Abstract 1908
Background
TITAN evaluated APA vs placebo (PBO), + ADT, in pts with mCSPC. APA improved overall survival (OS [HR, 0.67; 95% CI, 0.51-0.89; p = 0.0053]) vs PBO. We evaluated AR aberrations at baseline (BL) and end of treatment (EOT) and assessed associations of EOT AR aberrations with outcomes in TITAN.
Methods
From 265 pt samples (APA, n = 116; PBO, n = 149) available for evaluation, a subset was analyzed for circulating tumor (ct)DNA and AR aberrations (ARv7, AR amplification, AR ligand binding domain mutations) from cell-free (cf)DNA and cfRNA using next-generation sequencing and PCR, respectively. Associations with OS and duration on first subsequent therapy were assessed.
Results
BL characteristics of pts were balanced between biomarker-positive groups. Among aberrations at BL, AR amplification was associated with longer duration of prior ADT (4.2 mo vs 1.6 mo, pts with vs without AR amplification; p = 0.034). ctDNA % and frequency of AR aberrations increased from BL to EOT. At EOT, ctDNA % was similar in APA and PBO groups (60% and 66%), and AR aberrations were less frequent with APA vs PBO (Table). Regardless of treatment group, OS was significantly shorter with detection of any AR aberration at EOT (OS: 2.7 [1.1-6.6], p = 0.0278, APA; 6.1 [1.9-20.3], p = 0.0007, PBO). Detection of any AR aberration at EOT was significantly associated with duration on first subsequent therapy (2.0 [1.0-4.0], p = 0.0386).Table:
883P Frequency of AR aberrations at BL and EOT
BL | EOT | |||
---|---|---|---|---|
n, (n/N%) | APA + ADT | PBO + ADT | APA + ADT | PBO + ADT |
ARv7 | 2/15 (13) | 6/44 (14) | 9/46 (20) | 29/81 (36) |
AR mutation | 0 | 0 | 4/46 (9) | 7/81 (9) |
AR amplification | 1/15 (7) | 6/44 (14) | 19/46 (41) | 42/81 (52) |
Any AR aberrationa | 3/15 (20) | 10/44 (23) | 22/46 (48)b | 54/81 (67) |
Only pts with ARv7, AR amplification, and AR mutation measured are reported. bFrom Fisher’s exact test for comparison vs PBO, p = 0.04.
Conclusions
In TITAN, AR amplification at BL was associated with even brief ADT exposure. AR aberrations were fewer at EOT with APA vs PBO. Pts with AR aberrations at EOT had worse outcomes vs pts without. Taken together, these findings suggest that early APA + ADT provides long-term benefits vs ADT alone without increased acquisition of AR aberrations. The detailed biological mechanisms underlying these findings need to be further studied.
Clinical trial identification
NCT02489318.
Editorial acknowledgement
Larissa Belova, PhD, of Parexel.
Legal entity responsible for the study
Janssen Research & Development.
Funding
Janssen Research & Development.
Disclosure
K.N. Chi: Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Astellas Pharma; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Bayer; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Janssen; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Sanofi; Advisory / Consultancy: Amgen; Advisory / Consultancy: Essa; Advisory / Consultancy, Research grant / Funding (institution): Lilly/ImClone; Research grant / Funding (institution): Bristol-Myers Squibb; Research grant / Funding (institution): Merck; Research grant / Funding (institution): Roche; Research grant / Funding (institution): Tokai Pharmaceuticals; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Astellas Pharma; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Bayer; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Janssen; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Sanofi; Advisory / Consultancy: Amgen; Advisory / Consultancy: Essa; Advisory / Consultancy, Research grant / Funding (institution): Lilly/ImClone; Research grant / Funding (institution): Bristol-Myers Squibb; Research grant / Funding (institution): Merck; Research grant / Funding (institution): Roche; Research grant / Funding (institution): Tokai Pharmaceuticals. S. Thomas: Full / Part-time employment: Janssen Research & Development; Shareholder / Stockholder / Stock options: Johnson & Johnson. N. Agarwal: Advisory / Consultancy: Argos Therapeutics; AstraZeneca; Bayer; Bristol-Myers Squibb; Clovis Oncology; Eisai; EMD Serono; Exelixis; Foundation One Inc; Genentech/Roche; Lilly; Medivation/Astellas; Merck; Nektar; Novartis; Pfizer; Research grant / Funding (institution): Active Biotech; Amgen; AstraZeneca; Bavarian Nordic; Bayer; BN ImmunoTherapeutics; Bristol-Myers Squibb; Calithera Biosciences; Celldex; Eisai; Exelixis; Genentech; GlaxoSmithKline; Immunomedics; Janssen; Medivation; Merck; Newlink Geneti. F. Feng: Leadership role, Shareholder / Stockholder / Stock options: PFS Genomics; Advisory / Consultancy: Dendreon; Advisory / Consultancy: EMD Serono; Advisory / Consultancy: Janssen Oncology; Advisory / Consultancy: Ferring Pharmaceuticals; Advisory / Consultancy: Sanofi; Advisory / Consultancy: Bayer HealthCare Pharmaceuticals; Advisory / Consultancy: Blue Earth Diagnostics; Advisory / Consultancy: Celgene; Advisory / Consultancy: Medivation/Astellas Pharma; Research grant / Funding (institution): Zenith Epigenetics; Licensing / Royalties, I helped develop a molecular signature to predict radiation resistance in breast cancer, and this signature was patented by the University of Michigan, my employer; it is in the process of being licensed to PFS Genomics, a company that I helped found: Patents, Royalties, Other Intellectual Property. G. Attard: Honoraria (self), Advisory / Consultancy, Speaker Bureau / Expert testimony, Travel / Accommodation / Expenses: Astellas Pharma; Honoraria (self), Speaker Bureau / Expert testimony, Research grant / Funding (institution), Travel / Accommodation / Expenses: Janssen; Honoraria (self), Advisory / Consultancy, Travel / Accommodation / Expenses: Medivation; Advisory / Consultancy, Travel / Accommodation / Expenses: Abbott Laboratories; Advisory / Consultancy: ESSA; Advisory / Consultancy: Janssen-Cilag; Advisory / Consultancy: Millennium; Advisory / Consultancy: Novartis; Advisory / Consultancy, Speaker Bureau / Expert testimony, Travel / Accommodation / Expenses: Ventana Medical Systems; Advisory / Consultancy: Veridex; Speaker Bureau / Expert testimony: Sanofi; Speaker Bureau / Expert testimony: Takeda; Research grant / Funding (institution): Arno Therapeutics; Licensing / Royalties: The Institute of Cancer Research Rewards to Inventors list of abiraterone acetate; Non-remunerated activity/ies, Other relationship: Institute of Cancer Research. A.W. Wyatt: Advisory / Consultancy: Genzyme; Speaker Bureau / Expert testimony, Research grant / Funding (institution): Janssen. M. Gormley: Full / Part-time employment: Janssen Research & Development; Shareholder / Stockholder / Stock options: Johnson & Johnson. D.S. Ricci: Full / Part-time employment: Janssen Research & Development; Shareholder / Stockholder / Stock options: Johnson & Johnson. A. Lopez-Gitlitz: Full / Part-time employment: Janssen Research & Development; Shareholder / Stockholder / Stock options: Johnson & Johnson. K. Deprince: Full / Part-time employment: Janssen Research & Development; Shareholder / Stockholder / Stock options: Johnson & Johnson. J. Larsen: Full / Part-time employment: Janssen; Shareholder / Stockholder / Stock options: Johnson & Johnson. W. Chen: Full / Part-time employment: Janssen Research & Development; Shareholder / Stockholder / Stock options: Johnson & Johnson. B. Miladinovic: Full / Part-time employment: Janssen Research & Development; Shareholder / Stockholder / Stock options: Johnson & Johnson. V. Naini: Full / Part-time employment: Janssen Research & Development; Shareholder / Stockholder / Stock options: Johnson & Johnson. S. Chowdhury: Honoraria (self), Advisory / Consultancy: Clovis Oncology; Advisory / Consultancy: Astellas Pharma; Advisory / Consultancy: Bayer; Advisory / Consultancy, Speaker Bureau / Expert testimony: Pfizer; Advisory / Consultancy: Janssen-Cilag; Honoraria (self): Novartis; Research grant / Funding (institution): Sanofi/Aventis.
Resources from the same session
3290 - Identification of meningioma patients in high risk of tumor recurrence using microRNA profiling
Presenter: Josef Srovnal
Session: Poster Display session 3
Resources:
Abstract
2477 - Antecedent of cancer and mortality after the first ST segment elevation acute myocardial infarction treated with primary coronary angioplasty. A prospective cohort study
Presenter: Irene Sillero
Session: Poster Display session 3
Resources:
Abstract
1894 - Genomic characterisation of locally advanced pancreatic adenocarcinoma
Presenter: Sarah Picardo
Session: Poster Display session 3
Resources:
Abstract
3280 - Comparison of freshly prepared and frozen cells from colorectal cancer surgical samples for phenotyping experiments- a pilot study
Presenter: Sandra Mersakova
Session: Poster Display session 3
Resources:
Abstract
3419 - Hyaluronan (HA) Accumulation in the Tumor Microenvironment (TME) is Increased in Colorectal Cancer (CRC) and Associated with Consensus Molecular Subtypes (CMS) 4 Molecular Subtype
Presenter: Barbara Blouw
Session: Poster Display session 3
Resources:
Abstract
1833 - Evaluation of CT-based radiomics in patients with renal cell carcinoma
Presenter: An Zhao
Session: Poster Display session 3
Resources:
Abstract
5883 - Detection of Double Protein Expression in Diffuse Large B Cell Lymphoma
Presenter: Mohamed Gouda
Session: Poster Display session 3
Resources:
Abstract
5415 - Encyclopedic Tumor Analysis for organ agnostic treatment with Axitinib in combination regimens for advanced cancers
Presenter: Tim Crook
Session: Poster Display session 3
Resources:
Abstract
3297 - Computational model to predict response rate of clinical trials
Presenter: Orsolya Lorincz
Session: Poster Display session 3
Resources:
Abstract
4355 - Analysis of BRCA genes and homologous recombination deficiency (HRD) scores in tumours from patients (pts) with metastatic breast cancer (mBC) in the OlympiAD trial
Presenter: Mark Robson
Session: Poster Display session 3
Resources:
Abstract