Individualized Temozolomide in Treating Patients With Stage IV Melanoma That Cannot Be Removed By Surgery

NCT ID: NCT01328535

Last Updated: 2020-10-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 25 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-01-31
• Study Completion Date: 2018-07-11

Brief Summary

This clinical trial studies individualized temozolomide (TMZ) in treating patients with stage IV melanoma that cannot be removed by surgery. Drugs used in chemotherapy, such as TMZ, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving TMZ at different times, which are determined individually for each patient based on the phase (biorhythm) of the immune system response against the tumor may allow for a better drug response and may kill more tumor cells

Detailed Description

PRIMARY OBJECTIVES: I. To assess the clinical activity of timed administration of TMZ therapy in patients with stage IV melanoma who have or have not received prior chemotherapy for metastatic melanoma. SECONDARY OBJECTIVES: I. To assess the toxicity profile of timed administration of TMZ therapy in patients with stage IV melanoma who have or have not received prior chemotherapy for their metastatic disease. II. To evaluate the parameters of immune homeostasis that are associated with the anti-tumor immune biorhythm in order to gain insight into the mechanism of the observed clinical and immunological effect of timed TMZ chemotherapy. III. To evaluate the impact of timed TMZ chemotherapy on immune biomarkers and the anti-tumor immune biorhythms. OUTLINE: Prior to initiation of therapy patients will undergo a period of immunologic monitoring to analyze the bioperiodicity of their anti-tumor immune response. Patients with an established biorhythm will receive TMZ orally (PO) starting on the recommended day for 5 days. Treatment repeats every 21-42 days (based on the established biorhythm) until of disease progression or unacceptable toxicity. Patients without an established biorhythm are given the option to go off study or receive TMZ PO on days 1-5. Courses repeat every 28 days until disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up for up to 2 years.

Conditions

Recurrent Melanoma; Stage IV Melanoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment (individualized chemotherapy)

Patients with an established biorhythm receive TMZ PO on recommended day for 5 days. Treatment repeats every 21-42 days until disease progression or unacceptable toxicity. Patients without an established biorhythm receive TMZ PO on days 1-5. Courses repeat every 28 days until disease progression or unacceptable toxicity.

Group Type: EXPERIMENTAL

temozolomide

Intervention Type: DRUG

Given PO

flow cytometry

Intervention Type: OTHER

Correlative studies

staining method

Intervention Type: OTHER

Correlative studies

biopsy

Intervention Type: PROCEDURE

Optional correlative studies

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

Interventions

temozolomide

Given PO

Intervention Type: DRUG

flow cytometry

Correlative studies

Intervention Type: OTHER

staining method

Correlative studies

Intervention Type: OTHER

biopsy

Optional correlative studies

Intervention Type: PROCEDURE

laboratory biomarker analysis

Correlative studies

Intervention Type: OTHER

Other Intervention Names

SCH 52365; Temodal; Temodar; TMZ; Staining; biopsies

Eligibility Criteria

Inclusion Criteria

• Histologic/cytologic proof of stage IV malignant melanoma not amenable to surgery
• Any number of previous chemotherapy regimens (except those containing TMZ or dacarbazine [DTIC]) in the metastatic setting are allowed as long as >= 4 weeks have elapsed from last treatment
• Measurable disease defined as at least one lesion whose longest diameter can be accurately measured as >= 1.0 cm with spiral CT scan, or ≥ 2 cm with computed tomography (CT) component of a positron emission tomography (PET)/CT; Note: disease that is measurable by physical examination only is not eligible
• Life expectancy of >= 3 months
• Eastern Cooperative Oncology Group (ECOG) performance score of 0, 1, or 2
• Recovered from side effects that might interfere with the protocol therapy and: - >= 4 weeks must have elapsed from last radiation treatment to time of study entry - >= 4 weeks must have elapsed from the last chemotherapy administration to time of study entry
• Absolute neutrophil count (ANC) >= 1500/mL
• Platelet count >= 100,000/mcl
• Hemoglobin >= 9gm/mcl
• Creatinine =< 2.5 x upper limit of normal (ULN)
• Aspartate aminotransferase (AST) =< 3 x ULN
• Negative serum pregnancy test done =< 7 days prior to registration, for women of childbearing potential only
• Ability to understand and the willingness to sign a written informed consent document
• Willingness to return to Mayo Clinic Rochester for follow-up, except for some appointments that can be made with the local physician
• Patient willing to provide research blood samples

Exclusion Criteria

• Receiving any other investigational agents including those for symptom management
• Uncontrolled intercurrent illness including, but not limited to, the following: - Active infection - Congestive heart-failure (New York Heart Association [NYHA] grade III or IV)
• Pregnant or breast feeding women, or women of child-bearing potential (and/or their partners) who are unwilling to utilize an approved method of birth control during the study and for 1 month afterward
• History of other malignancy < 5 years with the exception of basal cell or squamous cell carcinoma of the skin treated with local resection only, limited stage prostate cancer treated with surgery or radiation therapy with currently undetectable prostate-specific antigen (PSA), or carcinoma in situ of the cervix
• Known standard therapy for the patient's disease that is potentially curative or proven capable of extending life expectancy
• Known immunosuppression (i.e. chronic steroid use) or autoimmune disorder
• Human immunodeficiency virus (HIV) positive
• Current or known history of hepatitis
• Previous treatment with DTIC or TMZ
• Previous immunotherapy treatment for metastatic disease in the preceding 2 months; Note: immunotherapy in the adjuvant setting is allowed
• Previously untreated brain metastases; Note: patients with previously treated brain metastases are allowed as long as these are radiologically stable for >= 3 months and the patient is off steroids for >= 4 weeks

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Mayo Clinic

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Roxana Dronca, M.D.

Role: STUDY_CHAIR

Mayo Clinic

Locations

Mayo Clinic

Rochester, Minnesota, United States

Countries

United States

Other Identifiers

NCI-2011-00449

Identifier Type: REGISTRY

Identifier Source: secondary_id

MC1076

Identifier Type: OTHER

Identifier Source: secondary_id

10-008497

Identifier Type: OTHER

Identifier Source: secondary_id

MC1076

Identifier Type: -

Identifier Source: org_study_id