RecruitingPhase 2ACTRN12616000151437

A Phase II study: Haematopoietic Stem Cell Transplantation for highly active treatment resistant multiple sclerosis .


Sponsor

Austin Health

Enrollment

20 participants

Start Date

Jan 15, 2016

Study Type

Interventional

Conditions

Summary

Over the past 15 years a number of new treatments have proved successful in the treatment of multiple sclerosis. There a remains though a small group of patients who do not respond and who continue to have attacks despite treatment causing further permanent neurological disability in a cumulative fashion. This disability can take the form of muscle weakness, impairing walking ability, visual loss, impaired balance, bladder and bowel dysfunction and loss of higher intellectual faculties. Patients with aggressive forms of MS also have a shortened life span as a result of their disease. Haematopoietic stem cell transplantation (HSCT) is a procedure originally used to treat patients with blood cancers. A high dose of chemotherapy is given which not only kills the malignant cells but also normal healthy bone marrow and blood cells. In order for the patient to survive these cells must be replaced by giving the patient a stem cell infusion following the chemotherapy . The stem cells replenish the bone marrow and a new blood and immune system then grows from it. Over the last 15 years, HSCT has become much safer. At the same time, numerous lines of evidence have emerged suggesting that a small number of patients with severe autoimmune diseases such as MS not controlled by other treatments could also respond to treatment with HSCT. This evidence came initially from patients with a co-existent auto-immune disease (AID) including multiple sclerosis (MS) who had chemotherapy for blood tumours. It was observed that not only did their cancers remain in prolonged remission after HSCT but so did the manifestations of their autoimmune disease. The procedure requires an initial dose of chemotherapy with a drug called cyclophosphamide to help stem cells to be collected via a vein in the arm. Subsequently the patient is admitted into hospital tohave high doses of chemotherapy that intensely suppresses the immune system. At this point the stem cells collected at the earlier time point are reinfused through the vein so they can re-grow a new immune system and protect the patient from the toxic effects of the chemotherapy. It takes about 14 days for the new stem cells to grow and then follow up is conducted carefully over several years to see if this method of immunosuppression and immune reconstitution prevents the reemergence of multiple sclerosis. The procedure is not without risk with the major complications of infection and death. Overall the risk of death where the procedure is done for an autoimmune disease is quoted at between 1-5 %. The Neurology Unit at Austin Health has conducted trials in MS since 1996 and the Haematology Unit performs HSCT on a regular basis for patients with blood malignancies. The unit’s morbidity and mortality results for HSCT are on par with the world’s leading hospitals. We intend to explore therapy in patients with an aggressive form of MS and then follow them in a rigorous fashion over 5 years to gauge its effectiveness.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 55 Yearss

Plain Language Summary

Simplified for easier understanding

This study tests whether a stem cell transplant procedure (HSCT) can stop or slow highly active multiple sclerosis (MS) that has not responded to standard treatments. The procedure resets the immune system using high-dose chemotherapy followed by the re-infusion of the patient's own stem cells. It carries real risks including serious infection and a 1–5% chance of death, but may prevent further disability in patients who keep relapsing despite medication. Participants are followed closely for five years. You may be eligible if: - You are between 18 and 55 years old - You have relapsing-remitting MS with a disability score (EDSS) between 2.5 and 5.5 - You were first diagnosed and treated for MS within the past 10 years - You have had at least one severe relapse and/or active brain lesions on MRI in the past two years despite ongoing approved MS therapy - Your heart, lungs, and other organs are functioning well enough for chemotherapy You may NOT be eligible if: - You have progressive MS with no recent disease activity on MRI - You have HIV, hepatitis B, or hepatitis C - You have a severe chronic infection - You cannot provide informed consent Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Patients are assessed using inclusion and exclusion criteria, specific for the highly active, treatment resistant multiple sclerosis in order to determine whether they are eligible for an Autologou

Patients are assessed using inclusion and exclusion criteria, specific for the highly active, treatment resistant multiple sclerosis in order to determine whether they are eligible for an Autologous Stem cell transplant. If eligible, all patients are given intravenous Cyclophosphamide 2g/m2 as per standard practice followed by G-CSF 10mcg/kg for the next 10-12 days until the following Monday when stem cells are collected by taking 150-200mls of blood which is processed in the laboratory. Minimum target CD34+ stem cell collection will be 2 x 10^6/kg. Patients will be admitted into hospital for their autologous stem cell transplant within 4-8 weeks of stem cell collection based on speed of laboratory processing to produce transplant cells. Patients will then undergo chemo-immunotherapy. with BEAM therapy combined with Horse ATG (Atgam). This includes intravenous administration of all the following agents carmustine 300mg/m2 on Day -6; then cytosine arabinoside 200mg/m2 /day and etoposide 200mg/m2 /day on Days -5, -4, -3, -2; then Melfalan 140mg/m2 on Day -1. Reinfusion of stem cells occurs on Day 0. This is followed by intravenous methylprednisolone 5mg/Kg /day and intravenous horse antithymocyte globulin 20mg/Kg /day on Days +1 and +2. Standard supportive measures including hydration, antiemetics, and antimicrobial prophylaxis are followed as per institutional protocols.


Locations(1)

Austin Health - Austin Hospital - Heidelberg

VIC, Australia

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ACTRN12616000151437


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