A Pilot Study of Trientine With Vemurafenib for the Treatment BRAF Mutated Metastatic Melanoma
Information source: Duke University
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Melanoma
Intervention: Vemurafenib and Trientine (Drug)
Phase: Phase 1
Status: Active, not recruiting
Sponsored by: Duke University Official(s) and/or principal investigator(s): April K Salama, MD, Principal Investigator, Affiliation: Duke University
Summary
The purpose of this study is to evaluate the safety of combination therapy with vemurafenib
and trientine in patients with BRAF mutated metastatic melanoma.
Vemurafenib is a drug that is currently approved by the United States Food and Drug
Administration (FDA) and by the European Medicines Agency (EMA) to treat adult patients with
melanoma that has spread to other parts of the body or cannot be removed by surgery. It can
only be used in patients whose cancer has a change (mutation) in the "BRAF" gene.
Preclinical data suggests that use of a copper chelator (reducer) is a strategy to block
cellular signaling activity which would result in anti-tumor effects (slow tumor growth).
Trientine is a copper chelator and is FDA approved for the treatment of Wilson's disease (a
disease of copper metabolism) and is generally well tolerated. It works by binding to copper
to help remove it from the body. Trientine is not FDA approved for the treatment of
melanoma and its use in this study is investigational. "Investigational" means the study
drug is still being tested in research studies.
All patients will receive vemurafenib at 960mg PO twice daily with continuous dosing in
combination with trientine in escalating doses. The dose of trientine will depend on what
portion of the study.
In order to participate in the study, patients must test positive for the change (mutation)
in the BRAF gene.
Clinical Details
Official title: A Pilot Study of Trientine With Vemurafenib for the Treatment BRAF Mutated Metastatic Melanoma
Study design: Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Maximum Tolerated Dose
Secondary outcome: Overall ResponseProgression Free Survival (PFS) Overall Survival (OS) The change in phosphorylated Erk kinase activity relative to total Erk kinase activity The change in phosphorylated MEK kinase activity relative to total MEK kinase activity The change in the expression of the copper transporter CTR1 Incidence of hyperproliferative skin lesions, specifically cutaneous squamous cell carcinomas and keratoacanthomas
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion criteria
1. Willing and able to give written informed consent.
2. ECOG performance status ≤ 1
3. Histologic diagnosis of unresectable stage IIIC or stage IV melanoma that is BRAF
V600 mutation positive
4. Stable, treated brain metastases are allowed. Stable brain metastases are defined as
stable on MRI 4 weeks after the completion of radiation, and currently asymptomatic
no longer requiring corticosteroids for 2 weeks prior to the initiation of study
drug.
5. Cutaneous tumor deposits that, in the opinion of the investigator are amenable to
sequential biopsies for correlative analyses. In addition to these, all patients must
have measurable disease (i. e., present with at least one measurable lesion per
RECIST, version 1. 1).
6. Able to swallow and retain oral medication and must not have any clinically
significant gastrointestinal abnormalities that may alter absorption such as
malabsorption syndrome or major resection of the stomach or bowels.
7. Required values for initial laboratory tests:
- WBC ≥ 2000/uL
- ANC ≥ 1000/uL
- Platelets ≥ 75 x 103/uL
- Hemoglobin ≥ 9 g/dL (≥ 80 g/L; may be transfused)
- Creatinine ≤ 2. 0 x ULN
- AST/ALT ≤ 2. 5 x ULN for patients without liver metastasis, ≤ 5 times for
liver metastases
- Bilirubin ≤ 2. 0 x ULN, (except patients with Gilbert's Syndrome, who must have
a total bilirubin less than 3. 0 mg/dL)
8. Women of childbearing potential (WOCBP) must be using an adequate method of
contraception to avoid pregnancy throughout the study and for up to 26 weeks after
the last dose of investigational product, in such a manner that the risk of pregnancy
is minimized. WOCBP include any female who has experienced menarche and who has not
undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation,
or bilateral oophorectomy) or is not post-menopausal. Post-menopause is defined as:
- Amenorrhea ≥ 12 consecutive months without another cause, or
- For women with irregular menstrual periods and taking hormone replacement
therapy (HRT), a documented serum follicle stimulating hormone (FSH) level ≥ 35
mIU/mL.
Women who are using oral contraceptives, other hormonal contraceptives (vaginal products,
skin patches, or implanted or injectable products), or mechanical products such as an
intrauterine device or barrier methods (diaphragm, condoms, spermicides) to prevent
pregnancy, or are practicing abstinence or where their partner is sterile (eg, vasectomy)
should be considered to be of childbearing potential.
WOCBP must have a negative serum pregnancy test (minimum sensitivity 25 IU/L or equivalent
units of HCG) within 72 hours.
Men of fathering potential must be using an adequate method of contraception to avoid
conception throughout the study [and for up to 26 weeks after the last dose of
investigational product] in such a manner that the risk of pregnancy is minimized.
Exclusion Criteria
1. Prior treatment with a BRAF or MEK inhibitor for metastatic melanoma (treatment in
the adjuvant setting is allowed)
2. Any other malignancy form which the patient has been disease-free for less than 2
years, with the exception of adequately treated and cured basal or squamous cell skin
cancer, superficial bladder cancer, carcinoma in situ of the cervix, or DCIS.
Patients with prior malignancies that are not considered to be an active problem may
be enrolled at the discretion of the investigator, regardless of time frame.
3. Women of childbearing potential (WOCBP), defined above in Section 4. 1, who:
1. are unwilling or unable to use an acceptable method of contraception to avoid
pregnancy for their entire study period and for at least 26 weeks after
cessation of study drug, or
2. have a positive pregnancy test at baseline, or
3. are pregnant or breastfeeding.
4. Anti-cancer therapy within 28 days prior to starting on therapy
5. Any serious or unstable pre-existing medical conditions psychiatric disorders, or
other conditions that could interfere with the subject's safety, obtaining informed
consent, or compliance with study procedures.
6. Known history of Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV), or
Hepatitis C Virus (HCV) infection (with the exception of chronic or cleared HBV and
HCV infection which will be allowed).
7. A history or evidence of cardiovascular risk including any of the following:
1. A QTc interval ≥ 500 ms at screening
2. A history or evidence of current clinically significant uncontrolled
arrhythmias; Exception: Subjects with atrial fibrillation controlled for > 30
days prior to randomization are eligible.
3. A history (within 6 months prior to randomization) of acute coronary syndromes
(including myocardial infarction or unstable angina), coronary angioplasty
4. A history or evidence of current ≥Class II congestive heart failure as defined
by the New York Heart Association (NYHA) guidelines
5. Treatment refractory hypertension defined as a blood pressure of systolic> 150
mmHg and/or diastolic > 100 mm Hg which cannot be controlled by antihypertensive
therapy;
6. Patients with intra-cardiac defibrillators or permanent pacemakers;
8. A history or current evidence/risk of retinal vein occlusion (RVO) or central serous
retinopathy (CSR) including:
a. Presence of predisposing factors to RVO or CSR (e. g., uncontrolled glaucoma or
ocular hypertension, uncontrolled hypertension, uncontrolled diabetes mellitus, or a
history of hyperviscosity or hypercoagulability syndromes)
9. Females who are nursing
10. A known diagnosis of Wilson's disease.
11. Patients with clinical symptoms consistent with active gastritis.
12. Patients with a condition that, in the opinion of the investigator, would interfere
with the absorption of oral medication will be excluded from the study.
13. Patients requiring iron supplementation will be excluded.
Locations and Contacts
Duke University Medical Center, Durham, North Carolina 27710, United States
Additional Information
Starting date: April 2014
Last updated: March 5, 2015
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