Abstract 5029
Background
In the randomized Phase III POLO trial (NCT02184195), progression-free survival (PFS) for pts with a germline BRCA1 and/or BRCA2 mutation (gBRCAm) and mPC was significantly prolonged with maintenance olaparib versus placebo. Maintenance treatment has the potential to prolong time without subsequent chemotherapies and their associated toxicities.
Methods
Eligible pts had a gBRCAm and mPC that had not progressed following ≥16 weeks of first-line platinum-based chemotherapy. Pts were randomized to receive maintenance olaparib tablets (300 mg bid) or placebo until investigator-assessed progression or unacceptable toxicity. Time from randomization to discontinuation of treatment (TDT), and initiation of first (TFST) and second (TSST) subsequent therapies following discontinuation of study treatment or death, were secondary endpoints, analysed by log-rank test. Follow-up for subsequent therapies took place 30 days after discontinuation, then every 8 weeks.
Results
92 and 62 pts were randomized to olaparib and placebo, respectively. TDT, TFST and TSST were meaningfully longer in the olaparib arm (Table). 30 olaparib (32.6%) and 8 placebo arm (12.9%) pts were on study treatment at the data cut-off. 54 (58.7%) and 49 (79.0%) pts, respectively, had discontinued treatment due to progression; 4 (4.3%) and 2 (3.2%), respectively, due to an adverse event. 45 olaparib (48.9%) and 46 placebo arm (74.2%) pts received subsequent treatment; all received chemotherapy in the second line, except for two placebo arm pts who received olaparib.Table:
693P
Olaparib (N = 92) | Placebo (N = 62) | |
---|---|---|
Time to discontinuation of treatment | ||
Events, n (%) | 60 (65.2) | 53 (85.5) |
Median, months (95% CI) | 7.2 (5.5, 10.8) | 3.8 (3.6, 4.8) |
Hazard ratio (95% CI) | 0.45 (0.30, 0.67) | |
Nominal P value | 0.0001 | |
Time to first subsequent therapy | ||
Events, n (%) | 58 (63.0) | 46 (74.2) |
Median, months (95% CI) | 8.6 (6.2, 12.5) | 5.7 (4.2, 6.3) |
Hazard ratio (95% CI) | 0.50 (0.32, 0.76) | |
Nominal P value | 0.0013 | |
Time to second subsequent therapy | ||
Events, n (%) | 50 (54.3) | 39 (62.9) |
Median, months (95% CI) | 13.2 (8.8, 20.0) | 9.2 (8.3, 13.1) |
Hazard ratio (95% CI) | 0.68 (0.44, 1.05) | |
Nominal P value | 0.083 |
Conclusions
Pts with a gBRCAm and mPC received maintenance olaparib for meaningfully longer than placebo. Initiation of subsequent second-line treatment, typically cytotoxic chemotherapy, was delayed for pts in the olaparib arm and data suggest this effect may be maintained through to subsequent third-line therapy.
Clinical trial identification
NCT02184195.
Editorial acknowledgement
Elin Pyke, MChem, from Mudskipper Business, Ltd, funded by AstraZeneca and Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, U.S.A. (MSD).
Legal entity responsible for the study
AstraZeneca and Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, U.S.A. (MSD).
Funding
AstraZeneca and Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, U.S.A. (MSD).
Disclosure
E. Van Cutsem: Advisory / Consultancy: AstraZeneca; Advisory / Consultancy, Research grant / Funding (institution): Bayer; Advisory / Consultancy: Bristol-Myers Squibb; Advisory / Consultancy, Research grant / Funding (institution): Celgene; Advisory / Consultancy, Research grant / Funding (institution): Lilly; Advisory / Consultancy, Research grant / Funding (institution): Merck Sharpe & Dohme; Advisory / Consultancy, Research grant / Funding (institution): Merck KGaA; Advisory / Consultancy, Research grant / Funding (institution): Novartis; Advisory / Consultancy, Research grant / Funding (institution): Roche; Advisory / Consultancy, Research grant / Funding (institution): Servier; Research grant / Funding (institution): Amgen; Research grant / Funding (institution): Boehringer Ingelheim; Research grant / Funding (institution): Ipsen. T. Golan: Honoraria (self), Research grant / Funding (institution), International coordinating investigator service fee: AstraZeneca; Research grant / Funding (institution): MSD Merck; Advisory / Consultancy, Speaker Bureau / Expert testimony, Personal fee for advisory board and speakers bureau: AbbVie; Advisory / Consultancy, Personal fees for consultancy: Teva. P. Hammel: Research grant / Funding (institution): Celgene; Research grant / Funding (institution): AstraZeneca; Research grant / Funding (institution), Travel / Accommodation / Expenses: Erythec; Honoraria (self), Research grant / Funding (institution): Halozyme. M. Reni: Honoraria (self), Advisory / Consultancy, Research grant / Funding (self), Travel / Accommodation / Expenses, Non-remunerated activity/ies: Celgene; Honoraria (self), Advisory / Consultancy: Baxalta; Honoraria (self), Advisory / Consultancy: Shire; Advisory / Consultancy: Eli Lilly; Advisory / Consultancy: Pfizer; Advisory / Consultancy: Novocure; Advisory / Consultancy: Novartis; Non-remunerated activity/ies: Boston Pharmaceutics; Non-remunerated activity/ies: AstraZeneca. T. Macarulla: Advisory / Consultancy: Genzyme, Sanofi/Aventis, Shire, Tesaro, Baxalta, QED Therapeutics; Advisory / Consultancy, Research grant / Funding (institution): Celgene; Advisory / Consultancy, Research grant / Funding (institution): Roche; Research grant / Funding (institution): Agios Pharmaceuticals Inc; Research grant / Funding (institution): Aslan Pharmaceuticals Pte Ltd; Research grant / Funding (institution): Bayer; Research grant / Funding (institution): Genentech; Research grant / Funding (institution): AstraZeneca; Research grant / Funding (institution): Halozyme Inc; Research grant / Funding (institution): Immunomedics; Research grant / Funding (institution): Lilly, S.A.; Research grant / Funding (institution): Merrimack; Research grant / Funding (institution): Millennium; Research grant / Funding (institution): Novartis Farmaceutica, S.A.; Research grant / Funding (institution): Novocure GmBH, Oncomed, Pfizer, S.L.U., Pharmacyclics; Travel / Accommodation / Expenses: Merck, H3 Biomedicine, Bayer, Sanofi. M.J. Hall: Non-remunerated activity/ies, Collaborative research only in which company data was shared and assessed and research published—no funding or payment: Myriad; Non-remunerated activity/ies, Collaborative research only in which company data was shared and assessed and research published—no funding or payment: Ambry; Non-remunerated activity/ies, Collaborative research only in which company data was shared and assessed and research published—no funding or payment: Invitae; Non-remunerated activity/ies, Collaborative research only in which company data was shared and assessed and research published—no funding or payment: Foundation Medicine; Travel / Accommodation / Expenses, Non-remunerated activity/ies, Collaborative research only in which company data was shared and assessed and research published—no funding or payment. Travel/accomodation/expenses as part of research collaboration Precision Oncology Alliance: Caris Lifesciences; Research grant / Funding (institution), Non-remunerated activity/ies, Keynote 177 trial site PI: Merck; Research grant / Funding (institution), Travel / Accommodation / Expenses, Non-remunerated activity/ies, As part of clinical trial leadership and steering committee; POLO trial site PI: AstraZeneca. J.O. Park: Honoraria (self), Advisory / Consultancy, Research grant / Funding (self): Celgene; Honoraria (self), Advisory / Consultancy: Shire; Advisory / Consultancy: Merck Serono. D. Arnold: Advisory / Consultancy: Lilly. D. Oh: Advisory / Consultancy, Research grant / Funding (self): AstraZeneca; Advisory / Consultancy, Research grant / Funding (self): Novartis; Research grant / Funding (self): Array; Research grant / Funding (self): Eli Lilly; Research grant / Funding (self): Green Cross; Advisory / Consultancy: Genentech/Roche; Advisory / Consultancy: Merck Serono; Advisory / Consultancy: Bayer; Advisory / Consultancy: Taiho; Advisory / Consultancy: ASLAN. A. Reinacher-Schick: Honoraria (self), Advisory / Consultancy, Travel / Accommodation / Expenses: Amgen; Honoraria (self), Advisory / Consultancy: Baxalta; Honoraria (self), Advisory / Consultancy: BMS; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Celgene; Honoraria (self), Research grant / Funding (institution): Ipsen; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Lilly; Honoraria (self), Advisory / Consultancy: Merck Serono; Honoraria (self), Advisory / Consultancy: MSD; Honoraria (self), Advisory / Consultancy: Pfizer; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Roche; Honoraria (self), Advisory / Consultancy: Sanofi-Aventis; Honoraria (self), Advisory / Consultancy, Travel / Accommodation / Expenses: Servier; Honoraria (self): Shire; Research grant / Funding (institution): AstraZeneca. G. Tortora: Honoraria (self), Advisory / Consultancy: Celgene; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Merck; Honoraria (self), Advisory / Consultancy: Incyte; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Novartis. H. Algül: Honoraria (self), Travel / Accommodation / Expenses: Celgene; Honoraria (self): Servier; Research grant / Funding (self): Chugai. E.M. O’Reilly: Advisory / Consultancy, Eileen M O’Reilly and spouse: 3DMedcare, Alignmed, Amgen, Antengene, Aptus, Aslan, Astellas, Bioline, Boston Scientific, Bridgebio, Carsgen, Cipla, CytomX, Daiichi, Debio, Delcath, Eisai, Genoscience, Hengrui, Inovio, Ipsen, Jazz, Jansen, Kyowa Kirin, LAM, Loxo, Merck, Mina, Novella,; Advisory / Consultancy, Research grant / Funding (institution), Eileen M O’Reilly and spouse: Agios, AstraZeneca, Bayer, Beigene, BMS, Casi, Celgene, Exelixis, Halozyme, Incyte, Lilly, QED; Research grant / Funding (institution), Eileen M O’Reilly and spouse: ActaBiologica, Array, Genentech, Mabvax, Novartis, Oncoquest, Polaris Puma, Roche; Advisory / Consultancy, Eileen M O’Reilly and spouse: Onxeo, PCI Biotech, Pfizer, Pieris, QED, Redhill, Sanofi, Servier, Silenseed, Sillajen, Sobi, Targovax, Tekmira, Twoxar, Vicus, Yakult, Yiviva. D. McGuinness: Full / Part-time employment, Contractor: AstraZeneca. K.Y. Cui: Full / Part-time employment: AstraZeneca; Research grant / Funding (institution), AstraZeneca receives payment from Merck to codevelop olaparib: Merck & Co. Inc. K. Schlienger: Travel / Accommodation / Expenses, Shareholder / Stockholder / Stock options, Full / Part-time employment: MSD. G.Y. Locker: Shareholder / Stockholder / Stock options, Full / Part-time employment: AstraZeneca. H.L. Kindler: Advisory / Consultancy, Research grant / Funding (institution): AstraZeneca; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Merck; Advisory / Consultancy: Aldeyra Therapeutics; Advisory / Consultancy: Astellas; Advisory / Consultancy, Travel / Accommodation / Expenses: Boehringer-Ingelheim; Advisory / Consultancy, Research grant / Funding (institution): Bristol-Myers Squibb; Advisory / Consultancy: Erytech; Advisory / Consultancy: Five Prime Therapeutics; Advisory / Consultancy: Ipsen Pharmaceuticals; Advisory / Consultancy: Kyowa; Advisory / Consultancy, Travel / Accommodation / Expenses: Paredox Therapeutics; Research grant / Funding (institution): Aduro; Research grant / Funding (institution): Bayer; Research grant / Funding (institution): Dicephera; Research grant / Funding (institution): GlaxoSmithKline; Research grant / Funding (institution): MedImmune; Research grant / Funding (institution): Lilly; Research grant / Funding (institution): Polaris; Research grant / Funding (institution): Verastem. All other authors have declared no conflicts of interest.
Resources from the same session
3191 - The efficacy and safety of lenvatinib in patients who did not meet the inclusion criteria of the phase 3 trial (REFLECT trial) and those with BCLC Stage B hepatocellular carcinoma - A nationwide multicenter study in Japan-
Presenter: Azusa Sakamoto
Session: Poster Display session 2
Resources:
Abstract
1529 - Prognostic and predictive value of baseline alpha-fetoprotein (AFP) in patients with advanced hepatocellular carcinoma (HCC) treated with ramucirumab from two phase 3 studies (REACH, REACH-2)
Presenter: Andrew Zhu
Session: Poster Display session 2
Resources:
Abstract
2767 - Effect of second-line cabozantinib on health states for patients with advanced hepatocellular carcinoma (aHCC) after sorafenib: QTWiST analysis from the CELESTIAL study
Presenter: Nicholas Freemantle
Session: Poster Display session 2
Resources:
Abstract
2150 - Alpha-fetoprotein (AFP) response in patients with unresectable hepatocellular carcinoma (HCC) in the phase 3 RESORCE trial
Presenter: Jordi Bruix
Session: Poster Display session 2
Resources:
Abstract
3437 - Phase I/II trial of NBTXR3 activated by SBRT in patients with hepatocellular carcinoma or liver metastasis
Presenter: Marc Pracht
Session: Poster Display session 2
Resources:
Abstract
1758 - Efficacy and safety of ramucirumab (RAM) for advanced hepatocellular carcinoma (HCC) with elevated alpha-fetoprotein (AFP) following first-line sorafenib across age subgroups in two global phase 3 trials (REACH and REACH-2)
Presenter: Masatoshi Kudo
Session: Poster Display session 2
Resources:
Abstract
1192 - Ramucirumab in patients with advanced hepatocellular carcinoma (HCC) and elevated alpha fetoprotein (AFP): An exposure–response analysis
Presenter: Josep Llovet
Session: Poster Display session 2
Resources:
Abstract
1600 - Outcomes of Hepatocellular Carcinoma (HCC) Patients Treated with Nivolumab: The Mount Sinai Hospital Experience.
Presenter: Sirish Dharmapuri
Session: Poster Display session 2
Resources:
Abstract
2364 - Pembrolizumab vs Chemotherapy in Patients With Advanced/Metastatic Adenocarcinoma (AC) or Squamous Cell Carcinoma (SCC) of the Esophagus as Second-Line Therapy: Analysis of the Chinese Subgroup in KEYNOTE-181
Presenter: Jia Chen
Session: Poster Display session 2
Resources:
Abstract
1933 - A national comparative effectiveness study to assess definitive chemoradiation regimens in proximal oesophageal squamous cell cancer
Presenter: Judith de Vos-Geelen
Session: Poster Display session 2
Resources:
Abstract