European Myeloma Network guidelines for the management of multiple myeloma-related complications
Jazyk angličtina Země Itálie Médium print
Typ dokumentu časopisecké články, směrnice pro lékařskou praxi
PubMed
26432383
PubMed Central
PMC4591757
DOI
10.3324/haematol.2014.117176
PII: haematol.2014.117176
Knihovny.cz E-zdroje
- MeSH
- anemie diagnóza etiologie terapie MeSH
- infekce diagnóza etiologie terapie MeSH
- lidé MeSH
- management bolesti MeSH
- management nemoci * MeSH
- mnohočetný myelom komplikace MeSH
- nemoci kostí diagnóza etiologie terapie MeSH
- nemoci ledvin diagnóza etiologie terapie MeSH
- nemoci periferního nervového systému diagnóza etiologie terapie MeSH
- žilní tromboembolie diagnóza etiologie terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- směrnice pro lékařskou praxi MeSH
The European Myeloma Network provides recommendations for the management of the most common complications of multiple myeloma. Whole body low-dose computed tomography is more sensitive than conventional radiography in depicting osteolytic disease and thus we recommend it as the novel standard for the detection of lytic lesions in myeloma (grade 1A). Myeloma patients with adequate renal function and bone disease at diagnosis should be treated with zoledronic acid or pamidronate (grade 1A). Symptomatic patients without lytic lesions on conventional radiography can be treated with zoledronic acid (grade 1B), but its advantage is not clear for patients with no bone involvement on computed tomography or magnetic resonance imaging. In asymptomatic myeloma, bisphosphonates are not recommended (grade 1A). Zoledronic acid should be given continuously, but it is not clear if patients who achieve at least a very good partial response benefit from its continuous use (grade 1B). Treatment with erythropoietic-stimulating agents may be initiated in patients with persistent symptomatic anemia (hemoglobin <10g/dL) in whom other causes of anemia have been excluded (grade 1B). Erythropoietic agents should be stopped after 6-8 weeks if no adequate hemoglobin response is achieved. For renal impairment, bortezomib-based regimens are the current standard of care (grade 1A). For the management of treatment-induced peripheral neuropathy, drug modification is needed (grade 1C). Vaccination against influenza is recommended; vaccination against streptococcus pneumonia and hemophilus influenza is appropriate, but efficacy is not guaranteed due to suboptimal immune response (grade 1C). Prophylactic aciclovir (or valacyclovir) is recommended for patients receiving proteasome inhibitors, autologous or allogeneic transplantation (grade 1A).
Department of Hematology Aalborg University Hospital Denmark
Department of Hematology and Oncology University of Freiburg Medical Center Germany
Department of Hematology Ankara University Turkey
Department of Hematology Azienda Ospedaliera dell'Annunziata Cosenza Italy
Department of Hematology Erasmus University Medical Center Rotterdam the Netherlands
Department of Hematology Memorial Sisli Hospital Istanbul Turkey
Department of Hematology University Medical Center Utrecht the Netherlands
Department of Hematology VU University Medical Center Amsterdam the Netherlands
Department of Internal Medicine 2 University Hospital Würburg Würzburg Germany
Division of Hematology S Giovanni Battista Hospital University of Turin Italy
Seràgnoli Institute of Hematology and Medical Oncology University of Bologna Italy
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