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TIL (Tumor Infiltrating Lymphocytes) and IL2 (Interleukin 2) Versus Abstention as Adjuvant Treatment in Melanoma With Only One Invaded Lymphnode After Lymphnodes Excision
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.
In this open, multicentric (Grenoble, Montpellier, Nantes, Angers, Caen, Le Mans, Poitiers, Rennes, Tours) randomized study, selected patients with only one invaded lymphnode confirmed by anatomopathological exam will be randomized to one of the following arms: 1-Control group: patients of this group will not receive any treatment and will have the same clinical follow-up as the treated group. 2- TIL-IL2 group: treated patients will receive two injections of TIL combined with IL2. Tumor Infiltrating Lymphocytes will be obtained from a small piece of tumour tissue removed from the invaded lymphnode after surgery. TIL will be grown in larger number in laboratory during 6 weeks. Patients randomized in treatment arm will receive two injection of TIL (the first about 6 and the second about 10 weeks post-surgery). Administration of TIL will be combined with a low dose of IL2 (6 million U.I. per day) injected subcutaneously from J1 to J5 and J8 to J12 following the day of TIL infusion. The same dose and duration of IL2 treatment will be used for the second injection of TIL performed one month later. After 2 months adjuvant therapy, patients received no other treatment. Only a regular follow-up was performed.
Age
0 - 75 years
Sex
ALL
Healthy Volunteers
No
CHU Angers
Angers, France
CHU Caen
Caen, France
Grenoble University Hospital
Grenoble, France
CH Le Mans
Le Mans, France
Montpellier University Hospital
Montpellier, France
Nantes University Hospital
Nantes, France
CHU Poitiers
Poitiers, France
CHU Rennes
Rennes, France
CHRU Tours
Tours, France
Start Date
May 1, 2005
Primary Completion Date
March 1, 2012
Completion Date
March 1, 2012
Last Updated
June 1, 2017
70
ACTUAL participants
TIL + IL2
DRUG
Lead Sponsor
Nantes University Hospital
NCT05039801
NCT06066138
Data Source & Attribution
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