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Intra Arterial (IA) Steroids Infusion for Hepatic Acute Hepatic Graft Versus Host Disease (aGVHD)

An Investigator Initiated Open Study to Evaluate the Efficacy and Safety of Intra Arterial Infusion for Treatment of Steroid Resistant Acute Hepatic Graft Versus Host Disease (AGVHD)

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01140984
Enrollment
2
Registered
2010-06-10
Start date
2010-09-30
Completion date
2015-03-31
Last updated
2015-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Graft Versus Host Disease

Keywords

acute graft versus host disease, intra arterial steroid infusion, steroid resistant acute hepatic graft versus host disease

Brief summary

Post allogeneic hematopoietic stem cell transplantation (HSCT) patients with steroid resistant acute GVHD localised to the liver will receive 24 hours continuous intra-arterial infusion of methylprednisolone.

Detailed description

The study population will include 30 patients with SR AGVHD having an index of B, C, or D on the IBMTR severity index localized to the liver. Standard treatment for SR AGVHD includes: IV cyclosporine or tacrolimus with adjusted doses depending on serum levels and methylprednisolone or prednisone 2 mg/kg/d. This treatment may be continued during the study period although steroid taper down should be attempted if clinically possible. GVHD diagnosis will be based upon clinical criteria and biopsy (if needed) from an involved organ. GVHD will be graded according to the International Bone Marrow Transplantation Registry (IBMTR) severity index. Intra-arterial treatment should be given in less than 72h from completion of inclusion criteria. Partially responding or non-responding patients may receive a second treatment within 14 days of the initial intra-arterial treatment, at the discretion of the treating physician. Definitions Hepatic response: * Initial response - the day in which bilirubin level began to decrease. * Partial response 75 - the day in which bilirubin level decreased below 75% of basal level. * Partial response 50 - the day in which bilirubin level decreased below 50% of basal level. * Partial response 25 - the day in which bilirubin level decreased below 25% of basal level. * Complete response - the day in which bilirubin level decreased to normal level.

Interventions

DRUGMethylprednisolone (Intra-arterial continuous infusion of corticosteroids)

Sedation/anesthesia of patient followed by placement of a 4F vascular sheath and a diagnostic and hepatic angiogram. Angiographic catheter tip to be placed in the proximal proper hepatic artery, secured in place externally and connected to an arterial line pressurized system which allows continuous drip infusion of methylprednisolone diluted in normal saline (600mg/m2 with maximal total dose of 100mg diluted in 480cc in normal saline administered at 20cc/hr for 24 hours).

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Recipient of allogeneic stem cell transplantation. * Age\>18 years. * Post stem cells transplant \<100 days. * AGVHD of liver, IBMTR index B, C, D. * Resistant AGVHD - Patients will be eligible for inclusion if they developed grade B-D AGVHD with progression after 3 days standard treatment OR unresponsive to at least 7 days standard treatment OR incomplete response to standard treatment after 14 days. * Has received no 1st line treatment for steroid refractory AGVHD. * Signed a written informed consent

Exclusion criteria

* Not fulfilling any of the inclusion criteria. * Active life-threatening infection. * Inability to comply with study requirements. * Inability to give informed consent. * Contraindication to arterial catheterization (uncorrectable coagulopathy, severe allergic reaction to contrast material or others). * Inability to give the first Intra-arterial treatment in less than 72h from completion of inclusion criteria * An IBMTR index ≤ A. * Refractory skin AGVHD or severe diarrhea.. * Pregnant or breast-feeding female or childbearing potential. * Known to be HIV positive. * Has been diagnosed with veno-occlusive disease. * Has been diagnosed with multi organ failure. * Known renal failure eGFR \<30

Design outcomes

Primary

MeasureTime frameDescription
Hepatic response180 daysThe degree to which serum bilirubin levels do or do not decrease

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026