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Spots Global Cancer Trial Database for Study of OFATUMUMAB as Part of the Scheme of Reduced Intensity Conditioning in High Risk Non-Hodgkin Lymphoma B Patients

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Trial Identification

Brief Title: Study of OFATUMUMAB as Part of the Scheme of Reduced Intensity Conditioning in High Risk Non-Hodgkin Lymphoma B Patients

Official Title: Ofatumumab as Part of the Reduced Intensity Conditioning Regimen (RIC) for Patients With High Risk B Non Hodgkin's Lymphoma Undergoing Allogeneic Hematopoietic Cell Transplantation

Study ID: NCT01613300

Interventions

Ofatumumab

Study Description

Brief Summary: The aim of this study is rate of acute graft-versus-host disease II-IV measured at day +365according to conventional criteria (Przepiorka et al. 1995) in patients with high risk non-Hodgkin lymphoma B subjects with Allogeneic Stem Cell Transplant

Detailed Description: In addition to above: * Rate of progression-free survival (PFS) at 12, 24, 36 and 60 months post-transplant defined as the time between the infusion of progenitors and the disease progression or death. Patients alive or in complete remission will be censored at the time of last follow up * Transplant-related mortality (TRM) at 12, 24, 36 and 60 months after transplantation, defined as any death not caused directly by lymphoma (any death caused by complications related to transplantation). * Overall survival (OS) defined as the time between infusion of progenitors and the patient's death from any cause. Alive Patients will be censored at the time of last follow-up * Incidence of chronic graft versus host disease (GVHD) wide at 1 and 5 years according to conventional criteria (Atkinson et al. 1989) and Filipovich et al. (BBMT, 2005). * Rate of event-free survival (DFS) defined as time interval between diagnosis of lymphoma and lymphoma progression or relapse or death if the above does not occur. * Successful graft implantation: is defined as: 1. º: three consecutive days with absolute neutrophil count greater than 0.5 \* 109 / L 2. ° thrombocythemia exceeds 20 \* 109 / L. * Reconstitution of the immune system: lymphocyte count populations CD20, CD3, CD4 and CD8 and immunoglobulinemia serum (days +100, 180, 360, 18 months and 24 months). * intercurrent infections. All sorts of infections (viral, fungal and bacterial)will be recorded * Safety assessment by the standards of Common Terminology Criteria for adverse events v. 4.0

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Hospital Vall d'Hebron, Barcelona, , Spain

Hospital Reina Sofia, Córdoba, , Spain

H.U. 12 de Octubre,, Madrid, , Spain

H.U. Gregorio Marañón,, Madrid, , Spain

H.U. La Paz, Madrid, , Spain

H. Morales Meseguer., Murcia, , Spain

Complejo Hospitalario Carlos Haya, Málaga, , Spain

H. Clinico de Salamanca, Salamanca, , Spain

Hospital Virgen del Rocío, Sevilla, , Spain

H. La Fe, Valencia, , Spain

Contact Details

Name: Maria Dolores Caballero, MD

Affiliation: Hospital Clinico de Salamanca

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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