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Normalized LST Is an Efficient Biomarker for Homologous Recombination Deficiency and Olaparib Response in Ovarian Carcinoma.

Authors :
Christinat, Yann
Ho, Liza
Clément, Sophie
Genestie, Catherine
Sehouli, Jalid
Cinieri, Saverio
Gonzalez Martin, Antonio
Denison, Ursula
Fujiwara, Keiichi
Vergote, Ignace
Tognon, Germana
Hietanen, Sakari
Ray-Coquard, Isabelle
Pujade-Lauraine, Eric
McKee, Thomas A.
Source :
JCO Precision Oncology; 6/26/2023, Vol. 7, p1-9, 9p
Publication Year :
2023

Abstract

PURPOSE: The efficiency of the Myriad Homologous Recombination Deficiency (HRD) test to guide the use of poly (ADP-ribose) polymerase (PARP) inhibitors has been demonstrated in several phase III trials. However, a need exists for alternative clinically validated tests. METHODS: A novel biomarker for HRD was developed using The Cancer Genome Atlas database and, as part of the ENGOT HRD European Initiative, applied to 469 samples from the PAOLA-1/ENGOT-ov25 trial. Results were compared with the Myriad myChoice Genomic Instability Score (GIS) with respect to the progression-free survival in the olaparib + bevacizumab and placebo + bevacizumab arms. RESULTS: Analysis of the TCGA cohort revealed that a normalization of the number of large-scale state transitions by the number of whole-genome doubling events allows a better separation and classification of HRD samples than the GIS. Analysis of the PAOLA-1 samples, using the Geneva test (OncoScan + nLST), yielded a lower failure rate (27 of 469 v 59 of 469) and a hazard ratio of 0.40 (95% CI, 0.28 to 0.57) compared with 0.37 for Myriad myChoice (BRCAm or GIS+) in the nLST-positive samples. In patients with BRCAwt, the Geneva test identified a novel subpopulation of patients, with a favorable 1-year PFS (85%) but a poor 2-year PFS (30%) on olaparib + bevacizumab treatment. CONCLUSION: The proposed test efficiently separates HRD-positive from HRD-negative patients, predicts response to PARP inhibition, and can be easily deployed in a clinical laboratory for routine practice. The performance is similar to the available commercial test, but its lower failure rate allows an increase in the number of patients who will receive a conclusive laboratory result. PARP inhibitors, such as olaparib, have greatly improved survival of patients with ovarian carcinoma. The Geneva HRD test can predict response to olaparib in combination with bevacizumab. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
24734284
Volume :
7
Database :
Complementary Index
Journal :
JCO Precision Oncology
Publication Type :
Academic Journal
Accession number :
164549326
Full Text :
https://doi.org/10.1200/PO.22.00555