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Erschienen in: Cancer Chemotherapy and Pharmacology 6/2012

01.06.2012 | Review Article

Lenalidomide in solid tumors

verfasst von: Angela Segler, Apostolia-Maria Tsimberidou

Erschienen in: Cancer Chemotherapy and Pharmacology | Ausgabe 6/2012

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Abstract

Background

Lenalidomide is a thalidomide analogue with immunomodulatory and anti-angiogenic properties that include altering cytokine production, activating T cells, and augmenting natural killer cell function. Lenalidomide is approved by the U.S. Food and Drug Administration (FDA) for single-agent treatment of myelodysplastic syndromes associated with a 5q deletion and as a combination therapy with dexamethasone for the treatment of multiple myeloma.

Methods

All prospective phase I–III clinical trials and preclinical data published until October 2011 and relevant literature were reviewed.

Results

In phase I and/or II studies of single-agent lenalidomide in patients with advanced cancer, responses were reported in patients with prostate, thyroid, hepatocellular, pancreatic, and renal cancer and melanoma. The most common toxicities were hematologic, and in the first clinical trials, thrombotic events were noted. When anticoagulation prophylaxis and exclusion of patients with a history of thrombosis were implemented, thrombotic complications became uncommon.

Conclusion

Monitoring of blood counts and for evidence of thromboembolic events is essential for patients treated with lenalidomide. Ongoing trials of lenalidomide combination therapy offer a treatment option for patients with advanced cancer and will better define the role of lenalidomide in solid tumors.
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Metadaten
Titel
Lenalidomide in solid tumors
verfasst von
Angela Segler
Apostolia-Maria Tsimberidou
Publikationsdatum
01.06.2012
Verlag
Springer-Verlag
Erschienen in
Cancer Chemotherapy and Pharmacology / Ausgabe 6/2012
Print ISSN: 0344-5704
Elektronische ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-012-1874-2

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