, B.
    Grivas, P.
    [J]. ANNALS OF ONCOLOGY, 2017, 28 (10) : 2458 - 2463
  • [6] Monitoring Treatment Response and Metastatic Relapse in Advanced Bladder Cancer by Liquid Biopsy Analysis
    Birkenkamp-Demtroder, Karin
    Christensen, Emil
    Nordentoft, Iver
    Knudsen, Michael
    Taber, Ann
    Hoyer, Soren
    Lamy, Philippe
    Agerbaek, Mads
    Jensen, Jorgen Bjerggaard
    Dyrskjot, Lars
    [J]. EUROPEAN UROLOGY, 2018, 73 (04) : 535 - 540
  • [7] Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia
    Bogliolo, Massimo
    Schuster, Beatrice
    Stoepker, Chantal
    Derkunt, Burak
    Su, Yan
    Raams, Anja
    Trujillo, Juan P.
    Minguillon, Jordi
    Ramirez, Maria J.
    Pujol, Roser
    Casado, Jose A.
    Banos, Rocio
    Rio, Paula
    Knies, Kerstin
    Zuniga, Sheila
    Benitez, Javier
    Bueren, Juan A.
    Jaspers, Nicolaas G. J.
    Schaerer, Orlando D.
    de Winter, Johan P.
    Schindler, Detlev
    Surralles, Jordi
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2013, 92 (05) : 800 - 806
  • [8] Cancer Susceptibility Mutations in Patients With Urothelial Malignancies
    Carlo, Maria I.
    Ravichandran, Vignesh
    Srinavasan, Preethi
    Bandlamudi, Chaitanya
    Kemel, Yelena
    Ceyhan-Birsoy, Ozge
    Mukherjee, Semanti
    Mandelker, Diana
    Chaim, Joshua
    Knezevic, Andrea
    Rana, Satshil
    Fnu, Zarina
    Breen, Kelsey
    Arnold, Angela G.
    Khurram, Aliya
    Tkachuk, Kaitlyn
    Cipolla, Catharine K.
    Regazzi, Ashley
    Hakimi, A. Ari
    Al-Ahmadie, Hikmat
    Dalbagni, Guido
    Cadoo, Karen A.
    Walsh, Michael F.
    Teo, Min-Yuen
    Funt, Samuel A.
    Coleman, Jonathan A.
    Bochner, Bernard H.
    Iyer, Gopa
    Solit, David B.
    Stadler, Zsofia K.
    Zhang, Liying
    Rosenberg, Jonathan E.
    Taylor, Barry S.
    Robson, Mark E.
    Berger, Michael F.
    Vijai, Joseph
    Bajorin, Dean F.
    Offit, Kenneth
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2020, 38 (05)
  • [9] Chakravarty D, 2017, JCO PRECIS ONCOL, V1
  • [10] Cancer Statistics in China, 2015
    Chen, Wanqing
    Zheng, Rongshou
    Baade, Peter D.
    Zhang, Siwei
    Zeng, Hongmei
    Bray, Freddie
    Jemal, Ahmedin
    Yu, Xue Qin
    He, Jie
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (02) : 115 - 132