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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00151645
Other study ID # AFSSAPS 990434
Secondary ID PHRC/02-06CIC020
Status Terminated
Phase Phase 2
First received September 8, 2005
Last updated December 30, 2005
Start date December 2003
Est. completion date July 2005

Study information

Verified date December 2005
Source Rennes University Hospital
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

Renal cell carcinoma represents today 3% of the solid tumors of the adult. Their bad prognosis is due to the frequency of metastasis and the resistance to chemotherapy. Immunotherapy (interferon-α, interleukin-2) has shown some good results but an important toxicity. In our study, we evaluate the response to a new therapeutic strategy which combines an injection of patient's own activated lymphocytes to a classic immunotherapy with interferon-α and interleukin-2.


Description:

Phase I and II trials for the treatment of melanoma or renal cell carcinoma have already evaluated lymphokine-activated killer cells and tumor-infiltrating cells. In metastatic renal cell carcinoma, these therapies have shown some complete responses and a low toxicity. In our study, we evaluate the response to a new therapeutic strategy which combines an injection of patient's own activated lymphocytes to a classic immunotherapy with interferon-α and interleukin-2. A secondary objective is to improve cell preparation methods and to characterize functionally and phenotypically injected cells.


Recruitment information / eligibility

Status Terminated
Enrollment 36
Est. completion date July 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients aged between 18 and 70 years

- Metastatic renal adenocarcinoma histologically proven

- Karnofsky performance status = 70%

- Life expectation > 3 months

- At least one target, in a non-irradiated area

- Objective response or steady-state after a treatment with cytokines

- Informed written consent

Exclusion Criteria:

- Patients presenting more than one metastatic site with one hepatic metastasis diagnosed within the last 12 months

- White blood cells count < 2.5 G/L, Platelet count < 100 G/L

- Serum creatinine rate > 150 µmol/L

- Positive serology for : hepatitis B, hepatitis C, retrovirus

- Patient not available for a long-term follow-up

- Bellini duct tumor

- History of allograft or tumor within the five past years

- Severe cardiovascular, hepatic, renal or pulmonary troubles

- Auto-immune disease

- Severe infection

- Pregnancy or breast-feeding

- Corticotherapy

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
activated lymphocytes


Locations

Country Name City State
France Service d'Urologie - Hôpital Pontchaillou Rennes

Sponsors (2)

Lead Sponsor Collaborator
Rennes University Hospital Ministry of Health, France

Country where clinical trial is conducted

France, 

References & Publications (4)

Belldegrun A, Pierce W, Kaboo R, Tso CL, Shau H, Turcillo P, Moldawer N, Golub S, deKernion J, Figlin R. Interferon-alpha primed tumor-infiltrating lymphocytes combined with interleukin-2 and interferon-alpha as therapy for metastatic renal cell carcinoma. J Urol. 1993 Nov;150(5 Pt 1):1384-90. — View Citation

Figlin RA, Pierce WC, Kaboo R, Tso CL, Moldawer N, Gitlitz B, deKernion J, Belldegrun A. Treatment of metastatic renal cell carcinoma with nephrectomy, interleukin-2 and cytokine-primed or CD8(+) selected tumor infiltrating lymphocytes from primary tumor. J Urol. 1997 Sep;158(3 Pt 1):740-5. — View Citation

Hayakawa M, Hatano T, Ogawa Y, Gakiya M, Ogura H, Osawa A. Treatment of advanced renal cell carcinoma using regional arterial administration of lymphokine-activated killer cells in combination with low doses of rIL-2. Urol Int. 1994;53(3):117-24. — View Citation

Mathiot C, Thiounn N, Tartour E, Flam T, Peyret C, Joyeux I, Zerbib M, Brandely M, Debré B, Fridman WH. Non-cytotoxic CD4 tumour-infiltrating lymphocytes induce responses in patients with metastatic renal cell carcinoma previously treated with interleukin-2. Eur J Cancer. 1995;31A(9):1551-2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Objective response rate: partial or complete response during at least 4 weeks from week 22 after the beginning of the first cycle of cytokines.
Secondary - Disease free survival
Secondary - Overall survival
Secondary - Functional and phenotypic characteristics of injected cells
Secondary - Biological response
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