New Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options

Philadelphia-negative myeloproliferative neoplasms (MPN) are aggressive diseases characterized by clonal proliferation of myeloid stem cells. The clonal process leads to excessive red cells production, platelets production, and bone marrow fibrosis. According to the phenotype, MPN can be classified...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autor principal: Domenico Penna
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
Acceso en línea:https://doaj.org/article/61c8db4b2543475f9aad70a2daa5087c
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:61c8db4b2543475f9aad70a2daa5087c
record_format dspace
spelling oai:doaj.org-article:61c8db4b2543475f9aad70a2daa5087c2021-11-25T18:18:22ZNew Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options10.3390/medicina571111811648-91441010-660Xhttps://doaj.org/article/61c8db4b2543475f9aad70a2daa5087c2021-10-01T00:00:00Zhttps://www.mdpi.com/1648-9144/57/11/1181https://doaj.org/toc/1010-660Xhttps://doaj.org/toc/1648-9144Philadelphia-negative myeloproliferative neoplasms (MPN) are aggressive diseases characterized by clonal proliferation of myeloid stem cells. The clonal process leads to excessive red cells production, platelets production, and bone marrow fibrosis. According to the phenotype, MPN can be classified as polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF). MPN patients have shortened survival due to the increased risk of thrombosis, hemorrhages, and transformation to acute myeloid leukemia (AML). Prognosis is variable, with a shorter life expectancy in myelofibrosis. Currently, drug therapy can reduce symptoms, splenomegaly, and risk of thrombosis. Still, some patients can be resistant or intolerant to the treatment. At the same time, allogeneic stem cell transplant (ASCT) is the only treatment modality with the potential to cure the disease. Nevertheless, the ASCT is reserved for high-risk leukemic progression patients due to the risk of treatment-related death and comorbidity. Therefore, there is a need for new drugs that can eradicate clonal hematopoiesis and prevent progression to more aggressive myeloid neoplasms. Thanks to the better understanding of the disease’s molecular pathogenesis, many new potentially disease-modifying drugs have been developed and are currently in clinical trials. This review explores the most promising new drugs currently in clinical trials.Domenico PennaMDPI AGarticleessential thrombocythemiamyelofibrosismyeloproliferative neoplasmsPolycythemia veratreatmentMedicine (General)R5-920ENMedicina, Vol 57, Iss 1181, p 1181 (2021)
institution DOAJ
collection DOAJ
language EN
topic essential thrombocythemia
myelofibrosis
myeloproliferative neoplasms
Polycythemia vera
treatment
Medicine (General)
R5-920
spellingShingle essential thrombocythemia
myelofibrosis
myeloproliferative neoplasms
Polycythemia vera
treatment
Medicine (General)
R5-920
Domenico Penna
New Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options
description Philadelphia-negative myeloproliferative neoplasms (MPN) are aggressive diseases characterized by clonal proliferation of myeloid stem cells. The clonal process leads to excessive red cells production, platelets production, and bone marrow fibrosis. According to the phenotype, MPN can be classified as polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF). MPN patients have shortened survival due to the increased risk of thrombosis, hemorrhages, and transformation to acute myeloid leukemia (AML). Prognosis is variable, with a shorter life expectancy in myelofibrosis. Currently, drug therapy can reduce symptoms, splenomegaly, and risk of thrombosis. Still, some patients can be resistant or intolerant to the treatment. At the same time, allogeneic stem cell transplant (ASCT) is the only treatment modality with the potential to cure the disease. Nevertheless, the ASCT is reserved for high-risk leukemic progression patients due to the risk of treatment-related death and comorbidity. Therefore, there is a need for new drugs that can eradicate clonal hematopoiesis and prevent progression to more aggressive myeloid neoplasms. Thanks to the better understanding of the disease’s molecular pathogenesis, many new potentially disease-modifying drugs have been developed and are currently in clinical trials. This review explores the most promising new drugs currently in clinical trials.
format article
author Domenico Penna
author_facet Domenico Penna
author_sort Domenico Penna
title New Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options
title_short New Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options
title_full New Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options
title_fullStr New Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options
title_full_unstemmed New Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options
title_sort new horizons in myeloproliferative neoplasms treatment: a review of current and future therapeutic options
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/61c8db4b2543475f9aad70a2daa5087c
work_keys_str_mv AT domenicopenna newhorizonsinmyeloproliferativeneoplasmstreatmentareviewofcurrentandfuturetherapeuticoptions
_version_ 1718411384346116096