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Genetic hallmarks of recurrent/metastatic adenoid cystic carcinoma.
Ho, Allen S; Ochoa, Angelica; Jayakumaran, Gowtham; Zehir, Ahmet; Valero Mayor, Cristina; Tepe, Justin; Makarov, Vladimir; Dalin, Martin G; He, Jie; Bailey, Mark; Montesion, Meagan; Ross, Jeffrey S; Miller, Vincent A; Chan, Lindsay; Ganly, Ian; Dogan, Snjezana; Katabi, Nora; Tsipouras, Petros; Ha, Patrick; Agrawal, Nishant; Solit, David B; Futreal, P Andrew; El Naggar, Adel K; Reis-Filho, Jorge S; Weigelt, Britta; Ho, Alan L; Schultz, Nikolaus; Chan, Timothy A; Morris, Luc Gt.
Afiliación
  • Ho AS; Department of Surgery and.
  • Ochoa A; Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Jayakumaran G; Marie-Josée and Henry R. Kravis Center for Molecular Oncology.
  • Zehir A; Diagnostic Molecular Pathology.
  • Valero Mayor C; Diagnostic Molecular Pathology.
  • Tepe J; Head and Neck Service, Department of Surgery, and.
  • Makarov V; Head and Neck Service, Department of Surgery, and.
  • Dalin MG; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center (MSKCC), New York, New York, USA.
  • He J; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center (MSKCC), New York, New York, USA.
  • Bailey M; Foundation Medicine, Cambridge, Massachusetts, USA.
  • Montesion M; Foundation Medicine, Cambridge, Massachusetts, USA.
  • Ross JS; Foundation Medicine, Cambridge, Massachusetts, USA.
  • Miller VA; Foundation Medicine, Cambridge, Massachusetts, USA.
  • Chan L; Foundation Medicine, Cambridge, Massachusetts, USA.
  • Ganly I; Foundation Medicine, Cambridge, Massachusetts, USA.
  • Dogan S; Head and Neck Service, Department of Surgery, and.
  • Katabi N; Diagnostic Molecular Pathology.
  • Tsipouras P; Diagnostic Molecular Pathology.
  • Ha P; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Agrawal N; Department of Otolaryngology-Head and Neck Surgery, UCSF, San Francisco, California, USA.
  • Solit DB; Department of Surgery, University of Chicago, Chicago, Illinois, USA.
  • Futreal PA; Marie-Josée and Henry R. Kravis Center for Molecular Oncology.
  • El Naggar AK; Head and Neck Service, Department of Surgery, and.
  • Reis-Filho JS; Department of Medicine.
  • Weigelt B; Department of Genomic Medicine and.
  • Ho AL; Department of Pathology, University of Texas MD Anderson Cancer Center (MDACC), Houston, Texas, USA.
  • Schultz N; Experimental Pathology Service, MSKCC, New York, New York, USA.
  • Chan TA; Experimental Pathology Service, MSKCC, New York, New York, USA.
  • Morris LG; Department of Medicine.
J Clin Invest ; 129(10): 4276-4289, 2019 10 01.
Article en En | MEDLINE | ID: mdl-31483290
BACKGROUNDAdenoid cystic carcinoma (ACC) is a rare malignancy arising in salivary glands and other sites, characterized by high rates of relapse and distant spread. Recurrent/metastatic (R/M) ACCs are generally incurable, due to a lack of active systemic therapies. To improve outcomes, deeper understanding of genetic alterations and vulnerabilities in R/M tumors is needed.METHODSAn integrated genomic analysis of 1,045 ACCs (177 primary, 868 R/M) was performed to identify alterations associated with advanced and metastatic tumors. Intratumoral genetic heterogeneity, germline mutations, and therapeutic actionability were assessed.RESULTSCompared with primary tumors, R/M tumors were enriched for alterations in key Notch (NOTCH1, 26.3% vs. 8.5%; NOTCH2, 4.6% vs. 2.3%; NOTCH3, 5.7% vs. 2.3%; NOTCH4, 3.6% vs. 0.6%) and chromatin-remodeling (KDM6A, 15.2% vs. 3.4%; KMT2C/MLL3, 14.3% vs. 4.0%; ARID1B, 14.1% vs. 4.0%) genes. TERT promoter mutations (13.1% of R/M cases) were mutually exclusive with both NOTCH1 mutations (q = 3.3 × 10-4) and MYB/MYBL1 fusions (q = 5.6 × 10-3), suggesting discrete, alternative mechanisms of tumorigenesis. This network of alterations defined 4 distinct ACC subgroups: MYB+NOTCH1+, MYB+/other, MYBWTNOTCH1+, and MYBWTTERT+. Despite low mutational load, we identified numerous samples with marked intratumoral genetic heterogeneity, including branching evolution across multiregion sequencing.CONCLUSIONThese observations collectively redefine the molecular underpinnings of ACC progression and identify further targets for precision therapies.FUNDINGAdenoid Cystic Carcinoma Research Foundation, Pershing Square Sohn Cancer Research grant, the PaineWebber Chair, Stand Up 2 Cancer, NIH R01 CA205426, the STARR Cancer Consortium, NCI R35 CA232097, the Frederick Adler Chair, Cycle for Survival, the Jayme Flowers Fund, The Sebastian Nativo Fund, NIH K08 DE024774 and R01 DE027738, and MSKCC through NIH/NCI Cancer Center Support Grant (P30 CA008748).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma Adenoide Quístico / Mutación Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Invest Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma Adenoide Quístico / Mutación Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Invest Año: 2019 Tipo del documento: Article
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