Clinical trial · Interventional
Interferon Alfa and Thalidomide in Treating Patients With Stage IV Melanoma
Evaluation of Interferon Alpha-2b and Thalidomide in Patients With Disseminated Malignant Melanoma, Phase II
NCT00026520CI-TRIAL-00010999completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Interferon alfa may interfere with the growth of cancer cells and slow the growth of the tumor. Thalidomide may stop the growth of cancer by stopping blood flow to the tumor. Combining interferon alfa with thalidomide may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining interferon alfa with thalidomide in treating patients who have stage IV melanoma.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Melanoma (Skin) | Melanoma | ONTOLOGY_EXACT | 0.85 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| recombinant interferon alfa | Biological | — | UNRESOLVED |
| thalidomide | Drug | Thalidomide | ALIAS |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically confirmed stage IV malignant melanoma * Surgically incurable disease * Measurable or evaluable disease * No brain metastases by CT scan or MRI * Prior brain metastases allowed only if completely resected and treated with whole brain radiotherapy * Must have received 1, and only 1, prior systemic therapy for metastatic disease * Chemotherapy, biologic/immunotherapy, hormonal therapy, or combination therapy PATIENT CHARACTERISTICS: Age: * Adult Performance status: * Zubrod 0-2 Life expectancy: * Not specified Hematopoietic: * Absolute neutrophil count at least 1,000/mm\^3 * Platelet count at least 75,000/mm\^3 Hepatic: * SGOT and/or SGPT no greater than 2.5 times upper limit of normal (ULN) * Bilirubin no greater than ULN Renal: * Creatinine no greater than 1.5 times ULN Other: * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use 2 methods of effective contraception 4 weeks before, during, and for 4 weeks after study * HIV negative * No AIDS or HIV-1-associated complex * No other serious illness * No serious active infections * No sensory neuropathy greater than grade 1 * No prior seizures or concurrent potential risk factors for the development of seizures * No other prior 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 currently in complete remission PRIOR CONCURRENT THERAPY: Biologic therapy: * See Disease Characteristics * At least 21 days since prior biologic therapy or immunotherapy in the adjuvant or metastatic setting and recovered * No concurrent filgrastim (G-CSF) * No other concurrent biologic therapy Chemotherapy: * See Disease Characteristics * At least 21 days since prior chemotherapy in the adjuvant or metastatic setting and recovered * No concurrent chemotherapy Endocrine therapy: * See Disease Characteristics * At least 21 days since prior hormonal therapy in the adjuvant or metastatic setting and recovered * No concurrent hormonal therapy * No concurrent systemic steroids (including creams) Radiotherapy: * See Disease Characteristics * At least 21 days since prior radiotherapy and recovered * Prior radiotherapy to all known sites of disease allowed if there is objective evidence of progression * No concurrent radiotherapy Surgery: * See Disease Characteristics * At least 21 days since prior surgery for primary or metastatic disease and recovered * No concurrent surgery Other: * At least 21 days since prior systemic therapy or combination regimen for metastatic disease and recovered * At least 21 days since prior adjuvant isolation limb perfusion therapy and recovered * No other concurrent therapy * No other concurrent investigational drugs * No concurrent immunosuppressive medications * Concurrent antihistamines allowed if no alternative medication available
References
Publications (2)
- RESULTHutchins LF, Moon J, Clark JI, Thompson JA, Lange MK, Flaherty LE, Sondak VK. Evaluation of interferon alpha-2B and thalidomide in patients with disseminated malignant melanoma, phase 2, SWOG 0026. Cancer. 2007 Nov 15;110(10):2269-75. doi: 10.1002/cncr.23035. PMID 17932881
- RESULTHutchins L, Moon J, Clark J, et al.: Interferon alpha-2b and thalidomide in previously treated patients with disseminated malignant melanoma: SWOG 0026. [Abstract] J Clin Oncol 22 (Suppl 14): A-7527, 716s, 2004.