Combination venetoclax and selinexor effective in relapsed refractory multiple myeloma with translocation t(11;14).
Nina NguyenSana I ChaudhryTulasigeri M TotigerRobert DiazEvan RobertsSkye MontoyaGabriel PardoAlejandro PardoJumana AfaghaniMaurizio AfferJacob JahnTerrence BradleyFrancesco MauraDickran KazandjianDaniel BilbaoJennifer ChapmanOla LandgrenJames HoffmanJustin TaylorPublished in: NPJ precision oncology (2022)
Patients with multiple myeloma-bearing translocation t(11;14) have recently been shown to benefit from the apoptosis-inducing drug venetoclax; however, the drug lacks FDA approval in multiple myeloma thus far due to a potential safety signal in the overall patient population. Selinexor is an inhibitor of nuclear export that is FDA-approved for patients with multiple myeloma refractory to multiple lines of therapy. Here, we report that in four patients with multiple myeloma with t(11;14), the concomitant administration of venetoclax and selinexor was safe and associated with disease response. Moreover, the combination was synergistic in t(11;14) multiple myeloma cell lines and caused decreased levels of Cyclin D1 (which is overexpressed due to the CCND1-IGH fusion) when given in combination as compared to single agents. These data suggest that the combination of venetoclax and selinexor is effective and t(11;14) may serve as a therapeutic marker for response and target for future clinical trials.
Keyphrases
- multiple myeloma
- clinical trial
- chronic lymphocytic leukemia
- oxidative stress
- randomized controlled trial
- emergency department
- cell cycle
- acute myeloid leukemia
- case report
- bone marrow
- cell cycle arrest
- drug delivery
- signaling pathway
- acute lymphoblastic leukemia
- drug induced
- cell proliferation
- open label
- study protocol
- adverse drug
- pi k akt