Assessment of Direct Biomarkers of Aspirin Action to Develop a Precision Chemoprevention Therapy of Colorectal Cancer

Colorectal Cancer Clinical Trial

Official title:

Assessment of Direct Biomarkers of Aspirin Action to Develop a Precision Chemoprevention Therapy of Colorectal Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03957902
• Other study ID #: PI17/01109
• Secondary ID: 2018-002101-65
• Status: Recruiting
• Phase: Phase 2
• Start date: May 6, 2019
• Est. completion date: May 2020

Study information

• Verified date: May 2019
• Source: Instituto de Investigación Sanitaria Aragón
• Contact: Ángel Lanas Arbeloa, MD
• Phone: 0034976765786
• Email: angel.lanas[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Acetylsalicylic acid (ASA) seems the ideal colorectal cancer (CRC) chemoprevention agent. Several ongoing trials are testing the effect of ASA as co-therapy in CRC. The mechanisms of action, the appropriate dose and the ideal target population are unknown. The investigators have demonstrated that doses of 100 mg of ASA induce direct and partial but persistent acetylation of the cyclooxygenase (COX) isoenzyme COX-1 in the normal colorectal mucosa. The primary objective is to perform a study of aspirin by using a proteomic assay for comparing platelet COX-1 and CRC mucosal COX-1 after different doses of ASA. Secondary objectives are: the measurement of prostaglandin E2 (PGE2) and phosphorylated S6 protein (p-S6) levels in CRC mucosa, the assessment of indirect biomarker of aspirin action (serum thromboxane B2 (TXB2) and urinary levels of 11-dehydro-TXB2 (TX-M)), the evaluation of systemic biomarkers of inflammatory/tumorigenic COX-2 by assessing urinary levels of major metabolite of PGE2 (PGE-M). Methods: Phase II randomized clinical trial in 60 patients with newly diagnosed CRC in 3 groups of 20 patients receiving 100 or 300 mg/day, or 100 mg/12 hours of enteric-coated ASA for 3±1 weeks, prior to definitive treatment by surgery. Main outcome: Acetylation of COX-1 and COX-2. Eicosanoid levels in target organs. Expected results: Evidence for the current uncertainty about the mechanisms of action and the dose required to obtain the best chemopreventive effect with ASA in CRC. Confirm acetylation of COX as a key biomarker of efficacy with ASA.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: May 2020
• Est. primary completion date: May 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 79 Years

Eligibility

Inclusion Criteria:

• age = 18 < 80 years old

• recent diagnosis (< 48h) of rectum or colon cancer, established by endoscopy and later confirmed by anatomo-pathologic study

• normal coagulation values and biochemical vales without clinically significant deviations that, at the discretion of the investigator, may interfere with the study procedures

Exclusion Criteria:

• Allergy to ASA or to any other NSAID.

• Rectal cancer requiring neoadjuvant treatment within the two weeks following the beginning of ASA treatment.

• Previous use of ASA, NSAIDs, antiplatelet agents, corticosteroids or misoprostol within the 15 days prior to diagnosis and/or anticipation of need for treatment with any of these drugs during the study period. History of peptic ulcer disease or active peptic ulcer or any other gastrointestinal disease that may be considered a contraindication to the use of ASA, without the concomitant use of proton pump inhibitors.

• Diagnosis of bleeding disorders.

• Diagnosis of cancer (excluding non-melanoma skin cancer) within the previous 3 years.

• Conditions supposing serious comorbidity, excluding diabetes, and including respiratory, cardiac, hepatic and renal diseases.

• Active smoking.

• Pregnancy or breastfeeding.

• History of drug or alcohol abuse.

Related Conditions & MeSH terms

• Colorectal Cancer
• Colorectal Neoplasms

Intervention

Drug:
• acetylsalicylic acid
Different dosage effect over platelet COX enzymes, non- neoplastic and neoplastic colonic tissues used as biomarkers of clinical efficacy in CRC chemoprevention

Locations

Country	Name	City	State
Spain	Hospital Clínico Universitario Lozano Blesa	Zaragoza

Sponsors (4)

Lead Sponsor	Collaborator
Instituto de Investigación Sanitaria Aragón	G. d'Annunzio University, Hospital Clínico Universitario Lozano Blesa, Instituto de Salud Carlos III

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of changes in acetylation levels of COX enzymes in platelets and non-neoplastic and neoplastic colonic tissues		before the beginning of the treatment and 3 ± 1 weeks of acetylsalicylic acid treatment
Secondary	Assessment of changes in prostaglandin E2 (PGE2) levels in colorectal mucosa depending on drug dosis		before the beginning of the treatment and 3 ± 1 weeks of acetylsalicylic acid treatment
Secondary	Assessment of changes in phosphorylated S6 protein (p-S6) levels in colorectal mucosa depending on drug dosis		before the beginning of the treatment and 3 ± 1 weeks of acetylsalicylic acid treatment
Secondary	Assessment of changes in thromboxane B2 (TxB2) levels in urine as indirect systemic biomarker depending on drug dosis		before the beginning of the treatment and 3 ± 1 weeks of acetylsalicylic acid treatment
Secondary	Assessment of changes in urinary metabolite 11-dehydro-TxB2 (TX-M) levels as indirect systemic biomarker depending on drug dosis		before the beginning of the treatment and 3 ± 1 weeks of acetylsalicylic acid treatment
Secondary	Assessment of changes in major urinary metabolite of PGE2 (PEG-M) levels depending on drug dosis		before the beginning of the treatment and 3 ± 1 weeks of acetylsalicylic acid treatment