Trial of Acetylsalicylic Acid and Atorvastatin in Patients With Castrate-resistant Prostate Cancer

About This Trial

This study is testing whether adding two common medications—aspirin and a cholesterol-lowering drug called atorvastatin—can help patients with advanced prostate cancer live longer.
It is designed for people whose cancer continues to grow or spread despite hormone-lowering therapy, and who have not yet received other treatments for this stage of the disease.
To take part, you must have reasonably good liver and kidney function and no conditions that put you at high risk for serious bleeding.
Importantly, you cannot join if you have taken daily aspirin or a daily statin medication within the past six months.

More Information

This is a 2x2 factorial randomized, multicenter, international, open phase III trial.
The primary objective is to evaluate the benefit of acetylsalicylic acid and atorvastatin on overall survival (OS) (main endpoint) for patients with castrate-resistant prostate cancer starting first line treatment for CRPC

Who Can Enroll

Age Range: 18 years and older
Gender: Male
Who This Trial is For: This study is testing whether adding two common medications—aspirin and a cholesterol-lowering drug called atorvastatin—can help patients with advanced prostate cancer live longer.

Study Details

Start Date: June 6, 2019
Lead Sponsor: Gustave Roussy, Cancer Campus, Grand Paris

Full Eligibility Criteria

Inclusion Criteria

Histologically confirmed adenocarcinoma of the prostate and no curative local therapy considered possible
Age ≥ 18 years, life expectancy of at least 6 months
CRPC defined as tumor progression (PSA increase on at least 2 separate values separated by at least 1 week or progression on imaging) while on Androgen Deprivation Therapy (orchiectomy, LHRH agonist or -antagonist) with documented serum testosterone levels ≤ 1.7 nmol/L (≤ 0.50 ng/mL). Ongoing concurrent use of LHRH agonist or antagonist is required if the patient has not been surgically castrated
Presence (M1) or absence (M0) of metastases on imaging
Performance status 0, 1 or 2
No previous use of life- prolonging treatments for CRPC (including abiraterone, enzalutamide, radium-223, docetaxel, cabazitaxel, and sipuleucel-T). The use of these agents together with Androgen Deprivation Therapy (ADT) for castrate-sensitive disease is allowed.
Adequate renal function within 30 days prior to registration: calculated creatinine clearance ≥ 50 mL/min, according to the formula of Cockcroft-Gault and adequate liver function with levels of AST and ALT ≤ 3xULN and no signs for cholestasis.
Participation in other clinical trials is allowed except for trials with the same primary endpoint, i.e. OS
Patient authorized to participate to a clinical trial by specific country regulation (eg patient affiliated to a social security system or beneficiary of the same)
Information delivered to patient and informed consent form signed by the patient.

Exclusion Criteria

Previous localised malignancy within 2 years with the exception of localized non-melanoma skin cancer and Ta or Tis bladder cancer (patients with asymptomatic Chronic Lymphocytic Leukemia can be included)
Previous metastatic malignancy within 5 years
Patient currently taking daily acetylsalicylic acid or a daily statin within the last 6 months
Patients with active liver disease (hepatitis B or C, cirrhosis) or unexplained persistent elevations of serum transaminases exceeding 3 times the upper limit of normal or cholestasis
Patients with excessive alcohol intake or history of a relevant liver disease
Known hypersensitivity or intolerance to acetylsalicylic acid or atorvastatin or hypersensitivity to any of its components
Contra-indication to acetylsalicylic acid or atorvastatin according to label, including known high-risk for haemorrhage,
History of or active myopathy or significantly elevated (> 5 times ULN) CK levels
History of recent stroke or transient ischemic attack (TIA).
Any concomitant drugs contraindicated for use with the trial drugs according to the product information (e.g. Fusidic acid, potent inhibitors of CYP3A4 or transport proteins: ciclosporin, telithromycin, clarithromycin, delavirdine, stiripentol, ketoconazole, voriconazole, itraconazole, posaconazole and HIV protease inhibitors including ritonavir, lopinavir, atazanavir, indinavir, darunavir, tipranavir, telaprevir, saquinavir, darunavir, fosamprenavir, boceprevir, gemfibrozil, fenofibrate, etc)
Any serious underlying medical condition (by the investigator's judgement) which could impair the ability of the patient to participate in the trial
Patients with hereditary galactose intolerance, Lapp-lactase deficiency or Glucose-Galactose-malabsorption
Compliance with trial medical follow-up impossible due to geographic, social or psychological reasons
Psychiatric disorder precluding understanding of information about trial related topics, providing informed consent, or interfering with compliance for oral drug intake