| Literature DB >> 29410295 |
Julia Suárez-González1, Carolina Martínez-Laperche2, Mi Kwon3, Pascual Balsalobre3, Diego Carbonell3, María Chicano3, Gabriela Rodríguez-Macías4, David Serrano3, Jorge Gayoso3, José Luis Díez-Martín5, Ismael Buño6.
Abstract
Development of de novo hematologic malignancies in donor cells after allogeneic stem cell transplantation (allo-SCT) provides a useful in vivo model to study the process of leukemogenesis. A systematic analysis of the cases reported in the literature was performed to identify risk factors and mechanisms involved in the pathogenesis of donor cell-derived hematologic neoplasms (DCHN) and leukemogenic transformation. Relevant data were extracted from 137 cases. Cases of DCHN show a wide heterogeneity with regard to recipient/donor age, sex mismatch, and conditioning regimen. Some characteristics, such as the type of primary disease, the type of hematologic malignancy of the DCHN, and the stem cell source used in the transplant procedure, differ from those expected. Mechanisms involved in the pathogenesis of DCHN are complex, and several hypotheses have been proposed, such as pre-existing hematologic neoplasms or premalignant clones in the donor, decreased immune surveillance, and damage to bone marrow microenvironment in the recipient. Most likely several if not all these mechanisms play a role in DCHN development. Novel approaches, such as next-generation sequencing to study consecutive samples after allo-SCT in these patients, appear to be promising to decipher the mechanisms of leukemogenesis.Entities:
Keywords: Allo-SCT; Donor cell leukemia; Donor cell–derived hematologic malignancy; Donor cell–derived neoplasm; Leukemogenesis; Systematic review
Mesh:
Year: 2018 PMID: 29410295 DOI: 10.1016/j.bbmt.2018.01.033
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742