Entinostat and Sorafenib Tosylate in Treating Patients With Advanced or Metastatic Solid Tumors or Refractory or Relapsed Acute Myeloid Leukemia

Unspecified Adult Solid Tumor, Protocol Specific Clinical Trial

Official title:

A Phase I Study of Sorafenib in Combination With the Histone Deacetylase Inhibitor, Entinostat in Patients With Advanced Cancers

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01159301
• Other study ID #: NCI-2011-01435
• Secondary ID: NCI-2011-01435CD
• Status: Terminated
• Phase: Phase 1
• First received: July 8, 2010
• Last updated: September 18, 2013
• Start date: June 2010

Study information

• Verified date: September 2013
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 44
• Est. primary completion date: September 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Must meet 1 of the following criteria:

• Histologically or cytologically confirmed solid tumors (dose-escalation only)

• Locally advanced, inoperable, or metastatic disease

• Evaluable or measurable disease

• 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)

• Refractory or relapsed disease

• Chronic myelogenous leukemia in blast crisis allowed

• No acute promyelocytic leukemia with t(15;17)

• Must consent to have fresh tumor, bone marrow aspirate, and biopsy obtained

• 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:

• NYHA class II-IV congestive heart failure

• Active coronary artery disease

• Prior diagnosis of bradycardia or other cardiac arrhythmia defined as = grade 2 or uncontrolled hypertension

• Myocardial infarction (MI) within the past 6 months

• Persistent tachycardia

• LVEF < 40% by MUGA

• Second- or third-degree heart block

• QTc > 490 msec

• ST-T wave changes consistent with acute MI or acute ischemia

• 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:

• Significant, uncontrolled inflammatory bowel disease

• Abdominal fistula or gastrointestinal perforation within the past 6 months

• Extensive small bowel resection

• Requiring tube feeding or parenteral hydration and/or nutrition

• 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:

• Valproic acid

• Rifampin

• Phenobarbital

• Phenytoin

• Carbamazepine

• Ketoconazole

• Erythromycin

• Grapefruit

• 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

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Adult Acute Basophilic Leukemia
• Adult Acute Eosinophilic Leukemia
• Adult Acute Megakaryoblastic Leukemia (M7)
• Adult Acute Minimally Differentiated Myeloid Leukemia (M0)
• Adult Acute Monoblastic Leukemia (M5a)
• Adult Acute Monocytic Leukemia (M5b)
• Adult Acute Myeloblastic Leukemia With Maturation (M2)
• Adult Acute Myeloblastic Leukemia Without Maturation (M1)
• Adult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities
• Adult Acute Myeloid Leukemia With Del(5q)
• Adult Acute Myeloid Leukemia With Inv(16)(p13;q22)
• Adult Acute Myeloid Leukemia With t(16;16)(p13;q22)
• Adult Acute Myeloid Leukemia With t(8;21)(q22;q22)
• Adult Acute Myelomonocytic Leukemia (M4)
• Adult Erythroleukemia (M6a)
• Adult Pure Erythroid Leukemia (M6b)
• Blast Crisis
• Blastic Phase Chronic Myelogenous Leukemia
• Hypereosinophilic Syndrome
• Leukemia
• Leukemia, Erythroblastic, Acute
• Leukemia, Megakaryoblastic, Acute
• Leukemia, Monocytic, Acute
• Leukemia, Myelogenous, Chronic, BCR-ABL Positive
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute
• Leukemia, Myelomonocytic, Acute
• Leukemia, Myelomonocytic, Chronic
• Recurrent Adult Acute Myeloid Leukemia
• Unspecified Adult Solid Tumor, Protocol Specific

Intervention

Drug:
• entinostat
Given orally (PO)
• sorafenib tosylate
Given PO

Other:
• pharmacological study
Correlative studies
• laboratory biomarker analysis
Correlative studies

Locations

Country	Name	City	State
United States	Roswell Park Cancer Institute	Buffalo	New York

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum-tolerated dose as assessed by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4.0		28 days	Yes
Primary	Safety as assessed by the NCI CTCAE version 4.0		Up to 30 days	Yes
Secondary	Pharmacokinetic profile of sorafenib tosylate		At baseline, and at days 15, 16, and 28 of course 1, and day 1 of course 2	No
Secondary	Pharmacokinetic profile of entinostat		At baseline and at days 1, 8, 15, 16, and 22	No
Secondary	Objective response rate (ORR) based on the best overall response recorded for each patients or according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1	For ORR the 95% confidence interval will be estimated. The 95% confidence interval for percent of patients in each RECIST response category (i.e., CR, PR, SD, and PD) and disease control rate will also be estimated.	Up to 30 days	No