Propranolol for the Treatment of Kaposi Sarcoma in Adults

Phase 2

Not yet recruiting

• Conditions: Kaposi Sarcoma
• Interventions: Drug: Propranolol Hydrochloride

• Registration Number: NCT06445166
• Lead Sponsor: Washington University School of Medicine

Brief Summary

Kaposi sarcoma (KS) lesions are initiated by endothelial cells infected with KS herpesvirus (KSHV), also known as human herpesvirus 8 (HHV-8). Lesion progression is driven by abnormal angiogenesis, chronic inflammation, and uncontrolled cell proliferation. KS remains one of the most commonly diagnosed cancers in many African countries where economic constrai...

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2024-05-31
• Study First Submitted QC: 2024-05-31
• Study First Posted: 2024-06-06
• Status Verified: 2024-11
• Last Update Submitted: 2024-11-13
• Last Update Posted: 2024-11-14
• Study Start: 2024-12-31
• Primary Completion: 2027-06-30
• Study Completion: 2027-12-31

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• Biopsy proven Kaposi Sarcoma that is measurable with a millimeter ruler. Patients presenting for both front-line therapy and subsequent-line therapy will be considered.

• Must have two lesions greater or equal to 4 x 4 mm that are accessible for 3-mm punch biopsy.

• Must be KS stage T0 (confined to skin and/or lymph nodes and/or minimal oral lesions) or T1 (limited to tumor-associated edema of cutaneous lesions without functional impairment or flat oral lesions).

• At least 18 years of age.

• Weight >40 kg

• ECOG performance status ≤ 2

• Meets the appropriate HIV-related criteria:

  • If HIV positive, patient must be on antiretroviral therapy (ART) that conforms to local standards of care for at least 12 weeks. HIV positive patients will not be excluded based on CD4 count or HIV viral load.

    • If on ART 12 to 24 weeks, must show evidence of KS progression requiring further systemic treatment.
    • If on ART for > 24 weeks, must show no evidence of regression in the last 8 weeks.

  • If HIV negative, must not show evidence of improvement in the 12 weeks prior to enrollment.

• Propranolol is US FDA pregnancy category C. For this reason, women of childbearing potential must agree to use adequate contraception prior to study entry, for the duration of study participation, and for one month after completion of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, s/e must inform her treating physician immediately.

• Able to take an oral pill.

• Ability to understand and willingness to sign an IRB approved written informed consent document.

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Exclusion Criteria

• Visceral disease causing functional impairment.
• Urgently clinically indicated for immediate cytotoxic chemotherapy. Patients who have received cytotoxic chemotherapy > 4 weeks prior to screening are eligible.
• Prior or concurrent malignancy whose natural history has the potential to interfere with the safety or efficacy assessment of the investigational regimen. Patients with prior or concurrent malignancy that does NOT meet that definition are eligible for this trial
• Currently taking beta-andrenergic antagonist(s) for other indications. Prior use is allowed.
• Currently receiving concurrent treatment with an anticancer therapy. Patients must not have received any anticancer therapies within 4 weeks prior to receiving the first dose of propranolol.
• Currently receiving any other investigational agents.
• A history of allergic reactions or hypersensitivity attributed to compounds of similar chemical or biologic composition to propranolol.
• History of asthma or current diagnosis of obstructive airway disease such as asthma, COPD, or bronchiolitis.
• History of diabetes mellitus, as defined by any of the following: A random blood glucose value of at least 200 mg/dL in the presence of hyperglycemia symptoms (weight loss, blurry vision, thirst, polyuria), fasting plasma glucose value of at least 126 mg/dL, A1c value of at least 6.5%, or two hour plasma glucose value of at least 200 mg/dL during a 75 g oral glucose tolerance test.
• History of uncompensated heart failure, severe sinus bradycardia, sick sinus syndrome, or heart block greater than first degree.
• History of hypotension (systolic blood pressure <90 mmHg or mean arterial pressure <65 mmHg) or orthostasis (>20 mmHg fall in systolic pressure or >10 mmHg fall in diastolic pressure with standing).
• Shortness of breath, hemoptysis, or moderate/severe cough not attributable to causes other than KS.
• Bleeding from the mouth or rectum not attributable to causes other than KS.
• Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.
• Concern for KSHV inflammatory cytokine syndrome.
• Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 21 days of study entry.
• Evidence of chronic hepatitis B virus (HBV) that is detectable on suppressive therapy. Patients with evidence of chronic HBV infection with undetectable HBV viral load on suppressive therapy are eligible. HBV testing not required in the absence of known history of infection.
• History of hepatitis C virus (HCV) infection that has not been cured or that has a detectable viral load. Patients with a history of HCV that has been treated and cured are eligible. Patients with HCV infection who are currently on treatment and have an undetectable HCV viral load are eligible. HCV testing not required in the absence of known history of infection.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Propranolol	Propranolol Hydrochloride	Begin at 1/2 the target dose for 2 days (4 doses), followed by a tolerability assessment. Patients who tolerate the 1/2 dose will begin the target dose on Day 3 for 2 days (4 doses), after which tolerability will be assessed. Patients who do not tolerate the target dose will decrease to a 1/2 dose for 2 days and then discontinue treatment; these patients will be withdrawn from the study and replaced. Those who continue will take the target dose for 12 weeks. At 12-week time point, one of the following paths will be taken: * Complete response: continue taking propranolol at the target dose for another 6 weeks, followed by a reduced dose (1/2 the target) for 7 days, then discontinue treatment * Partial response: continue taking propranolol at the target dose for another 12 weeks, followed by a reduced dose (1/2 the target) for 7 days, then discontinue treatment * No response (stable disease/disease progression):reduced dose (1/2 the target) for 7 days, then discontinue treatment

Primary Outcome Measures

Name	Time	Method
Objective response rate (ORR)	Through completion of treatment (estimated to be 25 weeks)	ORR is defined as the proportion of participants with complete response (CR) or partial response (PR) based on AMC KS Response Criteria.

Secondary Outcome Measures

Name	Time	Method
Incidence of intolerable toxicities and treatment-emergent adverse events (TEAEs) based on CTCAE v 5.0.	From start of treatment through 30 days after completion of treatment (estimated to be 29 weeks)
Time to recurrence or progression among responders overall.	Through completion of follow-up (estimated to be 6 months and 25 weeks)

Trial Locations

Locations (1)

Washington University School of Medicine; 🇺🇸 Saint Louis, Missouri, United States