Treatment of Gastro-Intestinal and/or Hepatic Graft Versus Host Disease With Budesonide in Patients Following Peripheral Blood Stem Cell Transplantation
Information source: Rafa Laboratories
Information obtained from ClinicalTrials.gov on March 21, 2008
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Graft Vs Host Disease
Intervention: Budesonide (Drug)
Phase: Phase 3
Status: Completed
Sponsored by: Rafa Laboratories Official(s) and/or principal investigator(s):
Michael Y Shapira, MD, Principal Investigator, Affiliation: Hadassah Medical Organization, Jerusalem Israel
Summary
Twenty-four (2 x 12) patients with intestinal graft versus host disease (GVHD) Grades 2, 3 or
4 will be treated with budesonide 3mg three times daily or placebo for 12 weeks. All of the
patients will receive cyclosporine and by mouth (po) prednisone or intravenous (IV)
methylprednisone with a starting dose of 2mg/kg/day (standard anti-GVHD treatment). Doses of
steroids will be decreased by approximately 10% or 10mg per week (depending upon patient’s
weight) upon response to therapy, defined as a decrease of volume of diarrhea by 50% per day,
decrease in abdominal pain and no presence of bloody stool. Patients with Grades 3 or 4 will
be withdrawn from the study if there is no response after one week of therapy. Patients with
Grade 2 may continue with no decrease in prednisone dose until response is achieved.
Clinical Details
Official title: A Phase 3 Study to Evaluate the Place of Budesonide in the Treatment of GVHD
Study design: Treatment, Randomized, Double-Blind, Placebo Control, Single Group Assignment, Efficacy Study
Detailed description:
Graft versus host disease (GVHD) is one of the most common complications of bone marrow
transplantation (BMT). Targets of GVHD are the gastro-intestinal tract (GIT) liver and skin,
causing severe diarrhea and mucosal aberration and hepatitis that can cause life threatening
liver failure. As a result of the mucosal aberration and the general immuno-suppression,
caused both by the GVHD process itself and by the anti GVHD therapy, these patients are
highly susceptible for severe, life threatening infections that usually originate from the
GIT. Systemic steroids are the backbone of anti GVHD therapy. However, in GVHD systemic
steroids have to be administered for a prolonged duration and in high doses, thus causing
prolonged immune suppression, and exposing the patients to steroid side effects such as
hypertension, diabetes, cataract formation etc.
Budesonide is a steroid that combines topical anti-inflammatory activity with high first-pass
hepatic extraction. It was shown to be effective in treatment of inflammatory bowel disease
with results slightly less then systemic steroids and fewer steroid-related adverse
reactions. Except for its influence on the gut, budesonide was also shown to benefit
inflammatory hepatic conditions such as primary biliary cirrhosis, liver transplantation and
autoimmune hepatitis. Recently, it has been shown that budesonide is an effective treatment
in acute GIT GVHD. The investigators propose to evaluate the effect of budesonide in GIT and
hepatic GVHD with the following study.
Patients:
Twelve patients after allogenic peripheral blood stem cell transplantation (PBSCT) with grade
>= 2 GIT and/or hepatic GVHD will be prospectively compared to 12 placebo controls.
Inclusion Criteria:
- Clinical and biopsy proven grade >/= 2 GIT AND/OR hepatic GVHD.
Exclusion Criteria:
- Preventive antimicrobial treatment (with the exception of Resprim) or somatostatin in
the GIT GVHD patients.
- Anti-GVHD treatment other then steroids (maximal dose ≤ 2 mg/kg methylprednisolone) and
cyclosporine A or tacrolimus.
Study Protocol:
All patients will be assessed for GVHD scoring (organ and general) according to standard
criteria and tested before inclusion for the following parameters –
- Colon and/or liver biopsy GVHD staging (including number of crypt abscesses).
- Liver function tests - blood albumin, AST, ALT, GGTP, Alk Phos, LDH, bilirubin,
coagulation function, cholesterol.
- Stool - volume and frequency.
- Radiological – CT scan for mucosal edema, wall thickening and ascites.
- Kidney function tests – blood creatinine, creatinine clearance.
- Blood pressure.
- Fasting blood glucose. If normal – oral glucose tolerance test, glycosylated
hemoglobin.
- Ophthalmologist evaluation for cataract formation and IOP.
- GIT absorption assessment - xylose absorption.
- Microbiological - stool culture and stool for CDT, CMV PCR, culture for CMV in blood
and urine.
- Bone density – by ultrasound.
After inclusion the patients will be treated with budesonide 9 or 15mg per day in divided
doses or placebo. Other anti-GVHD treatment or ursodeoxycholic acid will not be withheld but
tapering off will be tried.
Study parameters:
- LFT, albumin, PT, cholesterol, renal function, stool volume and frequency, CMV culture and PCR, clinical GVHD staging - every 2 weeks.
- Xylose test – every month.
- Ophthalmologist evaluation, diabetes control and CT scan – every 3 months.
- GIT and/or liver biopsy for GVHD staging (including number of crypt abscesses) and CMV
PCR, bone density – every 6 months
- Blood, urine and stool culture during every febrile episode.
Study duration: 14 weeks.
End points:
- Hospitalizations: due to GVHD and/or due to infections.
- Overall and GIT or hepatic GVHD staging.
- Time to response.
- Maximal daily diarrhea (volume and frequency).
- Weight.
- Liver function tests.
- Cataract formation and IOP.
- TNF level.
- Albumin.
- TPN consumption.
- Bone density.
- Hypertension.
- Diabetes – presence and control.
- Febrile episodes.
- Positive cultures.
- Days of antibiotic therapy.
- Survival.
Eligibility
Minimum age: 18 Years.
Maximum age: 70 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Patients with clinical and biopsy proven Grades 2, 3 or 4 intestinal GVHD
- Patients with a negative stool culture
- Male or female patients aged between 18 – 70 years
- Signed written informed consent of the patient
Exclusion Criteria:
- Uncertain GVHD diagnosis (other causes of intestinal disease are possible)
- Severe other disease which may influence the patient prognosis
- Contraindication to the use of steroids
- Patient’s inability to swallow the study medications
- Concurrent use of non-steroidal anti-inflammatory drug (NSAID)
- Known spontaneous or iatrogenic disturbances of thrombocyte aggregation or blood
clotting.
- Kidney dysfunction with creatinine level higher than 2mg/dl
- Patients on preventative antimicrobial therapy with the exception of Resprim®
(sulfamethoxazole and trimethoprim)
- Patients taking somatostatin
- Patients taking anti-GVHD medication with the exception of steroids (maximum dose of
prednisone or methylprednisolone 2mg/kg/day) and cyclosporine A or tacrolimus
- Pregnancy or lactation
- Insufficient contraception protection
- Participation in another clinical study within the last 30 days.
- Mental condition rendering the patient unable to understand the nature or scope and
possible consequences of the study and/or evidence of an uncooperative attitude.
Locations and Contacts
Hadassah Medical Organization,, Jerusalem 91120, Israel
Additional Information
Starting date: January 2001
Ending date: August 2005
Last updated: August 26, 2005
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