Zusammenfassung
Die systemische Behandlung des metastasierten Nierenzellkarzinoms hat in den letzten
Jahren eine rasante Wandlung erfahren. Hierzu haben Erkenntnisse über histologische
Subtypen und damit assoziierte genetische Aberrationen entscheidend beigetragen. Außerdem
sind verschiedene Signalwege identifiziert worden, die für eine Tumorprogression bzw.
therapeutische Beeinflussbarkeit bedeutsam sind. Bis vor wenigen Jahren stand lediglich
eine Immuntherapie unter Verwendung von Zytokinen zur Verfügung. In der vorliegenden
Übersichtsarbeit werden neue Medikamente zur Therapie des metastasierten Nierenzellkarzinoms
dargestellt. Diese beeinflussen insbesondere die VEGF-, EGFR- und mTOR-Signalwege.
Vier Substanzen sind in Phase-III-Studien geprüft worden und für die Therapie des
metastasierten Nierenzellkarzinoms zugelassen bzw. werden in Kürze zugelassen. Ferner
gibt es eine Vielzahl von Substanzen, die Phase-I und –II-Studien getestet wurden
oder werden. Derzeit existieren verschiedene Szenarien, welche die Therapieentscheidung
beeinflussen. Hierzu gehören verschiedene Prognosegruppen, der Einsatz in der Erstlinien-
bzw. Zeitlinientherapie, der Einsatz verschiedener Kombinationen sowie der Einfluss
der histologischen Subtypen.
Abstract
Systemic therapy of metastatic kidney cancer has undergone dramatic changes over the
past years. One reason for this is our increasing knowledge of different histological
subtypes and associated genetic aberrations. Furthermore, signalling pathways have
been identified to be relevant for tumour progression and therapeutic intervention.
Until some years ago, systemic therapy for kidney cancer consisted of cytokines. In
this review, new drugs for the treatment of metastatic kidney cancer are discussed.
These drugs predominantly interact the VEGF, EGFR and mTOR signalling pathways. Four
drugs have been studied in phase III trials and were (or will soon be) approved for
treatment of metastatic kidney cancer. Additionally, many drugs are currently being
tested in phase I and phase II trials. At present, the following scenarios have an
impact on therapy decisions: different prognostic groups, first-line and second-line
therapy, combination therapies and the impact of different histological subtypes.
Schlüsselwörter
Nierenzellkarzinom - Immuntherapie - Zytokine - Antikörper - Tyrosinkinase - small
molecules - VEGF - EGFR - mTOR
Key words
kidney cancer - immunotherapy - cytokines - antibodies - tyrosine kinase - small molecules
- VEGF - EGFR - mTOR
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Priv.-Doz. Dr. med. Christian Doehn
Ltd. Oberarzt der Klinik und Poliklinik für Urologie, Universitätsklinikum Schleswig-Holstein
(UK S-H), Campus Lübeck
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