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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Breast Cancer Detection and Treatment Monitoring Using a Noninvasive Prenatal Testing Platform: Utility in Pregnant and Nonpregnant Populations

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Autor(es):
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Lenaerts, Liesbeth [1] ; Che, Huiwen [2] ; Brison, Nathalie [3] ; Neofytou, Maria [2, 4] ; Jatsenko, Tatjana [2] ; Lefrere, Hanne [1] ; Maggen, Charlotte [1, 5] ; Villela, Darine [6, 2] ; Verheecke, Magali [7] ; Dehaspe, Luc [8] ; Croitor, Anca [9] ; Hatse, Sigrid [10] ; Wildiers, Hans [10, 11] ; Neven, Patrick [1, 5] ; Vandecaveye, Vincent [12, 13] ; Floris, Giuseppe [14, 15] ; Vermeesch, Joris Robert [2, 3, 8] ; Amant, Frederic [1, 5, 16, 17]
Número total de Autores: 18
Afiliação do(s) autor(es):
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[1] Katholieke Univ Leuven, Lab Gynecol Oncol, Dept Oncol, Leuven - Belgium
[2] Katholieke Univ Leuven, Lab Cytogenet & Genome Res, Dept Human Genet, Leuven - Belgium
[3] Univ Hosp Leuven, Ctr Human Genet, Leuven - Belgium
[4] Univ Cambridge, Canc Res UK Cambridge Inst, Mol & Computat Diagnost, Cambridge - England
[5] Univ Hosp Leuven, Dept Gynecol & Obstet, Leuven - Belgium
[6] Univ Sao Paulo, Dept Genet & Biol Evolut, Sao Paulo - Brazil
[7] Gen Hosp Turnhout, Gynaecol & Obstet Dept, Turnhout - Belgium
[8] Univ Hosp Leuven, Genom Core Facil, Leuven - Belgium
[9] Katholieke Univ Leuven, Unit Biomed MRI, Dept Imaging & Pathol, Leuven - Belgium
[10] Katholieke Univ Leuven, Lab Expt Oncol, Dept Oncol, Leuven - Belgium
[11] Univ Hosp Leuven, Dept Gen Med Oncol, Leuven - Belgium
[12] Katholieke Univ Leuven, Unit Translat MRI, Dept Imaging & Pathol, Leuven - Belgium
[13] Univ Hosp Leuven, Dept Radiol, Leuven - Belgium
[14] Katholieke Univ Leuven, Unit Translat Cell & Tissue Res, Dept Imaging & Pathol, Leuven - Belgium
[15] Univ Hosp Leuven, Dept Pathol, Leuven - Belgium
[16] Univ Amsterdam, Ctr Gynecol Oncol Amsterdam, Acad Med Ctr Amsterdam, Amsterdam - Netherlands
[17] Antoni van Leeuwenhoek Hosp, Netherlands Canc Inst, Amsterdam - Netherlands
Número total de Afiliações: 17
Tipo de documento: Artigo Científico
Fonte: CLINICAL CHEMISTRY; v. 66, n. 11, p. 1414-1423, NOV 2020.
Citações Web of Science: 0
Resumo

BACKGROUND: Numerous publications have reported the incidental detection of occult malignancies upon routine noninvasive prenatal testing (NIPT). However, these studies were not designed to evaluate the NIPT performance for cancer detection. METHODS: We investigated the sensitivity of a genome-wide NIPT pipeline, called GIPSeq, for detecting cancer-specific copy number alterations (CNAs) in plasma tumor DNA (ctDNA) of patients with breast cancer. To assess whether a pregnancy itself, with fetal cell-free DNA (cfDNA) in the maternal circulation, might influence the detection of ctDNA, results were compared in pregnant (n = 25) and nonpregnant (n = 25) cancer patients. Furthermore, the ability of GIPSeq to monitor treatment response was assessed. RESULTS: Overall GIPSeq sensitivity for detecting cancer-specific CNAs in plasma cfDNA was 26%. Fifteen percent of detected cases were asymptomatic at the time of blood sampling. GIPSeq sensitivity mainly depended on the tumor stage. Also, triple negative breast cancers (TNBC) were more frequently identified compared to hormone-positive or HER2-enriched tumors. This might be due to the presence of high-level gains and losses of cfDNA or high ctDNA loads in plasma of TNBC. Although higher GIPSeq sensitivity was noted in pregnant (36%) than in nonpregnant women (16%), the limited sample size prohibits a definite conclusion. Finally, GIPSeq profiling of cfDNA during therapy allowed monitoring of early treatment response. CONCLUSIONS: The results underscore the potential of NIPT-based tests, analyzing CNAs in plasma cfDNA in a genome-wide and unbiased fashion for breast cancer detection, cancer subtyping and treatment monitoring in a pregnant and nonpregnant target population. (AU)

Processo FAPESP: 17/23448-8 - Investigação global de número de cópias em DNA livre circulante no teste pré-natal não invasivo
Beneficiário:Darine Christina Maia Villela
Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Pós-Doutorado