Suspended

Phase II Trial of Temozolomide for the Treatment of Mycosis Fungoides and the Sezary Syndrome

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What is being tested

temozolomide

Drug
Who is being recruted

Hemic and Lymphatic Diseases+10

+ Immune System Diseases

+ Immunoproliferative Disorders

Over 18 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 2
Interventional
Study Start: May 1998
See protocol details

Summary

Principal SponsorNorthwestern University
Last updated: June 6, 2012
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 1998

Actual date on which the first participant was enrolled.

OBJECTIVES: Determine the response rate to temozolomide in patients with relapsed mycosis fungoides or Sezary syndrome. Determine the toxic effects of this drug in these patients. Correlate pretreatment AGT activity in tumor cells with response to this drug in these patients. OUTLINE: This is a multicenter study. Patients receive oral temozolomide once daily on days 1-5. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity for a maximum of 1 year. Patients are followed every 3 months. PROJECTED ACCRUAL: A total of 12-37 patients will be accrued for this study within 2 years.

NCT00004106
Principal SponsorNorthwestern University
Last updated: June 6, 2012
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

29 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Hemic and Lymphatic DiseasesImmune System DiseasesImmunoproliferative DisordersLymphatic DiseasesLymphoma, Non-HodgkinLymphoproliferative DisordersNeoplasmsNeoplasms by Histologic TypeLymphoma, T-CellLymphomaMycosis FungoidesSezary SyndromeLymphoma, T-Cell, Cutaneous

Criteria

DISEASE CHARACTERISTICS: Histologically confirmed mycosis fungoides or Sezary syndrome Stage IB-IVB disease Must have failed at least one prior systemic therapy Generalized erythroderma allowed Measurable disease and at least one indicator lesion OR evaluable disease for erythrodermic patients only Prior radiotherapy to areas of measurable disease allowed if disease progression is present in the site or if measurable disease is present outside irradiation port PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 OR WHO 0-2 Life expectancy: At least 3 months Hematopoietic: WBC at least 3,000/mm^3 Absolute granulocyte count at least 1,500/mm^3 Platelet count at least 100,000/mm^3 Hepatic: Bilirubin no greater than 2.2 mg/dL SGOT or SGPT no greater than 2 times upper limit of normal (ULN) Alkaline phosphatase no greater than 2 times ULN Renal: Creatinine no greater than 2.0 mg/dL Cardiovascular: No New York Heart Association class III or IV heart disease No clinically significant peripheral venous insufficiency Other: HIV negative No poorly controlled diabetes mellitus No acute infection requiring IV antibiotics No other medical condition that would prevent ingestion or absorption of oral medication No other neoplasm within the past 5 years except curatively treated squamous cell or basal cell skin cancer, melanoma in situ, or carcinoma in situ of the cervix Not pregnant or nursing Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: At least 4 weeks since prior biologic therapy and recovered No concurrent growth factors or epoetin alfa Chemotherapy: At least 4 weeks since prior chemotherapy and recovered Endocrine therapy: At least 4 weeks since prior topical steroids Radiotherapy: See Disease Characteristics At least 2 weeks since prior radiotherapy for local control or palliation and recovered Surgery: Recovered from prior major surgery Other: No other concurrent investigational drugs

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 3 locations

Yale Comprehensive Cancer Center at Yale University School of Medicine

New Haven, United StatesOpen Yale Comprehensive Cancer Center at Yale University School of Medicine in Google Maps

Robert H. Lurie Comprehensive Cancer Center at Northwestern University

Chicago, United States

University of Chicago Cancer Research Center

Chicago, United States
Suspended3 Study Centers