Clinical trial · Interventional
Tumor Infiltrating Lymphocytes Adjuvant Therapy of Melanoma
TIL (Tumor Infiltrating Lymphocytes) and IL2 (Interleukin 2) Versus Abstention as Adjuvant Treatment in Melanoma With Only One Invaded Lymphnode After Lymphnodes Excision
- 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)
The objective of this multicentric Phase III study is to confirm the results of the phase I-II study (Dreno B \& Al. Cancer Immunol Immunother 2002; 51: 539-456) which demonstrated the preventive effect of a treatment by TIL (Tumor Infiltrating Lymphocytes) combined with IL2 (Interleukin 2; low dose injected subcutaneously) on the metastatic relapse in the stage III melanoma patients with only one invaded lymphnode.
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 | Melanoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| TIL + IL2 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- TIL+IL2
- description
- TIL + IL2
- interventionNames
- Drug: TIL + IL2
- type
- NO_INTERVENTION
- label
- control
- description
- Patients are not treated
Primary outcomes (4)
- measure
- Determination of the duration of the relapse-free interval.
- timeFrame
- 5 years
- measure
- Physical examination, every 2 months until M18 then every 3 months until M36 then every 4 months up to 5 years, then once per year with a clinical examination only.
Eligibility
Eligibility (as posted)
- Sex
- All
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Melanoma stage III (regional lymph node recurrence). Will be selected the patients with only one invaded lymph node confirmed by anatomopathological exam after lymph nodes excision. * Absence of visceral metastases verified by physical examination, chest radiography, liver echography and brain-chest-liver CT-Scan. * Age \< 75 years, both genders * ECOG 0-2, Karnofsky \> 80%. * Negative pregnancy test performed at the screening visit for fertile women. * The potentially fertile women must use an oral contraception or an intra-uterine device (IUD) until three months following the last injection of the study treatment. * The patients must have fully recovered from surgery. * HIV 1/2: The patients must be negative for antibodies HIV 1 and HIV 2 and for Ag P24 or DGV HIV. * HBV: The patients must be negative for the antigen, but can be positive for the antibodies but with a negative DNA PCR. * HCV: The patients must be negative for the antibodies. * HTLV ½: The patients must be negative for the antibodies. * Following laboratory results: * Hemoglobin: ≥ 10 g/dl * WBC: ≥ 4000/µl * Lymphocytes: ≥ 700/µl * Platelet count: ≥ 100.000/µl * Serum creatinine: \< 2.0 mg/dl or £ 177 mmol/l * Serum Bilirubin: \< 2.0 mg/dl or £ 34.2 mmol/l * ASAT and ALAT: \< 2.5 x the upper limit of normal. Exclusion criteria: * Patient with more than one invaded lymph node confirmed by anatomopathological exam. * Presence of melanoma metastases discovered by clinical or radiological examination at the screening visit. * Patients must not have received any Chemotherapy, immunotherapy or radiotherapy within the preceding 4 weeks (6 weeks since prior nitrosurea and mitomycin C therapies). * Presence of cardiac affections (congestive cardiac insufficiency, coronaropathy, not controlled HTA). * Any serious active medical illnesses, for example: Active systemic infections requiring of antibiotics, coagulation disorders or any other condition which requires concomitant medications not allowed during this study. * Presence of the second active cancer other than surgically cured non-melanoma skin cancer or cervical carcinoma in-situ. * Any affection requiring a systemic corticotherapy or a treatment by Interferon A. * Any active auto-immune disease including the insulin-dependent diabetes or a immunodeficiency. The vitiligo is not an exclusion criteria. * Thyroid dysfunction not responsive to therapy. * Positive Serology for HIV, HVB, HVC or HTLV1/2. * Woman pregnant or nursing or without an effective contraception. * Incapacity to give written consent.
References
Publications (0)
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