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Lenalidomide at the dose of 25 mg every other day in patients affected by multiple myeloma and renal failure

Authors :
Vincenzo Martinelli
Fabrizio Pane
Marco Picardi
Claudio Cerchione
Anna Emanuele Pareto
Davide Nappi
A. Romano
Lucio Catalano
Cerchione, Claudio
Nappi, Davide
Pareto, Anna E.
Romano, Alessandra
Martinelli, Vincenzo
Picardi, Marco
Pane, Fabrizio
Catalano, Lucio
Source :
Anti-Cancer Drugs. 29:371-372
Publication Year :
2018
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2018.

Abstract

Renal impairment (RI) is a relevant complication of patients affected by multiple myeloma (MM); it can be present in up to 30-35% of newly diagnosed MM and is linked to a poor outcome. However, early recognition and early treatment with novel agents can overcome the negative impact of RI and even reverse kidney damage in most cases. Lenalidomide, available as an oral compound, is an immunomodulatory drug with both antiproliferative and immunomodulatory activity that is largely used in the management of MM. Dose reduction is mandatory in RI; however, there is no theoretical assumption against the possibility that protracting the time of full standard doses can be equally effective and tolerated by patients requiring reduced doses. In this report, we describe our retrospective experience, in 18 patients, with the administration of lenalidomide 25 mg every other day for patients with MM and RI. The overall response ratio was 66.5%. More than half (61.1%) of the patients had a renal response. The median progression-free survival was 8 months (range: 3-18 months). No serious adverse event occurred during treatment, and it was never necessary to disrupt or delay treatment for toxicity. These preliminary observations point to a significant therapeutic effect of lenalidomide, at the dose of 25 mg every other day for 21 days, with logistic and economic advantages. However, these results should be validated by controlled studies involving larger numbers of patients.

Details

ISSN :
09594973
Volume :
29
Database :
OpenAIRE
Journal :
Anti-Cancer Drugs
Accession number :
edsair.doi.dedup.....956ef111df547515c3cb158e04e9dca6