Introduction: Multiple myeloma (MM) patients who relapse, or become refractory to currently available novel agents, have limited treatment options with poor outcomes. The introductions of the newer proteasome inhibitor carfilzomib and the immunomodulatory agent pomalidomide have provided new treatment strategies within the relapse setting. Pomalidomide, a novel 4-amino derived from thalidomide, was recently introduced for the treatment of MM. In addition to being immune-adjuvant with anti-inflammatory properties, pomalidomide has shown several biological activities that directlyand indirectly inhibit MM cells. Areas covered: Herein, the authors review the chemistry, the mechanism of action and the pharmacokinetic properties of pomalidomide. The data reviewed within this article based on the relevant literature pertaining to pomalidomide's Phase I, II and III clinical trials. Expert opinion: Pomalidomide has shown to be a safe and active agent, both alone and in combination with dexamethasone, in heavily pretreated patients. Furthermore, pomalidomide represents an effective treatment option for relapsed/refractory patients. Results from the ongoing trials evaluating the synergistic activity of pomalidomide combined with conventional chemotherapy or novel agents look promising and may prove to be viable treatment options in the future. © 2013 Informa UK, Ltd.
Pharmacokinetic evaluation of pomalidomide for the treatment of myeloma
Gay F.First
;Mina R.;Troia R.;Bringhen S.
Last
2013-01-01
Abstract
Introduction: Multiple myeloma (MM) patients who relapse, or become refractory to currently available novel agents, have limited treatment options with poor outcomes. The introductions of the newer proteasome inhibitor carfilzomib and the immunomodulatory agent pomalidomide have provided new treatment strategies within the relapse setting. Pomalidomide, a novel 4-amino derived from thalidomide, was recently introduced for the treatment of MM. In addition to being immune-adjuvant with anti-inflammatory properties, pomalidomide has shown several biological activities that directlyand indirectly inhibit MM cells. Areas covered: Herein, the authors review the chemistry, the mechanism of action and the pharmacokinetic properties of pomalidomide. The data reviewed within this article based on the relevant literature pertaining to pomalidomide's Phase I, II and III clinical trials. Expert opinion: Pomalidomide has shown to be a safe and active agent, both alone and in combination with dexamethasone, in heavily pretreated patients. Furthermore, pomalidomide represents an effective treatment option for relapsed/refractory patients. Results from the ongoing trials evaluating the synergistic activity of pomalidomide combined with conventional chemotherapy or novel agents look promising and may prove to be viable treatment options in the future. © 2013 Informa UK, Ltd.File | Dimensione | Formato | |
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[POST-PRINT Vsn] Gay et al - 2013 - Pomalidomide review_EOMT.pdf
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Descrizione: Restricted access - Author's version. Gay F, Mina R, Troia R, Bringhen S. Pharmacokinetic evaluation of pomalidomide for the treatment of myeloma. Expert Opin Drug Metab Toxicol. 2013 Nov;9(11):1517-27. doi: 10.1517/17425255.2013.827169. Epub 2013 Aug 21. PMID: 23961770. © 2013 Informa UK, Ltd. The published version is available at: https://www.tandfonline.com/doi/abs/10.1517/17425255.2013.827169?journalCode=iemt20 | https://doi.org/10.1517/17425255.2013.827169 . When citing, please refer to the published version.
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[Published Vsn] Gay et al - 2013 - Expert Opin Drug Metab Toxicol - Pharmacokinetic evaluation.pdf
Accesso riservato
Descrizione: Restricted access - Published version. Gay F, Mina R, Troia R, Bringhen S. Pharmacokinetic evaluation of pomalidomide for the treatment of myeloma. Expert Opin Drug Metab Toxicol. 2013 Nov;9(11):1517-27. doi: 10.1517/17425255.2013.827169. Epub 2013 Aug 21. PMID: 23961770. © 2013 Informa UK, Ltd. The published version is available at: https://www.tandfonline.com/doi/abs/10.1517/17425255.2013.827169?journalCode=iemt20 | https://doi.org/10.1517/17425255.2013.827169
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