Et. Walpole et al., SURVIVAL AFTER PHASE-II TREATMENT OF ADVANCED RENAL-CELL CARCINOMA WITH TAXOL OR HIGH-DOSE INTERLEUKIN-2, Journal of immunotherapy with emphasis on tumor immunology, 13(4), 1993, pp. 275-281
Citations number
22
Categorie Soggetti
Immunology,Oncology,"Medicine, Research & Experimental
From 1986 to 1989, 71 patients with advanced renal cell carcinoma were
treated at one institution with either the Phase II agent, taxol, or
one of several high dose interleukin-2 (IL-2) protocols. As no respons
es to taxol were seen, that group may represent the natural history of
renal cell carcinoma in a Phase II population. The results of treatme
nt with IL-2 were examined against this background. Concurrently, 17 p
atients received taxol and 14 patients IL-2. An additional 40 patients
subsequently received IL-2. Five taxol patients with Eastern Cooperat
ive Oncology Group (ECOG) performance status (PS) 2 were excluded from
the comparison as similar patients were ineligible for the IL-2 studi
es. There were more patients in the IL-2 groups with non-liver/lung me
tastases and ECOG PS 0 than in the taxol group. Six (43%) of concurren
t IL-2 patients responded [complete response (CR) = 14%; partial respo
nse (PR) = 29%]. The response rate for all IL-2-treated patients was 2
2% (CR +/- 7%, PR +/- 15%). The response rate to IL-2 was higher in ca
ses with ECOG PS 0, time to treatment <12 months, and no prior chemoth
erapy. The median time to progression for the concurrent IL-2 group wa
s 4.5 months (4.0 months for all IL-2 patients) and 2.5 months for tax
ol patients. Median survival for concurrent IL-2 patients was 12.5 mon
ths (12 months for all IL-2 patients) and 10 months for taxol patients
. Durable remissions resulted in a 21% overall survival at 40 months f
or all IL-2 patients. These data show prolonged time to treatment fail
ure after treatment with IL-2 and evidence of improvement in survival
for patients eligible for Phase II studies.