Homologous recombination deficiency test validation in patients with high-grade advanced ovarian cancer.

Journal: Frontiers In Molecular Biosciences
Published:
Abstract

Along with BRCA mutation status, homologous recombination deficiency (HRD) testing is a prognostic and predictive biomarker for poly-ADP-ribose polymerase (PARP) inhibitor therapy indication in high-grade epithelial ovarian, fallopian tube, or peritoneal cancer. Approximately 50% of high-grade serous ovarian cancers exhibit HRD, even in the absence of germline or somatic BRCA1/2 loss-of-function mutations. In this scenario, access to a validated diagnostic HRD test can optimize treatment selection and increase the effectiveness of the intervention. To technically validate an in-house next-generation sequencing (NGS)-based HRD test, QIAseq Custom Panel (QIAGEN), by comparing it with the reference assay, MyChoice CDx® Plus HRD (Myriad Genetics), which is used in routine care. This is a prospective cohort study conducted at the Oncoclínicas Precision Medicine (OCPM) laboratory using samples from patients with advanced or relapsed platinum-sensitive ovarian cancer eligible for HRD testing in a diagnostic clinical setting at Oncoclínicas and Co. We assessed the performance of the in-house test (GS Focus HRD) using Cohen's kappa statistic to measure agreement with the gold standard assay (MyChoice® HRD Plus CDx) in HRD status classification, along with other accuracy metrics. In total, 41 samples were analyzed (20 HRD-positive, 19 HRD-negative, and 2 inconclusive results with the MyChoice® HRD Plus CDx assay). The GS Focus HRD test demonstrated high concordance for HRD status with the reference test (kappa: 0.8 and 95% CI: 0.60-0.98). Overall accuracy, sensitivity, and specificity were 90%. Six samples had BRCA1/2 mutations identified by the MyChoice® HRD Plus CDx, all of which were detected by the GS Focus HRD test. In summary, the results demonstrate substantial agreement and high accuracy of the NGS-based GS Focus HRD test compared to MyChoice® HRD Plus CDx. Our in-house assay is eligible for diagnostic test approval and market access as per Brazilian regulations.

Authors
Angelica Nogueira Rodrigues, Andreza Karine De Barros Souto, Diocésio Alves De Andrade, Larissa Gomes, Sandra Koide, Renata De E Silva, Bruno De Souza, Juliana Massaro, Andréia De Melo, Andrea Borges, Camila Giro, Carlos Augusto De Andrade, Cesar Da Costa, Daniel Gimenes, Eduardo Caminha De Mello, Fernanda De Oliveira, Frederico Müller De Lima, Gabriel Lopes, Gustavo De Bretas, Gustavo Jacob, Herika Lucia Da Silva, Juliana Notaro, Lara Alves, Marcos Moitinho, Mirian Da Silva, Roberto Abramoff, Thais Amaral Da Rauber, Rodrigo Dienstmann, Fernanda Koyama
Relevant Conditions

Ovarian Cancer