Recommendations for the diagnosis and initial evaluation of patients with Waldenström Macroglobulinaemia: A Task Force from the 8th International Workshop on Waldenström Macroglobulinaemia.
Identifieur interne : 001729 ( PubMed/Curation ); précédent : 001728; suivant : 001730Recommendations for the diagnosis and initial evaluation of patients with Waldenström Macroglobulinaemia: A Task Force from the 8th International Workshop on Waldenström Macroglobulinaemia.
Auteurs : Jorge J. Castillo [États-Unis] ; Ramon Garcia-Sanz [Espagne] ; Evdoxia Hatjiharissi [Grèce] ; Robert A. Kyle [États-Unis] ; Xavier Leleu [France] ; Mary Mcmaster [États-Unis] ; Giampaolo Merlini [Italie] ; Monique C. Minnema [Pays-Bas] ; Enrica Morra [Italie] ; Roger G. Owen [Royaume-Uni] ; Stephanie Poulain [France] ; Marvin J. Stone [États-Unis] ; Constantine Tam [Australie] ; Marzia Varettoni [Italie] ; Meletios A. Dimopoulos [Grèce] ; Steven P. Treon [États-Unis] ; Efstathios Kastritis [Grèce]Source :
- British journal of haematology [ 1365-2141 ] ; 2016.
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- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
Abstract
The diagnosis of Waldenström macroglobulinaemia (WM) can be challenging given the variety of signs and symptoms patients can present. Furthermore, once the diagnosis of WM is established, the initial evaluation should be thorough as well as appropriately directed. During the 8th International Workshop for WM in London, United Kingdom, a multi-institutional task force was formed to develop consensus recommendations for the diagnosis and initial evaluation of patients with WM. In this document, we present the results of the deliberations that took place to address these issues. We provide recommendations for history-taking and physical examination, laboratory studies, bone marrow aspiration and biopsy analysis and imaging studies. We also provide guidance on the initial evaluation of special situations, such as anaemia, hyperviscosity, neuropathy, Bing-Neel syndrome and amyloidosis. We hope these recommendations serve as a practical guidance to clinicians taking care of patients with a suspected or an established diagnosis of WM.
DOI: 10.1111/bjh.14196
PubMed: 27378193
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<front><div type="abstract" xml:lang="en">The diagnosis of Waldenström macroglobulinaemia (WM) can be challenging given the variety of signs and symptoms patients can present. Furthermore, once the diagnosis of WM is established, the initial evaluation should be thorough as well as appropriately directed. During the 8th International Workshop for WM in London, United Kingdom, a multi-institutional task force was formed to develop consensus recommendations for the diagnosis and initial evaluation of patients with WM. In this document, we present the results of the deliberations that took place to address these issues. We provide recommendations for history-taking and physical examination, laboratory studies, bone marrow aspiration and biopsy analysis and imaging studies. We also provide guidance on the initial evaluation of special situations, such as anaemia, hyperviscosity, neuropathy, Bing-Neel syndrome and amyloidosis. We hope these recommendations serve as a practical guidance to clinicians taking care of patients with a suspected or an established diagnosis of WM.</div>
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<Abstract><AbstractText>The diagnosis of Waldenström macroglobulinaemia (WM) can be challenging given the variety of signs and symptoms patients can present. Furthermore, once the diagnosis of WM is established, the initial evaluation should be thorough as well as appropriately directed. During the 8th International Workshop for WM in London, United Kingdom, a multi-institutional task force was formed to develop consensus recommendations for the diagnosis and initial evaluation of patients with WM. In this document, we present the results of the deliberations that took place to address these issues. We provide recommendations for history-taking and physical examination, laboratory studies, bone marrow aspiration and biopsy analysis and imaging studies. We also provide guidance on the initial evaluation of special situations, such as anaemia, hyperviscosity, neuropathy, Bing-Neel syndrome and amyloidosis. We hope these recommendations serve as a practical guidance to clinicians taking care of patients with a suspected or an established diagnosis of WM.</AbstractText>
<CopyrightInformation>© 2016 John Wiley & Sons Ltd.</CopyrightInformation>
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<Initials>JJ</Initials>
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<AffiliationInfo><Affiliation>Bing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA. jorgej_castillo@dfci.harvard.edu.</Affiliation>
</AffiliationInfo>
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<ForeName>Ramon</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Hospital Universitario de Salamanca, Salamanca, Spain.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hatjiharissi</LastName>
<ForeName>Evdoxia</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Department of Haematology, Theageneion Hospital of Thessaloniki, Thessaloniki, Greece.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Kyle</LastName>
<ForeName>Robert A</ForeName>
<Initials>RA</Initials>
<AffiliationInfo><Affiliation>Division of Hematology, Mayo Clinic, Rochester, MN, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Leleu</LastName>
<ForeName>Xavier</ForeName>
<Initials>X</Initials>
<AffiliationInfo><Affiliation>La Miletrie Hospital, CHU Poitiers, Poitiers, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>McMaster</LastName>
<ForeName>Mary</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Merlini</LastName>
<ForeName>Giampaolo</ForeName>
<Initials>G</Initials>
<AffiliationInfo><Affiliation>Amyloidosis Research and Treatment Centre, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Minnema</LastName>
<ForeName>Monique C</ForeName>
<Initials>MC</Initials>
<AffiliationInfo><Affiliation>Department of Haematology, UMC Utrecht Cancer Centre, Utrecht, the Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Morra</LastName>
<ForeName>Enrica</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Division of Haematology, Niguarda Ca' Granda Hospital, Milano, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Owen</LastName>
<ForeName>Roger G</ForeName>
<Initials>RG</Initials>
<AffiliationInfo><Affiliation>St James's Institute of Oncology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Poulain</LastName>
<ForeName>Stephanie</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Service d'Hématologie-Immunologie-Cytogénétique, Centre Hospitalier de Valenciennes, Valenciennes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Stone</LastName>
<ForeName>Marvin J</ForeName>
<Initials>MJ</Initials>
<AffiliationInfo><Affiliation>Department of Oncology, Baylor Charles A Sammons Cancer Center, Dallas, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Tam</LastName>
<ForeName>Constantine</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Department of Haematology, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Varettoni</LastName>
<ForeName>Marzia</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Haematology Oncology, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Dimopoulos</LastName>
<ForeName>Meletios A</ForeName>
<Initials>MA</Initials>
<AffiliationInfo><Affiliation>Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Treon</LastName>
<ForeName>Steven P</ForeName>
<Initials>SP</Initials>
<AffiliationInfo><Affiliation>Bing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Kastritis</LastName>
<ForeName>Efstathios</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
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<Agency>Intramural NIH HHS</Agency>
<Country>United States</Country>
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<Month>07</Month>
<Day>05</Day>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D026683" MajorTopicYN="N">Advisory Committees</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008131" MajorTopicYN="N">London</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017410" MajorTopicYN="N">Practice Guidelines as Topic</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008258" MajorTopicYN="N">Waldenstrom Macroglobulinemia</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Bing-Neel syndrome</Keyword>
<Keyword MajorTopicYN="N">Waldenström macroglobulinaemia</Keyword>
<Keyword MajorTopicYN="N">amyloidosis</Keyword>
<Keyword MajorTopicYN="N">anaemia</Keyword>
<Keyword MajorTopicYN="N">hyperviscosity</Keyword>
<Keyword MajorTopicYN="N">neuropathy</Keyword>
</KeywordList>
<CoiStatement>JJC received honoraria from Celgene and Pharmacyclics, and research funding from Abbvie, Gilead, Millennium and Pharmacyclics. RGS received honoraria from Bristol-Myers Squibb, Janssen and Takeda and. EH received honoraria from Amgen, Gilead and Janssen. GM received honoraria from GlaxoSmithKline, Janssen and Millennium-Takeda. RGO received honoraria from Celgene, Janssen, Pharmacyclics and Roche, and research funding from Celgene. CT received honoraria and research funding from Janssen and Roche. MAD received honoraria from Amgen, Celgene, Janssen and Novartis. SPT received research funding and/or honoraria from Gilead, Janssen, Onyx and Pharmacyclics. EK received honoraria from Amgen, Janssen and Takeda and. RAK, XL, MM, MCM, EM, SP, MJS, MV have no conflict of interest to disclose.</CoiStatement>
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<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year>
<Month>03</Month>
<Day>17</Day>
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<PubMedPubDate PubStatus="accepted"><Year>2016</Year>
<Month>05</Month>
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