Hydroxyurea in Ph negative myeloproliferative neoplasms: experience in Argentina
Revista Hematología ENERO - ABRIL 2019
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Keywords

Myeloproliferative Neoplasm, Hydroxyurea, Thrombosis, JAK2 Mutation

How to Cite

Bendek, G. E., Vicente, A., Varela, A., Sackman, F., Heller, P., Galeazzi, A., Cabrejo, M., Moiraghi, B., Enrico, A., Nucifora, E., Arbelbide, J., Cardenas, M., Beligoy, L., Seehaus, C., Agra, M., Aguilera, E., Benzadon, R., Bonacina, A., Braidot, G., Canonico, M., Carvani, A., Casale, M., Casali, C., Castano, V., Cazap, N., Celebrin, L., Celina, V., Macchiavello, E., Fernández Grecco, H., Ferrari, L., Pavlovsky, C., Pavlovsky, A., Fontana, S., Garate, G., Gomez, M., Gonzalez, F., Gotta, D., Longordo, I., Jerez, J., Kornblihtt, L., Rojas, F., Lafalce, D., Mahuad, C., Maradei, J., Marquez, M., Masachessi, N., Melillo, L., Perez, M., Roveri, E., Ruades, A., Salto, A., Sanchez Avalos, J., Sfeir, Z., Cruset, S., Williams, M., Zani, C., Tosin, M., Musso, A., Gilli, V., Fernández, V., Minissale, C., & Castro Rios, M. (2019). Hydroxyurea in Ph negative myeloproliferative neoplasms: experience in Argentina. Journal of Hematology, 23(1), 24–30. Retrieved from https://revistahematologia.com.ar/index.php/Revista/article/view/70

Abstract

Ph negative myeloproliferative neoplasms (NMP), polycythemia vera (PV), essential thrombocythemia
(ET) and primary myelofibrosis (MF), are clonal hematopoietic disorders characterized in their chronic
phase by an overproduction of differentiated hematopoietic cells. Hydroxyurea (HU) is an antineoplastic
agent belonging to the family of antimetabolites.  (According to ELN guidelines, it is recommended as first-line cytoreductive therapy). It is the cytoreductive agent recommended in the first line by the European Leukemia Net (ELN). The aim of this work was to describe the criteria for the initiation of cytoreductive treatment, vascular complications and response rates, intolerance, resistance and progression to myelofibrosis or AML in a population of patients with NMP treated with hydroxyurea in Argentina. 419 patients referred by 63 members of the SAH, belonging to 37 institutions, diagnosed between 1986 and 2017 were included, of which 417 were available for analysis. We observed that the main reason for starting treatment was age (51%), followed by the presence of vascular risk factors (26.6%), thrombocytosis (24.7%) with an average platelet count 1.052 x 109/L (DS 360.32) and previous thrombosis (16.8%). Complete hematological responses lasting at least three months were obtained in PV and TE (61 and 66%). The presence of arterial and venous thrombosis had a similar frequency (14%). The use of HU significantly reduced the risk of thrombosis in the higher risk group. The clinical course and complications of the patients studied with PV JAK2 and positive JAK2 TE were similar and adverse events due to the use of HU were mild but frequent (32.6%).

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