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Extended continuous infusion low-dose recombinant interleukin-2 in advanced cancer: prolonged immunomodulation without significant toxicity.

Publication ,  Journal Article
Caligiuri, MA; Murray, C; Soiffer, RJ; Klumpp, TR; Seiden, M; Cochran, K; Cameron, C; Ish, C; Buchanan, L; Perillo, D
Published in: Journal of Clinical Oncology
December 1991

In previous clinical trials, recombinant interleukin-2 (rIL-2) has been infused at high doses over short periods of time to generate lymphokine-activated killer (LAK) cells in vivo. These trials have been limited by severe toxicities, and the immunologic effects of rIL-2 have been transient. The present study was designed to assess the toxicity and immunologic effects of prolonged administration of low doses of rIL-2. In this phase I study, patients with advanced cancer were scheduled to receive intravenous (IV) infusion of rIL-2 without interruption for 3 months in an outpatient setting. Twenty-one patients received rIL-2 at doses ranging from 0.5 x 10(5) to 6.0 x 10(5) U/m2/d. Treatment was extremely well tolerated, and no patient experienced grade 3 or grade 4 toxicity. The lowest dose level (0.5 x 10(5) U/m2/d) did not have demonstrable immunologic activity. At doses of 1.5 x 10(5) and 4.5 x 10(5) U/m2/d, rIL-2 infusion resulted in the specific expansion of natural-killer (NK) cells (sixfold and ninefold increases, respectively, at these two dose levels) without any changes in B cells, T cells, neutrophils, or monocytes. Grade 2 toxicity was observed at the dose of 6.0 x 10(5) U/m2/d, as three patients required interruption of therapy and two patients who completed therapy developed transient hypothyroidism. In patients with increased NK cells, enhancement of non-major histocompatibility complex (MHC)-restricted cytotoxicity and increased generation of LAK cells in vitro were also demonstrated. Therapy with low-dose rIL-2 can be given safely in an uninterrupted fashion for prolonged periods of time in an outpatient setting. This results in selective expansion of NK cells in vivo with minimal toxicity. Further investigation of this schedule for immunomodulation in vivo should be pursued in phase II studies of both malignant and immunodeficient disease states.

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Published In

Journal of Clinical Oncology

DOI

EISSN

1527-7755

ISSN

0732-183X

Publication Date

December 1991

Volume

9

Issue

12

Start / End Page

2110 / 2119

Publisher

American Society of Clinical Oncology (ASCO)

Related Subject Headings

  • Oncology & Carcinogenesis
  • 1112 Oncology and Carcinogenesis
  • 1103 Clinical Sciences
 

Citation

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Chicago
ICMJE
MLA
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Caligiuri, M. A., Murray, C., Soiffer, R. J., Klumpp, T. R., Seiden, M., Cochran, K., … Perillo, D. (1991). Extended continuous infusion low-dose recombinant interleukin-2 in advanced cancer: prolonged immunomodulation without significant toxicity. Journal of Clinical Oncology, 9(12), 2110–2119. https://doi.org/10.1200/jco.1991.9.12.2110
Caligiuri, M. A., C. Murray, R. J. Soiffer, T. R. Klumpp, M. Seiden, K. Cochran, C. Cameron, C. Ish, L. Buchanan, and D. Perillo. “Extended continuous infusion low-dose recombinant interleukin-2 in advanced cancer: prolonged immunomodulation without significant toxicity.Journal of Clinical Oncology 9, no. 12 (December 1991): 2110–19. https://doi.org/10.1200/jco.1991.9.12.2110.
Caligiuri MA, Murray C, Soiffer RJ, Klumpp TR, Seiden M, Cochran K, et al. Extended continuous infusion low-dose recombinant interleukin-2 in advanced cancer: prolonged immunomodulation without significant toxicity. Journal of Clinical Oncology. 1991 Dec;9(12):2110–9.
Caligiuri, M. A., et al. “Extended continuous infusion low-dose recombinant interleukin-2 in advanced cancer: prolonged immunomodulation without significant toxicity.Journal of Clinical Oncology, vol. 9, no. 12, American Society of Clinical Oncology (ASCO), Dec. 1991, pp. 2110–19. Crossref, doi:10.1200/jco.1991.9.12.2110.
Caligiuri MA, Murray C, Soiffer RJ, Klumpp TR, Seiden M, Cochran K, Cameron C, Ish C, Buchanan L, Perillo D. Extended continuous infusion low-dose recombinant interleukin-2 in advanced cancer: prolonged immunomodulation without significant toxicity. Journal of Clinical Oncology. American Society of Clinical Oncology (ASCO); 1991 Dec;9(12):2110–2119.

Published In

Journal of Clinical Oncology

DOI

EISSN

1527-7755

ISSN

0732-183X

Publication Date

December 1991

Volume

9

Issue

12

Start / End Page

2110 / 2119

Publisher

American Society of Clinical Oncology (ASCO)

Related Subject Headings

  • Oncology & Carcinogenesis
  • 1112 Oncology and Carcinogenesis
  • 1103 Clinical Sciences