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A Phase II Trial of AZD6244 (Selumetinib, ARRY-142886), an Oral MEK1/2 Inhibitor, in Relapsed/Refractory Multiple Myeloma.

Authors :
Holkova B
Zingone A
Kmieciak M
Bose P
Badros AZ
Voorhees PM
Baz R
Korde N
Lin HY
Chen JQ
Herrmann M
Xi L
Raffeld M
Zhao X
Wan W
Tombes MB
Shrader E
Weir-Wiggins C
Sankala H
Hogan KT
Doyle A
Annunziata CM
Wellons M
Roberts JD
Sullivan D
Landgren O
Grant S
Source :
Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2016 Mar 01; Vol. 22 (5), pp. 1067-75. Date of Electronic Publication: 2015 Oct 07.
Publication Year :
2016

Abstract

Purpose: AZD6244 is a MEK1/2 inhibitor with significant preclinical activity in multiple myeloma cells. This phase II study used a two-stage Simon design to determine the AZD6244 response rate in patients with relapsed or refractory multiple myeloma.<br />Experimental Design: AZD6244 (75 mg) was administered orally, twice a day, continuously for 28-day cycles. Response was evaluated after three cycles.<br />Results: Thirty-six patients received therapy. The median age was 65 years (range: 43-81) and the median number of prior therapies was 5 (range: 2-11). The most common grade 3 and 4 toxicities included anemia, neutropenia, thrombocytopenia, diarrhea, and fatigue. Three deaths occurred possibly related to AZD6244 (2 due to sepsis, 1 due to acute kidney injury). After AZD6244 discontinuation, three additional deaths occurred due to disease progression. The response rate (CR + PR) was 5.6% with a mean duration of response of 4.95 months and median progression-free survival time of 3.52 months. One patient had a very good partial response (VGPR), 1 patient had a partial response, 17 patients had stable disease, 13 patients had progressive disease, and 4 patients could not be assessed for response. Pharmacodynamic studies revealed variable effects on bone marrow CD138(+) cell MEK1/2 and ERK1/2 phosphorylation. The best clinical response, a prolonged VGPR, occurred in a patient with an MMSET translocation.<br />Conclusions: Single-agent AZD6244 was tolerable and had minimal activity in this heavily pretreated population.<br /> (©2015 American Association for Cancer Research.)

Details

Language :
English
ISSN :
1557-3265
Volume :
22
Issue :
5
Database :
MEDLINE
Journal :
Clinical cancer research : an official journal of the American Association for Cancer Research
Publication Type :
Academic Journal
Accession number :
26446942
Full Text :
https://doi.org/10.1158/1078-0432.CCR-15-1076