Homologous recombination deficiency (HRD) testing on cell-free tumor DNA from peritoneal fluid.


Journal

Molecular cancer
ISSN: 1476-4598
Titre abrégé: Mol Cancer
Pays: England
ID NLM: 101147698

Informations de publication

Date de publication:
06 11 2023
Historique:
received: 20 04 2023
accepted: 19 09 2023
medline: 8 11 2023
pubmed: 7 11 2023
entrez: 6 11 2023
Statut: epublish

Résumé

Knowing the homologous recombination deficiency (HRD) status in advanced epithelial ovarian cancer (EOC) is vital for patient management. HRD is determined by BRCA1/BRCA2 pathogenic variants or genomic instability. However, tumor DNA analysis is inconclusive in 15-19% of cases. Peritoneal fluid, available in > 95% of advanced EOC cases, could serve as an alternative source of cell-free tumor DNA (cftDNA) for HRD testing. Limited data show the feasibility of cancer panel gene testing on ascites cfDNA but no study, to date, has investigated HRD testing. We collected ascites/peritoneal washings from 53 EOC patients (19 from retrospective cohort and 34 from prospective cohort) and performed a Cancer Gene Panel (CGP) using NGS for TP53/HR genes and shallow Whole Genome Sequencing (sWGS) for genomic instability on cfDNA. cfDNA was detectable in 49 out of 53 patients (92.5%), including those with limited peritoneal fluid. Median cfDNA was 3700 ng/ml, with a turnaround time of 21 days. TP53 pathogenic variants were detected in 86% (42/49) of patients, all with HGSOC. BRCA1 and BRCA2 pathogenic variants were found in 14% (7/49) and 10% (5/49) of cases, respectively. Peritoneal cftDNA showed high sensitivity (97%), specificity (83%), and concordance (95%) with tumor-based TP53 variant detection. NGS CGP on cftDNA identified BRCA2 pathogenic variants in one case where tumor-based testing failed. sWGS on cftDNA provided informative results even when tumor-based genomic instability testing failed. Profiling cftDNA from peritoneal fluid is feasible, providing a significant amount of tumor DNA. This fast and reliable approach enables HRD testing, including BRCA1/2 mutations and genomic instability assessment. HRD testing on cfDNA from peritoneal fluid should be offered to all primary laparoscopy patients.

Sections du résumé

BACKGROUND
Knowing the homologous recombination deficiency (HRD) status in advanced epithelial ovarian cancer (EOC) is vital for patient management. HRD is determined by BRCA1/BRCA2 pathogenic variants or genomic instability. However, tumor DNA analysis is inconclusive in 15-19% of cases. Peritoneal fluid, available in > 95% of advanced EOC cases, could serve as an alternative source of cell-free tumor DNA (cftDNA) for HRD testing. Limited data show the feasibility of cancer panel gene testing on ascites cfDNA but no study, to date, has investigated HRD testing.
METHODS
We collected ascites/peritoneal washings from 53 EOC patients (19 from retrospective cohort and 34 from prospective cohort) and performed a Cancer Gene Panel (CGP) using NGS for TP53/HR genes and shallow Whole Genome Sequencing (sWGS) for genomic instability on cfDNA.
RESULTS
cfDNA was detectable in 49 out of 53 patients (92.5%), including those with limited peritoneal fluid. Median cfDNA was 3700 ng/ml, with a turnaround time of 21 days. TP53 pathogenic variants were detected in 86% (42/49) of patients, all with HGSOC. BRCA1 and BRCA2 pathogenic variants were found in 14% (7/49) and 10% (5/49) of cases, respectively. Peritoneal cftDNA showed high sensitivity (97%), specificity (83%), and concordance (95%) with tumor-based TP53 variant detection. NGS CGP on cftDNA identified BRCA2 pathogenic variants in one case where tumor-based testing failed. sWGS on cftDNA provided informative results even when tumor-based genomic instability testing failed.
CONCLUSION
Profiling cftDNA from peritoneal fluid is feasible, providing a significant amount of tumor DNA. This fast and reliable approach enables HRD testing, including BRCA1/2 mutations and genomic instability assessment. HRD testing on cfDNA from peritoneal fluid should be offered to all primary laparoscopy patients.

Identifiants

pubmed: 37932736
doi: 10.1186/s12943-023-01864-1
pii: 10.1186/s12943-023-01864-1
pmc: PMC10626673
doi:

Substances chimiques

BRCA1 protein, human 0
BRCA1 Protein 0
BRCA2 protein, human 0
BRCA2 Protein 0
Circulating Tumor DNA 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

178

Informations de copyright

© 2023. The Author(s).

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Auteurs

Cyril Roussel-Simonin (C)

Drug Development Department (DITEP), Gustave-Roussy Cancer Campus, Villejuif. Sorbonne Université, Paris, France. Cyril.ROUSSEL-SIMONIN@gustaveroussy.fr.

Felix Blanc-Durand (F)

Departement of Medecine, Gustave-Roussy Cancer Campus, INSERM U981, Université Paris-Saclay, Villejuif, France.
Université Paris-Saclay, Gustave-Roussy Cancer Campus, Inserm U981, Villejuif, France.

Roseline Tang (R)

Cancer Genetics Laboratory, Medical Biology and Pathology Department, Gustave-Roussy Cancer Campus, Villejuif, France.

Damien Vasseur (D)

Cancer Genetics Laboratory, Medical Biology and Pathology Department, Gustave-Roussy Cancer Campus, Villejuif, France.

Audrey Le Formal (A)

Université Paris-Saclay, Gustave-Roussy Cancer Campus, Inserm U981, Villejuif, France.

Laure Chardin (L)

Université Paris-Saclay, Gustave-Roussy Cancer Campus, Inserm U981, Villejuif, France.

Elisa Yaniz (E)

Université Paris-Saclay, Gustave-Roussy Cancer Campus, Inserm U981, Villejuif, France.

Sébastien Gouy (S)

Department of Pathology and Medical Biology, Gustave-Roussy Cancer Campus, Villejuif, France.

Amandine Maulard (A)

Department of Pathology and Medical Biology, Gustave-Roussy Cancer Campus, Villejuif, France.

Stéphanie Scherier (S)

Department of Pathology and Medical Biology, Gustave-Roussy Cancer Campus, Villejuif, France.

Claire Sanson (C)

Department of Pathology and Medical Biology, Gustave-Roussy Cancer Campus, Villejuif, France.

Ludovic Lacroix (L)

Department of Gynecologic Surgery, Gustave-Roussy Cancer Campus, Villejuif, France.

Sophie Cotteret (S)

Cancer Genetics Laboratory, Medical Biology and Pathology Department, Gustave-Roussy Cancer Campus, Villejuif, France.

Lea Mauny (L)

Department of Pathology and Medical Biology, Gustave-Roussy Cancer Campus, Villejuif, France.

François Zaccarini (F)

Department of Pathology and Medical Biology, Gustave-Roussy Cancer Campus, Villejuif, France.

Etienne Rouleau (E)

Université Paris-Saclay, Gustave-Roussy Cancer Campus, Inserm U981, Villejuif, France.
Cancer Genetics Laboratory, Medical Biology and Pathology Department, Gustave-Roussy Cancer Campus, Villejuif, France.

Alexandra Leary (A)

Departement of Medecine, Gustave-Roussy Cancer Campus, INSERM U981, Université Paris-Saclay, Villejuif, France.
Université Paris-Saclay, Gustave-Roussy Cancer Campus, Inserm U981, Villejuif, France.

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Classifications MeSH