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Genomic profiling of uterine aspirates and cfDNA as an integrative liquid biopsy strategy in endometrial cancer

Authors :
Victoria Sampayo
Carlos Casas-Arozamena
Silvia Cabrera
Carlos López Gil
Alba Ferreirós
Miguel Abal
Juan Cueva
Gema Moreno-Bueno
Sara S Oltra
Cristian Pablo Moiola
Marta Bouso
Eva Colas
Antonio Gil-Moreno
Lorena Alonso-Alconada
Javier De Santiago
Eva C. Diaz
Alicia Abalo
Efigenia Arias
Laura Muinelo-Romay
Ana Vilar
UAM. Departamento de Bioquímica
Instituto de Investigaciones Biomédicas 'Alberto Sols' (IIBM)
Source :
Biblos-e Archivo. Repositorio Institucional de la UAM, instname, Journal of Clinical Medicine, Biblos-e Archivo: Repositorio Institucional de la UAM, Universidad Autónoma de Madrid, Dipòsit Digital de Documents de la UAB, Universitat Autònoma de Barcelona, Volume 9, Issue 2, Journal of Clinical Medicine, Vol 9, Iss 2, p 585 (2020)
Publication Year :
2020
Publisher :
MDPI, Basel, Switzerland, 2020.

Abstract

The incidence and mortality of endometrial cancer (EC) have risen in recent years, hence more precise management is needed. Therefore, wecombined di erent 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 e cacy 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<br />This work was supported by grants and support from the Instituto de Salud Carlos III (ISCIII) and FEDER (PI17/01919, PI17/02071), CIBERONC (CB16/12/00328), and the AECC (Grupos Estables de Investigacion 2018-AECC) to A.G.-M. and M.A.; Instituto de Salud Carlos III (ISCIII) and FEDER (PI16/00134), CIBERONC (CB16/12/00295), and the AECC (Grupos Estables de Investigacion 2018-AECC) to G.M.-B.; and the AECC to L.M.-R.

Details

Database :
OpenAIRE
Journal :
Biblos-e Archivo. Repositorio Institucional de la UAM, instname, Journal of Clinical Medicine, Biblos-e Archivo: Repositorio Institucional de la UAM, Universidad Autónoma de Madrid, Dipòsit Digital de Documents de la UAB, Universitat Autònoma de Barcelona, Volume 9, Issue 2, Journal of Clinical Medicine, Vol 9, Iss 2, p 585 (2020)
Accession number :
edsair.doi.dedup.....a5eb80dc2c9dccfdfc774e009fba742b