| Literature DB >> 19034614 |
Livio Pagano1, Caterina Giovanna Valentini2, Morena Caira2, Michela Rondoni3, Maria Teresa Van Lint4, Anna Candoni5, Bernardino Allione6, Chiara Cattaneo7, Laura Marbello8, Cecilia Caramatti9, Enrico Maria Pogliani10, Emilio Iannitto11, Fiorina Giona12, Felicetto Ferrara13, Rosangela Invernizzi14, Rosa Fanci15, Monia Lunghi16, Luana Fianchi2, Grazia Sanpaolo17, Pietro Maria Stefani18, Alessandro Pulsoni12, Giovanni Martinelli3, Giuseppe Leone2, Pellegrino Musto19.
Abstract
The aim of the study is to evaluate clinical features, treatments and outcome of patients with systemic mast cell disease (MCD) who arrived to the attention of hematologists. A retrospective study was conducted over 1995-2006 in patients admitted in 18 Italian hematological divisions. Twenty-four cases of advanced MCD were collected: 12 aggressive SM (50%), 8 mast cell leukemia (33%), 4 SM with associated clonal non-mast cell-lineage hematologic disease (17%). Spleen and liver were the principal extramedullary organ involved. The c-kit point mutation D816V was found in 13/18 patients in which molecular biology studies were performed (72%). Treatments were very heterogeneous: on the whole Imatinib was administered in 17 patients, alpha-Interferon in 8, 2-CdA in 3; 2 patients underwent allogeneic hematopoietic stem cell transplantation. The overall response rate to Imatinib, the most frequently employed drugs, was of 29%, registering one complete remission and four partial remission; all responsive patients did not present D816V c-kit mutation. Overall three patients (12%) died for progression of disease. We conclude that MCD is characterized by severe mediator-related symptoms but with a moderate mortality rate. D816V c-kit mutation is frequent and associated with resistance against Imatinib. Because of the rarity of these forms, an effective standard of care is lacking. More data are needed to find new and successful therapeutic strategies.Entities:
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Year: 2008 PMID: 19034614 DOI: 10.1007/s12185-008-0166-4
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490