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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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00436605
Enrollment
39
Registered
2007-02-19
Start date
2006-12-31
Completion date
2010-11-30
Last updated
2014-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent Melanoma, Stage IIIA Melanoma, Stage IIIB Melanoma, Stage IIIC Melanoma, Stage IV Melanoma

Brief summary

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.

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.

Interventions

DRUGdasatinib

Sponsors

National Cancer Institute (NCI)
Lead SponsorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Number of Subjects With Objective Response(Partial Response and Complete Response) as Measured by RECIST CriteriaAfter every 8 weeks (or 2 courses), assessed up to 4 weeks after completion of treatmentOnly 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.
Progression-free SurvivalTime from start treatment to time of progression, assessed up to 6 monthsProgression 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

Countries

United States

Participant flow

Participants by arm

ArmCount
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
39
Total39

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyProtocol Violation3

Baseline characteristics

CharacteristicTreatment (Kinase Inhibitor Therapy)
Age, Continuous64 years
Sex: Female, Male
Female
13 Participants
Sex: Female, Male
Male
26 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
39 / 39
serious
Total, serious adverse events
20 / 39

Outcome results

Primary

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.

Time frame: After every 8 weeks (or 2 courses), assessed up to 4 weeks after completion of treatment

ArmMeasureValue (NUMBER)
Treatment (Kinase Inhibitor Therapy)Number of Subjects With Objective Response(Partial Response and Complete Response) as Measured by RECIST Criteria2 participants
Primary

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 frame: Time from start treatment to time of progression, assessed up to 6 months

ArmMeasureValue (MEAN)
Treatment (Kinase Inhibitor Therapy)Progression-free Survival8 weeks

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026