Outpatient Hematopoietic Grafting in Multiple Sclerosis Employing Autologous Peripheral Blood Stem Cells
What it found
A paper reports the results; we have not read it yet. See Papers below.
What was tested
Treatment tested
- Hematopoietic stem cell transplantation
What it measured
Main measures
Expanded Disability Status Scale
4 years
Disability progression
Other measures (1)
Overall survival
4 years
Who could take part
Relapsing and progressive
Inclusion Criteria: * Patients with MS having a relapsing-remitting course, even though other forms could also qualify: Secondary progressive (SPMS) or primary progressive (PPMS) * Patients must have a Karnofsky performance status above 70% and a EDSS score of 8 or below. * In cases of patients with score between 6 and 8 patients will be accepted provided a carer accompanies the patient. * A recent central nervous system (CNS) MRI study (less than two months). * Patient has to be able to travel to and remain in Puebla, México during an 4-week period, accompanied by a caregiver. * Discontinue Immune Modulation or suppression medications 3 months before. Exclusion criteria: * EDSS score higher than 8 * Karnofsky performance status lower than 70% * Been exposed to chemotherapy in the past
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
Multiple sclerosis (MS) is a chronic, inflammatory, debilitating disease that causes destruction of central nervous system (CNS) myelin, with varying degrees of axonal damage. It mainly affects young adults and is twice as common in women as in men (1). Studies published from the 1990s brought animal models and theoretical considerations of hematopoietic stem cell transplantation (HSCT) being useful in the prevention and treatment of autoimmune diseases, with clinical responses in some patients, suggesting that high-dose chemotherapy followed by HSCT rescue could "reset" the immunological changes through the control of autoreactive clones, followed by immunological tolerance after immune reconstitution (2); this led to the conclusion that HSCT may be a viable therapeutic option for MS (1-6). Autologous HSCT have been done in patients with MS since 1996 and more than 700 HSCTs have been performed around the world (1-6). Most patients have been treated in small trials or in multicenter studies. In retrospective analyzes, a progression-free survival of more than five years after transplant has been observed, the neurological outcomes being considerably more favorable in patients with the relapsing-remitting type and/or those who showed an inflammatory pattern in magnetic resonance imaging (MRI) during the pre-transplant screening. Reports of good results, particularly in the aggressive forms of MS reinforce the effectiveness HSCT in MS patients with prominent inflammatory activity. The risk of transplant related mortality in HSCT for MS was conventionally considered very high but has declined since 2001 to 1.3% (2-6), this probably being the result of the changes in the conditioning regimens, thus reducing toxicity. Recent data, with more than 700 autologous transplants for MS in Europe, showed an overall survival of 92% in five years and a progression-free survival of 46%, the main cause of mortality and morbidity being the recurrence of the autoimmune disease (2-6). The consensus provides an indication of HSCT in patients with progressive MS unresponsive to conventional therapy and Expanded Disability Status Scale (EDSS) (1) between 3.0 and 6.0. The forms of the disease that might benefit from transplantation are: relapsing remitting, primary or secondary progressive, and the "malignant" form, provided there is evidence of inflammatory activity at the time of transplant indication.
Papers
Results
Self-reported changes in the expanded disability status scale score in patients with multiple sclerosis after autologous stem cell transplants: real-world data from a single center.Clin Exp Immunol · 2019
Results
A Feasibility Study of the Full Outpatient Conduction of Hematopoietic Transplants in Persons with Multiple Sclerosis Employing Autologous Non-Cryopreserved Peripheral Blood Stem Cells.Acta Haematol · 2017
Results
Pastelin-Martinez ML, Gallardo-Perez MM, Gomez-de-Leon A, Olivares-Gazca JC, Hernandez-Flores EJ, Sanchez-Bonilla D, Montes-Robles M, Robles-Nasta M, Ocana-Ramm G, Soto-Olvera S, Gomez-Almaguer D, Ruiz-Delgado GJ, Ruiz-Arguelles GJ. The consequences of delayed diagnosis and treatment in persons with multiple sclerosis given autologous hematopoietic stem cell transplantation. Diagnosis (Berl). 2024Results
Hernandez-Flores EJ, Gallardo-Perez MM, Robles-Nasta M, Montes-Robles MA, Sanchez-Bonilla D, Pastelin-Martinez ML, Ocana-Ramm G, Olivares-Gazca JC, Ruiz-Delgado GJ, Ruiz-Arguelles GJ. Second Autologous Hematopoietic Stem Cell Transplantation in Multiple Sclerosis: A Single-Center Prospective Experience. Transplant Proc. 2024 Jan-Feb;56(1):211-214. doi: 10.1016/j.transproceed.2023.12.004. Epub 2024Results
Montes-Robles MA, Gallardo-Perez MM, Hernandez-Flores EJ, Pastelin-Martinez ML, Sanchez-Bonilla D, Robles-Nasta M, Ocana-Ramm G, Olivares-Gazca JC, Ruiz-Delgado GJ, Ruiz-Arguelles GJ. In persons with CIDP, auto-HSCT can be conducted fully on an outpatient basis and induces significant clinical responses: A prospective study in a single center. Transpl Immunol. 2023 Dec;81:101944. doi: 10.1016/j.trBackground
Gale RP, Gomez-Cruz GB, Olivares-Gazca JC, Leon-Pena AA, Gomez-Almaguer D, Gomez-De-Leon A, Gonzalez-Lopez EE, Ruiz-Arguelles A, Soto-Vega E, Munoz-Perez MJ, Ruiz-Delgado GJ, Ruiz-Arguelles GJ. Determine safety of outpatient chemotherapy and autotransplants using refrigerated, non-frozen grafts in persons with multiple sclerosis. Clin Transplant. 2019 Jun;33(6):e13567. doi: 10.1111/ctr.13567. Epub
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History
Started
May 2015
Main results due
Dec 2025
Finished
Dec 2025
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