Aspirin in Colorectal Cancer Liver Metastases

Colorectal Cancer Clinical Trial

— ASAC  

Official title:

Acetylsalicylic Acid as Secondary Prevention in Colorectal Cancer

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03326791
• Other study ID #: 2014/2217
• Status: Active, not recruiting
• Phase: Phase 2/Phase 3
• Start date: December 15, 2017
• Est. completion date: February 2025

Study information

• Verified date: December 2023
• Source: Oslo University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The ASAC trial is a Scandinavian, multi-center, double-blinded, randomized, placebo-controlled study to determine whether adjuvant treatment with low-dose acetylsalicylic acid (ASA) can improve disease free survival in patients treated with resection for colorectal cancer liver metastases (CRCLM).

Several studies have shown beneficial effect of ASA on primary prevention of CRC and the investigators group and others have shown a potential association of ASA also taken after the diagnosis on CRC survival in registry-based studies (secondary prevention). Up to 800 patients operated for CRCLM will be randomized to Arm#1 ASA 160 mg once daily or Arm#2 Placebo for a period of 3 years or till disease recurrence. The patients will be treated and followed up according to standard of care and the National Guidelines.

The ASAC trial will be the first clinical interventional trial to assess the beneficial role of ASA in recurrence of CRC liver metastases and survival. ASA is an inexpensive, well tolerated, and easily accessible drug that will be highly potential as adjuvant drug in secondary prevention of CRC liver metastases if the study shows a beneficial effect. This trial will also investigate the effect of ASA as adjuvant treatment on Health-related Quality of Life and the cost-effectiveness.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 466
• Est. completion date: February 2025
• Est. primary completion date: February 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• First time CRCLM (synchronous or metachronous).

• Recurrence of CRCLM (not previously included in this trial).

• In synchronous CRCLM and "Liver first" approach, the primary tumor must be resected within 6 weeks after the liver

• Macroscopic (surgical) free resection margins (R0 or R1 resection).

• Must be ambulatory with a performance status Eastern Cooperative Oncology Group (ECOG) 0-2.

• Must be at least 18 years of age.

• Signed informed consent and expected cooperation of the patients for the treatment and follow up must be obtained and documented according to International Conference on Harmonization - Good Clinical Practice (ICH GCP), and national/local regulations.

Exclusion Criteria:

• Concomitant use of ASA or other anticoagulants or platelet inhibitors such as warfarin or clopidogrel.

• Ongoing regular use of corticosteroids or NSAIDs.

• Inherited or acquired coagulopathy (haemophilia).

• Blood platelets (thrombocytes) < 100 x 10^9/L.

• Severe heart failure (classified as New York Heart Association (NYHA) class >III)

• Severe kidney failure >Stage 3b

• CRCLM previously treated with radiofrequency or microwave ablation technique

• Pregnancy or breastfeeding. For women in childbearing age there will be pregnancy test at monthly intervals (urine human chorionic gonadotropin (HCG) pregnancy tests (for home testing) will be given to the patients for monthly tests and the patient will self-report the results at each control). Furthermore, highly effective contraceptives will be required.

• Childbearing potential without proper contraceptive measures such as oral contraceptives, other hormonal contraceptives (vaginal products, skin patches, or implanted or injectable products), or mechanical products such as an intrauterine device to avoid pregnancy for the entire study period.

• Liver cirrhosis with a Child-Pugh score >B7.

• Alcoholism.

• Contraindication listed on the Summary of Product Characteristics (SmPC) of Trombyl:

Hypersensitivity/allergies to ASA, Thrombocytopenia, Previous severe gastrointestinal haemorrhage/peptic ulcer due to ASA/NSAID, Active peptic ulcer, Haemophilia, Liver cirrhosis, Severe congestive heart failure.

• Need to use concomitant medications contraindicated according to SmPC of Trombyl.

Related Conditions & MeSH terms

• Colorectal Cancer
• Colorectal Cancer Liver Metastases
• Colorectal Neoplasms
• Liver Metastases
• Liver Neoplasms
• Neoplasm Metastasis
• Neoplasms, Second Primary

Intervention

Drug:
• Acetylsalicylic acid
Trombyl 160 mg once daily
• Placebo Oral Tablet
Placebo one tablet daily

Locations

Country	Name	City	State
Denmark	Aarhus University Hospital	Aarhus
Denmark	Rigshospitalet, Copenhagen	Copenhagen
Denmark	Odense University Hospital	Odense
Norway	Haukeland University Hospital	Bergen
Norway	Oslo University Hospital	Oslo
Norway	Stavanger University Hospital	Stavanger
Norway	University Hospital of North-Norway	Tromsø
Norway	St Olavs Hospital	Trondheim
Sweden	Sahlgranska University Hospital	Gothenburg
Sweden	Linköping University Hospital	Linköping
Sweden	Skåne University Hospital Lund	Lund
Sweden	Karolinska University Hospital	Stockholm
Sweden	University Hospital of Umeå	Umeå
Sweden	Uppsala University Hospital	Uppsala

Sponsors (4)

Lead Sponsor	Collaborator
Oslo University Hospital	Klinbeforsk, Norwegian Cancer Society, The Research Council of Norway

Countries where clinical trial is conducted

Denmark,  Norway,  Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Disease Free Survival (DFS) after three years treatment	DFS three years after initiation of treatment with ASA or Placebo after resection of liver metastases.	3 years
Secondary	Time to recurrence (TTR) of disease after randomization	Time to recurrence of liver metastases three years after start of treatment.	3 years
Secondary	Overall survival (OS) three years after treatment start	OS at three years after initiation of treatment with ASA or Placebo	3 years
Secondary	Health-related Quality of Life with 36-item Short Form Health Survey (SF-36)	SF-36 has been proven useful in monitoring population health, estimating the burdens of different diseases, monitoring outcome in clinical practice, and evaluating medical treatment effects. Health-related Quality of Life (HR-QoL) will be assessed with SF-36.	3 years
Secondary	Health-related Quality of Life with EuroQoL 5 Dimensions (EQ-5D)	The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. The EQ VAS records the patient's self-rated health on a vertical visual analogue scale. This will be used as a quantitative measure of health outcome that reflects the patient's own judgement. The scores on these five dimensions will be presented as a health profile. Health-related Quality of Life (HR-QoL) will be assessed with EuroQoL 5 Dimensions (EQ-5D).	3 years
Secondary	ASA in CRC and Cost-Effectiveness Analyses I	Changes in HR-QoL will be used in calculation of the quality-adjusted life-year (QALY), a key outcome used in economic evaluations to compare treatments.	3 years
Secondary	ASA in CRC and Cost-Effectiveness Analyses II	Cost-effectiveness measured from a health care perspective by assessing the use of Health care provider in primary and specialized medicine.	3 years
Secondary	ASA in CRC and Cost-Effectiveness Analyses III	Cost-effectiveness measured from a societal perspective by assessing records in Statistics Norway (SSB).	3 years

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