A Phase I Study of Sorafenib in Combination With the Histone Deacetylase Inhibitor, Entinostat in Patients With Advanced Cancers
A Phase I Study of Sorafenib in Combination With the Histone Deacetylase Inhibitor, Entinostat in Patients With Advanced Cancers
This phase I trial is studying the side effects and the best dose of entinostat when given together with sorafenib tosylate in treating patients with advanced or metastatic solid tumors or refractory or relapsed acute myeloid leukemia. Entinostat and sorafenib tosylate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.
PRIMARY OBJECTIVES:
I. To determine the maximum-tolerated dose of entinostat in combination with sorafenib tosylate in patients with advanced, inoperable, or metastatic solid tumors.
II. To determine the safety and tolerability of this regimen in these patients.
SECONDARY OBJECTIVES:
I. To determine the pharmacokinetic profile of this regimen in patients with refractory/relapsed acute myeloid leukemia (AML).
II. To assess the preliminary anti-tumor activity of this regimen in patients with advanced, inoperable, or metastatic solid tumors or refractory/relapsed AML.
III. To evaluate histone deacetylase (HDAC) inhibition of histone acetylation in leukemia blast cells.
TERTIARY OBJECTIVES (EXPLORATORY):
I. To evaluate the expression of downstream markers of drug activity such as p38, MCL-1, FLT-3, and VEGFR-2 in leukemia blast cells.
II. To evaluate SNDX-induced expression of p21^WAF1/CIP1 in leukemia blast cells.
OUTLINE: This is a multicenter, dose-escalation study of entinostat.
Patients receive oral entinostat once daily on days 1 and 15 and oral sorafenib tosylate twice daily on days 1-28 (days 15-28 only of course 1). Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Patients in the expansion cohort undergo blood, bone marrow aspiration, or biopsy for pharmacokinetic studies and biomarker analysis.
After completion of study therapy, patients are followed up for up to 24 months.
Inclusion Criteria:
Must meet 1 of the following criteria:
Histologically or cytologically confirmed solid tumors (dose-escalation only)
Diagnosis of acute myeloid leukemia (AML) for which no other standard therapy, including stem cell transplantation, is expected to result in meaningful clinical response (expansion cohort only)
No untreated, symptomatic, or unstable brain metastases
No active CNS involvement for patients with AML
ECOG performance status 0-1
ANC ≥ 1,500/mm³ (dose-escalation only)
Platelet count ≥ 100,000/mm³ (dose-escalation only)
Hemoglobin ≥ 10 g/dL (dose-escalation only)
Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
ALT and AST ≤ 3 times ULN (≤ 5 times ULN for liver metastasis)
Creatinine clearance ≥ 40 mL/min
Albumin > 3.0 g/dL
Plasma phosphorus > lower limit of normal (with supplementation)
INR ≤ 1.5
APTT ≤ 1.5 times ULN (if not on anticoagulants)
Able to swallow oral medications
≥ 16 years old (expanded cohort patients recruited at the University of Colorado site)
Must have tolerated prior sorafenib tosylate (dose: 400 mg twice daily), if applicable
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective double-barrier contraception during the study and for 90 days after completion of study therapy
No history of cardiac disease, including any of the following:
No clinically active serious infections defined as ≥ grade 2
No substance abuse, medical, psychological, or social conditions that may, in the opinion of the Investigator, interfere with the patient's participation or evaluation of the study results
No condition that is unstable or that could jeopardize the safety of the patient and his/her study compliance
No known HIV infection
No significant gastrointestinal disorder that, in the opinion of the Investigator, could interfere with the absorption of entinostat and/or sorafenib tosylate including any of the following:
No concurrent immunosuppressive therapies, including high-dose systemic corticosteroids (> 0.5 mg/kg/day prednisone or equivalent) unless used intermittently or as a tapered course for ≤ 4 weeks
Concurrent hydroxyurea and/or anagrelide allowed
Concurrent warfarin allowed provided the dose has been stable for the past 2 months and INR has been between 2 and 3
More than 4 weeks since prior chemotherapy, immunotherapy, or investigational agents (=< 2 weeks for leukemia patients in expansion cohort)
More than 2 weeks since prior palliative radiotherapy
More than 4 weeks since major surgery
More than 2 weeks since minor surgery (e.g., talc pleurodesis, excisional biopsy, etc.)
Concurrent hormonal therapies (e.g., LHRH antagonists, megestrol, octreotide, calcitonin, etc.) allowed
No concurrent strong CYP3A4 inducers or inhibitors, including, but not limited to, any of the following:
No other concurrent anticancer therapy including chemotherapy, radiotherapy (including palliative), or immunotherapy (except hydroxyurea in leukemia patients during course 1)
No other concurrent investigational agents