Literature DB >> 23538263

Carfilzomib: a next-generation proteasome inhibitor for multiple myeloma treatment.

Elizabeth Bilotti1.   

Abstract

Although the incidence of multiple myeloma (MM) is increasing, the median overall survival and the number of agents in the pipeline for treating MM also are increasing. Response rates higher than 80% are not uncommon in the frontline setting when the novel agents thalidomide, lenalidomide, and bortezomib are used in combination. Response rates and survival also have improved in disease that has relapsed after treatment with conventional therapies. The focus of research has now shifted to improving survival and disease response in patients refractory to current treatment paradigms. New agents are targeting new pathways, as well as existing mechanisms known to be effective, but with different safety profiles. Carfilzomib is a potent, selective, irreversible inhibitor of the ubiquitin-proteasome pathway. The drug is a next-generation proteasome inhibitor found to be safe and effective for patients with relapsed and refractory MM, where treatment options are limited. As with any newly approved agent, one should recognize that drugs within the same class will be administered differently and often cause dissimilar treatment-related toxicities. Oncology nurses are crucial to the successful administration of chemotherapeutic agents such as carfilzomib, and an understanding of management techniques is paramount to quality patient care.

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Year:  2013        PMID: 23538263     DOI: 10.1188/13.CJON.E35-E44

Source DB:  PubMed          Journal:  Clin J Oncol Nurs        ISSN: 1092-1095            Impact factor:   1.027


  2 in total

1.  Reversal of Mutant KRAS-Mediated Apoptosis Resistance by Concurrent Noxa/Bik Induction and Bcl-2/Bcl-xL Antagonism in Colon Cancer Cells.

Authors:  Koichi Okamoto; Aziz Zaanan; Hisato Kawakami; Shengbing Huang; Frank A Sinicrope
Journal:  Mol Cancer Res       Date:  2014-12-29       Impact factor: 5.852

2.  Proteasome Inhibitors Decrease the Viability of Pulmonary Arterial Smooth Muscle Cells by Restoring Mitofusin-2 Expression under Hypoxic Conditions.

Authors:  I-Chen Chen; Yi-Ching Liu; Yen-Hsien Wu; Shih-Hsing Lo; Shu-Chi Wang; Chia-Yang Li; Zen-Kong Dai; Jong-Hau Hsu; Chung-Yu Yeh; Yu-Hsin Tseng
Journal:  Biomedicines       Date:  2022-04-09
  2 in total

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