Phase II Study Incorporating Pegylated Interferon In the Treatment For Children With High-Risk Melanoma

NCT ID: NCT00539591

Last Updated: 2025-12-23

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 29 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-05-09
• Study Completion Date: 2026-05-31

Brief Summary

The main goal of this study is to estimate the tumor response rate of temozolomide administered in combination with peginterferon alfa-2b to pediatric patients with unresectable Stage III, metastatic, or recurrent cutaneous melanoma.

Detailed Description

This study is for children with malignant melanoma and high risk features (at high risk of melanoma returning or spreading to other parts of the body) or who have recurrent disease. The study has two treatment groups based on the stage of the disease. Patients with stage IIC, IIIA or IIIB melanoma whose tumors have been removed by surgery will be treated in study group A. These patients will receive 4 weeks of high dose interferon alfa-2b followed by 48 weeks of peginterferon. Patients with stage IIIC or IV melanoma, stage III melanoma that could not be removed by surgery and those with recurrent disease will be treated in study group B. These patients will receive peginterferon alfa-2b and temozolomide.

Stratum A: Resected Stages IIC, IIIA, and IIIB patients

Induction therapy (weeks 1-4): Subjects will receive recombinant interferon alfa-2b 20 million units/m2 per day intravenously over 20-30 minutes on 5 consecutive days per week for 4 weeks. Subjects will receive peginterferon alfa-2b 1 mcg/kg/week subcutaneously for a total of 48 weeks.

Stratum B: Resected Stage IIIC, unresectable Stage III, Stage IV, and recurrent patients

Stratum B is divided into 2 groups based on the presence (Stratum B1) or absence (Stratum B2) of measurable disease. Subjects will receive 8 weekly doses of peginterferon alfa-2b 0.5 mcg/kg/dose subcutaneously in combination with temozolomide 75mg/m2/dose by mouth daily for 6 weeks followed by 2 week break. The duration of each treatment course will be 8 weeks. Strata B2 (no measurable disease) will proceed with 7 courses as outlined.

Surgery interventions -Associated with both Strata A and B Surgery description: All subjects with initial presentation of melanoma (T1-4) will be treated with primary wide local excision with a minimum of 1cm margin (if anatomically feasible) surrounding the primary lesion or biopsy scar. For lesions with Breslow's thickness of > 1mm or <or= with ulceration or Clark's level IV/V, a 2 cm margin is preferred when anatomically feasible. Subjects with sentinel lymph node(s) positive for disease, will undergo complete lymph node dissection of the involved nodal basin.

Additional objectives include:

• To assess the safety of temozolomide administered in combination with peginterferon α-2b to pediatric patients with resected AJCC Stage IIIC, unresectable Stage III, metastatic, or recurrent cutaneous melanoma (Stratum B).
• To study the feasibility and safety of administering peginterferon α-2b weekly for 48 weeks following an initial induction phase with intravenous high dose interferon α-2b for 4 weeks to pediatric patients with resected thick melanomas (> 4mm) with ulcerations (AJCC Stage IIC) and resected melanomas with regional lymph node metastases (AJCC Stage IIIA and IIIB) (Stratum A).

Conditions

Malignant Melanoma

Keywords

Cutaneous Melanoma

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Temozolomide/peginterferon alfa-2b

Stratum B: Resected Stage IIIC, unresectable Stage III, Stage IV, and recurrent patients

Stratum B is divided into 2 groups based on the presence (Stratum B1) or absence (Stratum B2) of measurable disease. Subjects will receive 8 weekly doses of peginterferon alfa-2b 0.5 mcg/kg/dose subcutaneously (SQ) in combination with temozolomide 75mg/m2/dose by mouth (PO) daily for 6 weeks followed by 2 week break. The duration of each treatment course will be 8 weeks. Strata B2 (no measurable disease) will proceed with 7 courses as outlined.

Group Type: EXPERIMENTAL

Peginterferon alfa-2b

Intervention Type: DRUG

Given either IV or SQ. Therapeutic drug class: interferon.

Temozolomide

Intervention Type: DRUG

Given PO. Therapeutic drug class: antineoplastic agent.

Peginterferon alfa-2b/non-pegylated interferon alfa-2b

Stratum A: Resected Stages IIC, IIIA, and IIIB patients will receive recombinant interferon alfa-2b 20 million units/m2/day intravenously (IV) 5 consecutive days per week for 4 weeks followed by peginterferon alfa-2b 1mcg/kg subcutaneously (SQ) once a week for 48 weeks.

Group Type: EXPERIMENTAL

Peginterferon alfa-2b

Intervention Type: DRUG

Given either IV or SQ. Therapeutic drug class: interferon.

Temozolomide

Intervention Type: DRUG

Given PO. Therapeutic drug class: antineoplastic agent.

Recombinant interferon alfa-2b

Intervention Type: DRUG

Given IV. Therapeutic drug classes: antineoplastic agent, immunomodulatory agent, interferon

Interventions

Peginterferon alfa-2b

Given either IV or SQ. Therapeutic drug class: interferon.

Intervention Type: DRUG

Temozolomide

Given PO. Therapeutic drug class: antineoplastic agent.

Intervention Type: DRUG

Recombinant interferon alfa-2b

Given IV. Therapeutic drug classes: antineoplastic agent, immunomodulatory agent, interferon

Intervention Type: DRUG

Other Intervention Names

PEG-Intron(R); pegylated interferon alfa-2b; Temodar(R), SCH 52365; Intron®; non-pegylated interferon alfa-2b

Eligibility Criteria

Inclusion Criteria

• AJCC stage IIC, III, IV or recurrent cutaneous melanoma
• Adequate bone marrow function
• Age less than or equal to 21 years of age at diagnosis
• Adequate liver and kidney function

Exclusion Criteria

• Prior Therapy with dacarbazine or temozolomide
• Patients who have uncontrolled infection
• Patients with autoimmune hepatitis
• Patients who have a history of depression or other psychiatric diseases requiring hospitalization
• Patients taking systemic corticosteroids including oral steroids (i.e. prednisone, dexamethasone) or topical steroid creams/ointments. Steroid containing inhalers, steroid replacement for adrenal insufficiency and steroid premedication for prevention of transfusion or imaging contrast-agent related allergic reaction will be permitted.
• Patients with hypersensitivity reaction to non-pegylated interferon α-2b are not eligible for study
• Patients with diabetes mellitus not adequately controlled with medication
• Patients with hypo- or hyperthyroidism not adequately controlled with medication.
• Patients with a history of myocardial infarction, severe or unstable angina, or severe peripheral vascular disease.

• Maximum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Schering-Plough

INDUSTRY

Sponsor Role: collaborator

St. Jude Children's Research Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Alberto Pappo, MD

Role: PRINCIPAL_INVESTIGATOR

St. Jude Children's Research Hospital

Locations

Rady Children's Hospital

San Diego, California, United States

St. Jude Children's Research Hospital

Memphis, Tennessee, United States

The Children's Cancer Hospital at UT M.D. Anderson Cancer Center

Houston, Texas, United States

Countries

United States

Related Links

http://www.stjude.org

St. Jude Children's Research Hospital

http://www.stjude.org/protocols

Clinical Trials Open at St. Jude

Other Identifiers

NCI-2011-01192

Identifier Type: REGISTRY

Identifier Source: secondary_id

MEL06

Identifier Type: -

Identifier Source: org_study_id