Clinical trial · Interventional
Comparison of Methotrexate Versus Interferon-alfa 2b in Patients With Primary Cutaneous T-cell Lymphomas
Comparison of Methotrexate Versus Interferon-alfa 2b on Efficacy, Safety and Quality of Life in Patients With Primary Cutaneous T-cell Lymphomas
NCT02323659CI-TRIAL-00055954terminatedPhase 4ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Slow recruitment
Summary
Brief summary (as posted)
Comparison of methotrexate versus interferon-alfa 2b on efficacy, safety and quality of life in patients with primary cutaneous T-cell lymphomas after failure of topical or phototherapy treatment.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lymphoma, T-Cell, Cutaneous | Lymphoma | ONTOLOGY_EXACT | 0.85 |
| Mycosis Fungoides | Mycosis Fungoides | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Interferon Alfa-2b | Drug | Interferon Alfa-2b | ALIAS |
| Methotrexate | Drug | Methotrexate | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Methotrexate arm
- description
- Patients assigned to receive methotrexate
- interventionNames
- Drug: Methotrexate
- type
- ACTIVE_COMPARATOR
- label
- Interferon Alfa-2b
- description
- Patients assigned to receive Interferon alfa 2b
- interventionNames
- Drug: Interferon Alfa-2b
Primary outcomes (1)
- measure
- Objective response rate as measured by the modified Severity Weighted Assessment Tool (mSWAT scoring system)
- timeFrame
- 3 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically confirmed primary cutaneous T-cell lymphoma (CTCL) 2. Age ≥ 18 years 3. Performance status WHO\<=2 4. Subject must have adequate bone marrow, renal and hepatic function 5. Topical and phototherapy treatment failure in the past 6. Signed informed consent Exclusion Criteria: 1. Subject has received prior systemic methotrexate or interferon therapy 2. Unacceptable methotrexate or interferon treatment toxicity in the past 3. Inadequate bone marrow, renal or hepatic function as follows: * Bone Marrow: Absolute neutrophil count (ANC) \< 1,500/mm 3 (1.5 × 10 9 /L); Platelets \<100,000/mm 3 (100 × 10 9 /L); Hemoglobin \< 9.0 g/dL (1.4 mmol/L); * Renal function: Creatinine \>1.5 x Upper limit of normal (ULN) * Hepatic function: Aspartate and Alanine transaminase (AST and ALT) \>3× ULN; bilirubin \> 1.5 × ULN * Active hepatitis B or hepatitis C 4. anorexia 5. major depression with suicidal ideation or suicide attempt in the past 6. Symptomatic congestive heart failure 7. Epilepsia or other symptomatic central nervous system dysfunction 8. active skin infection not related to underlying CTCL, active Tuberculosis, HIV infection 9. Subject is pregnant or lactating 10. Psychiatric illness/social situation that would limit compliance with study requirements
References
Publications (1)
- DERIVEDValipour A, Jager M, Wu P, Schmitt J, Bunch C, Weberschock T. Interventions for mycosis fungoides. Cochrane Database Syst Rev. 2020 Jul 7;7(7):CD008946. doi: 10.1002/14651858.CD008946.pub3. PMID 32632956