Status:
COMPLETED
Tumor Infiltrating Lymphocytes Adjuvant Therapy of Melanoma
Lead Sponsor:
Nantes University Hospital
Conditions:
Melanoma
Eligibility:
All Genders
Up to 75 years
Phase:
PHASE3
Brief Summary
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 effe...
Detailed Description
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 anatomopatho...
Eligibility Criteria
Inclusion
- 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.
Exclusion
Key Trial Info
Start Date :
May 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2012
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT00200577
Start Date
May 1 2005
End Date
March 1 2012
Last Update
June 1 2017
Active Locations (9)
Enter a location and click search to find clinical trials sorted by distance.
1
CHU Angers
Angers, France
2
CHU Caen
Caen, France
3
Grenoble University Hospital
Grenoble, France
4
CH Le Mans
Le Mans, France