TY - JOUR
T1 - Combination of interleukin-2 and gamma interferon in metastatic renal cell carcinoma
AU - Escudier, B.
AU - Antoun, S.
AU - Leclercq, B.
AU - Nitenberg, G.
AU - Farace, F.
AU - Angevin, E.
AU - Triebel, F.
AU - Hercend, T.
AU - Aboudaram, A.
AU - Brandely, M.
PY - 1993/1/1
Y1 - 1993/1/1
N2 - The use of high-dose interleukin-2 (IL2), alone or in association with lymphokine activated killer cells in patients with metastatic renal cell carcinoma (MRCC) results in a 20-25% response rate. However, the toxicity of IL2 is substantial and despite many clinical trials, response rates initially reported have not been improved. The aim of this study was to evaluate a combination of IL2 and gamma interferon (IFN) in MRCC with respect to both efficacy and tolerance. IL2 was given by continuous intravenous infusion at a daily dose of 24 × 106 U/m2 for 2 consecutive days during 5 consecutive weeks. Gamma IFN was given subcutaneously at a daily dose of 5 × 106 U/m2 on the same days as IL2. 33 patients with MRCC entered the study. Clinical responses were comparable with other published series: 7 patients (21%) achieved partial response, 13 (39%) were stable and 13 had progression, despite therapy. Immunological profile observed with this regimen showed a major increase in natural killer cells which became the predominant lymphocyte population at the end of the therapy. Tolerance was good with 92.5% of the planned doses actually received by the patients. This was reflected by an early discharge from the hospital in 95% of the cycles, increasing acceptability of the regimen by the patients.
AB - The use of high-dose interleukin-2 (IL2), alone or in association with lymphokine activated killer cells in patients with metastatic renal cell carcinoma (MRCC) results in a 20-25% response rate. However, the toxicity of IL2 is substantial and despite many clinical trials, response rates initially reported have not been improved. The aim of this study was to evaluate a combination of IL2 and gamma interferon (IFN) in MRCC with respect to both efficacy and tolerance. IL2 was given by continuous intravenous infusion at a daily dose of 24 × 106 U/m2 for 2 consecutive days during 5 consecutive weeks. Gamma IFN was given subcutaneously at a daily dose of 5 × 106 U/m2 on the same days as IL2. 33 patients with MRCC entered the study. Clinical responses were comparable with other published series: 7 patients (21%) achieved partial response, 13 (39%) were stable and 13 had progression, despite therapy. Immunological profile observed with this regimen showed a major increase in natural killer cells which became the predominant lymphocyte population at the end of the therapy. Tolerance was good with 92.5% of the planned doses actually received by the patients. This was reflected by an early discharge from the hospital in 95% of the cycles, increasing acceptability of the regimen by the patients.
UR - http://www.scopus.com/inward/record.url?scp=0027464902&partnerID=8YFLogxK
U2 - 10.1016/S0959-8049(05)80354-5
DO - 10.1016/S0959-8049(05)80354-5
M3 - Article
C2 - 8471331
AN - SCOPUS:0027464902
SN - 0959-8049
VL - 29
SP - 724
EP - 728
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 5
ER -