Unraveling germline predisposition in hematological neoplasms: Navigating complexity in the genomic era.

Fecha de publicación: Fecha Ahead of Print:

Autores de IIS La Fe

Participantes ajenos a IIS La Fe

  • Jerez, Joaquin

Grupos

Abstract

Genomic advancements have yielded pivotal insights into hematological neoplasms, particularly concerning germline predisposition mutations. Following the WHO 2016 revisions, dedicated segments were proposed to address these aspects. Current WHO 2022, ICC 2022, and ELN 2022 classifications recognize their significance, introducing more mutations and prompting integration into clinical practice. Approximately 5-10% of hematological neoplasm patients show germline predisposition gene mutations, rising with risk factors such as personal cancer history and familial antecedents, even in older adults. Nevertheless, technical challenges persist. Optimal DNA samples are skin fibroblast-extracted, although not universally applicable. Alternatives such as hair follicle use are explored. Moreover, the scrutiny of germline genomics mandates judicious test selection to ensure precise and accurate interpretation. Given the significant influence of genetic counseling on patient care and post-assessment procedures, there arises a demand for dedicated centers offering specialized services.

Copyright © 2023 Elsevier Ltd. All rights reserved.

Datos de la publicación

ISSN/ISSNe:
0268-960X, 1532-1681

BLOOD REVIEWS  Churchill Livingstone

Tipo:
Article
Páginas:
101143-101143
Factor de Impacto:
2,799 SCImago
Cuartil:
Q1 SCImago

Documentos

  • No hay documentos

Métricas

Filiaciones

Filiaciones no disponibles

Keywords

  • Genetic counseling; Germline predisposition; Technical challenges

Campos de estudio

Proyectos asociados

Programa piloto de cribado de susceptibilidad a neoplasias hematológicas hereditarias.

Investigador Principal: ESPERANZA SUCH TABOADA

2019_0070_CRC_AECC_SANTIAGO . FUNDACIÓN CIENTÍFICA AECC . 2019

New approaches for the identification and functional characterization of prognostic genetic biomarkers in inherited childhood myelodysplastic/acute leukemia syndromes. Acronym: GEMMA

Investigador Principal: JOSÉ VICENTE CERVERA ZAMORA

PROJECT 228/C/2020 . FUNDACIÓ LA MARATÓ DE TV3 . 2021

Diagnóstico citogenético mediante citogenética de nueva generación en pacientes con neoplasias oncohematológicas y cariotipo no valorable (CNG-Oncohemato).

Investigador Principal: ESPERANZA SUCH TABOADA

PID2021-126138OB-I00 . MINISTERIO DE CIENCIA E INNOVACION . 2022

Ampliar el espectro molecular y evaluar la aplicabilidad clínica de la secuenciación del genoma y del transcriptoma en las neoplasias mieloides.

Investigador Principal: JOSÉ VICENTE CERVERA ZAMORA

PI22/01633 . INSTITUTO DE SALUD CARLOS III . 2023

Contratos Río Hortega 2022. Marta Santiago Balsera

Investigador Principal: JOSÉ VICENTE CERVERA ZAMORA

CM22/00191 . INSTITUTO DE SALUD CARLOS III . 2023

Caracterización funcional de variantes germinales en neoplasias mieloides hereditarias (GERMVAR)

Investigador Principal: ALEJANDRA SANJUAN PLA

PID2022-136660OB-I00 . MINISTERIO DE CIENCIA E INNOVACION . 2023

Análisis clínico-biológico de los procedimientos y productos de transfusión de componentes sanguíneos, aféresis y terapia celular.

Investigador Principal: PILAR SOLVES ALCAINA

2142_23 . 2024

Cita

Compartir