A Randomized, 2x2 Factorial Design Biomarker Prevention Trial of Low-dose ASA and Metformin in Stage I-III Crc Patients (ASAMET)

Ente Ospedaliero Ospedali Galliera

Status and phase: Terminated; Phase 2

Conditions: Tertiary Prevention in Colon Cancer

Treatments: Other: Placebo; Drug: ASA; Drug: MET

Study type: Interventional

Funder types: Other

Identifiers

NCT03047837

2015-004824-77 (EudraCT Number)

27UCS2015

Details and patient eligibility

About

It has been shown that Aspirin (ASA) as well as Metformin (Met) can inhibit the incidence and mortality of colorectal cancer (CRC). In this randomized, placebo controlled clinical trial we compare the effect of these two drugs alone and their combination to prevent recurrent CRC after surgery.

Full description

Epidemiological studies and cardiovascular prevention trials have shown that low-dose aspirin (ASA) can inhibit colorectal cancer (CRC) incidence and mortality, including inhibition of distant metastases. Metformin (MET) has also been associated with decreased CRC incidence and mortality in meta-analyses of epidemiological studies in diabetics and has been shown to decrease by 40% colorectal adenoma recurrence in a randomized trial. Recent studies have shown that ASA is an inhibitor of mTOR/S6K1 and an activator of AMPK, targeting regulators of intracellular energy homeostasis and metabolism, and that the combination of ASA and MET, another AMPK activator and S6K1 inhibitor, has a striking additive effect on AMPK activation and mTOR inhibition, with increased autophagy and decreased cell growth in CRC cell lines. While both drugs are being tested as single agents, their combination has not been tested in trials.

This is a randomized, placebo-controlled, double blind, 2x2 biomarker trial of ASA and MET to test the activity of either agent alone and the potential synergism of their combination on a set of surrogate biomarkers of colorectal carcinogenesis. After surgery 160 patients with stage I-III colon cancer will randomly be assigned in a four-arm trial to either ASA, 100 mg day, MET 850 mg bid, their combination, or placebo for one year. The primary endpoint biomarker is the change, defined as the difference between pre- and post-treatment expression of nuclear factor kappa-B (NFκB), in the unaffected mucosa of proximal and distal colon obtained by multiple biopsies in two paired colonoscopies one year apart. Additional biomarkers will include: 1) the genomic profile of candidate genes, pathways, and overall genomic patterns in tissue biopsies by genome wide gene expression arrays; 2) the IHC expression of tissue pS6K, p53, beta-catenin, PI3K; 3) the associations of mutations and SNPs with treatment response by next generation sequencing of primary tumors; 4) the measurement of circulating IL-6, CRP and VEGF and 5) plasma and colonic MET concentrations and their correlation with biomarker profiles.

Enrollment: 160 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients aged > 18 and ≤ 80 years.

• Patients with completely resected stage I, II, or III primary colorectal cancer within 24 months prior to randomization, regardless of (neo-)adjuvant chemotherapy. Patients with pT1 CRC treated with endoscopic polypectomy.

• Adjuvant chemotherapy and (neo-)adjuvant radiotherapy terminated at least 3 months before randomization.

• ECOG performance status ≤ 1.

• Satisfactory hematological and biochemical functions:

  • Platelets ≥ 100 x 10^9/L
  • Creatinine clearance estimated with the Cockcroft - Gault formula ≥ 60 mL/min. Patients with Gault formula ≥ 45-59 ≤ ml/min are eligible but they will receive a single (evening) tablet of MET, 850 mg.
  • AST and ALT ≤ 2.5 times ULN.

• Females of childbearing potential/males with partners of childbearing potential participating in the study are to use effective methods of birth control during study participation. Female participants must provide a pregnancy test, according to local/national guidelines.

• Able to understand and sign an informed consent (or have a legal representative who is able and willing to do so).

Exclusion criteria

• Patients who are not able to undergo colonoscopy.
• Patients who are allergic or intolerant to ibuprofen or naproxen,or who have MET-, or ASA-, or salicylate intolerance or more generalized drug intolerance to non-steroidal anti-inflammatory drugs (NSAIDs).
• Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the patient from signing or participating in the study and/or comply with study procedures.
• Chronic treatment with ASA or other NSAIDs or MET or patients who are on current long term treatment (≥ 4 consecutive weeks) with ASA, NSAID or COX -2 inhibitors or MET.
• Diabetic patients on drug treatment are excluded.
• Anticoagulant therapy (dicumarol, heparin, fondaparinux, apixaban, dabigatran etexilate, rivaroxaban) or active current treatment with antiplatelet agents (e.g. off-study ASA, clopidogrel, prasugrel, ticagrelor, or ticlopidine).
• Any other invasive malignancies (with the exclusion of basal cell carcinoma or cutaneous squamous cell carcinoma) diagnosed during the last 5 years before randomization. Past history of any other invasive CRC than the one the patient is currently being treated for
• Alcohol or drug abuse.
• Prior history of gastro-intestinal bleeding or hemorrhagic diathesis (e.g. hemophilia).
• Erosive-ulcerative lesions in the gastrointestinal tract.
• History of erosive GERD or active erosive GERD on gastroscopy.
• Concomitant corticosteroid treatment.
• Known deficiency of glucose-6-phosphate dehydrogenase (G6PD).
• Treatment with another investigational drug < 28 days prior to study entry.
• Concurrent participation in a clinical trial with the same endpoints.
• History of hemorrhagic stroke.
• Lynch Syndrome (HNPCC).
• Crohn's disease (CD) and Ulcerative Colitis (UC).
• Pregnant or lactating females.
• History of lactic acidosis.
• Liver dysfunction including chronic active hepatitis and cirrhosis not compensated.
• History of vitamin B12 deficiency or megaloblastic anemia.
• Uncontrolled coronary syndrome or symptomatic congestive heart failure (e.g. Class III or IV New York Heart Association's Functional Classification).
• Inability or unwillingness to swallow tablets.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: Quadruple Blind

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160 participants in 4 patient groups, including a placebo group

Placebo

Placebo Comparator group

Description:

placebo Aspirin (1 tablet daily) + placebo Metformin (1 tablet BID) for 12 months

Treatment:

Other: Placebo

Metformin

Experimental group

Description:

placebo Aspirin (1 tablet daily) + active Metformin (850 mg, 1 tablet BID), for 12 months

Treatment:

Drug: MET

Aspirin

Experimental group

Description:

active Aspirin (100 mg, 1 tablet daily) + placebo Metformin (1 tablet BID), for 12 months

Treatment:

Drug: ASA

Apirin plus Metformin

Experimental group

Description:

active Asprin (100 mg, 1 tablet daily) + active Metformin (850 mg, 1 tablet BID), for 12 months

Treatment:

Drug: MET

Drug: ASA