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dc.date.accessioned2020-06-19T18:16:57Z
dc.date.available2020-06-19T18:16:57Z
dc.date.created2019-06-23T13:56:30Z
dc.date.issued2019
dc.identifier.citationHillengass, Jens Usmani, Saad Rajkumar, S. Vincent Durie, Brian G.M. Mateos, María-Victoria Lonial, Sagar Joao, Cristina Anderson, Kenneth C. García-Sanz, Ramón Serra, Eloísa Riva Du, Juan van de Donk, Niels Berdeja, Jesús G. Terpos, Evangelos Zamagni, Elena Kyle, Robert A. San Miguel, Jesús Goldschmidt, Hartmut Giralt, Sergio Kumar, Shaji Raje, Noopur Ludwig, Heinz Ocio, Enrique Schots, Rik Einsele, Hermann Schjesvold, Fredrik Hellem Chen, Wen-Ming Abildgaard, Niels Lipe, Brea C. Dytfeld, Dominik Wirk, Baldeep Mona Drake, Matthew Cavo, Michele Lahuerta, Juan José Lentzsch, Suzanne . International myeloma working group consensus recommendations on imaging in monoclonal plasma cell disorders. The Lancet Oncology. 2019, 20(6), e302-e312
dc.identifier.urihttp://hdl.handle.net/10852/77067
dc.description.abstractRecent advances in the treatment of multiple myeloma have increased the need for accurate diagnosis of the disease. The detection of bone and bone marrow lesions is crucial in the investigation of multiple myeloma and often dictates the decision to start treatment. Furthermore, detection of minimal residual disease is important for prognosis determination and treatment planning, and it has underscored an unmet need for sensitive imaging methods that accurately assess patient response to multiple myeloma treatment. Low-dose whole-body CT has increased sensitivity compared with conventional skeletal survey in the detection of bone disease, which can reveal information leading to changes in therapy and disease management that could prevent or delay the onset of clinically significant morbidity and mortality as a result of skeletal-related events. Given the multiple options available for the detection of bone and bone marrow lesions, ranging from conventional skeletal survey to whole-body CT, PET/CT, and MRI, the International Myeloma Working Group decided to establish guidelines on optimal use of imaging methods at different disease stages. These recommendations on imaging within and outside of clinical trials will help standardise imaging for monoclonal plasma cell disorders worldwide to allow the comparison of results and the unification of treatment approaches for multiple myeloma.
dc.languageEN
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleInternational myeloma working group consensus recommendations on imaging in monoclonal plasma cell disorders
dc.typeJournal article
dc.creator.authorHillengass, Jens
dc.creator.authorUsmani, Saad
dc.creator.authorRajkumar, S. Vincent
dc.creator.authorDurie, Brian G.M.
dc.creator.authorMateos, María-Victoria
dc.creator.authorLonial, Sagar
dc.creator.authorJoao, Cristina
dc.creator.authorAnderson, Kenneth C.
dc.creator.authorGarcía-Sanz, Ramón
dc.creator.authorSerra, Eloísa Riva
dc.creator.authorDu, Juan
dc.creator.authorvan de Donk, Niels
dc.creator.authorBerdeja, Jesús G.
dc.creator.authorTerpos, Evangelos
dc.creator.authorZamagni, Elena
dc.creator.authorKyle, Robert A.
dc.creator.authorSan Miguel, Jesús
dc.creator.authorGoldschmidt, Hartmut
dc.creator.authorGiralt, Sergio
dc.creator.authorKumar, Shaji
dc.creator.authorRaje, Noopur
dc.creator.authorLudwig, Heinz
dc.creator.authorOcio, Enrique
dc.creator.authorSchots, Rik
dc.creator.authorEinsele, Hermann
dc.creator.authorSchjesvold, Fredrik Hellem
dc.creator.authorChen, Wen-Ming
dc.creator.authorAbildgaard, Niels
dc.creator.authorLipe, Brea C.
dc.creator.authorDytfeld, Dominik
dc.creator.authorWirk, Baldeep Mona
dc.creator.authorDrake, Matthew
dc.creator.authorCavo, Michele
dc.creator.authorLahuerta, Juan José
dc.creator.authorLentzsch, Suzanne
cristin.unitcode185,53,18,75
cristin.unitnameK.G. Jebsen senter for B-cellekreft - del UiO
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2
dc.identifier.cristin1707070
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=The Lancet Oncology&rft.volume=20&rft.spage=e302&rft.date=2019
dc.identifier.jtitleThe Lancet Oncology
dc.identifier.volume20
dc.identifier.issue6
dc.identifier.startpagee302
dc.identifier.endpagee312
dc.identifier.doihttps://doi.org/10.1016/S1470-2045(19)30309-2
dc.identifier.urnURN:NBN:no-80204
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1470-2045
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/77067/5/INTERN%257E1.pdf
dc.type.versionAcceptedVersion


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