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Drug Evaluation

The Role of Carfilzomib in Treatment of Newly Diagnosed Multiple Myeloma

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Pages 3123-3134 | Received 16 Jan 2018, Accepted 29 Jun 2018, Published online: 30 Jul 2018
 

Abstract

Despite improvement of prognosis since approval of proteasome inhibitors and immunomodulatory drugs, myeloma remains largely incurable. The outcome of first-line treatment is known to be crucial for survival and, therefore, implementation of novel strategies remains one of the key aims of clinical myeloma research. Since approval of carfilzomib for relapsed and refractory multiple myeloma, a new therapeutic option with a favorable safety profile regarding neuropathy is available. Regarding its superior response rates and progression-free survival (PFS) when combined with other agents in heavily pretreated patients, the compound rapidly became a matter of great interest in search for first-line treatment. With an ORR up to 98% and promising PFS data, it might become an important partner in treatment of newly diagnosed myeloma.

This article is part of the following collections:
Multiple Myeloma

Financial & competing interests disclosure

S Knop received lecture fees from AMGEN GmbH; Celgene GmbH; BristolMyers Squibb GmbH and Janssen GmbH. S Strifler declares no financial interest or relationships of interest regarding the subject’s matter. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

No writing assistance was utilized inthe production of this manuscript.

Company review

In addition to the peer-review process, with the author’s consent, the manufacturer of the product discussed in this article was given the opportunity to review the manuscript for factual accuracy. Changes were made by the author at their discretion and based on scientific or editorial merit only. The author maintained full control over the manuscript, including content, wording and conclusions.

Additional information

Funding

S Knop received lecture fees from AMGEN GmbH; Celgene GmbH; BristolMyers Squibb GmbH and Janssen GmbH. S Strifler declares no financial interest or relationships of interest regarding the subject’s matter. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. No writing assistance was utilized inthe production of this manuscript.

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