A Phase II Study of Vemurafenib Combined With Acitretin in Patients With Advanced Melanoma

We propose to conduct a phase 2 study to assess whether the addition of acitretin to vemurafenib therapy is able to decrease the rate of cutaneous squamous cell carcinoma (cSCC) development, a known side effect of vemurafenib therapy, in patients with advanced melanoma. Further, we seek a preliminary assessment as to whether the addition of acitretin to vemurafenib enhances the clinical efficacy of this anti-melanoma agent.

Study Overview

• Status: Terminated
• Conditions: Malignant Melanoma
• Intervention / Treatment: Drug: Acitretin; Drug: Vemurafenib

• Study Type: Interventional
• Enrollment (Actual): 2
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • Arizona
    • Tucson, Arizona, United States, 85724
      • University of Arizona Cancer Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Histologically or cytologically confirmed advanced melanoma.
• BRAF mutation detected by DNA sequencing of exon 15.
• Age 18 or older.
• ECOG Performance Status 0-2.
• Appropriate tumor imaging studies (i.e. CT scan chest, abdomen and pelvis or PET/CT scan) performed within 28 days of study registration.
• Patients with melanoma measurable by RECIST 1.1 criteria will be monitored using this system for evidence of disease response/progression.
• Patients with a known history of brain metastases must have a diagnostic quality MRI of the brain or contrasted CT scan of the head performed within 28 days prior to registration.
• Female patients of child bearing capacity must have had 2 negative urine or serum pregnancy tests with a sensitivity of at least 25 mIU/mL before receiving the initial acitretin prescription. The first test (a screening test) is obtained by the prescriber when the decision is made to pursue acitretin therapy. The second pregnancy test (a confirmation test) should be done during the first 5 days of the menstrual period immediately preceding the beginning of acitretin therapy. The second test will be need to be repeated if not performed within 14 days prior to registration.
• Willingness to use at least two forms of contraception during sexual intercourse, including at least one form of barrier contraception, for at least 30 days prior to receiving the first dose of acitretin AND during the study period, AND up to 3 years after receiving the last dose of acitretin.
• Patients must agree not to consume alcoholic beverages while receiving acitretin and for 2 months after cessation of therapy.
• Electrocardiogram with QTc <450 ms at baseline.

• Patients must be evaluated for the following within 14 days prior to registration:

  • leukocytes >3,000/mcL
  • absolute neutrophil count >1,500/mcL
  • platelets >100,000/mcL
  • Hemoglobin >9.0 g/dL
  • AST(SGOT)/ALT(SGPT) <2.5 X institutional upper limit of normal
  • Alkaline phosphatase <2.5 X institutional upper limit of normal
  • Total bilirubin <1.5 X institutional upper limit of normal
  • Renal function serum creatinine <1.5 mg/dL OR 1.5 x institutional normal; alternatively, creatinine clearance as assessed by 24-hour urine collection ≥60 ml/min
  • Total cholesterol < 239 mg/dL or < 6.1 mmol/L
  • LDL < 159 mg/d or < 4.1mmol/L
  • HDL > 40 mg/dL or >1.0 mmol/L
  • Serum triglycerides < 199 mg/dL or < 2.2 mmol/L
  • Potassium 3.5-5.5 mMol/L
  • Magnesium 1.7-2.6mg/dL
  • Calcium 8.5-10.6 mg/dL

Exclusion Criteria:

• Known hypersensitivity to vemurafenib, acitretin, or vitamin A analogues.
• Uncontrolled hypertension.
• Serious and uncontrolled hypertriglyceridemia.
• Uncontrolled coronary artery disease or active anginal symptoms.
• Uncontrolled brain metastases.
• Concomitant malignancies or previous malignancies within the last 5 years, with the exception of adequately treated basal or squamous cell carcinoma of the skin, carcinoma in situ of the cervix, or low-grade prostate cancer.
• Myocardial Infarction, Transient Ischemic Attack (TIA), Cerebrovascular Accident (CVA) or symptomatic Congestive Heart Failure (CHF) within 6 months of study registration.
• Corrected QTc interval >450ms at baseline, history of congenital long QT syndrome, or known and uncorrectable electrolyte abnormalities.
• History of organ or hematologic transplant.
• Underlying defined genetic syndrome based on individual or family history predisposing to high risk of non-melanoma or melanoma skin cancer as assessed by the treating Oncologist.
• Concurrent use of St John's Wort.
• Concurrent (or within 60 days prior to acitretin dosing) use of methotrexate or other tetracyclines, phenytoin, vitamin A supplements, Tegison (etretinate) or progestin-only oral contraceptives.
• Pregnant or nursing.
• Receipt of any other investigational agents.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: Acitretin and Vemurafenib; Vemurafenib is self-administered at a dose of 960 mg (four 240 mg tablets) twice daily. The first dose should be taken in the morning and the second dose should be taken in the evening approximately 12 hours later. Each dose can be taken with or without a meal. Acitretin will initially be dosed at 25 mg orally per day with dosing altered every two weeks with a 50 mg dose.

Drug: Acitretin; A combination of Acitretin and Vemurafenib will be administered to determine if it reduces the incidence of biopsy-confirmed cSCC at 6 months; Other Names: Soriatane; Drug: Vemurafenib; A combination of Acitretin and Vemurafenib will be administered to determine if it reduces the incidence of biopsy-confirmed cSCC at 6 months; Other Names: Zelboraf

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Rate of Development of cSCC at 6 Months (Biopsy Confirmed).	6 months post treatment

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Participants With Adverse Events	The study period during which all AEs must be reported begins after informed consent is obtained and initiation of study treatment and ends 30 days following the last administration of study treatment or study discontinuation/termination, whichever is earlier. All adverse events will be classified using either the MedDRA term or NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.0	Baseline through 30 Days post Treatment

Collaborators and Investigators

• Sponsor: University of Arizona
• Investigators: Principal Investigator: Lee Cranmer, MD, PhD, University of Arizona

Study record dates

Study Major Dates

• Study Start: December 1, 2013
• Primary Completion (Actual): December 1, 2014
• Study Completion (Actual): July 1, 2015

Study Registration Dates

• First Submitted: January 24, 2014
• First Submitted That Met QC Criteria: January 28, 2014
• First Posted (Estimate): January 30, 2014

Study Record Updates

• Last Update Posted (Actual): December 26, 2018
• Last Update Submitted That Met QC Criteria: December 4, 2018
• Last Verified: December 1, 2018

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Neuroectodermal Tumors; Neoplasms, Germ Cell and Embryonal; Neoplasms, Nerve Tissue; Neuroendocrine Tumors; Nevi and Melanomas; Melanoma; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Antineoplastic Agents; Dermatologic Agents; Protein Kinase Inhibitors; Keratolytic Agents; Vemurafenib; Acitretin
• Other Study ID Numbers: 1312167559