Mb. Atkins et al., High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: Analysis of 270 patients treated between 1985 and 1993, J CL ONCOL, 17(7), 1999, pp. 2105-2116
Purpose: To determine the short- and long-term efficacy and toxicity of the
high-dose intravenous bolus interleukin 2 (IL-2) regimen in patients with
metastatic melanoma,
Patients and Methods: Two hundred seventy assessable patients were entered
onto eight clinical trials conducted between 1985 and 1993. IL-2 (Proleukin
[aldesleukin]; Chiron Corp, Emeryville, CA) 600,000 or 720,000 IU/kg was a
dministered by 15-minute intravenous infusion every 8 hours for up to 14 co
nsecutive doses over 5 days as clinically tolerated with maximum support, i
ncluding pressors, A second identical treatment cycle was scheduled after 6
to 9 days of rest, and courses could be repeated every 6 to 12 weeks in st
able or responding patients, Data were analyzed through fall 1996.
Results: The overall objective response rate was 16% (95% confidence interv
al, 12% to 21%); there were 17 complete responses (CRs) (6%) and 26 partial
responses (PRs) (10%), Responses occurred with ail sites of disease and in
patients with large tumor burdens. The median response duration for patien
ts who achieved a CR has not been reached and was 5.9 months for those who
achieved a PR, Twelve (28%) of the responding patients, including 10 (59%)
of the patients who achieved a CR, remain progression-free. Disease did not
progress in any patient responding for more than 30 months. Baseline perfo
rmance status and whether patients had received prior systemic therapy were
the only predictive prognostic factors for response to IL-2 therapy. Toxic
ities, although severe, generally reversed rapidly after therapy was comple
ted. Six patients (2%) died from adverse events, all related to sepsis,
Conclusion: High-dose IL-2 treatment seems to benefit some patients with me
tastatic melanoma by producing durable CRs or PRs and should be considered
for appropriately selected melanoma patients. (C) 1999 by American Society
of Clinical Oncology.