Allo After Allo Stem Cell Transplantation Following Relapse After Allogeneic Transplant in Haematological Malignancies: Retrospective Results of the GETH
NCT ID: NCT01212796
Last Updated: 2010-10-01
Study Results
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Basic Information
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UNKNOWN
350 participants
OBSERVATIONAL
2010-09-30
2011-06-30
Brief Summary
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Another therapeutic approach after relapse post allogeneic transplant is to resubmit the allogeneic transplant patient to patient. In this clinical situation is little known. All previous studies are retrospective, the data provided are of little statistical value and heterogeneous patient samples.
The GETH (Grupo Espanol de trasplantes hematopoyeticos y terapia celular) has included in its database a figure around 350 seconds allogeneic transplants. Comparing this with the studies published so far, this would be the largest retrospective series published size compared to second allogeneic transplants.
Detailed Description
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To collect these forms of EBMT, patients have previously authorized through the informed consent of this information collection.
It will include basic descriptive characteristics of the cohort and comparisons between groups were conducted to check if the sample is homogeneous.
The analysis is divided into descriptive data collection related to the transplant, both prior to transplantation and on during it. It also collected data related to transplant once done this.
FINDINGS AND PURPOSE The main variables to be analyzed are: overall survival, disease-free survival and progression, relapse rate and transplant-related mortality.
Secondary endpoints to be analyzed can vary once made the data collection. Yet between them will include: incidence of graft-versus-host disease (both acute and chronic), incidence of infections.
The purpose of this study is the description of variables that can predict the success or failure of making a second allogeneic transplant after the first relapse. These variables were also analyzed for third or subsequent transplants.
Also seeks to differentiate risk groups among patients. The novelty of this study could provide regarding previously published studies is the description of third or subsequent transplants, so far there are few references to this in the literature to date.
FINANCING This study does not require funding.
CONFLICT OF INTEREST There is no conflict of interest
DATA COLLECTION PERIOD AEMET submission and acceptance: 1-2 months. Aceppt (SEPT-10-2010) Data collection: 3 - 6 months Results: at 6 - 9 months Publication and presentation at conferences, at 12 months
Conditions
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Study Design
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RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
Yes
Sponsors
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Grupo Espanol de trasplantes hematopoyeticos y terapia celular
OTHER
Responsible Party
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GETH
Principal Investigators
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Duarte R Palomino, MD
Role: PRINCIPAL_INVESTIGATOR
Grupo Espanol de trasplantes hematopoyeticos y terapia celular
Central Contacts
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Other Identifiers
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get-alo-2010-01
Identifier Type: -
Identifier Source: secondary_id
GET-ALO-2010-01
Identifier Type: -
Identifier Source: org_study_id