Phase I/II Trial of the MEK1/2 Inhibitor GSK1120212 (GSK212) in Patients with Relapsed/ Refractory...
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Transcript of Phase I/II Trial of the MEK1/2 Inhibitor GSK1120212 (GSK212) in Patients with Relapsed/ Refractory...
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Phase I/II Trial of the MEK1/2 Inhibitor GSK1120212 (GSK212) in Patients with Relapsed/Refractory Myeloid Malignancies: Evidence of Activityin Pts with RAS Mutation
Borthakur G et al.Proc ASCO 2011;Abstract 6506.
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Borthakur G et al. Proc ASCO 2011;Abstract 6506.
Background
– Signaling through the RAS/RAF/MEK pathway is activated in many human cancers.
– GSK212 is a potent, selective allosteric inhibitor of MEK1/2 that inhibits proliferation of myeloid cell lines in vitro.
– A Phase I/II study of a single, daily, oral dosing regimen was conducted.
Study Objectives:– Define the recommended Phase II dose (RP2D) of GSK212.– Evaluate pharmacokinetics, toxicity and preliminary
activity in patients with previously treated hematologic malignancies.
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Phase I/II Study Design
Eligibility
Relapsed/refractory AML, poor-risk MDS (>5% blasts), ALL, CMMLECOG PS 0-2Adequate organ function
Borthakur G et al. Proc ASCO 2011;Abstract 6506.
ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; CMML, chronic myelomonocytic leukemia; MDS, myelodysplatic syndrome
Recommended Phase II dose = 2 mg QD
3 mg loading1 mg QD
n = 3
1 mg QDn = 2
2 mg QDn = 9
Cohort 1RAS-mutant AML MDS
Cohort 2RAS wild type or unknown
Cohort 3RAS-mutant CMML
RP2D
3 + 3 doseescalation
Phase 1 — Dose escalation Phase 2 — Expansion
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Patient Characteristics: 2 mg/Day Dose
Characteristic n = 47
Median age, years (range) 64 (21-87)
Number of prior therapies, median 2
ECOG PS, n (%) 0-1 2
34 (72)13 (28)
Diagnosis, n (%) AML Other
42 (89)5 (11)
RAS mutation, n (%) 16 (34)
FLT3 mutation, n (%) 18 (38)
Cytogenetics, n (%) Complex Core-binding factor Normal Other/unknown
9 (19)2 (4)
8 (17)17 (37)
Borthakur G et al. Proc ASCO 2011;Abstract 6506.
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Clinical Activity
Best Response, n (%)N or KRAS Mutated
(n = 16)
RAS Wild Type or Unknown
(n = 31)
CR/CRp 3 (19) 0
MLFS 1 (6) 0
Partial response 0 1 (3)
HI/HI-N/HI-P 1 (6) 5 (16)
Stable disease 10 (63) 8 (26)
Progressive disease 0 13 (42)
Overall response rate 4 (25) 1 (3)
Borthakur G et al. Proc ASCO 2011;Abstract 6506.
• MLFS = morphologic leukemic-free state• ORR = CR/CRp/MLFS/PR
6 patients not evaluable
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Select Adverse Events*
AEs (N = 47) All Grades Grade 3/4
Diarrhea 47% 4%
Pyrexia 30% 6%
Rash 26% 4%
Fatigue 25% 4%
AST increase 24% 11%
ALT increase 23% 11%
Pneumonia 23% 17%
Febrile neutropenia 23% 19%
Borthakur G et al. Proc ASCO 2011;Abstract 6506.
* Occurring in greater than 20% of patients
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Events of Special Interest
Borthakur G et al. Proc ASCO 2011;Abstract 6506.
• Decrease in LVEF
– Six percent (3/47) of patients had drug-related left ventricular dysfunction (1 Grade 1 event and 2 Grade 2 events).
• Transaminase elevations
– Two patients had drug held due to transaminase elevations — on rechallenge, 1 positive and 1 negative.
• Ocular toxicity
– Central Serous Retinopathy: Fluid accumulation in the macular region between retinal pigment epithelium and out segment.
– One patient developed a reversible retinopathy.
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Borthakur G et al. Proc ASCO 2011;Abstract 6506.
Author Conclusions
Acceptable safety profile:– Monotherapy safety profile suggests potential to
combine with other antileukemic therapies
Preliminary efficacy:– Overall response rates of 25 percent (4 of 16) among
patients with RAS mutation
Enrolling patients with RAS-mutant AML, MDS and CMML:– Centralized RAS mutation analysis– Up to 30 sites in US and Europe open to accrual