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Low-dose interleukin-2 immunotherapy does not improve outcome of patients age 60 years and older with acute myeloid leukemia in first complete remission: Cancer and Leukemia Group B Study 9720.

Publication ,  Journal Article
Baer, MR; George, SL; Caligiuri, MA; Sanford, BL; Bothun, SM; Mrózek, K; Kolitz, JE; Powell, BL; Moore, JO; Stone, RM; Anastasi, J; Larson, RA ...
Published in: J Clin Oncol
October 20, 2008

PURPOSE: Cancer and Leukemia Group B (CALGB) 9720 evaluated subcutaneous low-dose recombinant interleukin-2 (rIL-2) maintenance immunotherapy as a strategy for prolonging remission in older patients with acute myeloid leukemia (AML). PATIENTS AND METHODS: AML patients age 60 years and older in first complete remission after induction and consolidation chemotherapy were randomly assigned to no further therapy or a 90-day regimen of 14-day cycles of low-dose rIL-2, aimed at expanding natural killer (NK) cells, followed by 3-day higher doses aimed at activating cytotoxicity of expanded NK cells to lyse residual AML cells. All randomly assigned patients were included in an intention-to-treat analysis. RESULTS: A total of 163 (64%) of 254 patients who completed induction and consolidation chemotherapy on CALGB 9720 were randomly assigned to rIL-2 (n = 81) or no further therapy (n = 82); the most common reasons for lack of random assignment were patient refusal and relapse. Fifteen patients randomly assigned to rIL-2 never initiated it because of refusal, intercurrent medical problems, or relapse, and 24 patients initiated rIL-2 but stopped early because of toxicity or relapse. Grade 4 toxicities during rIL-2 therapy included thrombocytopenia (65%) and neutropenia (64%), and grade 3 toxicities included anemia (33%), infection (24%) and malaise/fatigue (14%). Forty-two patients (52%) randomly assigned to rIL-2 completed the full 90-day course. Patients in both arms had similar distributions of both disease-free (combined median = 6.1 months; P = .47) and overall survival (combined median = 14.7 months; P = .61) after random assignment. Moreover, the 42 patients who completed all planned therapy did not show prolongation of disease-free or overall survival. CONCLUSION: Low-dose rIL-2 maintenance immunotherapy is not a successful strategy in older AML patients.

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Published In

J Clin Oncol

DOI

EISSN

1527-7755

Publication Date

October 20, 2008

Volume

26

Issue

30

Start / End Page

4934 / 4939

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Survival Rate
  • Remission Induction
  • Oncology & Carcinogenesis
  • Middle Aged
  • Male
  • Leukemia, Myeloid, Acute
  • Interleukin-2
  • Immunotherapy
  • Humans
 

Citation

APA
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Baer, M. R., George, S. L., Caligiuri, M. A., Sanford, B. L., Bothun, S. M., Mrózek, K., … Larson, R. A. (2008). Low-dose interleukin-2 immunotherapy does not improve outcome of patients age 60 years and older with acute myeloid leukemia in first complete remission: Cancer and Leukemia Group B Study 9720. J Clin Oncol, 26(30), 4934–4939. https://doi.org/10.1200/JCO.2008.17.0472
Baer, Maria R., Stephen L. George, Michael A. Caligiuri, Ben L. Sanford, Sandra M. Bothun, Krzysztof Mrózek, Jonathan E. Kolitz, et al. “Low-dose interleukin-2 immunotherapy does not improve outcome of patients age 60 years and older with acute myeloid leukemia in first complete remission: Cancer and Leukemia Group B Study 9720.J Clin Oncol 26, no. 30 (October 20, 2008): 4934–39. https://doi.org/10.1200/JCO.2008.17.0472.
Baer MR, George SL, Caligiuri MA, Sanford BL, Bothun SM, Mrózek K, Kolitz JE, Powell BL, Moore JO, Stone RM, Anastasi J, Bloomfield CD, Larson RA. Low-dose interleukin-2 immunotherapy does not improve outcome of patients age 60 years and older with acute myeloid leukemia in first complete remission: Cancer and Leukemia Group B Study 9720. J Clin Oncol. 2008 Oct 20;26(30):4934–4939.

Published In

J Clin Oncol

DOI

EISSN

1527-7755

Publication Date

October 20, 2008

Volume

26

Issue

30

Start / End Page

4934 / 4939

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Survival Rate
  • Remission Induction
  • Oncology & Carcinogenesis
  • Middle Aged
  • Male
  • Leukemia, Myeloid, Acute
  • Interleukin-2
  • Immunotherapy
  • Humans