Propranolol Hydrochloride in Treating Patients With Locally Recurrent or Metastatic Solid Tumors That Cannot Be Removed By Surgery

Sponsor

William Carson (Other)

Overall Status

Active, not recruiting

CT.gov ID

NCT02013492

Collaborator

(none)

Enrollment

Location

Arm

95.3

Anticipated Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This pilot trial studies propranolol hydrochloride in treating patients with locally recurrent or metastatic solid tumors that cannot be removed by surgery. Propranolol hydrochloride may slow the growth of tumor cells by blocking the use of hormones by the tumor cells.

Condition or Disease	Intervention/Treatment	Phase
Male Breast Cancer Recurrent Melanoma Stage IV Breast Cancer Stage IV Melanoma Stage IV Ovarian Epithelial Cancer Stage IV Ovarian Germ Cell Tumor Unspecified Adult Solid Tumor, Protocol Specific Hepatocellular Carcinoma	Drug: propranolol hydrochloride Other: Correlative Studies	Early Phase 1

Detailed Description

PRIMARY OBJECTIVES:

To determine the feasibility and tolerability of beta-adrenergic blockade in patients with metastatic or locally advanced cancer.
To determine the effects of beta-adrenergic blockade on the tumor microenvironment and host immune system via a series of correlative laboratory studies using cancer tumor tissue and peripheral blood mononuclear cells from the study patients.

SECONDARY OBJECTIVES:

Evaluate the effects of beta-adrenergic blockade on progression-free survival and overall survival.

OUTLINE:

Patients receive propranolol hydrochloride orally (PO) twice daily (BID) for 4 months in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up every 3 months for up to 1 year.

Study Design

Study Type:

Interventional

Actual Enrollment :

1 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Pilot Study of Beta-Blockers in Patients With Advanced Cancer

Actual Study Start Date :

Jan 21, 2014

Actual Primary Completion Date :

Jun 12, 2015

Anticipated Study Completion Date :

Dec 31, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Treatment (propranolol hydrochloride) Patients receive propranolol hydrochloride PO BID for 4 months in the absence of disease progression or unacceptable toxicity. Propranolol will be administered on an out-patient basis. Blood for correlative studies (30 ml - green top tube) will be drawn at baseline and at each clinic visit. Tumor tissue for analysis will be obtained via core needle biopsy (or other appropriate modality) pre-study and at approximately the two month time point.	Drug: propranolol hydrochloride Given PO Other Names: Inderal Other: Correlative Studies Correlative studies will be conducted using the following materials: Plasma derived from peripheral blood. Peripheral blood mononuclear cells (PBMC) derived from patient blood Tumor tissue obtained at the time of core needle biopsy at the 2 month time point. Paraffin-embedded tumor tissue obtained pre-therapy to make the diagnosis of metastatic disease.

Arm

Intervention/Treatment

Experimental: Treatment (propranolol hydrochloride)

Patients receive propranolol hydrochloride PO BID for 4 months in the absence of disease progression or unacceptable toxicity. Propranolol will be administered on an out-patient basis. Blood for correlative studies (30 ml - green top tube) will be drawn at baseline and at each clinic visit. Tumor tissue for analysis will be obtained via core needle biopsy (or other appropriate modality) pre-study and at approximately the two month time point.

Drug: propranolol hydrochloride

Given PO

Other Names:

Inderal

Other: Correlative Studies

Correlative studies will be conducted using the following materials: Plasma derived from peripheral blood. Peripheral blood mononuclear cells (PBMC) derived from patient blood Tumor tissue obtained at the time of core needle biopsy at the 2 month time point. Paraffin-embedded tumor tissue obtained pre-therapy to make the diagnosis of metastatic disease.

Outcome Measures

Primary Outcome Measures

Incidence of toxicity graded according to Common Terminology Criteria for Adverse Events (CTCAE) V. 4.0 [Up to 4 months]
A dose-limiting toxicity (DLT) will be considered as any grade 3 or higher hematologic or non- hematologic toxicity that is probably or definitely related to treatment.
Change in vascular endothelial growth factor (VEGF) [Baseline to 4 months]
Effect of beta-adrenergic blockade on the tumor microenvironment [Up to 4 months]
Measured via a series of correlative laboratory studies using cancer tumor tissue and peripheral blood mononuclear cells.
Effect of beta-adrenergic blockade on the host immune system [Up to 4 months]
Measured via a series of correlative laboratory studies using cancer tumor tissue and peripheral blood mononuclear cells.

Secondary Outcome Measures

Progression-free survival [Up to 1 year]
Overall survival [Up to 1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Patients must have histologically-proven locally-recurrent or metastatic solid tumor; the first 10 patients may have cancer of any histology; preference will be given to patients with metastatic ovarian cancer, breast cancer, and malignant melanoma, as these malignancies have been shown to be sensitive to manipulation of the beta-adrenergic receptor; the final twenty-five patients to be accrued must have locally-recurrent or metastatic malignant melanoma that is not surgically resectable. An additional cohort of 10 patients with BCLC stages A to C locally advanced or metastatic hepatocellular carcinoma (HCC) that is not surgically resectable will also be enrolled (See appendix for BCLC staging system). Patients with liver transplantation will not be eligible.
The diagnosis of hepatocellular carcinoma may be made by one of the following methods:

Pathologically (histologically or cytologically) proven diagnosis of HCC.
At least one solid liver lesion or vascular tumor thrombosis (involving portal vein, IVC and/or hepatic vein) > 1 cm with arterial enhancement and delayed washout on multiphasic computerized tomography (CT) or magnetic resonance imaging (MRI) in the setting of cirrhosis or chronic hepatitis B or C without cirrhosis.
For patients whose CURRENT disease is vascular only: Enhancing vascular thrombosis (involving portal vein, IVC and/or hepatic vein) demonstrating early arterial enhancement and delayed washout on multi-phasic CT or MRI, in a patient with known HCC (diagnosed according to criteria in (a) or (b).

Patients may have had any number of prior systemic therapies; patients need not have exhausted standard therapy for their disease, but must be stable and must not have actively progressing
Eastern Cooperative Oncology Group (ECOG) performance status =< 2
Karnofsky >= 60%
Life expectancy of greater than 6 months
Patients (except for the HCC cohort) must have normal organ and marrow function as defined below:
Leukocytes >= 3,000/mcL
Absolute neutrophil count >= 1,500/mcL
Platelets >= 100,000/mcL
Total bilirubin within normal institutional limits
Aspartate aminotransferase (AST)(serum glutamic oxaloacetic transaminase [SGOT])/alanine aminotransferase (ALT)(serum glutamate pyruvate transaminase [SGPT]) =< 2.5 X institutional upper limit of normal
Creatinine within normal institutional limits OR
Creatinine clearance >= 60 mL/min/1.73 m^2 for patients with creatinine levels above institutional normal
Parameters for the HCC cohort:
leukocytes > or = 3000/mcl
absolute neutrophil count > or =1000/mcl
platelets > or = 70,000
total bilirubin < or = 2mg/dL
AST/ALT <6 times ULN
creatinine within normal institutional limits OR
creatinine clearance > or = 60mL/min/1.73m2 for patients with creatinine levels above institutional normal level
INR < or = 1.7
The effects of propranolol on the developing human fetus may be detrimental. For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately
Ability to understand and the willingness to sign a written informed consent document
Patients with brain metastases may participate in this clinical study provided that symptoms have been controlled with standard therapies and/or appropriate medications; the principal investigator (P.I.) will carefully evaluate the suitability of patient participation when brain metastases are present

Exclusion Criteria:

Patients who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier
Patients may not be receiving any other investigational agents
History of allergic reactions attributed to compounds of similar chemical or biologic composition to propranolol
Uncontrolled hypertension
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
Patients with significant lung disease, an ejection fraction less than 40%, or a resting heart rate less than 60/min will not be enrolled
Pregnant women are excluded from this study because propranolol is an agent with the potential for teratogenic or abortifacient effects
Patients who are currently receiving a beta-blocker for another medical condition will be excluded from this study; patients with extremes of blood pressure (e.g., systolic blood pressure [SBP] > 150 or < 100) may be excluded from participation if the treating physician feels that this medical condition has not been adequately addressed by the patient's primary care physician
Patients with worsening depression that has not been addressed clinically will be excluded from this study