Title :

How to capture cytogenetic and molecular abnormalities into promise database for hematological malignancies: guidelines from the francophone society of bone marrow transplantation and cellular therapy (sfgm-tc)

Author(s) :

Raus, Nicole [Auteur]
Karam, Micheline [Auteur]
Chebel, Reda [Auteur]
Dantin, Carole [Auteur]
Pereira, Maguy [Auteur]
Wallart, Anne [Auteur]
Yakoub-Agha, Ibrahim [Auteur]
Lille Inflammation Research International Center - U 995 [LIRIC]
Srour, Micha [Auteur]

Journal title :

Bulletin du Cancer

Abbreviated title :

Bull Cancer

Volume number :

107

Pages :

S52-S61

Publication date :

2020-01

ISSN :

1769-6917

English keyword(s) :

SFGM-TC recommendations
Cytogenetics
Molecular biology
Entering ProMISe

HAL domain(s) :

Sciences du Vivant [q-bio]

English abstract : [en]

In an effort to standardize hematopoietic stem cell allograft procedures, the Francophone bone marrow transplantation and Cell Therapy Society (SFGM-TC) organized the 9th Allograft Harmonization Practice Workshop in Lille ...
Show more >In an effort to standardize hematopoietic stem cell allograft procedures, the Francophone bone marrow transplantation and Cell Therapy Society (SFGM-TC) organized the 9th Allograft Harmonization Practice Workshop in Lille in September 2018. The purpose of these workshops is to propose a consensual attitude to the centers that wish it. In this workshop, we discuss how to capture the cytogenetic and molecular abnormalities of acute leukaemias, myelomas, myelodysplasias, myeloproliferative syndromes and myelodysplastic/myeloproliferative syndromes in the database common to all European transplant centers called ProMISe and managed by the European Society for Blood and Marrow Transplantation (EBMT). The complexity of cytogenetic and molecular data makes it difficult to enter data into the ProMISe registry. This workshop proposes a tool for input assistance, in tabular form by pathology. The main recommendation for the karyotype remains that of the complex karyotype that must be entered in "Full caryotype". Concerning the molecular anomalies, it is necessary to enter all the items proposed by ProMISe. In reviewing all the sheets proposed by ProMise, we note the absence of some relevant elements that can be added later.Show less >

Language :

Anglais

Audience :

Internationale

Popular science :

Non

Collections :

• Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286

Submission date :

2024-01-30T10:28:19Z
2024-01-30T15:08:21Z