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The landscape of new drugs in lymphoma

Identifieur interne : 001568 ( Main/Exploration ); précédent : 001567; suivant : 001569

The landscape of new drugs in lymphoma

Auteurs : Anas Younes [États-Unis] ; Stephen Ansell [États-Unis] ; Nathan Fowler [États-Unis] ; Wyndham Wilson [États-Unis] ; Sven De Vos [États-Unis] ; John Seymour [Australie] ; Ranjana Advani [États-Unis] ; Andres Forero [États-Unis] ; Franck Morschhauser [France] ; Marie Jose Kersten [Pays-Bas] ; Kensei Tobinai [Japon] ; Pier Luigi Zinzani [Italie] ; Emanuele Zucca [Suisse] ; Jeremy Abramson [États-Unis] ; Julie Vose [États-Unis]

Source :

RBID : PMC:5611863

Descripteurs français

English descriptors

Abstract

The landscape of drugs for the treatment of lymphoma has become crowded in light of the plethora of new agents, necessitating the efficient prioritization of drugs for expedited development. The number of drugs available, and the fact that many can be given for an extended period of time, has resulted in the emergence of new challenges; these include determining the optimal duration of therapy, and the need to balance costs, benefits, and the risk of late-onset toxicities. Moreover, with the increase in the number of available investigational drugs, the number of possible combinations is becoming overwhelming, which necessitates prioritization plans for the selective development of novel combination regimens. In this Review, we describe the mospromising agents in clinical development for the treatment of lymphoma, and provide expert opinion on new strategies that might enable more streamlined drug development. We also address new approaches for patient selection and for incorporating new end points into clinical trials.


Url:
DOI: 10.1038/nrclinonc.2016.205
PubMed: 28031560
PubMed Central: 5611863


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Drug Discovery (trends)</term>
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<term>Lymphoma</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Drug Discovery</term>
<term>Immunotherapy</term>
<term>Molecular Targeted Therapy</term>
</keywords>
<keywords scheme="MESH" qualifier="tendances" xml:lang="fr">
<term>Découverte de médicament</term>
<term>Thérapie moléculaire ciblée</term>
</keywords>
<keywords scheme="MESH" qualifier="therapeutic use" xml:lang="en">
<term>Antineoplastic Combined Chemotherapy Protocols</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Lymphomes</term>
</keywords>
<keywords scheme="MESH" qualifier="trends" xml:lang="en">
<term>Drug Discovery</term>
<term>Molecular Targeted Therapy</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr">
<term>Antinéoplasiques</term>
<term>Facteurs immunologiques</term>
<term>Protocoles de polychimiothérapie antinéoplasique</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Humans</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Découverte de médicament</term>
<term>Humains</term>
<term>Immunothérapie</term>
<term>Thérapie moléculaire ciblée</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p id="P1">The landscape of drugs for the treatment of lymphoma has become crowded in light of the plethora of new agents, necessitating the efficient prioritization of drugs for expedited development. The number of drugs available, and the fact that many can be given for an extended period of time, has resulted in the emergence of new challenges; these include determining the optimal duration of therapy, and the need to balance costs, benefits, and the risk of late-onset toxicities. Moreover, with the increase in the number of available investigational drugs, the number of possible combinations is becoming overwhelming, which necessitates prioritization plans for the selective development of novel combination regimens. In this Review, we describe the mospromising agents in clinical development for the treatment of lymphoma, and provide expert opinion on new strategies that might enable more streamlined drug development. We also address new approaches for patient selection and for incorporating new end points into clinical trials.</p>
</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Australie</li>
<li>France</li>
<li>Italie</li>
<li>Japon</li>
<li>Pays-Bas</li>
<li>Suisse</li>
<li>États-Unis</li>
</country>
<region>
<li>Hollande-Septentrionale</li>
<li>Maryland</li>
</region>
<settlement>
<li>Amsterdam</li>
</settlement>
</list>
<tree>
<country name="États-Unis">
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<name sortKey="Younes, Anas" sort="Younes, Anas" uniqKey="Younes A" first="Anas" last="Younes">Anas Younes</name>
</noRegion>
<name sortKey="Abramson, Jeremy" sort="Abramson, Jeremy" uniqKey="Abramson J" first="Jeremy" last="Abramson">Jeremy Abramson</name>
<name sortKey="Advani, Ranjana" sort="Advani, Ranjana" uniqKey="Advani R" first="Ranjana" last="Advani">Ranjana Advani</name>
<name sortKey="Ansell, Stephen" sort="Ansell, Stephen" uniqKey="Ansell S" first="Stephen" last="Ansell">Stephen Ansell</name>
<name sortKey="De Vos, Sven" sort="De Vos, Sven" uniqKey="De Vos S" first="Sven" last="De Vos">Sven De Vos</name>
<name sortKey="Forero, Andres" sort="Forero, Andres" uniqKey="Forero A" first="Andres" last="Forero">Andres Forero</name>
<name sortKey="Fowler, Nathan" sort="Fowler, Nathan" uniqKey="Fowler N" first="Nathan" last="Fowler">Nathan Fowler</name>
<name sortKey="Vose, Julie" sort="Vose, Julie" uniqKey="Vose J" first="Julie" last="Vose">Julie Vose</name>
<name sortKey="Wilson, Wyndham" sort="Wilson, Wyndham" uniqKey="Wilson W" first="Wyndham" last="Wilson">Wyndham Wilson</name>
</country>
<country name="Australie">
<noRegion>
<name sortKey="Seymour, John" sort="Seymour, John" uniqKey="Seymour J" first="John" last="Seymour">John Seymour</name>
</noRegion>
</country>
<country name="France">
<noRegion>
<name sortKey="Morschhauser, Franck" sort="Morschhauser, Franck" uniqKey="Morschhauser F" first="Franck" last="Morschhauser">Franck Morschhauser</name>
</noRegion>
</country>
<country name="Pays-Bas">
<region name="Hollande-Septentrionale">
<name sortKey="Kersten, Marie Jose" sort="Kersten, Marie Jose" uniqKey="Kersten M" first="Marie Jose" last="Kersten">Marie Jose Kersten</name>
</region>
</country>
<country name="Japon">
<noRegion>
<name sortKey="Tobinai, Kensei" sort="Tobinai, Kensei" uniqKey="Tobinai K" first="Kensei" last="Tobinai">Kensei Tobinai</name>
</noRegion>
</country>
<country name="Italie">
<noRegion>
<name sortKey="Zinzani, Pier Luigi" sort="Zinzani, Pier Luigi" uniqKey="Zinzani P" first="Pier Luigi" last="Zinzani">Pier Luigi Zinzani</name>
</noRegion>
</country>
<country name="Suisse">
<noRegion>
<name sortKey="Zucca, Emanuele" sort="Zucca, Emanuele" uniqKey="Zucca E" first="Emanuele" last="Zucca">Emanuele Zucca</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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