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Study Summary
No. 2005-0143:.......Melanoma......Wen-Jen Hwu......Melanoma Medical Oncology
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Study Summary Title
Study Summary
Number:
2005-0143
Study Title:Randomized Phase II Neoadjuvant Study of Temozolomide alone or with Pegylated Interferon-alpha 2b in Patients with Resectable AJCC Stage IIIB/IIIC or Stage IV (M1a) Metastatic Melanoma
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Physician New Patient Referral
Name:Wen-Jen HwuPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Melanoma Medical OncologyReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-792-7217
Contact us about clinical trials
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General Information
Disease Group:MelanomaSupported By:N/A
Phase of Study:Phase IIReturn
Visit:
During neo-adjuvant therapy, every 2 weeks for 8 weeks. During adjuvant
therapy, every 4 weeks for 24 weeks. During follow-up, every 3 months for Year
1, every 4 months for Year 2, every 6 months for Years 3-5, and annually for
Year 6 and beyond.
Treatment
Agents:
Pegylated Interferon-alpha 2b
Temozolomide
Home Care:N/A
Treatment Loc:Independent Multicenter Arrangements
Estimated
Length of Stay
in Houston:
Length of stay for surgery ranges 2-5 days.
Description/
Intervention:
The goal of this clinical research study is to learn if temozolomide alone or
given with pegylated interferon alpha-2b can help to control metastatic
melanoma. Researchers also want to study the safety of these 2 treatments.
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Study Objectives / Outcomes
1. To determine the anti-tumor activity (pathological response CR+PR) and toxicity of temozolomide (TMZ) alone or in combination with pegylated interferon alpha-2b (PGI) in patients with resectable stage IIIC or stage IV (M1a) metastatic melanoma prior to definitive surgical resection.
2. To determine the relapse-free survival, overall survival and the impact of tumor response to chemotherapy in these patients.
3. To differentiate the in vivo treatment effects of TMZ alone vs.TMZ plus PGI and correlate with clinical outcome by analysis the pre- and post-treatment tumors and peripheral blood mononuclear cells with respect to:
      1) Known cellular and molecular markers of apoptosis and cell proliferation,
      2) Promotor methylation status of the DNA repair enzyme O6-methylguanine-DNA methyltransferase (MGMT),
      3) DNA sequence variability of tumor suppressor genes and DNA repair enzymes,
      4) Tumor genomic expression profiles analysis by cDNA microarray and protein array
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Study Status Information
Study Activation / Registration Date:08/31/2006
IRB Review and Approval Date:12/07/2005
Study Type:Phase Ii Or Phase I/Ii
Recruitment Status:Open
Projected Accrual:124
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Histologically documented diagnosis of melanoma metastases.

2) Stage IIIB/IIIC (N2b, N2c and N3) or stage IV (M1a) melanoma patients with measurable and potentially resectable metastases without clinical and radiological evidence of other distant metastases.

3) An ECOG performance status of 0-1.

4) Age 18 or older.

5) Adequate organ function defined as follows: a.) Absolute granulocytes greater than or equal to 1,000/mm^3 and Platelets greater than or equal to 100,000/mm^3, b.) Serum bilirubin and serum creatinine of less than or equal to 1.5 times upper limit of laboratory normal. If serum creatinine is greater than 1.5 times upper limit of laboratory normal, the urine creatinine clearance must be greater than 60 ml/min., c.) SGOT (AST), SGPT (ALT) and alkaline phosphatase less than or equal to 3 times upper limit of laboratory normal.

6) Patients have not had any previous systemic chemotherapy for metastatic melanoma. Prior biologic therapy, targeted therapy or immunotherapy are allowable, but must be at least 2 weekssince prior therapy before starting study drugs. No other concurrent chemotherapy, immunotherapy, or radiotherapy.

7) Prior radiation therapy used to enhance local regional control is permitted, but must be at least 2 weeks since prior therapy before starting study drugs. In addition, the patient must have unirradiated metastatic sites for response evaluation and has fully recovered from its toxicity. Lesions within the prior field of radiation may only be used as indicator lesions if there has been recent evidence of disease progression after .

8) Ability to understand and sign an informed consent form, indicating awareness of the investigational nature of this study.

Exclusion Criteria:1) Significant cardiac or pulmonary dysfunction, such as a history of severe cardiovascular disease, myocardial infarction within 6 months of the start of treatment, unstable angina, Class III or Class IV congestive heart failure, ventricular arrhythmia, or any uncontrolled arrhythmia.

2) Current significant psychiatric illness.

3) Serious infection requiring intravenous antibiotics, or any non-malignant medical illnesses that are uncontrolled or whose control may be jeopardized by complications of this therapy.

4) Frequent vomiting or any medical condition (e.g. partial bowel obstruction) that could interfere with oral medication intake.

5) Autoimmune or immunosuppressive disorders (e.g. HIV or AIDS-related illness).

6) Patients who require therapy with systemic corticosteroids.

7) No evidence of active secondary malignancy that requires chemotherapy within the past 2 years (excluding non-melanoma skin cancer, and/or all carcinoma in-situ)

8) Pregnant or lactating women are ineligible. Women of childbearing potential must have a negative urine pregnancy test within a week of initiation of therapy. All patients must agree to use medically approved contraceptive measures to prevent pregnancy during treatment.

9) Any other medical condition or reason that, in the principal investigator's opinion, makes the patient unsuitable to participate in a clinical trial.

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Links
Registration Number: NCT00525031
Study Information on Clinical Trials Registry (clinicaltrials.gov)

Other Links:
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Results


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