TY - JOUR
T1 - Traitement du cancer du rein métastatique avec un nouveau schéma d'interleukine 2
T2 - expérience de l'institut Gustave-Roussy
AU - Escudier, B.
AU - Farace, F.
AU - Théodore, C.
AU - Angevin, E.
AU - Court, B.
AU - Couanet, D.
AU - Dietrich, P. Y.
AU - Culine, S.
AU - Pallardy, M.
AU - Hercend, T.
AU - Droz, J. P.
PY - 1995/4/1
Y1 - 1995/4/1
N2 - Treatment of metastatic renal cell carcinoma with interleukin 2 (IL2) remains controversial despite the authorisation from the French government for IL2 with the West schedule in this disease. We report herein the study of the Institut Gustave-Roussy of 73 patients, who received from 1989 to 1991 a new schedule of high dose IL2. Seventy three patients received high dose IL2 according to the following schedule: IL2 by continuous infusion at 24·106 IU/m2/d, on 2 consecutive days per week, during 5 weeks. This treatment was associated in the first 33 patients with gamma interferon at a dose of 5.106 IU/m2/d subcutaneously the days of IL2 infusion, during the 5 weeks of therapy. Immunotherapy was further continued in responding patients, either as an association of IL2 and LANAK (lymphokine-activated naturel killer) cells, or as IL2 alone. Finally, when possible, surgery was performed on residual masses. Twenty five percent of objective responses (PR + CR) have been observed. Moreover, 12.3% CR has been obtained after the overall therapy. The global mean survival is 15 months, with a mean survival of 8, 18 and 24 + months depending on the status of the disease (progressive, stable or responsing) after initial treatment with IL2. Tolerance of this schedule was good with an actual received dose of 90% of the planned doses, and patients could leave the hospital within 2 hours after the end of IL2 in 87% of the cycles. No toxic death was observed. Among the parameters observed for correlation with the clinical response, only performance status and level of sTNF-αR were significantly associated with the response.
AB - Treatment of metastatic renal cell carcinoma with interleukin 2 (IL2) remains controversial despite the authorisation from the French government for IL2 with the West schedule in this disease. We report herein the study of the Institut Gustave-Roussy of 73 patients, who received from 1989 to 1991 a new schedule of high dose IL2. Seventy three patients received high dose IL2 according to the following schedule: IL2 by continuous infusion at 24·106 IU/m2/d, on 2 consecutive days per week, during 5 weeks. This treatment was associated in the first 33 patients with gamma interferon at a dose of 5.106 IU/m2/d subcutaneously the days of IL2 infusion, during the 5 weeks of therapy. Immunotherapy was further continued in responding patients, either as an association of IL2 and LANAK (lymphokine-activated naturel killer) cells, or as IL2 alone. Finally, when possible, surgery was performed on residual masses. Twenty five percent of objective responses (PR + CR) have been observed. Moreover, 12.3% CR has been obtained after the overall therapy. The global mean survival is 15 months, with a mean survival of 8, 18 and 24 + months depending on the status of the disease (progressive, stable or responsing) after initial treatment with IL2. Tolerance of this schedule was good with an actual received dose of 90% of the planned doses, and patients could leave the hospital within 2 hours after the end of IL2 in 87% of the cycles. No toxic death was observed. Among the parameters observed for correlation with the clinical response, only performance status and level of sTNF-αR were significantly associated with the response.
KW - adoptive immunotherapy
KW - cancer du rein métastatique
KW - chirurgie des métastases
KW - immunothérapie adoptive
KW - interleukin 2
KW - interleukine 2
KW - metastatic renal cell carcinoma
KW - surgery of metastases
UR - http://www.scopus.com/inward/record.url?scp=0028916345&partnerID=8YFLogxK
U2 - 10.1016/0007-4551(96)82702-0
DO - 10.1016/0007-4551(96)82702-0
M3 - Article
C2 - 10846540
AN - SCOPUS:0028916345
SN - 0007-4551
VL - 82
SP - 296
EP - 302
JO - Bulletin du Cancer
JF - Bulletin du Cancer
IS - 4
ER -