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International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma.

Identifieur interne : 001C50 ( Main/Exploration ); précédent : 001C49; suivant : 001C51

International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma.

Auteurs : Shaji Kumar [États-Unis] ; Bruno Paiva [Espagne] ; Kenneth C. Anderson [États-Unis] ; Brian Durie [États-Unis] ; Ola Landgren [États-Unis] ; Philippe Moreau [France] ; Nikhil Munshi [États-Unis] ; Sagar Lonial [États-Unis] ; Joan Bladé [Espagne] ; Maria-Victoria Mateos [Espagne] ; Meletios Dimopoulos [Grèce] ; Efstathios Kastritis [Grèce] ; Mario Boccadoro [États-Unis] ; Robert Orlowski [États-Unis] ; Hartmut Goldschmidt [Allemagne] ; Andrew Spencer [Australie] ; Jian Hou [République populaire de Chine] ; Wee Joo Chng [Singapour] ; Saad Z. Usmani [États-Unis] ; Elena Zamagni [Italie] ; Kazuyuki Shimizu [Japon] ; Sundar Jagannath [États-Unis] ; Hans E. Johnsen [Danemark] ; Evangelos Terpos [Grèce] ; Anthony Reiman [Canada] ; Robert A. Kyle [États-Unis] ; Pieter Sonneveld [Pays-Bas] ; Paul G. Richardson [États-Unis] ; Philip Mccarthy [États-Unis] ; Heinz Ludwig [Autriche] ; Wenming Chen [République populaire de Chine] ; Michele Cavo [Italie] ; Jean-Luc Harousseau [France] ; Suzanne Lentzsch [États-Unis] ; Jens Hillengass [Allemagne] ; Antonio Palumbo [Italie] ; Alberto Orfao [Espagne] ; S Vincent Rajkumar [États-Unis] ; Jesus San Miguel [Espagne] ; Herve Avet-Loiseau [France]

Source :

RBID : pubmed:27511158

Descripteurs français

English descriptors

Abstract

Treatment of multiple myeloma has substantially changed over the past decade with the introduction of several classes of new effective drugs that have greatly improved the rates and depth of response. Response criteria in multiple myeloma were developed to use serum and urine assessment of monoclonal proteins and bone marrow assessment (which is relatively insensitive). Given the high rates of complete response seen in patients with multiple myeloma with new treatment approaches, new response categories need to be defined that can identify responses that are deeper than those conventionally defined as complete response. Recent attempts have focused on the identification of residual tumour cells in the bone marrow using flow cytometry or gene sequencing. Furthermore, sensitive imaging techniques can be used to detect the presence of residual disease outside of the bone marrow. Combining these new methods, the International Myeloma Working Group has defined new response categories of minimal residual disease negativity, with or without imaging-based absence of extramedullary disease, to allow uniform reporting within and outside clinical trials. In this Review, we clarify several aspects of disease response assessment, along with endpoints for clinical trials, and highlight future directions for disease response assessments.

DOI: 10.1016/S1470-2045(16)30206-6
PubMed: 27511158


Affiliations:


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Le document en format XML

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<name sortKey="Terpos, Evangelos" sort="Terpos, Evangelos" uniqKey="Terpos E" first="Evangelos" last="Terpos">Evangelos Terpos</name>
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<name sortKey="Ludwig, Heinz" sort="Ludwig, Heinz" uniqKey="Ludwig H" first="Heinz" last="Ludwig">Heinz Ludwig</name>
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<name sortKey="Cavo, Michele" sort="Cavo, Michele" uniqKey="Cavo M" first="Michele" last="Cavo">Michele Cavo</name>
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<name sortKey="Harousseau, Jean Luc" sort="Harousseau, Jean Luc" uniqKey="Harousseau J" first="Jean-Luc" last="Harousseau">Jean-Luc Harousseau</name>
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<name sortKey="Lentzsch, Suzanne" sort="Lentzsch, Suzanne" uniqKey="Lentzsch S" first="Suzanne" last="Lentzsch">Suzanne Lentzsch</name>
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<nlm:affiliation>Columbia University, New York, NY, USA.</nlm:affiliation>
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<name sortKey="Hillengass, Jens" sort="Hillengass, Jens" uniqKey="Hillengass J" first="Jens" last="Hillengass">Jens Hillengass</name>
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<nlm:affiliation>Department of Hematology, Oncology and Rheumatology, University of Heidelberg, Heidelberg, Germany.</nlm:affiliation>
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<wicri:regionArea>Department of Hematology, Oncology and Rheumatology, University of Heidelberg, Heidelberg</wicri:regionArea>
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<region type="land" nuts="1">Bade-Wurtemberg</region>
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<name sortKey="Palumbo, Antonio" sort="Palumbo, Antonio" uniqKey="Palumbo A" first="Antonio" last="Palumbo">Antonio Palumbo</name>
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<nlm:affiliation>Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Citta della Salute e della Scienza di Torino, Torino, Italy.</nlm:affiliation>
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<name sortKey="Orfao, Alberto" sort="Orfao, Alberto" uniqKey="Orfao A" first="Alberto" last="Orfao">Alberto Orfao</name>
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<nlm:affiliation>University Hospital of Salamanca/IBSAL, Salamanca, Spain.</nlm:affiliation>
<country xml:lang="fr">Espagne</country>
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<name sortKey="Rajkumar, S Vincent" sort="Rajkumar, S Vincent" uniqKey="Rajkumar S" first="S Vincent" last="Rajkumar">S Vincent Rajkumar</name>
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<title xml:lang="en">International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma.</title>
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<nlm:affiliation>Clinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Pamplona, Spain.</nlm:affiliation>
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</author>
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<nlm:affiliation>University Hospital of Salamanca/IBSAL, Salamanca, Spain.</nlm:affiliation>
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<nlm:affiliation>Department of Clinical Therapeutics, University of Athens, School of Medicine, Athens, Greece.</nlm:affiliation>
<country xml:lang="fr">Grèce</country>
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<nlm:affiliation>Department of Clinical Therapeutics, University of Athens, School of Medicine, Athens, Greece.</nlm:affiliation>
<country xml:lang="fr">Grèce</country>
<wicri:regionArea>Department of Clinical Therapeutics, University of Athens, School of Medicine, Athens</wicri:regionArea>
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<settlement type="city">Athènes</settlement>
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<country xml:lang="fr">Allemagne</country>
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<country xml:lang="fr">République populaire de Chine</country>
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<country xml:lang="fr">Danemark</country>
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<nlm:affiliation>Department of Clinical Therapeutics, University of Athens, School of Medicine, Athens, Greece.</nlm:affiliation>
<country xml:lang="fr">Grèce</country>
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<country xml:lang="fr">États-Unis</country>
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<nlm:affiliation>Erasmus Medical Center, Rotterdam, Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
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<nlm:affiliation>Dana-Farber Cancer Institute, Boston, MA, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Dana-Farber Cancer Institute, Boston, MA</wicri:regionArea>
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<region type="state">Massachusetts</region>
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<name sortKey="Mccarthy, Philip" sort="Mccarthy, Philip" uniqKey="Mccarthy P" first="Philip" last="Mccarthy">Philip Mccarthy</name>
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<nlm:affiliation>Roswell Park Cancer Institute, Buffalo, NY, USA.</nlm:affiliation>
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<region type="state">État de New York</region>
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<name sortKey="Ludwig, Heinz" sort="Ludwig, Heinz" uniqKey="Ludwig H" first="Heinz" last="Ludwig">Heinz Ludwig</name>
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<name sortKey="Chen, Wenming" sort="Chen, Wenming" uniqKey="Chen W" first="Wenming" last="Chen">Wenming Chen</name>
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<country xml:lang="fr">République populaire de Chine</country>
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<region type="land" nuts="1">Bade-Wurtemberg</region>
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<country xml:lang="fr">Espagne</country>
<wicri:regionArea>University Hospital of Salamanca/IBSAL, Salamanca</wicri:regionArea>
<wicri:noRegion>Salamanca</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Rajkumar, S Vincent" sort="Rajkumar, S Vincent" uniqKey="Rajkumar S" first="S Vincent" last="Rajkumar">S Vincent Rajkumar</name>
<affiliation wicri:level="2">
<nlm:affiliation>Division of Hematology, Mayo Clinic, Rochester, MN, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Division of Hematology, Mayo Clinic, Rochester, MN</wicri:regionArea>
<placeName>
<region type="state">Minnesota</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Miguel, Jesus San" sort="Miguel, Jesus San" uniqKey="Miguel J" first="Jesus San" last="Miguel">Jesus San Miguel</name>
<affiliation wicri:level="1">
<nlm:affiliation>Clinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Pamplona, Spain.</nlm:affiliation>
<country xml:lang="fr">Espagne</country>
<wicri:regionArea>Clinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Pamplona</wicri:regionArea>
<wicri:noRegion>Pamplona</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Avet Loiseau, Herve" sort="Avet Loiseau, Herve" uniqKey="Avet Loiseau H" first="Herve" last="Avet-Loiseau">Herve Avet-Loiseau</name>
<affiliation wicri:level="3">
<nlm:affiliation>University of Toulouse, Toulouse, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>University of Toulouse, Toulouse</wicri:regionArea>
<placeName>
<region type="region">Occitanie (région administrative)</region>
<region type="old region">Midi-Pyrénées</region>
<settlement type="city">Toulouse</settlement>
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</analytic>
<series>
<title level="j">The Lancet. Oncology</title>
<idno type="eISSN">1474-5488</idno>
<imprint>
<date when="2016" type="published">2016</date>
</imprint>
</series>
</biblStruct>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Antineoplastic Combined Chemotherapy Protocols (adverse effects)</term>
<term>Consensus</term>
<term>Humans</term>
<term>Multiple Myeloma (drug therapy)</term>
<term>Neoplasm, Residual (chemically induced)</term>
<term>Neoplasm, Residual (diagnosis)</term>
<term>Practice Guidelines as Topic (standards)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Consensus</term>
<term>Guides de bonnes pratiques cliniques comme sujet (normes)</term>
<term>Humains</term>
<term>Maladie résiduelle ()</term>
<term>Maladie résiduelle (diagnostic)</term>
<term>Myélome multiple (traitement médicamenteux)</term>
<term>Protocoles de polychimiothérapie antinéoplasique (effets indésirables)</term>
</keywords>
<keywords scheme="MESH" qualifier="adverse effects" xml:lang="en">
<term>Antineoplastic Combined Chemotherapy Protocols</term>
</keywords>
<keywords scheme="MESH" qualifier="chemically induced" xml:lang="en">
<term>Neoplasm, Residual</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Neoplasm, Residual</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr">
<term>Maladie résiduelle</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Multiple Myeloma</term>
</keywords>
<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr">
<term>Protocoles de polychimiothérapie antinéoplasique</term>
</keywords>
<keywords scheme="MESH" qualifier="normes" xml:lang="fr">
<term>Guides de bonnes pratiques cliniques comme sujet</term>
</keywords>
<keywords scheme="MESH" qualifier="standards" xml:lang="en">
<term>Practice Guidelines as Topic</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Myélome multiple</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Consensus</term>
<term>Humans</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Consensus</term>
<term>Humains</term>
<term>Maladie résiduelle</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Treatment of multiple myeloma has substantially changed over the past decade with the introduction of several classes of new effective drugs that have greatly improved the rates and depth of response. Response criteria in multiple myeloma were developed to use serum and urine assessment of monoclonal proteins and bone marrow assessment (which is relatively insensitive). Given the high rates of complete response seen in patients with multiple myeloma with new treatment approaches, new response categories need to be defined that can identify responses that are deeper than those conventionally defined as complete response. Recent attempts have focused on the identification of residual tumour cells in the bone marrow using flow cytometry or gene sequencing. Furthermore, sensitive imaging techniques can be used to detect the presence of residual disease outside of the bone marrow. Combining these new methods, the International Myeloma Working Group has defined new response categories of minimal residual disease negativity, with or without imaging-based absence of extramedullary disease, to allow uniform reporting within and outside clinical trials. In this Review, we clarify several aspects of disease response assessment, along with endpoints for clinical trials, and highlight future directions for disease response assessments.</div>
</front>
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<li>France</li>
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<li>États-Unis</li>
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<li>Californie</li>
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<li>Massachusetts</li>
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<li>Minnesota</li>
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<li>Pays de la Loire</li>
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<li>Texas</li>
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<li>Université Columbia</li>
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