Temozolomide and Sunitinib Malate in Treating Patients With Stage III or Stage IV Malignant Melanoma

Completed · Phase 1

Conditions studied: Metastatic Melanoma

In brief

RATIONALE: Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Sunitinib malate 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. Giving temozolomide together with sunitinib malate may kill more tumor cells. Phase II was never conducted due to toxicity in phase I. PURPOSE: This phase I/II trial is studying the side effects and best dose of sunitinib malate when given together with temozolomide and to see how well they work in treating patients with stage III or stage IV malignant melanoma.

Key facts

Study ID

NCT01005472

Run by

Jonsson Comprehensive Cancer Center

People needed

16

Starts

2008-12-01

Expected to finish

2018-01-17

Last updated by the study team

2020-08-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically confirmed Stage IIIC unresectable cutaneous or mucosal melanoma with measureable disease or stage IV cutaneous, mucosal or ocular melanoma with measureable disease.
• ECOG performance status of 0-2
• age greater than or equal to 18 years
• ANC ≥ 1,500/µL
• Platelet count ≥ 100,000/µL
• Hemoglobin ≥ 10.0 g/dL
• Creatinine ≤ 2 times upper limit of normal (ULN)
• Total bilirubin ≤ 2 times ULN
• LDH ≤ 5 times ULN
• AST or ALT ≤ 2.5 times ULN (≤ 5 times ULN if liver metastasis is present)
• LVEF ≥ 50% on screening ECHO
• women of childbearing potential must have a negative urine or serum pregnancy test upto 28 days prior to commencement of dosing.
• Fertile patients must use effective contraception during and for ≥ 6 months after completion of study treatment
• Willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures
• before study entry , written informed consent must be obtained. Written informed consent must be obtained from patient prior to performing any study related procedures.

You may not qualify if…

• pregnant or nursing
• any following within the past 12 months:
• Myocardial infarction
• Severe and/or unstable angina
• Coronary and/or peripheral artery bypass graft
• Symptomatic congestive heart failure
• Cerebrovascular accident or transient ischemic attack
• Pulmonary embolism
• ongoing cardiac dysrhythmias ≥ grade 2, according to NCI CTCAE v3.0
• prolonged QTc interval on baseline EKG
• uncontrolled hypertension (i.e., blood pressure > 150/100 mm Hg despite optimal medical therapy)
• pre-existing thyroid abnormality with thyroid function that cannot be maintained in the normal range with medication
• any known clinically uncontrolled infectious disease, including HIV positivity or AIDS-related illness
• severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration or may interfere with the interpretation of study results, and, in the judgment of the investigator, would make the patient inappropriate for study entry
• prior chemotherapy for melanoma, except for chemotherapy given during isolated limb perfusion for stage IIIC disease
• Prior adjuvant immunotherapy and/or immunotherapy for metastatic disease allowed
• prior major surgery, radiotherapy, or immunotherapy within 4 weeks of starting therapy
• treatment with potent CYP3A4 inhibitors 7 days before study dosing
• treatment with potent CYP3A4 inducers 12 days before study dosing
• concurrent treatment on another clinical trial (Concurrent participation on supportive care trials or non-treatment trials (e.g., quality-of-life trials) allowed).
• concurrent chemotherapy, immunotherapy, biological therapy, or investigational drugs
• concurrent drugs with dysrhythmic potential, including any of the following:
• Terfenadine
• Quinidine
• Procainamide

Where it is running

• University of California Los Angeles (UCLA) — Los Angeles, California, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.