Dtsch Med Wochenschr 2012; 137(20): 1057-1061
DOI: 10.1055/s-0032-1304921
Übersicht | Review article
Onkologie
© Georg Thieme Verlag KG Stuttgart · New York

Prophylaxe und Therapie beim multiplen Myelom und anderen tumorbedingten Knochenveränderungen

Von Bisphosphonaten zu zielgerichteten TherapeutikaCurrent approaches in multiple myeloma and other cancer-related bone diseases From bisphosphonates through to targeted therapy
M. Engelhardt
1   Hämatologie und Onkologie, Medizin I, Universitätsklinik Freiburg
,
M. Kleber
1   Hämatologie und Onkologie, Medizin I, Universitätsklinik Freiburg
,
J. Udi
1   Hämatologie und Onkologie, Medizin I, Universitätsklinik Freiburg
,
R. Wäsch
1   Hämatologie und Onkologie, Medizin I, Universitätsklinik Freiburg
› Author Affiliations
Further Information

Publication History

24 November 2011

17 February 2012

Publication Date:
27 April 2012 (online)

Zusammenfassung

Das multiple Myelom ist die 2. häufigste hämatologische Neoplasie und betrifft vorwiegend ältere Patienten. Ca. 90 % aller Patienten mit Myelom erleiden im Laufe ihrer Erkrankung skelettale Komplikationen wie Frakturen, Myelonkompression, Querschnittssymptomatik oder Hyperkalzämie. Für die Diagnostik dieser Knochenläsionen stehen neben dem Nativ-Röntgen auch sensitivere radiologische Verfahren wie CT, NMR und PET zur Verfügung, letztere um das Ausmaß der Osteolysen eindeutiger zu verifizieren. Zur Therapie dieser Osteolysen sind Bisphosphonate der Goldstandard; zudem die effektive MyelomTherapie unter Einschluss innovativer Substanzen, wie des Proteasominhibitors Bortezomib oder immunmodulatorischer Substanzen (IMIDs), wie Thalidomid und Lenalidomid. Zahlreiche klinische Studien prüfen aktuell den RANKL-(receptor activator of NF-κB ligand) neutralisierenden Antikörper Denosumab, Anti-Sclerostin (Antikörper gegen Sclerostin, den Wnt-Signalweg wiederherstellend und die Osteoklastenaktivität steigernd) oder Sotatercept (Inhibierung von Aktivin-A) in ihrem therapeutischen Potenzial. Der vorliegende Beitrag gibt einen Überblick über die Pathogenese, Diagnostik, Therapie und Prävention ossärer Komplikationen beim multiplen Myelom, welche in ähnlicher oder gleicher Weise auch für andere tumorbedingte Knochenmetastasen gelten.

Abstract

Multiple myeloma (MM) ranges second of all hematological malignancies and occurs most commonly in elderly patients. Almost all MM patients develop bone lesions in the course of their disease or have evidence of bone loss at initial diagnosis. Whole-body conventional radiography remains the gold standard in the diagnostic evaluation, albeit computed tomography (CT) and magnetic resonance imaging (MRI) are increasingly used as complementary techniques in the more sensitive detection of osteolytic processes. Bisphosphonates like zoledronate or pamidronate represent the cornerstone therapeutics in osteolytic disease, and are effective supportives to potent anti-myeloma therapies, including novel agents such as the proteasome inhibitor bortezomib or immunomodulatory drugs (IMIDs, e. g. thalidomide or lenalidomide). Several studies are ongoing to investigate the effects of alternative bone-seeking agents and their therapeutic potential for the management of myeloma bone disease, such as denosumab (RANKL-neutralizing antibody), anti-sclerostin (monoclonal antibody, generated against sclerostin) or sotatercept (potent activin-A inhibitor). This review summarizes the most prominent data on myeloma bone disease pathogenesis, the role of imaging techniques as well as therapy and prevention of lytic complications in myeloma which may similarly or equally be true for other bone metastases-inducing solid tumors.

 
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