Expert review on soft-tissue plasmacytomas in multiple myeloma: definition, disease assessment and treatment considerations

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3102101 36 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Expert review on soft-tissue plasmacytomas in multiple myeloma: definition, disease assessment and treatment considerations
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
In this review, two types of soft-tissue involvement in multiple myeloma are defined: (i) extramedullary (EMD) with haematogenous spread involving only soft tissues and (ii) paraskeletal (PS) with tumour masses arising from skeletal lesions. The incidence of EMD and PS plasmacytomas at diagnosis ranges from 1·7% to 4·5% and 7% to 34·4% respectively. EMD disease is often associated with high-risk cytogenetics, resistance to therapy and worse prognosis than in PS involvement. In patients with PS involvement a proteasome inhibitor-based regimen may be the best option followed by autologous stem cell transplantation (ASCT) in transplant eligible patients. In patients with EMD disease who are not eligible for ASCT, a proteasome inhibitor-based regimen such as lenalidomide-bortezomib-dexamethasone (RVD) may be the best option, while for those eligible for high-dose therapy a myeloma/lymphoma-like regimen such as bortezomib, thalidomide and dexamethasone (VTD)-RVD/cisplatin, doxorubicin, cyclophosphamide and etoposide (PACE) followed by SCT should be considered. In both EMD and PS disease at relapse many strategies have been tried, but this remains a high-unmet need population. © 2021 British Society for Haematology and John Wiley & Sons Ltd
Έτος δημοσίευσης:
2021
Συγγραφείς:
Rosiñol, L.
Beksac, M.
Zamagni, E.
Van de Donk, N.W.C.J.
Anderson, K.C.
Badros, A.
Caers, J.
Cavo, M.
Dimopoulos, M.-A.
Dispenzieri, A.
Einsele, H.
Engelhardt, M.
Fernández de Larrea, C.
Gahrton, G.
Gay, F.
Hájek, R.
Hungria, V.
Jurczyszyn, A.
Kröger, N.
Kyle, R.A.
Leal da Costa, F.
Leleu, X.
Lentzsch, S.
Mateos, M.V.
Merlini, G.
Mohty, M.
Moreau, P.
Rasche, L.
Reece, D.
Sezer, O.
Sonneveld, P.
Usmani, S.Z.
Vanderkerken, K.
Vesole, D.H.
Waage, A.
Zweegman, S.
Richardson, P.G.
Bladé, J.
Περιοδικό:
British Journal of Haematology
Εκδότης:
John Wiley and Sons Inc
Τόμος:
194
Αριθμός / τεύχος:
3
Σελίδες:
496-507
Λέξεις-κλειδιά:
bortezomib; carfilzomib; carmustine; cisplatin; cyclophosphamide; cytarabine; daratumumab; dexamethasone; doxorubicin; etoposide; fluorodeoxyglucose; ixazomib; lenalidomide; melphalan; methotrexate; paraprotein; pomalidomide; prednisone; thalidomide; antineoplastic agent, abdominal mass; autologous stem cell transplantation; bone graft; bone marrow; cancer incidence; cerebrospinal fluid; cytogenetics; disease assessment; fluorescence in situ hybridization; gene overexpression; human; immunohistochemistry; incidence; lymphoma; multiple myeloma; nuclear magnetic resonance imaging; overall survival; plasmacytoma; positron emission tomography; Review; sensitivity and specificity; severe combined immunodeficiency; soft tissue cancer; stem cell transplantation; whole body imaging; animal; autotransplantation; complication; disease management; hematopoietic stem cell transplantation; multiple myeloma; pathology; plasmacytoma; prognosis, Animals; Antineoplastic Combined Chemotherapy Protocols; Bortezomib; Cisplatin; Cyclophosphamide; Dexamethasone; Disease Management; Doxorubicin; Etoposide; Hematopoietic Stem Cell Transplantation; Humans; Lenalidomide; Multiple Myeloma; Plasmacytoma; Prognosis; Transplantation, Autologous
Επίσημο URL (Εκδότης):
DOI:
10.1111/bjh.17338
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