TY - JOUR
T1 - Treatment of stage IIIB non-small-cell lung cancer with surgery followed by infusion of tumor infiltrating lymphocytes and recombinant interleukin-2
T2 - A pilot study
AU - Melioli, Giovanni
AU - Ratto, Giovanni Battista
AU - Ponte, Marco
AU - Guastella, Marina
AU - Semino, Claudia
AU - Fantino, Giovanni
AU - Tassara, Elisabetta
AU - Pasquetti, Wanda
AU - Mereu, Carlo
AU - Merlo, Franco
AU - Reggiardo, Giorgio
AU - Morasso, Gabriella
AU - Santi, Leonardo
AU - Moretta, Lorenzo
PY - 1996
Y1 - 1996
N2 - Stage IIIb non-small-cell lung cancer (NSCLC) has a poor prognosis. The median survival is ~6 months, and only 30% of patients are alive 1 year after diagnosis. The need for effective treatment is evident. The aim of this study was to evaluate whether the infusion of tumor-infiltrating lymphocytes (TILs), isolated from resected tumor, expanded in vitro and injected together with recombinant Interleukin-2, is feasible and may at least partially modify the poor prognosis in these patients. The infusion of TILs, derived from surgically resected NSCLC and expanded in vitro, together with subcutaneous (s.c.) injections of recombinant interleukin-2 (rIL-2) was attempted in a group of 11 patients. Treated patients were infused i.v. with in vitro expanded TILs (from 4 to 70 x 109 cells), and rIL-2 was injected s.c. at doses varying from 61 to 378 x 106 IU. Toxic side effects (fever and, in some cases, hypotension) were observed and limited the dose of rIL-2 infused. Follow-up was continued for 40 months. The mean survival time was 13.8 months. Three of five TIL-treated patients with residual disease have no evident disease after 1 year, and two of them are still alive and have no evidence of disease after 40 months. This pilot study suggests that the infusion of in vitro expanded TILs, derived from surgical samples, is feasible and seems to prolong overall survival and to control the residual disease in patients with advanced NSCLC.
AB - Stage IIIb non-small-cell lung cancer (NSCLC) has a poor prognosis. The median survival is ~6 months, and only 30% of patients are alive 1 year after diagnosis. The need for effective treatment is evident. The aim of this study was to evaluate whether the infusion of tumor-infiltrating lymphocytes (TILs), isolated from resected tumor, expanded in vitro and injected together with recombinant Interleukin-2, is feasible and may at least partially modify the poor prognosis in these patients. The infusion of TILs, derived from surgically resected NSCLC and expanded in vitro, together with subcutaneous (s.c.) injections of recombinant interleukin-2 (rIL-2) was attempted in a group of 11 patients. Treated patients were infused i.v. with in vitro expanded TILs (from 4 to 70 x 109 cells), and rIL-2 was injected s.c. at doses varying from 61 to 378 x 106 IU. Toxic side effects (fever and, in some cases, hypotension) were observed and limited the dose of rIL-2 infused. Follow-up was continued for 40 months. The mean survival time was 13.8 months. Three of five TIL-treated patients with residual disease have no evident disease after 1 year, and two of them are still alive and have no evidence of disease after 40 months. This pilot study suggests that the infusion of in vitro expanded TILs, derived from surgical samples, is feasible and seems to prolong overall survival and to control the residual disease in patients with advanced NSCLC.
KW - In vivo infusion
KW - Non-small-cell lung cancer
KW - Recombinant interleukin-2
KW - Surgery
KW - Tumor-infiltrating lymphocytes
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U2 - 10.1097/00002371-199605000-00007
DO - 10.1097/00002371-199605000-00007
M3 - Article
C2 - 8811497
AN - SCOPUS:8944253774
SN - 1053-8550
VL - 19
SP - 224
EP - 230
JO - Journal of Immunotherapy
JF - Journal of Immunotherapy
IS - 3
ER -