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

September 18, 2013 updated by: National Cancer Institute (NCI)

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.

Study Overview

Status

Terminated

Conditions

Intervention / Treatment

Detailed 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.

Study Type

Interventional

Enrollment (Actual)

44

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • New York
      • Buffalo, New York, United States, 14263
        • Roswell Park Cancer Institute

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Treatment (entinostat, sorafenib tosylate)
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.
Other: laboratory biomarker analysis
Correlative studies
Other: pharmacological study
Correlative studies
Other Names:
  • pharmacological studies
Drug: sorafenib tosylate
Given PO
Other Names:
  • BAY 43-9006
  • BAY 43-9006 Tosylate Salt
  • BAY 54-9085
  • Nexavar
  • SFN
Drug: entinostat
Given orally (PO)
Other Names:
  • HDAC inhibitor SNDX-275
  • SNDX-275

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Maximum-tolerated dose as assessed by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4.0
Time Frame: 28 days
28 days
Safety as assessed by the NCI CTCAE version 4.0
Time Frame: Up to 30 days
Up to 30 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pharmacokinetic profile of sorafenib tosylate
Time Frame: At baseline, and at days 15, 16, and 28 of course 1, and day 1 of course 2
At baseline, and at days 15, 16, and 28 of course 1, and day 1 of course 2
Pharmacokinetic profile of entinostat
Time Frame: At baseline and at days 1, 8, 15, 16, and 22
At baseline and at days 1, 8, 15, 16, and 22
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
Time Frame: Up to 30 days
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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

National Cancer Institute (NCI)

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2010

Primary Completion (ACTUAL)

September 1, 2013

Study Registration Dates

First Submitted

July 8, 2010

First Submitted That Met QC Criteria

July 8, 2010

First Posted (ESTIMATE)

July 9, 2010

Study Record Updates

Last Update Posted (ESTIMATE)

September 19, 2013

Last Update Submitted That Met QC Criteria

September 18, 2013

Last Verified

September 1, 2013

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • NCI-2011-01435 (REGISTRY: CTRP (Clinical Trial Reporting Program))
  • CDR0000675600
  • I-165409 (OTHER: Roswell Park Cancer Institute)
  • 8272 (CTEP)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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