Genomic Profiling of Uterine Aspirates and cfDNA as an Integrative Liquid Biopsy Strategy in Endometrial Cancer

被引:27
作者
Casas-Arozamena, Carlos [1 ]
Diaz, Eva [2 ]
Pablo Moiola, Cristian [3 ]
Alonso-Alconada, Lorena [4 ]
Ferreiros, Alba [4 ]
Abalo, Alicia [1 ]
Lopez Gil, Carlos [3 ]
Oltra, Sara S. [2 ]
de Santiago, Javier [5 ]
Cabrera, Silvia [3 ]
Sampayo, Victoria [6 ]
Bouso, Marta [7 ]
Arias, Efigenia [6 ]
Cueva, Juan [1 ]
Colas, Eva [3 ,8 ]
Vilar, Ana [6 ]
Gil-Moreno, Antonio [3 ,8 ]
Abal, Miguel [1 ,4 ,8 ]
Moreno-Bueno, Gema [2 ,8 ,9 ]
Muinelo-Romay, Laura [1 ,8 ]
机构
[1] Univ Hosp Santiago De Compostela SERGAS, Hlth Res Inst Santiago De Compostela IDIS, Translat Med Oncol Grp Oncomet, Trav Choupana S-N, Santiago De Compostela 15706, Spain
[2] Fdn MD Anderson Int, C Gomez Hemans 2, Madrid 28033, Spain
[3] Univ Autonoma Barcelona, Vall dHebron Res Inst VHIR, Biomed Res Grp Gynecol, 119-129 Pg Vall dHebron, Barcelona 08035, Spain
[4] Nasasbiotech SL, Canton Grande 3, La Coruna 15003, Spain
[5] MD Anderson Canc Ctr, Dept Gynecol, Madrid 28029, Spain
[6] Univ Hosp Santiago De Compostela SERGAS, Dept Gynecol, Trav Choupana S-N, Santiago De Compostela 15706, Spain
[7] Univ Hosp Santiago De Compostela SERGAS, Dept Pathol, Trav Choupana S-N, Santiago De Compostela 15706, Spain
[8] Ctr Invest Biomed Red Canc CIBERONC, Monforte Lemos 3-5, Madrid 28029, Spain
[9] Auton Univ Madrid UAM, Biomed Res Inst Alberto Sols CSIC UAM, Dept Biochem, IdiPaz, Arzobispo Morcillo 4, Madrid 28029, Spain
关键词
endometrial cancer; uterine aspirates; circulating biomarkers; circulating tumor DNA (ctDNA); circulating tumor cells (CTCs); PDX models; targeted therapies; DNA;
D O I
10.3390/jcm9020585
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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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页数:16
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