Diagnosis, treatment, and response assessment in solitary plasmacytoma: updated recommendations from a European Expert Panel

Jo Caers(Centre Hospitalier Universitaire de Liège), Bruno Paiva(Navarre Institute of Health Research), Elena Zamagni, Xavier Leleu(Centre Hospitalier Universitaire de Poitiers), Joan Bladé(Hospital Clínic de Barcelona), Sigurður Y. Kristinsson(National University Hospital of Iceland), Cyrille Touzeau, Niels Abildgaard(Odense University Hospital), Evangelos Terpos(National and Kapodistrian University of Athens), Roy Heusschen(Centre Hospitalier Universitaire de Liège), Enrique M. Ocio(Instituto de Investigación Biomédica de Salamanca), Michel Delforge(KU Leuven), Orhan Sezer(Eppendorf (Germany)), Meral Beksaç(Ankara University), Heinz Ludwig(Wilhelminen Hospital), Giampaolo Merlini(University of Pavia), Philippe Moreau, Sonja Zweegman(Amsterdam UMC Location Vrije Universiteit Amsterdam), Monika Engelhardt(University of Freiburg), Laura Rosiñol(Hospital Clínic de Barcelona)
Journal of Hematology & Oncology
January 16, 2018
Cited by 319Open Access
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Abstract

Solitary plasmacytoma is an infrequent form of plasma cell dyscrasia that presents as a single mass of monoclonal plasma cells, located either extramedullary or intraosseous. In some patients, a bone marrow aspiration can detect a low monoclonal plasma cell infiltration which indicates a high risk of early progression to an overt myeloma disease. Before treatment initiation, whole body positron emission tomography-computed tomography or magnetic resonance imaging should be performed to exclude the presence of additional malignant lesions. For decades, treatment has been based on high-dose radiation, but studies exploring the potential benefit of systemic therapies for high-risk patients are urgently needed. In this review, a panel of expert European hematologists updates the recommendations on the diagnosis and management of patients with solitary plasmacytoma.


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