Evaluation of Lucanthone to Whole Brain Radiation Therapy in Patients With Brain Metastases From Non-Small Cell Lung Cancer

Phase 2

Withdrawn

• Conditions: Brain Metastases; Non-small Cell Lung Cancer
• Interventions: Other: Placebo; Drug: Lucanthone

• Registration Number: NCT02014545
• Lead Sponsor: Wake Forest University Health Sciences

Brief Summary

This is a randomized, double blind placebo controlled study to evaluate safety and efficacy of lucanthone administered as an adjunct to patients receiving whole brain radiation therapy (WBRT) as primary treatment for brain metastases secondary to non-small cell lung cancer.

Detailed Description

Eligible patients for this trial will be randomized to lucanthone or placebo in a ratio of 1:1. The treatment will consist of WBRT given in a dose of 30 Gy in ten fractions. Lucanthone/placebo will be given as an adjunct to the WBRT on days that WBRT is administered. Tumor assessments will be done with a brain MRI. Radiological assessments on the tumor will be made periodically throughout the study and will be discontinued at the time of tumor progression. Safety will be evaluated for one year during the study period and survival data will be collected thereafter.

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: 2013-12-12
• Study First Submitted QC: 2013-12-12
• Study First Posted: 2013-12-18
• Study Start: 2016-01
• Primary Completion: 2017-11-29
• Study Completion: 2017-11-29
• Status Verified: 2018-07
• Last Update Submitted: 2018-07-03
• Last Update Posted: 2018-07-05

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• The patient has given informed consent.
• The patient is willing and able to abide by the protocol.
• The patient is between age 18 and 70 (between 19 and 70 in Alabama).
• The patient has histologically proven NSCLC with radiologically documented brain metastases.
• Newly diagnosed or stable systemic disease, on or off systemic therapy.
• If receiving systemic therapy for NSCLC, at least two weeks since patient received systemic therapy.
• Able to withhold systemic therapy for duration of WBRT therapy.
• If the patient is of childbearing potential, he/she is using an acceptable/effective method of contraception.
• The patient's Karnofsky Score is greater than or equal to 70%.

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Exclusion Criteria

• Patient has a diagnosis of recurrent brain metastases.
• The patient has an absolute neutrophil count less than or equal to 1.5 X 10 9/L.
• The patient has a screening platelet count less than 100,000/uL.
• The patient has a screening bilirubin greater than 1.6 mg/dL.
• The patient has a screening creatinine greater than 2.25 mg/dL in men and 1.8 mg/dL in women.
• The patient has a screening ALT/AST greater than 2.5 times the upper limit of the laboratory reference range.
• The patient has an unstable medical condition or significant comorbid pathophysiology (e.g. active infection, poorly controlled diabetes, unstable angina, severe heart failure) that would interfere with his/her participation in the study.
• The patient is enrolled, or plans to enroll, in a concurrent treatment protocol with another investigational product.
• The patient has received prior chemotherapy or radiation therapy within two weeks of beginning WBRT on protocol.
• The patient is allergic to gadolinium contrast.
• More than 21 days has or will elapse between the brain MRI documenting the brain metastases and the initiation of WBRT.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
WBRT + Placebo	Placebo	Patients will receive prophylactic cranial irradiation at 3 Gy per fraction, 5 days per week, for 2 weeks to a total dose of 30 Gy.
WBRT + Lucanthone	Lucanthone	Treatment will consist of WBRT given in a dose of 30 Gy in ten fractions with lucanthone given as an adjunct. Lucanthone will be administered as 25 mg and 100 mg tablets to be swallowed. Dosage will be one of the following: 250 mg bid, 250 tid, or 375 mg tid.

Primary Outcome Measures

Name	Time	Method
Determine the efficacy of lucanthone when given during WBRT	2 weeks to 13 months	Progression free survival at 6 months and one year, overall response rate at months 1, 4, 7, 10, and 13 months and overall survival at 13 months will be evaluated. MRI brain scans will be performed baseline and months 1, 4, 7, 10, and 13. Objective assessments of overall response will be based on tumor assessments from MRI scans interpreted using the Revised Assessment in Neuro-Oncology (RANO) criteria.

Secondary Outcome Measures

Name	Time	Method
Evaluate the safety and toxicity of lucanthone when used in combination with standard doses of WBRT in the primary treatment of brain metastases secondary to non-small cell lung cancer	2 weeks to 13 months	Safety will be monitored throughout the study by physical exams, review of adverse events, and laboratory studies.

Trial Locations

Locations (1)

Comprehensive Cancer Center of Wake Forest University; 🇺🇸 Winston-Salem, North Carolina, United States