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SWOG-9430: Surgery in Treating Patients With Metastatic Melanoma

A Phase II Trial of Complete Surgical Resection For Stage IV Melanoma -- Surgical Resection With Biological Evaluation and Clinical Follow-Up

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002860
Enrollment
77
Registered
2003-01-27
Start date
1996-11-30
Completion date
2010-12-31
Last updated
2012-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Melanoma (Skin)

Keywords

stage IV melanoma, recurrent melanoma

Brief summary

RATIONALE: Surgery may be effective therapy in treating patients with metastatic melanoma. PURPOSE: This phase II trial is studying how well surgery works in treating patients with metastatic melanoma.

Detailed description

OBJECTIVES: * Assess overall and progression-free survival in patients with metastatic melanoma (beyond the draining lymph nodes) after complete surgical resection of all known disease. * Determine the ability of the Southwest Oncology Group Melanoma Committee to enroll patients with metastatic melanoma who can be resected to a disease-free state. OUTLINE: This is a multicenter study. All patients undergo gross total resection of all known disease. Patients whose disease cannot be completely resected or who have disease recurrence after surgery are removed from study. Patients found to have microscopic residual disease after surgery are considered completely resected. Resected tissue is submitted for analysis on protocol SWOG-9431. Patients may receive any adjuvant therapy (e.g., radiotherapy, interferon, and/or vaccines) deemed clinically appropriate by the treating physician. Patients are followed periodically for 5 years after study entry. PROJECTED ACCRUAL: A total of 100 eligible patients with completely surgically resected disease will be accrued for this study.

Interventions

PROCEDURESurgery

Complete surgical resection of metastatic melanoma

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Eastern Cooperative Oncology Group
CollaboratorNETWORK
SWOG Cancer Research Network
Lead SponsorNETWORK

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed metastatic melanoma that is deemed grossly surgically resectable * Multiple resected sites or metastatic melanoma of unknown primary allowed provided all known disease can be grossly resected * Recurrence in iliac lymph nodes after inguinal lymph dissection allowed * No metastatic disease beyond the lesions planned for resection * Confirmed by CT scan of chest, abdomen, pelvis, and CT or MRI of brain within 42 days of study * Concurrent registration on protocol SWOG-9431 required PATIENT CHARACTERISTICS: Age: * 18 and over Performance status: * SWOG 0-2 Hematopoietic: * Not specified Hepatic: * Not specified Renal: * Not specified Other: * No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or adequately treated stage I or II cancer from which patient is currently disease free * Not pregnant PRIOR CONCURRENT THERAPY: Biologic therapy: * Prior immunotherapy in the adjuvant or metastatic setting allowed Chemotherapy: * Prior chemotherapy in the adjuvant or metastatic setting allowed Endocrine therapy: * Prior hormonal therapy in the adjuvant or metastatic setting allowed Radiotherapy: * Prior radiotherapy in the adjuvant or metastatic setting allowed Surgery: * See Disease Characteristics * At least 14 days since prior surgery in the adjuvant or metastatic setting Other: * Recovered from prior therapy

Design outcomes

Primary

MeasureTime frame
Overall survival1-year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026