Dietary Intervention in Follicular Lymphoma

• Status: Unknown status
• Trial end date: 2009-12-01
• Target enrollment: 0
• Participant gender: All

Summary

A dietary intervention study in patients with Follicular Lymphoma (FL) Stage III/IV to assess the ability of several dietary factors to induce apoptosis, inhibit cell proliferation and modulate tumor cell infiltrate in vivo.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Oslo University Hospital
• Collaborator: University of Oslo
• Treatments: Allicin; Quercetin; Resveratrol; Selenium

Criteria

Inclusion Criteria:

• Age 18 years or more.

• Permanent address in Norway, located in health region south or east. People living outside these areas in other health regions in Norway may be able to participate but after individual evaluation.

• Histologically verified follicular lymphoma grade I or II without clinical signs of transformation to aggressive lymphoma.

• Stage III/IV.

• Previously untreated or at least 1 year since rituximab treatment or 6 months since cytotoxic chemotherapy.

• Not scheduled for disease specific treatment for the next 3 months.

• At least one pathological superficial lymph node available for ultrasound guided biopsy.

• Cytologically and/or immunocytologically compatible with follicular lymphoma.

• Women with childbearing potential, only with use of safe contraceptives

Exclusion Criteria:

• Gross abnormalities in blood samples. (Hematologic values Hgb< 10, leukocytes< 2,5, trombocytes <100, liver enzymes (ALAT,ASAT,GT,ALP) > 2,5 x upper normal values,bilirubin >35 creatinine >130)

• Other serious medical illness (unstable cardiovascular disease, unstable pulmonary disease, uncontrolled diabetes, autoimmunity, chronic infection or other active cancer).

• Use of NSAID, ASA the last two weeks prior to enrollment.

• Use of systemic corticosteroids the last two months prior to enrollment.

• Regular use of anticoagulants as LMW Heparin or warfarin.

• Use of carbamazepin, nifedipin and other drugs metabolized with CYP 3A4 where interaction might cause hazardous side effects which cannot be controlled with serum measurements or organ function monitoring.

• Inclusion in another clinical trial which involves medication or nutritional supplements.

• Use of complementary medicine/alternative medicine which includes high dose* vitamins or antioxidants/nutritional supplements 2 weeks prior to sampling procedures .

• Regularly use of omega 3 fatty acids more than 1g / day

• History of serious or unstable medical or psychiatric disorder.

• History of heavy alcohol consumption > 3 units / day.

• Pregnancy

• Individuals judged by the clinical investigator to be unable to follow instructions and procedures of the study.

(*high dose is defined as vitamins or antioxidant supplements exceeding what is present in regular multi-vitamin supplements covering regular RDAs)