9PPlasma gene conversions after one cycle (C) abiraterone acetate (AA) for metastatic castration-resistant prostate cancer (mCRPC): A biomarker analysis of a multi-centre, international trial. (7th November 2019)
- Record Type:
- Journal Article
- Title:
- 9PPlasma gene conversions after one cycle (C) abiraterone acetate (AA) for metastatic castration-resistant prostate cancer (mCRPC): A biomarker analysis of a multi-centre, international trial. (7th November 2019)
- Main Title:
- 9PPlasma gene conversions after one cycle (C) abiraterone acetate (AA) for metastatic castration-resistant prostate cancer (mCRPC): A biomarker analysis of a multi-centre, international trial
- Authors:
- Jayaram, A K
Shen, D
Wingate, A
Wetterskog, D
Sternberg, C
Jones, R
Berruti, A
Lefresne, F
Lahaye, M
Thomas, S
Joshi, S
Gormley, M
Tombal, B
Merseburger, A
Ricci, D
Attard, G - Abstract:
- Abstract: Background: A number of genomic alterations detected in plasma DNA have been associated with worse outcome in mCRPC (Jayaram et al Cancer Discov). We hypothesized that patients (pts) who harbored a genomic alteration that decreased after 1C of treatment derive treatment benefit and this would distinguish them from truly resistant pts. Methods: Plasma DNA (128 C1 day (D) 1, 134 C2 D1, and 41 progression [PD] from chemotherapy-naïve mCRPC pts in a phase 2 study of AA (NCT01867710), recently reported (Attard et al, Jama Onc) were subjected to custom targeted-capture NGS. Assay was optimised and validated to detect pathogenic point mutations (PM), deletions and copy number alterations (CNA) inAR, TP53, RB1, PIK3CA and DNA repair deficient genes (DRD): BRCA1, BRCA2, FANCA, ATM, CHEK2, HDAC2, BRIP1, and PALB2. Pts were followed up for overall survival (OS) and radiographic progression-free survival (rPFS) (48 months). Results: Pts were classified into 4 groups based on whether a gene alteration was detectable (+) or not (-) at C1D1 and C2D1 respectively. At C1D1, 49 pts (37.5%) had + alterations. Pts who converted from + to - (+/-) had similar outcomes as pts who remained - (-/-) and those that did not convert had worst outcomes (+/+) (Table). In matched C1D1 and PD samples pts with ARgain (G) at C1D1 were more ARG at PD (p = <0.01) while ARPM were only detected in PD samples that were ARnormal (N) at C1D1. DRD + pts at C1D1 were more likely DRD + at PD (p = <0.1).Abstract: Background: A number of genomic alterations detected in plasma DNA have been associated with worse outcome in mCRPC (Jayaram et al Cancer Discov). We hypothesized that patients (pts) who harbored a genomic alteration that decreased after 1C of treatment derive treatment benefit and this would distinguish them from truly resistant pts. Methods: Plasma DNA (128 C1 day (D) 1, 134 C2 D1, and 41 progression [PD] from chemotherapy-naïve mCRPC pts in a phase 2 study of AA (NCT01867710), recently reported (Attard et al, Jama Onc) were subjected to custom targeted-capture NGS. Assay was optimised and validated to detect pathogenic point mutations (PM), deletions and copy number alterations (CNA) inAR, TP53, RB1, PIK3CA and DNA repair deficient genes (DRD): BRCA1, BRCA2, FANCA, ATM, CHEK2, HDAC2, BRIP1, and PALB2. Pts were followed up for overall survival (OS) and radiographic progression-free survival (rPFS) (48 months). Results: Pts were classified into 4 groups based on whether a gene alteration was detectable (+) or not (-) at C1D1 and C2D1 respectively. At C1D1, 49 pts (37.5%) had + alterations. Pts who converted from + to - (+/-) had similar outcomes as pts who remained - (-/-) and those that did not convert had worst outcomes (+/+) (Table). In matched C1D1 and PD samples pts with ARgain (G) at C1D1 were more ARG at PD (p = <0.01) while ARPM were only detected in PD samples that were ARnormal (N) at C1D1. DRD + pts at C1D1 were more likely DRD + at PD (p = <0.1). Conclusions: These findings suggest that tracking gene aberrations in plasma DNA could be an early marker of treatment efficacy. Clinical trial identification: NCT01867710. Legal entity responsible for the study: The authors. Funding: Janssen Pharmaceuticals. Disclosure: D. Shen: Shareholder / Stockholder / Stock options, Full / Part-time employment: Janssen Research and Development. A. Wingate: Honoraria (self), Research grant / Funding (self), Travel / Accommodation / Expenses: Janssens. C. Sternberg: Honoraria (self): Astellas Pharma; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Pfizer; Honoraria (self), Research grant / Funding (institution): Sanofi; Honoraria (self), Advisory / Consultancy: Ipsen; Honoraria (self), Research grant / Funding (institution): AstraZeneca; Honoraria (self), Research grant / Funding (institution): Janssen; Advisory / Consultancy, Research grant / Funding (institution): Bristol-Myers Squibb; Advisory / Consultancy: Novartis; Advisory / Consultancy, Research grant / Funding (institution): Bayer; Advisory / Consultancy: Eisai; Advisory / Consultancy, Research grant / Funding (institution): Clovis Oncology; Advisory / Consultancy, Research grant / Funding (institution): Incyte; Advisory / Consultancy: Roche; Advisory / Consultancy: Ipsen; Advisory / Consultancy, Research grant / Funding (institution): Merck; Advisory / Consultancy: Medscape; Advisory / Consultancy: UroToday; Advisory / Consultancy: Genentech; Advisory / Consultancy: Medivation; Research grant / Funding (institution): Exelixis. R. Jones: Honoraria (self), Research grant / Funding (institution), Travel / Accommodation / Expenses: Astellas Pharma; Honoraria (self), Travel / Accommodation / Expenses: Janssen; Honoraria (self), Research grant / Funding (institution): AstraZeneca; Honoraria (self), Travel / Accommodation / Expenses: MSD Oncology; Honoraria (self): BMS; Honoraria (self), Research grant / Funding (institution): Pfizer; Honoraria (self), Research grant / Funding (institution): Novartis; Honoraria (self), Travel / Accommodation / Expenses: Ipsen; Research grant / Funding (institution): Roche; Advisory / Consultancy, Research grant / Funding (institution): Clovis Oncology; Research grant / Funding (institution): Exelixis; Honoraria (self): Sanofi; Honoraria (self): Genentech; Honoraria (self): Eusa Pharma; Honoraria (self): Pharmacyclics. A. Berruti: Advisory / Consultancy, Speaker Bureau / Expert testimony, Research grant / Funding (institution), Travel / Accommodation / Expenses: Janssen-Cilag; Advisory / Consultancy, Research grant / Funding (institution): Astellas Pharma; Travel / Accommodation / Expenses: Sanofi. F. Lefresne: Honoraria (self), Research grant / Funding (self), Travel / Accommodation / Expenses, Shareholder / Stockholder / Stock options, Full / Part-time employment: Johnson & Johnson. M. Lahaye: Honoraria (self), Advisory / Consultancy, Leadership role, Shareholder / Stockholder / Stock options, Full / Part-time employment: Janssen-Cilag. S. Thomas: Leadership role, Research grant / Funding (self), Travel / Accommodation / Expenses, Shareholder / Stockholder / Stock options, Licensing / Royalties, Full / Part-time employment: Janssen Research and Development. S. Joshi: Honoraria (self), Travel / Accommodation / Expenses, Full / Part-time employment: Janssen Research and Development. M. Gormley: Travel / Accommodation / Expenses, Licensing / Royalties, Full / Part-time employment: Janssen Research and Development. B. Tombal: Honoraria (self), Advisory / Consultancy, Travel / Accommodation / Expenses: Astellas Pharma; Honoraria (institution), Speaker Bureau / Expert testimony, Travel / Accommodation / Expenses: Amgen; Honoraria (self), Advisory / Consultancy, Travel / Accommodation / Expenses: Bayer; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Ferring; Honoraria (self), Advisory / Consultancy, Travel / Accommodation / Expenses: Sanofi; Honoraria (self), Advisory / Consultancy, Speaker Bureau / Expert testimony, Travel / Accommodation / Expenses: Janssen; Advisory / Consultancy: Takeda; Advisory / Consultancy: Steba Biotech; Honoraria (self): Myovant Sciences. A. Merseburger: Honoraria (self), Research grant / Funding (institution), Travel / Accommodation / Expenses: Janssen-Cilag; Honoraria (self), Advisory / Consultancy, Travel / Accommodation / Expenses: Astellas Pharma; Honoraria (self), Advisory / Consultancy, Speaker Bureau / Expert testimony, Travel / Accommodation / Expenses: Ipsen; Honoraria (self): Roche; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): BMS; Honoraria (self): Eisai; Honoraria (self): Takeda; Honoraria (self): Pfizer; Honoraria (self), Research grant / Funding (self): Novartis; Research grant / Funding (institution): Clovis Oncology. D. Ricci: Travel / Accommodation / Expenses, Shareholder / Stockholder / Stock options, Licensing / Royalties, Full / Part-time employment: Janssen. G. Attard: Honoraria (self), Honoraria (institution), Speaker Bureau / Expert testimony, Travel / Accommodation / Expenses: Janssen; Honoraria (self), Advisory / Consultancy, Speaker Bureau / Expert testimony, Travel / Accommodation / Expenses: Astellas Pharma; Advisory / Consultancy: Janssen-Cilag; Research grant / Funding (institution): Innocrin; Research grant / Funding (institution): Arno; Advisory / Consultancy, Travel / Accommodation / Expenses: Ventana Medical Systems; Travel / Accommodation / Expenses: Abbott Laboratories; Licensing / Royalties: ICR Rewards to Inventors; Honoraria (self), Travel / Accommodation / Expenses: Abbott; Advisory / Consultancy, Travel / Accommodation / Expenses: ESSA; Advisory / Consultancy, Travel / Accommodation / Expenses: Bayer; Advisory / Consultancy, Travel / Accommodation / Expenses: Pfizer. All other authors have declared no conflicts of interest. … (more)
- Is Part Of:
- Annals of oncology. Volume 30(2019)Supplement 7
- Journal:
- Annals of oncology
- Issue:
- Volume 30(2019)Supplement 7
- Issue Display:
- Volume 30, Issue 7 (2019)
- Year:
- 2019
- Volume:
- 30
- Issue:
- 7
- Issue Sort Value:
- 2019-0030-0007-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-11-07
- Subjects:
- Oncology -- Periodicals
616.992 - Journal URLs:
- https://www.journals.elsevier.com/annals-of-oncology ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/annonc/mdz413.014 ↗
- Languages:
- English
- ISSNs:
- 0923-7534
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1043.320000
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