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Phase I studies of interleukin (IL)-2 and rituximab in B-cell non-hodgkin's lymphoma: IL-2 mediated natural killer cell expansion correlations with clinical response.

Publication ,  Journal Article
Gluck, WL; Hurst, D; Yuen, A; Levine, AM; Dayton, MA; Gockerman, JP; Lucas, J; Denis-Mize, K; Tong, B; Navis, D; Difrancesco, A; Milan, S ...
Published in: Clin Cancer Res
April 1, 2004

PURPOSE: Expansion and activation of natural killer (NK) cells with interleukin-2 (IL-2) may enhance antibody-dependent cellular cytotoxicity (ADCC), an important mechanism of rituximab activity. Two parallel Phase I studies evaluated combination therapy with rituximab and IL-2 in relapsed or refractory B-cell non-Hodgkin's lymphoma (NHL). EXPERIMENTAL DESIGN: Thirty-four patients with advanced NHL received rituximab (375 mg/m(2) i.v. weekly, weeks 1-4) and escalating doses of s.c. IL-2 [2-7.5 MIU daily (n = 19) or 4.5-14 million international units three times weekly (n = 15), weeks 2-5]. Safety, tolerability, clinical responses, NK cell counts, and ADCC activity were evaluated. RESULTS: Maximally tolerated doses (MTD) of IL-2 were 6 MIU daily and 14 million international units thrice weekly. The most common adverse events were fever, chills, and injection site reactions. Dose-limiting toxicities were fatigue and reversible liver enzyme test elevations. Of the 9 patients enrolled at the daily schedule MTD, 5 showed clinical response. On the thrice-weekly schedule at the MTD, 4 of 5 patients responded. Responders showed median time to progression of 14.9 and 16.1 months, respectively, for the two studies. For the same total weekly dose, thrice-weekly IL-2 administration induced greater increases in NK cell counts than daily dosing, and NK cells correlated with clinical response on the thrice-weekly regimen. ADCC activity was increased and maintained after IL-2 therapy in responding and stable disease patients. CONCLUSIONS: Addition of IL-2 to rituximab therapy is safe and, using thrice-weekly IL-2 dosing, results in NK cell expansion that correlates with response. This combination treatment regimen merits additional evaluation in a randomized clinical trial.

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Published In

Clin Cancer Res

DOI

ISSN

1078-0432

Publication Date

April 1, 2004

Volume

10

Issue

7

Start / End Page

2253 / 2264

Location

United States

Related Subject Headings

  • Time Factors
  • Rituximab
  • Oncology & Carcinogenesis
  • Middle Aged
  • Maximum Tolerated Dose
  • Male
  • Lymphoma, B-Cell
  • Lymphocytes
  • Lymphocyte Subsets
  • Liver
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Gluck, W. L., Hurst, D., Yuen, A., Levine, A. M., Dayton, M. A., Gockerman, J. P., … Wolin, M. (2004). Phase I studies of interleukin (IL)-2 and rituximab in B-cell non-hodgkin's lymphoma: IL-2 mediated natural killer cell expansion correlations with clinical response. Clin Cancer Res, 10(7), 2253–2264. https://doi.org/10.1158/1078-0432.ccr-1087-3
Gluck, William Larry, Deborah Hurst, Alan Yuen, Alexandra M. Levine, Mark A. Dayton, Jon P. Gockerman, Jennifer Lucas, et al. “Phase I studies of interleukin (IL)-2 and rituximab in B-cell non-hodgkin's lymphoma: IL-2 mediated natural killer cell expansion correlations with clinical response.Clin Cancer Res 10, no. 7 (April 1, 2004): 2253–64. https://doi.org/10.1158/1078-0432.ccr-1087-3.
Gluck WL, Hurst D, Yuen A, Levine AM, Dayton MA, Gockerman JP, et al. Phase I studies of interleukin (IL)-2 and rituximab in B-cell non-hodgkin's lymphoma: IL-2 mediated natural killer cell expansion correlations with clinical response. Clin Cancer Res. 2004 Apr 1;10(7):2253–64.
Gluck, William Larry, et al. “Phase I studies of interleukin (IL)-2 and rituximab in B-cell non-hodgkin's lymphoma: IL-2 mediated natural killer cell expansion correlations with clinical response.Clin Cancer Res, vol. 10, no. 7, Apr. 2004, pp. 2253–64. Pubmed, doi:10.1158/1078-0432.ccr-1087-3.
Gluck WL, Hurst D, Yuen A, Levine AM, Dayton MA, Gockerman JP, Lucas J, Denis-Mize K, Tong B, Navis D, Difrancesco A, Milan S, Wilson SE, Wolin M. Phase I studies of interleukin (IL)-2 and rituximab in B-cell non-hodgkin's lymphoma: IL-2 mediated natural killer cell expansion correlations with clinical response. Clin Cancer Res. 2004 Apr 1;10(7):2253–2264.

Published In

Clin Cancer Res

DOI

ISSN

1078-0432

Publication Date

April 1, 2004

Volume

10

Issue

7

Start / End Page

2253 / 2264

Location

United States

Related Subject Headings

  • Time Factors
  • Rituximab
  • Oncology & Carcinogenesis
  • Middle Aged
  • Maximum Tolerated Dose
  • Male
  • Lymphoma, B-Cell
  • Lymphocytes
  • Lymphocyte Subsets
  • Liver