Overview

Effect of Atorvastatin on 5-Fluorouracil Induced Mucositis

Status:
Unknown status
Trial end date:
2020-09-30
Target enrollment:
0
Participant gender:
All
Summary
5-Fuorouracil (5-Fu) remains one of the most effective and most commonly used drugs to treat colorectal cancer. Mucositis is a major complication that occurs in approximately 80% of patients receiving 5-FU and results in abdominal bloating as well as vomiting and diarrhea. oral mucositis (OM) are often very painful and compromise nutrition and oral hygiene as well as increase risk for local and systemic infection. OM is characterized by an intense inflammatory reaction on the mucosa lamina propria cells, which results in activation of the transcription factor NF-kB. The activation of NF-kB leads to transcription of genes involved in the synthesis of pro-inflammatory cytokines, such as IL-1β, IL-6 and TNF-α. Agents known to attenuate the expression of cytokines have demonstrated efficacy in the prevention of experimental mucositis. The use of atorvastatin were associated with reduced production of TNF-α and IL-1β and decreased neutrophil infiltration evidenced by histopathological analysis and Myeloperoxidase (MPO) activity. In addition, atorvastatin also reduced oxidative stress and induced an increase in non-protein sulfhydryl groups showing anti-inflammatory and immunomodulatory action.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Ain Shams University
Collaborator:
Nasser Institute For Research and Treatment
Treatments:
Atorvastatin
Fluorouracil
Criteria
Inclusion Criteria:

1. Adult patients (>18 years old).

2. Colon cancer patients ???? who will receive adjuvant FOLFOX 6& FOLFIRI 6 for 6 cycles.

3. ECOG performance status 0-2

4. Adequate bone marrow function (white blood count ≥4,000/mm3, platelet count
≥100,000/mm3), liver function (serum total bilirubin <1.5 mg/dl), renal function
(creatinine <1.5 mg/dl).

Exclusion Criteria:

1. Patients who have Clinical GIT mucositis or Periodontal disease.

2. Patients with other primary malignancy.

3. Patients receiving mTOR inhibitors (eg, rapamycin, everolimus, and temsirolimus), EGFR
inhibitors (eg, bevacizumab and erlotinib) and tyrosine-kinase inhibitors (eg,
sorafenib and sunitinib).

4. Hypersensitivity to Atorvastatin.

6-Pregnant and lactating women. 7- Patients treated with ATV for any other indication. 8-
Patient who already have a mucositis