Suspended

Adjuvant Ganglioside GM2-KLH/QS-21 Vaccination: Post-Operative Adjuvant Ganglioside GM2-KLH/QS-21 (BMS-248479) Vaccination Treatment After Resection of Primary Cutaneous Melanoma Thicker Than 1.5mm (AJCC/UICC Stage II, T3-T4N0M0), a 2-Arm Multicenter Randomized Phase III Trial vs. Observation

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What is being tested

GM2-KLH vaccine

+ QS21

+ adjuvant therapy

BiologicalProcedure
Who is being recruted

Neoplasms+9

+ Neoplasms by Histologic Type

+ Neoplasms by Site

From 18 to 80 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 3
Interventional
Study Start: December 1999
See protocol details

Summary

Principal SponsorEuropean Organisation for Research and Treatment of Cancer - EORTC
Last updated: February 9, 2009
Sourced from a government-validated database.Claim as a partner

Study start date: December 1, 1999

Actual date on which the first participant was enrolled.

OBJECTIVES: Compare the effect of immunization with GM2-KLH and QS21 to observation on the disease-free survival of patients with primary cutaneous stage II melanoma after adequate surgery. Determine overall survival and toxicity in the two treatment arms. OUTLINE: This is a randomized, open-label, parallel, multicenter study. Patients are stratified according to participating center, tumor thickness (greater than 1.5 to 3.0 mm vs greater than 3.0 to 4.0 mm vs greater than 4.0 mm), gender, ulceration (yes vs no), and presence of additional staging procedures of regional lymph nodes (yes vs no). Patients are randomized to one of two arms. Arm I: Patients are vaccinated with GM2-KLH and QS21 subcutaneously on day 1 of weeks 1-4, 12, 24, 36, 48, 60, 72, 84, 96, 120, and 144 for a total of 14 vaccinations. Arm II: Patients undergo observation. Patients are followed every 6 months for 7 years. PROJECTED ACCRUAL: A total of 1300 patients (650 per arm) will be accrued for this study within 36 months.

NCT00005052
Principal SponsorEuropean Organisation for Research and Treatment of Cancer - EORTC
Last updated: February 9, 2009
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.

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.

From 18 to 80 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

NeoplasmsNeoplasms by Histologic TypeNeoplasms by SiteNeoplasms, Germ Cell and EmbryonalNeoplasms, Nerve TissueSkin DiseasesSkin NeoplasmsSkin and Connective Tissue DiseasesNeuroectodermal TumorsNevi and MelanomasNeuroendocrine TumorsMelanoma

Criteria

DISEASE CHARACTERISTICS: Histologically confirmed primary stage II melanoma greater than 1.5 mm without evidence of lymph node metastases T3 or T4, N0, M0 Must originate in the skin Wide excision with a minimum of 1-2 cm margin surrounding primary lesion or biopsy scar No more than 56 days since definitive surgical treatment (wide excision) No more than 12 weeks since primary surgery No clinical, radiological, or pathological evidence of incompletely resected disease, lymph node metastases, in-transit metastasis, or any distant metastatic disease PATIENT CHARACTERISTICS: Age: 18 to 80 Performance status: ECOG 0-1 Life expectancy: Not specified Hematopoietic: WBC at least 3,000/mm^3 Platelet count at least 100,000/mm^3 Hemoglobin at least 9.8 g/dL Hepatic: SGOT/SGPT no greater than 2 times upper limit of normal (ULN) Alkaline phosphatase no greater than 2 times ULN LDH no greater than 2 times ULN Bilirubin no greater than 2 times ULN Hepatitis B and C negative Renal: Creatinine normal Other: Not pregnant or nursing Negative pregnancy test No prior or other concurrent cancer except carcinoma in situ of the cervix or basal or squamous cell skin cancer No autoimmune disorders No conditions requiring systemic treatment with immunosuppressive drugs including treatment with systemic corticosteroids No history of CNS demyelinating or inflammatory disease No hereditary or acquired peripheral neuropathy No other significant medical or surgical condition or psychiatric disorders requiring medication that would preclude study No history of severe allergic reaction to shellfish HIV negative PRIOR CONCURRENT THERAPY: Biologic therapy: No prior immunotherapy No other concurrent biologic therapy Chemotherapy: No prior systemic chemotherapy No concurrent cytotoxic chemotherapy Endocrine therapy: No concurrent hormonal therapy except replacement therapy No concurrent corticosteroids No concurrent chronic systemic steroids Radiotherapy: No prior adjuvant radiotherapy No concurrent radiotherapy Surgery: See Disease Characteristics Other: No prior preoperative infusion or perfusion therapy No concurrent immunosuppressive medications No other concurrent anticancer therapy

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

Secondary 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 80 locations

Royal Perth Hospital

Perth, AustraliaOpen Royal Perth Hospital in Google Maps

Hopital Universitaire Erasme

Brussels, Belgium

Cliniques Universitaires Saint-Luc

Brussels, Belgium

Universitair Ziekenhuis Antwerpen

Edegem, Belgium
Suspended80 Study Centers