Skip to main content
Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging 8/2007

01.08.2007 | Guidelines

EANM procedure guideline for 32P phosphate treatment of myeloproliferative diseases

verfasst von: Jan Tennvall, Boudewijn Brans

Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging | Ausgabe 8/2007

Einloggen, um Zugang zu erhalten

Abstract

Introduction

32P phosphate was the first therapeutic radioisotope, used in leukaemia about 70 years ago. Since then, many new agents for haematological proliferations have been introduced successfully. Today there remains a distinct subgroup of elderly patients with polycythaemia vera and essential thrombocythaemia for whom 32P is the most optimal treatment option, an assertion supported by two large studies with long follow-up.

Purpose

The purpose of this guideline is to assist the nuclear medicine physician in treating and managing patients who may be candidates for 32P phosphate therapy.
Literatur
1.
Zurück zum Zitat Najean Y, Rain JD for the French Polycythemia Study Group. Treatment of polycythemia vera: use of 32P alone or in combination with maintenance therapy using hydroxyurea in 461 patients greater than 65 years of age. Blood 1997;89(7):2319–27.PubMed Najean Y, Rain JD for the French Polycythemia Study Group. Treatment of polycythemia vera: use of 32P alone or in combination with maintenance therapy using hydroxyurea in 461 patients greater than 65 years of age. Blood 1997;89(7):2319–27.PubMed
2.
Zurück zum Zitat Brandt L, Anderson H. Survival and risk of leukaemia in polycythemia vera and essential thrombocythemia treated with oral radiophosphorus. Eur J Haematol 1995;54(1):21–6.PubMedCrossRef Brandt L, Anderson H. Survival and risk of leukaemia in polycythemia vera and essential thrombocythemia treated with oral radiophosphorus. Eur J Haematol 1995;54(1):21–6.PubMedCrossRef
3.
Zurück zum Zitat Fruchtman SM. Treatment paradigms in the management of myeloproliferative disorders. Semin Hematol 2004;41 (2 suppl 3):18–22.CrossRefPubMed Fruchtman SM. Treatment paradigms in the management of myeloproliferative disorders. Semin Hematol 2004;41 (2 suppl 3):18–22.CrossRefPubMed
4.
Zurück zum Zitat Barbui T. The leukaemia controversy in myeloprolifertive disorders: is it a natural progression of disease, a secondary sequela of therapy, or a combination of both? Semin Hematol 2004;41 (2 Suppl 3):15–7.CrossRefPubMed Barbui T. The leukaemia controversy in myeloprolifertive disorders: is it a natural progression of disease, a secondary sequela of therapy, or a combination of both? Semin Hematol 2004;41 (2 Suppl 3):15–7.CrossRefPubMed
5.
Zurück zum Zitat Fruchtman SM, Petitt RM, Gilbert HS, Fiddler G, Lyne A. Anagrelide Study Group. Anagrelide: analysis of long-term efficacy, safety and leukemogenic potential in myeloproliferative disorders. Leukemia Res 2005;29:481–91.CrossRef Fruchtman SM, Petitt RM, Gilbert HS, Fiddler G, Lyne A. Anagrelide Study Group. Anagrelide: analysis of long-term efficacy, safety and leukemogenic potential in myeloproliferative disorders. Leukemia Res 2005;29:481–91.CrossRef
Metadaten
Titel
EANM procedure guideline for 32P phosphate treatment of myeloproliferative diseases
verfasst von
Jan Tennvall
Boudewijn Brans
Publikationsdatum
01.08.2007
Verlag
Springer-Verlag
Erschienen in
European Journal of Nuclear Medicine and Molecular Imaging / Ausgabe 8/2007
Print ISSN: 1619-7070
Elektronische ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-007-0407-4

Weitere Artikel der Ausgabe 8/2007

European Journal of Nuclear Medicine and Molecular Imaging 8/2007 Zur Ausgabe