Abstract
Background
Quantification of circulating tumour DNA methylation is a promising novel approach for predicting and monitoring treatment efficacy in cancer. The currently frequently employed biomarker CA-125, has been recently shown to not be prognostic for overall survival in platinum-resistant patients, making it further relevant for identifying novel biomarkers. HOXA9 promoter methylation has been observed in a large proportion of patients with high grade serous ovarian carcinoma (OC), and hypermethylation of HOXA9 is associated with worse progression-free survival and overall survival. The aim of the current study was to investigate whether HOXA9 methylation at baseline and during treatment, could predict treatment efficacy in BRCA-mutated ovarian cancer patients treated with the PARP inhibitor, Veliparib.
Methods
Plasma from OC patients was retrieved at baseline before initiation of daily oral single agent Veliparib, as well as following each treatment cycle, as part of a phase II investigator initiated trial (NCT01472783). DNA was purified from 4 ml of plasma, bisulfite converted and analysed by droplet digital PCR with a HOXA9 methylation-specific assay. Beta-2-microglobulin alleles/mL were used for normalization, and the fractional abundance of methylated HOXA9 was calculated.
Results
32 patients were enrolled in a phase II trial, of which 24 had methylated HOXA9 at baseline. There was no significant different in overall survival based on HOXA9 methylation at baseline (p = 0.4), however patients with HOXA9 methylation following three treatment cycles had a significantly worse overall survival compared to patients with non-methylated HOXA9 (median overall survival was 8 months vs. 19 months for patients with methylated vs. non-methylated HOXA9, respectively, p = 0.0001). A similar trend was noted for progression free survival.
Conclusions
Methylation of HOXA9 detected in circulating tumor DNA may serve as a prognostic and treatment efficacy biomarker in BRCA-mutated ovarian cancer patients undergoing treatment with PARP inhibitors.
Clinical trial identification
NCT01472783.
Quantification of circulating tumour DNA methylation is a promising novel approach for predicting and monitoring treatment efficacy in cancer. The currently frequently employed biomarker CA-125, has been recently shown to not be prognostic for overall survival in platinum-resistant patients, making it further relevant for identifying novel biomarkers. HOXA9 promoter methylation has been observed in a large proportion of patients with high grade serous ovarian carcinoma (OC), and hypermethylation of HOXA9 is associated with worse progression-free survival and overall survival. The aim of the current study was to investigate whether HOXA9 methylation at baseline and during treatment, could predict treatment efficacy in BRCA-mutated ovarian cancer patients treated with the PARP inhibitor, Veliparib.
Methods
Plasma from OC patients was retrieved at baseline before initiation of daily oral single agent Veliparib, as well as following each treatment cycle, as part of a phase II investigator initiated trial (NCT01472783). DNA was purified from 4 ml of plasma, bisulfite converted and analysed by droplet digital PCR with a HOXA9 methylation-specific assay. Beta-2-microglobulin alleles/mL were used for normalization, and the fractional abundance of methylated HOXA9 was calculated.
Results
32 patients were enrolled in a phase II trial, of which 24 had methylated HOXA9 at baseline. There was no significant different in overall survival based on HOXA9 methylation at baseline (p = 0.4), however patients with HOXA9 methylation following three treatment cycles had a significantly worse overall survival compared to patients with non-methylated HOXA9 (median overall survival was 8 months vs. 19 months for patients with methylated vs. non-methylated HOXA9, respectively, p = 0.0001). A similar trend was noted for progression free survival.
Conclusions
Methylation of HOXA9 detected in circulating tumor DNA may serve as a prognostic and treatment efficacy biomarker in BRCA-mutated ovarian cancer patients undergoing treatment with PARP inhibitors.
Clinical trial identification
NCT01472783.
| Original language | English |
|---|---|
| Article number | 954P |
| Journal | Annals of Oncology |
| Volume | 29 |
| Issue number | Suppl. 8 |
| Pages (from-to) | viii341 |
| Number of pages | 1 |
| ISSN | 0923-7534 |
| DOIs | |
| Publication status | Published - 20. Oct 2018 |
| Event | ESMO 2018 Congress: Securing access to optimal cancer care - Munchen, Germany Duration: 19. Oct 2018 → 23. Oct 2018 https://www.esmo.org/Conferences/ESMO-2018-Congress |
Conference
| Conference | ESMO 2018 Congress |
|---|---|
| Country/Territory | Germany |
| City | Munchen |
| Period | 19/10/2018 → 23/10/2018 |
| Internet address |