E6201 and Dabrafenib for the Treatment of Central Nervous System Metastases From BRAF V600 Mutated Metastatic Melanoma
Study Details
Study Description
Brief Summary
This phase I tests the safety, side effects, and best dose of E6201 in combination with dabrafenib in treating patients with BRAF V600 mutated melanoma that has spread to the central nervous system (central nervous system metastases). E6201 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Dabrafenib is used in patients whose cancer has a mutated (changed) form of a gene called BRAF. It is in a class of medications called kinase inhibitors. It works by blocking the action of an abnormal protein that signals tumor cells to multiply. This helps stop the spread of tumor cells. Giving E6201 and dabrafenib together may work better in treating patients with BRAF V600 mutated melanoma that has spread to the central nervous system than either drug alone.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Detailed Description
PRIMARY OBJECTIVE:
- To determine the maximum tolerated dose of MEK-1/MEKK-1 inhibitor E6201 (E6201) in combination with dabrafenib in patients with central nervous system (CNS) metastases from BRAF V600- mutated metastatic melanoma.
SECONDARY OBJECTIVES:
-
To assess the time to first progression in subjects with CNS metastases due to metastatic melanoma with a BRAF V600 mutation treated with E6201 + dabrafenib.
-
To assess overall survival (OS) in subjects with CNS metastases due to metastatic melanoma with a BRAF V600 mutation treated with E6201 + dabrafenib.
-
To assess the adverse events profile of E6201 in combination with dabrafenib in subjects with CNS metastases due to metastatic melanoma with a BRAF V600 mutation treated with E6201 + dabrafenib.
CORRELATIVE RESEARCH OBJECTIVE:
- To assess the impact of BRAF mutational status (e.g., type, heterozygosity or homozygosity) in archival tissue with clinical outcome.
OUTLINE: This is a dose-escalation study of MEK-1/MEKK-1 inhibitor E6201 followed by a dose-expansion study.
Patients receive MEK-1/MEKK-1 inhibitor E6201 intravenously (IV) over 2 hours on days 1, 4, 8, 11, 15, and 18, and dabrafenib orally (PO) twice daily (BID) on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up every 6 months for up to 2 years from time of registration.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Treatment (E6201, dabrafenib) Patients receive MEK-1/MEKK-1 inhibitor E6201 IV over 2 hours on days 1, 4, 8, 11, 15, and 18, and dabrafenib PO BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. |
Drug: Dabrafenib
Given PO
Other Names:
Drug: MEK-1/MEKK-1 Inhibitor E6201
Given IV
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Maximum tolerated dose [Up to end of cycle 1 (1 cycle = 28 days)]
Secondary Outcome Measures
- Overall intracranial response rate [Up to 2 years]
Defined as the number of patients who have achieved CR or PR per Response Assessment in Neuro-oncology (RANO) for brain metastases criteria during treatment with E6201 plus dabrafenib divided by total number of evaluable patients. Responses will be summarized by simple descriptive summary statistics delineating complete and partial responses as well as stable and progressive disease in this patient population.
- Overall extracranial response rate [Up to 2 years]
Defined by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. Systemic response by RECIST 1.1 criteria for extracranial disease will be estimated using systemic response rate (SRR) - where SRR is defined as the number of evaluable patients achieving a response (partial response or complete response per RECIST 1.1) during treatment with study therapy divided by the total number of evaluable patients. Responses will be summarized by simple descriptive summary statistics delineating complete and partial responses as well as stable and progressive disease in this patient population.
- Incidence of adverse events [Up to 2 years]
The maximum grade for each type of adverse event will be recorded for each patient, and frequency tables will be reviewed to determine patterns. Additionally, the relationship of the adverse event(s) to the study treatment will be taken into consideration.
- Time to first progression [Up to 2 years]
Will be summarized descriptively.
- Overall survival [Up to 2 years]
Will be summarized descriptively.
Other Outcome Measures
- BRAF mutational status [Up to 2 years]
Correlations between BRAF mutational status (e.g., type, heterozygosity or homozygosity) and other outcome measures like response, and dose levels will be carried out in an exploratory manner. Descriptive statistics will form the basis of presentation of these data.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age >= 18 years
-
Histologically or cytologically confirmed stage IV metastatic BRAF V600-mutated melanoma
-
Documented metastasis of the primary tumor to the CNS
-
BRAF-mutation melanoma tumor status will be established prior to entry based on previous BRAF-gene analysis reports from a Clinical Laboratory Improvement Act (CLIA) qualified laboratory. If a report is not available, the mutation analysis will be performed at screening on archival tissue
-
At least one measurable brain metastasis 0.5 - 3.0 cm, as assessed by magnetic resonance imaging (MRI) or computed tomography (CT) with contrast =< 3 weeks prior to registration and does not require immediate local intervention (surgery or radiosurgery) NOTE: Tumor lesions in a previously irradiated area are not considered measurable disease; disease that is measurable by physical examination only is not eligible
-
Asymptomatic or symptomatic CNS metastasis
-
Other metastatic melanoma systemic disease is allowed, including leptomeningeal disease
-
Prior stereotactic radiosurgery and/or excision of up to 3 brain metastases is allowed
3 weeks before initiation of study treatment, provided neurological sequelae have resolved completely and at least one measurable metastasis with documented disease progression is present on MRI
-
Prior immunotherapy for metastatic disease is allowed, if >= 2 weeks have elapsed between the end of therapy and initiation of study treatment
-
Prior treatment with BRAF/MEK inhibitor therapy is allowed, if >= 2 weeks have elapsed between the end of therapy and initiation of study treatment
-
Prior melanoma adjuvant immunotherapy is allowed, if >= 6 months has elapsed between the end of therapy and initiation of study treatment
-
Prior melanoma adjuvant BRAF/MEK inhibitor treatment is allowed if >= 12 months has elapsed between the end of therapy and initiation of study treatment
-
Able to swallow and retain oral medication with no clinically significant gastrointestinal abnormalities that may alter absorption, such as malabsorption syndrome or major resection of the stomach or bowels
-
Stable dose of corticosteroids for CNS metastasis is allowed if >= 7 days
-
Seizures due to CNS metastases must be controlled with stable anti-epileptic treatment for >= 14 days
-
Bisphosphonates and/or denosumab are allowed
-
Life expectancy >= 3 months
-
Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2
-
Hemoglobin (Hb) >= 9 g/dL without ongoing transfusional support (obtained =< 15 days prior to registration)
-
Absolute neutrophil count (ANC) >= 1.0 x 10^9 cells/L without ongoing transfusional support (obtained =< 15 days prior to registration)
-
Platelets >= 75 x 10^9 cells/L without ongoing transfusional support (obtained =< 15 days prior to registration)
-
Creatinine =< 1.5 x the upper limit of normal (ULN), or calculated creatinine clearance >= 50 mL/minute per the Cockcroft-Gault formula (obtained =< 15 days prior to registration)
-
Total bilirubin =< 2 times ULN unless due to Gilbert's disease (obtained =< 15 days prior to registration)
-
Alanine aminotransferase (ALT)/aspartate aminotransferase (AST) =< 2.5 times ULN, or < 5 times ULN for subjects with liver metastases (obtained =< 15 days prior to registration)
-
Negative serum pregnancy test done =< 14 days prior to registration, for persons of childbearing potential only, defined as a female who has not undergone a hysterectomy or who has not been naturally post-menopausal for at least 24 consecutive months (i.e., who has had menses any time in the preceding 24 consecutive months)
-
Willing to use contraception
-
Sexually active persons of childbearing potential (PCBP) and persons able to father a child must agree to use adequate methods to avoid pregnancy throughout the study and for 28 days after the completion of study treatment
-
Provide written informed consent
-
Willing to return to enrolling institution for follow-up (during the Active Monitoring Phase of the study)
-
Ability to complete Patient Medication Diaries by themselves or with assistance
-
Willingness to have institution procure previous BRAF-gene analysis report(s) from a CLIA qualified laboratory, or if a report is not available, willingness to have institution procure archived tumor sample to establish BRAF-mutational melanoma tumor status prior to study
-
Ability to swallow
Exclusion Criteria:
-
Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm
-
Urgent need of treatment to prevent acute neurologic deterioration, including urgent neurosurgery or radiotherapy
-
Symptoms of uncontrolled intracranial pressure
-
Symptomatic or untreated spinal cord compression
-
Prior treatment with any chemotherapeutic or investigational agent for =< 4 weeks prior to registration
-
Prior treatment with > 2 lines of immunotherapy for metastatic disease
-
Prior treatment with > 1 line of a BRAF and/or MEK inhibitor for metastatic disease
-
Serious cardiac condition =< 6 months prior to registration, such as uncontrolled arrhythmia, myocardial infarction, unstable angina, or heart disease defined by the New York Heart Association (NYHA) class III or class IV
-
Failure to recover from acute, reversible effects of prior therapy regardless of interval since last treatment
-
Uncontrolled intercurrent non-cardiac illness including, but not limited to:
-
Ongoing or active infection requiring IV antibiotic usage within the last week prior to study treatment
-
Any other conditions that would limit compliance with study requirements or confound the interpretation of study results
-
Immunocompromised patients and patients known to be human immunodeficiency virus (HIV) positive and currently receiving antiretroviral therapy
-
NOTE: Patients known to be HIV positive, but without clinical evidence of an immunocompromised state, are eligible for this trial
-
Any of the following, because this study involves an agent that has known genotoxic, mutagenic and teratogenic effects:
-
Pregnant persons
-
Nursing persons
-
Persons of childbearing potential who are unwilling to employ adequate contraception
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Mayo Clinic in Florida | Jacksonville | Florida | United States | 32224-9980 |
Sponsors and Collaborators
- Mayo Clinic
- National Cancer Institute (NCI)
Investigators
- Principal Investigator: Hani M Babiker, Mayo Clinic
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- MC210703
- NCI-2022-04133
- MC210703
- P30CA015083