| Literature DB >> 32511022 |
Shambavi Richard1, Joshua Richter1, Sundar Jagannath1.
Abstract
The progression of multiple myeloma is accompanied by complex cytogenetic and epigenetic alterations that include mutation or functional inactivation of tumor suppressor proteins and overexpression of oncoproteins. Patients whose myeloma is refractory to the three major classes of drugs including immunomodulatory agents, proteasome inhibitors and anti-CD38 monoclonal antibodies have a very poor prognosis. Drugs with novel mechanisms of action that can bypass resistance mechanisms are sorely needed for this group of patients. Selinexor represents a novel, oral agent with an innovative mechanism of action that offers a significant therapeutic advance in this group of heavily treated patients. Moreover, this novel mechanism may provide additional options for patients with less refractory disease.Entities:
Keywords: SINE; XPO1; exportin 1; karyopherin; multiple myeloma; refractory; relapsed; selective inhibitor of nuclear export; selinexor
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Year: 2020 PMID: 32511022 DOI: 10.2217/fon-2020-0054
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404