Myeloproliferative Neoplasms (eBook)

Critical Concepts and Management
eBook Download: PDF
2012 | 2012
VIII, 240 Seiten
Springer Berlin (Verlag)
978-3-642-24989-1 (ISBN)

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This book focuses on three of the main categories of myeloproliferative neoplasm: polycythemia vera, essential thrombocythemia, and primary myelofibrosis. Relevant laboratory and clinical advances are comprehensively covered, and great emphasis is placed on the practical issues that challenge physicians in their daily practice. The main topics considered thus include contemporary diagnostic  approaches, the value and limitations of mutation screening for diagnostic and  prognostic purposes, risk stratification in terms of both survival and other  disease complications such as leukemic transformation and thrombosis, and  modern therapeutic strategies, including conventional drugs, allogeneic stem cell  transplantation, and experimental drugs still under study. The reader will find Critical Concepts and Management Recommendations in Myeloproliferative Neoplasms to be an invaluable and up-to-date source of information from leading authorities in the field.



The discovery of the JAK2 V617F mutation in the majority of patients with bcr/abl-negative myeloproliferative neoplasms has stimulated a number of questions regarding the diagnosis, prognosis, and treatment of polycythemia vera, essential thrombocythemia, and primary myelofibrosis. This book provides evidence-based reviews and expert consensus results concerning the key clinical issues for patient management. Practical recommendations are provided for the optimization and standardization of management of all three types of myeloproliferative neoplasm. Risk stratification, treatment goals, and first- and second-line therapies are discussed in detail, and other relevant diagnostic and research issues are also addressed. The reader will find Critical Concepts and Management Recommendations in Myeloproliferative Neoplasms to be an invaluable and up-to-date source of information from leading authorities in the field.

The discovery of the JAK2 V617F mutation in the majority of patients with bcr/abl-negative myeloproliferative neoplasms has stimulated a number of questions regarding the diagnosis, prognosis, and treatment of polycythemia vera, essential thrombocythemia, and primary myelofibrosis. This book provides evidence-based reviews and expert consensus results concerning the key clinical issues for patient management. Practical recommendations are provided for the optimization and standardization of management of all three types of myeloproliferative neoplasm. Risk stratification, treatment goals, and first- and second-line therapies are discussed in detail, and other relevant diagnostic and research issues are also addressed. The reader will find Critical Concepts and Management Recommendations in Myeloproliferative Neoplasms to be an invaluable and up-to-date source of information from leading authorities in the field.

Biology: UpdateDo we need biology studies for patient management?Gerneral Issues in the Management of MPNs:Critical Issues about the Diagnosis of MPNsPatient's Information and Examinations Needed before Planning Therapy Specific Issues of Treatment in PV and ET:Risk classificationGoal of TherapyFirst-line Therapy and Monitoring the Response in the Individual PatientPrimary and Secondary Antithrombotic ProphylaxisWhen to change Therapy: Second Line OptionsThe Evolution in Myelofibrosis and LeukemiaTreatment of PMF:Current Clinical NeedsRisk StratificationGoal of Therapy: Palliation and CurativeResearch Issues and Perspectives:New drugsOngoing Clinical TrialsHow to Design Clinical Studies in Rare Diseases

Erscheint lt. Verlag 10.1.2012
Reihe/Serie Hematologic Malignancies
Hematologic Malignancies
Zusatzinfo VIII, 240 p. 22 illus., 13 illus. in color.
Verlagsort Berlin
Sprache englisch
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Innere Medizin
Medizin / Pharmazie Medizinische Fachgebiete Onkologie
Schlagworte Myeloproliferative • Neoplasms • polycythemia vera • Primary Myelofibrosis • Thrombocythemia
ISBN-10 3-642-24989-2 / 3642249892
ISBN-13 978-3-642-24989-1 / 9783642249891
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