Randomized Study of High-Dose and Low-Dose Interleukin-2 in Patients With Metastatic Renal Cancer

This three-arm randomized study compares response rates and overall survival of patients with metastatic renal cell cancer (RCC) receiving high-dose or one of two low-dose interleukin-2 (IL-2) regimens. Patients with measurable metastatic RCC and a good performance status were randomized to receive...

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Veröffentlicht in:Journal of clinical oncology 2003-08, Vol.21 (16), p.3127-3132
Hauptverfasser: YANG, James C, SHERRY, Richard M, LIEWEHR, David J, MERINO, Maria J, ROSENBERG, Steven A, STEINBERG, Seth M, TOPALIAN, Suzanne L, SCHWARTZENTRUBER, Douglas J, HWU, Patrick, SEIPP, Claudia A, ROGERS-FREEZER, Linda, MORTON, Kathleen E, WHITE, Donald E
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Sprache:eng
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Zusammenfassung:This three-arm randomized study compares response rates and overall survival of patients with metastatic renal cell cancer (RCC) receiving high-dose or one of two low-dose interleukin-2 (IL-2) regimens. Patients with measurable metastatic RCC and a good performance status were randomized to receive either 720,000 U/kg (high-dose [HD]) or 72,000 U/kg (low-dose [LD]), both given by intravenous (IV) bolus every 8 hours. After randomly assigning 117 patients, a third arm of low-dose daily subcutaneous IL-2 was added, and an additional 283 patients were randomly assigned. A total of 156 patients were randomly assigned to HD IV IL-2, and 150 patients to LD IV IL-2. Toxicities were less frequent with LD IV IL-2 (especially hypotension), but there were no IL-2-related deaths in any arm. There was a higher response proportion with HD IV IL-2 (21%) versus LD IV IL-2 (13%; P =.048) but no overall survival difference. The response rate of subcutaneous IL-2 (10%, partial response and complete response) was similar to that of LD IV IL-2, differing from HD IV (P =.033). Response durability and survival in completely responding patients was superior with HD IV compared with LD IV therapy (P =.04). Major tumor regressions, as well as complete responses, were seen with all regimens tested. IL-2 was more clinically active at maximal doses, although this did not produce an overall survival benefit. The immunological factors which constrain the curative potential of IL-2 to only a small percentage of patients need to be further elucidated.
ISSN:0732-183X
1527-7755
DOI:10.1200/JCO.2003.02.122