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Spots Global Cancer Trial Database for Sequential Trial on Reduced Intensity Conditioning (RIC) Allogeneic Transplantation

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Trial Identification

Brief Title: Sequential Trial on Reduced Intensity Conditioning (RIC) Allogeneic Transplantation

Official Title: European Myeloma Network Sequential Phase I / Phase II Trial on RIC Allogeneic Transplantation: an Optimized Program for High Risk Relapsed Patients

Study ID: NCT01460420

Study Description

Brief Summary: The aim of the current study is to improve the outcome of patients with hematologic malignancies (in a phase I trial) and more specifically multiple myeloma (in a phase II trial) by 2 interventions: reduce the risk of graft-versus-host disease (GVHD) and improve the efficacy of the procedure decreasing the risk of relapses after transplant. Currently, the standard approach used in most centers to prevent graft-versus-host disease after allogeneic transplantation is based on the combination of a calcineurin inhibitor (cyclosporine or tacrolimus) plus a short course of methotrexate. Unfortunately, this strategy is far from ideal, since the risk of acute GVHD is in the range of 30-40% among patients receiving a matched related donor transplantation and even higher among patients receiving transplantation from an unrelated donor while the incidence of chronic GVHD is 60-70% among patients receiving peripheral blood progenitor cells from either a related or unrelated donor. As far as the patients with multiple myeloma (MM) is concerned, although the development of new drugs has markedly changed the outcome and management of these patients, allogeneic transplantation so far appears to be the only curative option, especially among those patients relapsing after first line treatment. Nevertheless, still new strategies within the allogeneic transplant setting are needed to improve its results. Relapses may occur either extramedullary (very common in this setting) or systemic. In order to reduce the risk of systemic relapses the investigators will use maintenance therapy with Lenalidomide (Len) which, together with bortezomib (Bz) should contribute to eradicate minimal residual disease (MRD). In case the patient do not obtain complete remission or near complete remission after transplant, in addition to the maintenance therapy, the investigators will use four intensification cycles with VRD (Bz-Len-Dexamethasone). In summary, the goal is to optimize the efficacy of allogeneic transplantation by two interventions: one focused on reducing the risk of relapse and the other on reducing the incidence of GVHD.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Medizinische Klinik and Poliklinik II, University Hospital, Würzburg,, , Germany

S Giovanni Battista Hospital, Torino, , Italy

Azienda Ospedaliera Universitaria di Udine, Udine, , Italy

Hospital Clinic i Provincial,, Barcelona,, , Spain

Hospital Santa Creu I Sant Pau,, Barcelona,, , Spain

Hospital Universitario Ramón y Cajal, Madrid, , Spain

Hospital Gregorio Marañón,, Madrid, , Spain

Hospital Clinico Universitario Salamanca,, Salamanca,, , Spain

Hospital Universitario Virgen del Rocío,, Sevilla, , Spain

Karolinska University Hospital, Huddinge, Stockholm, , Sweden

Contact Details

Name: Jose-Antonio Perez-Simon, MD-PhD

Affiliation: University Hospital Virgen del Rocio

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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