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Genomic Profiling of Uterine Aspirates and cfDNA as an Integrative Liquid Biopsy Strategy in Endometrial Cancer.
Casas-Arozamena, Carlos; Díaz, Eva; Moiola, Cristian Pablo; Alonso-Alconada, Lorena; Ferreirós, Alba; Abalo, Alicia; Gil, Carlos López; Oltra, Sara S; de Santiago, Javier; Cabrera, Silvia; Sampayo, Victoria; Bouso, Marta; Arias, Efigenia; Cueva, Juan; Colas, Eva; Vilar, Ana; Gil-Moreno, Antonio; Abal, Miguel; Moreno-Bueno, Gema; Muinelo-Romay, Laura.
Afiliación
  • Casas-Arozamena C; Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago de Compostela (IDIS), University Hospital of Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
  • Díaz E; Foundation MD Anderson International, C/Gómez Hemans 2, 28033 Madrid, Spain.
  • Moiola CP; Biomedical Research Group in Gynecology, Vall d'Hebron Research Institute (VHIR), Universitat Autonoma de Barcelona, 119-129 Pg. Vall d'Hebron, 08035 Barcelona, Spain.
  • Alonso-Alconada L; Nasasbiotech, S.L., Canton Grande 3, 15003 A Coruña, Spain.
  • Ferreirós A; Nasasbiotech, S.L., Canton Grande 3, 15003 A Coruña, Spain.
  • Abalo A; Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago de Compostela (IDIS), University Hospital of Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
  • Gil CL; Biomedical Research Group in Gynecology, Vall d'Hebron Research Institute (VHIR), Universitat Autonoma de Barcelona, 119-129 Pg. Vall d'Hebron, 08035 Barcelona, Spain.
  • Oltra SS; Foundation MD Anderson International, C/Gómez Hemans 2, 28033 Madrid, Spain.
  • de Santiago J; Department of Gynecology, MD Anderson Cancer Center, 28029 Madrid, Spain.
  • Cabrera S; Biomedical Research Group in Gynecology, Vall d'Hebron Research Institute (VHIR), Universitat Autonoma de Barcelona, 119-129 Pg. Vall d'Hebron, 08035 Barcelona, Spain.
  • Sampayo V; Department of Gynecology, University Hospital of Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
  • Bouso M; Department of Pathology, University Hospital of Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
  • Arias E; Department of Gynecology, University Hospital of Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
  • Cueva J; Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago de Compostela (IDIS), University Hospital of Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
  • Colas E; Biomedical Research Group in Gynecology, Vall d'Hebron Research Institute (VHIR), Universitat Autonoma de Barcelona, 119-129 Pg. Vall d'Hebron, 08035 Barcelona, Spain.
  • Vilar A; Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Monforte de Lemos 3-5, 28029 Madrid, Spain.
  • Gil-Moreno A; Department of Gynecology, University Hospital of Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
  • Abal M; Biomedical Research Group in Gynecology, Vall d'Hebron Research Institute (VHIR), Universitat Autonoma de Barcelona, 119-129 Pg. Vall d'Hebron, 08035 Barcelona, Spain.
  • Moreno-Bueno G; Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Monforte de Lemos 3-5, 28029 Madrid, Spain.
  • Muinelo-Romay L; Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago de Compostela (IDIS), University Hospital of Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
J Clin Med ; 9(2)2020 Feb 21.
Article en En | MEDLINE | ID: mdl-32098121
The incidence and mortality of endometrial cancer (EC) have risen in recent years, hence more precise management is needed. Therefore, we combined different types of liquid biopsies to better characterize the genetic landscape of EC in a non-invasive and dynamic manner. Uterine aspirates (UAs) from 60 patients with EC were obtained during surgery and analyzed by next-generation sequencing (NGS). Blood samples, collected at surgery, were used for cell-free DNA (cfDNA) and circulating tumor cell (CTC) analyses. Finally, personalized therapies were tested in patient-derived xenografts (PDXs) generated from the UAs. NGS analyses revealed the presence of genetic alterations in 93% of the tumors. Circulating tumor DNA (ctDNA) was present in 41.2% of cases, mainly in patients with high-risk tumors, thus indicating a clear association with a more aggressive disease. Accordingly, the results obtained during the post-surgery follow-up indicated the presence of ctDNA in three patients with progressive disease. Moreover, 38.9% of patients were positive for CTCs at surgery. Finally, the efficacy of targeted therapies based on the UA-specific mutational landscape was demonstrated in PDX models. Our study indicates the potential clinical applicability of a personalized strategy based on a combination of different liquid biopsies to characterize and monitor tumor evolution, and to identify targeted therapies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Clin Med Año: 2020 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Clin Med Año: 2020 Tipo del documento: Article País de afiliación: España
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