Sorafenib and Isolated Limb Infusion of Melphalan in Treating Patients With Stage III Melanoma of the Arm or Leg

Melanoma (Skin) Clinical Trial

Official title:

A Phase I Dose Escalation Trial to Evaluate Safety and Efficacy of Oral Sorafenib (Nexavar) With Regional Melphalan Via Normothermic Isolated Limb Infusion (ILI) in Patients With Intransit Extremity Melanoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00565968
• Other study ID #: Pro00001344
• Secondary ID: CDR0000575427
• Status: Completed
• Phase: Phase 1
• First received: November 29, 2007
• Last updated: March 5, 2015
• Start date: October 2007

Study information

• Verified date: March 2015
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as melphalan, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Sorafenib may also make tumor cells more sensitive to melphalan. Giving sorafenib together with an isolated limb infusion of melphalan may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of sorafenib when given together with an isolated limb infusion of melphalan in treating patients with stage III melanoma of the arm or leg.

Description:

OBJECTIVES:

Primary

• To determine the dose-limiting toxicities and maximum tolerate dose of systemic sorafenib tosylate in combination with regionally administered melphalan by isolated limb infusion in patients with stage IIIB or IIIC intransit extremity melanoma.

Secondary

• To characterize the safety and tolerability of this regimen in these patients.

• To assess the antitumor activity of this regimen, as evidenced by best overall response and duration of response, in these patients.

• To characterize the duration of progression-free survival of these patients.

• To characterize the pharmacokinetics of melphalan.

• To assess alterations in selected gene and protein expression profiles following treatment.

OUTLINE: This is a multicenter, dose-escalation study of sorafenib tosylate.

Patients receive oral sorafenib tosylate twice daily on days 1-14 and melphalan via isolated limb infusion into the upper or lower extremities on day 8.

Patients undergo tumor biopsies at baseline and in weeks 2 and 12 for gene expression analysis and western blot analysis. Patients also undergo blood sample collection periodically for pharmacokinetic analysis of melphalan.

After completion of study treatment, patients are followed every 3 months for 1 year and then every 6 months for 2 years.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. primary completion date: August 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed primary or recurrent extremity melanoma

• Stage IIIB or IIIC disease

• Patients with stage IIIC disease must have had regional lymph nodes previously removed

• Disease to be treated by regional therapy must be distal to the planned site of tourniquet placement

• Bidimensionally measurable disease by caliper or radiological method

• Must have identifiable target lesions for disease assessment

• Patients with a single lesion must have archived tumor tissue available for research analysis

• No stage IV disease

• No known brain metastasis

• Patients with neurological symptoms must have undergone a CT scan or MRI of the brain within the past 4 weeks to exclude brain metastasis

PATIENT CHARACTERISTICS:

• ECOG or Zubrod performance status 0-1

• Life expectancy > 6 months

• Hemoglobin = 9.0 g/dL

• WBC = 3,000/mm^3

• ANC = 1,500/mm^3

• Platelet count = 100,000/mm^3

• Total bilirubin = 1.5 x upper limit of normal (ULN)

• ALT and AST = 2.5 x ULN

• INR < 1.5 or PT/PTT normal

• Creatinine = 1.5 x ULN

• Not pregnant or nursing

• Negative serum pregnancy test

• Fertile patients must use effective contraception

• Must have a palpable femoral or axillary pulse in the extremity to be treated

• No cardiac disease, including any of the following:

• NYHA class III or IV congestive heart failure

• Unstable angina (i.e., angina symptoms at rest) or new onset angina within the past 3 months

• Myocardial infarction within the past 6 months

• No cardiac ventricular arrhythmias requiring antiarrhythmic therapy

• No uncontrolled hypertension, defined as systolic blood pressure (BP) > 150 mm Hg or diastolic BP > 90 mm Hg, despite optimal medical management

• No known HIV infection

• No chronic hepatitis B or C

• No active clinically serious infection > CTCAE grade 2

• No thrombotic or embolic events (e.g., cerebrovascular accident or transient ischemic attacks) within the past 6 months

• No signs or symptoms of vascular insufficiency (i.e., any history of blood clots or other ischemic peripheral vascular disease)

• No evidence or history of bleeding diathesis or coagulopathy

• No pulmonary hemorrhage or bleeding event = CTCAE grade 2 within the past 4 weeks

• No other hemorrhage or bleeding event = CTCAE grade 3 within the past 4 weeks

• No serious nonhealing wound, ulcer, or bone fracture

• No significant traumatic injury within the past 4 weeks

• No condition that impairs the patient's ability to swallow whole pills

• No malabsorption problem

• No known history of allergic reactions and/or hypersensitivity to melphalan, sorafenib tosylate, or any other agent used in the study

• No psychiatric condition or diminished capacity that would compromise giving informed consent, or interfere with study compliance

• No history of other malignancies, except for any of the following:

• Adequately treated basal cell or squamous cell carcinoma of the skin

• Curatively treated in situ carcinoma of the uterine cervix, prostate cancer, or superficial bladder cancer

• Other curatively treated solid tumor with no evidence of disease for = 5 years

PRIOR CONCURRENT THERAPY:

• Recovered from prior therapy

• No prior sorafenib tosylate

• Prior melphalan via isolated limb infusion allowed

• No antineoplastic therapy, radiotherapy, or any other investigational drug within the past 4 weeks

• No major surgery or open biopsy within the past 4 weeks

• No concurrent Hypericum perforatum (St. John wort) or rifampin

• Concurrent anti-coagulation treatment with warfarin or heparin allowed

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Melanoma
• Melanoma (Skin)

Intervention

Drug:
• melphalan

• sorafenib tosylate

Genetic:
• gene expression analysis

• protein expression analysis

• western blotting

Other:
• pharmacological study

Locations

Country	Name	City	State
United States	Memorial Sloan-Kettering Cancer Center	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
Duke University	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum tolerated dose		1 year	Yes
Secondary	Safety and tolerability		2 years	Yes
Secondary	Antitumor activity, as evidenced by best overall response and duration of response		3 years	No
Secondary	Duration of progression-free survival		3 years	No
Secondary	Pharmacokinetics of melphalan		3 years	No
Secondary	Tumor gene and protein expression profiles following treatment		3 years	No