Dasatinib in Treating Patients With Stage III Melanoma That Cannot Be Removed By Surgery or Stage IV Melanoma

A Phase 2 Study of Dasatinib in Advanced Melanoma

This phase II trial is studying how well dasatinib works in treating patients with stage III melanoma that cannot be removed by surgery or stage IV melanoma. Dasatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Study Overview

• Status: Completed
• Conditions: Recurrent Melanoma; Stage IV Melanoma; Stage IIIA Melanoma; Stage IIIB Melanoma; Stage IIIC Melanoma
• Intervention / Treatment: Drug: dasatinib

Detailed Description

PRIMARY OBJECTIVES:

I. Determine the objective response rate in patients with stage III unresectable or stage IV melanoma treated with dasatinib.

II. Determine the progression-free survival of patients treated with this drug.

SECONDARY OBJECTIVES:

I. To assess the expression of targets of Dasatinib prior to treatment by obtaining pre-treatment biopsies or examining paraffin-embedded tissues from previous tumor resections.

II. In selected patients (approximately 5-10) where tumor tissue is available pre-treatment and can be obtained post-treatment with Dasatinib (21 days after initiation of therapy), to determine if Dasatinib induces changes in expression of selected targets and downstream mediators, including MEK, ERK and RSK-1.

III. To assess toxicity.

OUTLINE:

Patients receive oral dasatinib twice daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 4 weeks.

• Study Type: Interventional
• Enrollment (Actual): 39
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • Connecticut
    • New Haven, Connecticut, United States, 06520
      • Yale University
  • Minnesota
    • Minneapolis, Minnesota, United States, 55455
      • Masonic Cancer Center, University of Minnesota

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 confirmed stage III unresectable or stage IV melanoma
• Measurable disease
• Must have evidence of tumor growth or new lesions within the past 6 months
• No large pleural effusions

• No known brain metastases or leptomeningeal metastases

  • Previously treated brain metastases allowed provided there is no requirement for steroids AND no evidence of progression for ≥ 8 weeks after treatment
• ECOG performance status (PS) 0-1 OR Karnofsky PS 70-100%
• Life expectancy > 3 months
• WBC ≥ 3,000/mm³
• Absolute neutrophil count ≥ 1,500/mm³
• Platelet count ≥ 100,000/mm³
• Hemoglobin ≥ 9.0 g/dL (transfusions allowed)
• Bilirubin ≤ 1.5 mg/mL
• AST and ALT ≤ 2.5 times upper limit of normal (ULN)
• PT/INR and PTT normal
• Creatinine ≤ 1.5 times ULN OR creatinine clearance ≥ 60 mL/min

• No medical condition that may affect the ability to swallow and retain dasatinib tablets, including any of the following:

  • Gastrointestinal tract disease resulting in an inability to take oral medication
  • Requirement for IV alimentation
  • Prior surgical procedures affecting absorption
  • Active peptic ulcer disease

• No clinically significant cardiovascular disease, including any of the following:

  • Myocardial infarction or ventricular tachyarrhythmia within the past 6 months
  • Prolonged QTc > 480 msec
  • Major conduction abnormality (unless a cardiac pacemaker is present)

• No uncontrolled intercurrent illness including, but not limited to, any of the following:

  • Ongoing or active infection

  • History of significant congenital or acquired bleeding disorder, including any of the following:

    • Von Willebrand's disease
    • Antifactor VIII antibodies
  • Dyspnea at rest or with minimal exertion
  • Uncontrolled seizure disorder
  • Psychiatric illness or social situations that would preclude study compliance
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No other active malignancy within the past 3 years except curatively treated stage I malignancies or resected skin carcinomas
• Recovered from prior therapy
• Prior adjuvant therapy for stage II or III melanoma allowed
• No prior cytotoxic therapy for metastatic melanoma
• No prior dasatinib or other inhibitors of src, bcr-abl, c-Kit, EPHA2, and PDGFRβ
• No more than 2 prior immunomodulator therapies for metastatic melanoma
• At least 1 week since prior and no concurrent warfarin or other anticoagulants or medications that inhibit platelet function (including acetylsalicylic acid)

• At least 1 week since prior and no concurrent steroids or other immunosuppressive agents

  • Concurrent steroids to treat induced pleural effusions allowed

• At least 3 weeks since prior immunomodulators including, but not limited to, any of the following:

  • Aldesleukin
  • Cancer vaccines
  • T-cell-activating monoclonal antibodies

• At least 4 weeks since prior radiotherapy

  • Prior palliative radiotherapy to a single site of disease allowed (tumor is not considered evaluable for response unless there is tumor progression at the site of radiation)
• More than 7 days since prior and no concurrent CYP3A4 inhibitors
• At least 7 days since prior and no concurrent agents with proarrhythmic potential
• No other concurrent investigational agents
• No other concurrent anticancer agents or therapies
• No concurrent enzyme-inducing anticonvulsant agents
• No concurrent grapefruit or grapefruit juice
• No concurrent combination antiretroviral therapy for HIV-positive patients
• No concurrent CYP3A4 inducers

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: Treatment (kinase inhibitor therapy); Patients receive oral dasatinib twice daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.	Drug: dasatinib; Other Names: BMS-354825; Sprycel

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Subjects With Objective Response(Partial Response and Complete Response) as Measured by RECIST Criteria	Only those patients who have measurable disease present at baseline, have received at least one course of therapy, and have had their disease re-evaluated will be considered evaluable for response. A Simon's optimum two-stage design will be used.	After every 8 weeks (or 2 courses), assessed up to 4 weeks after completion of treatment
Progression-free Survival	Progression will be evaluated in this study using the new international criteria proposed by the RECIST Committee. A Simon's optimum two-stage design will be used	Time from start treatment to time of progression, assessed up to 6 months

Collaborators and Investigators

• Sponsor: National Cancer Institute (NCI)
• Investigators: Principal Investigator: Harriet Kluger, Yale University

Study record dates

Study Major Dates

• Study Start: December 1, 2006
• Primary Completion (Actual): March 1, 2010
• Study Completion (Actual): November 1, 2010

Study Registration Dates

• First Submitted: February 15, 2007
• First Submitted That Met QC Criteria: February 15, 2007
• First Posted (Estimate): February 19, 2007

Study Record Updates

• Last Update Posted (Estimate): May 15, 2014
• Last Update Submitted That Met QC Criteria: April 29, 2014
• Last Verified: October 1, 2011

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; Protein Kinase Inhibitors; Dasatinib
• Other Study ID Numbers: NCI-2009-00219 (Registry Identifier: CTRP (Clinical Trial Reporting Program)); CDR0000528937; UMN-2007UC009; YALE-HIC-0608001765; HIC#0608001765 (Other Identifier: Yale University); 7758 (Other Identifier: CTEP); P30CA016359 (U.S. NIH Grant/Contract)