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  • Open Access

Stable disease after high dose interleukin-2 (HD IL-2) immunotherapy: observations on long term survival and clinical benefit of additional HD IL-2

  • 1,
  • 2,
  • 3,
  • 4,
  • 5,
  • 6 and
  • 7
Journal for ImmunoTherapy of Cancer20142 (Suppl 3) :P88

  • Published:


  • Melanoma
  • Renal Cell Carcinoma
  • Stable Disease
  • Metastatic Melanoma
  • Metastatic Renal Cell Carcinoma
Patients with stable disease (SD) following cancer treatment have traditionally not been considered responders. We, and others, have previously shown that SD is an important response criteria in cancer patients treated with HD IL-2 immunotherapy [15]. Here we summarize findings from 13 sites, including 97 mRCC and 170 mM patients enrolled in the retrospective cohort of a national HD IL-2 database ( Patients in the database were enrolled between 2006-2011, in an era of immune checkpoint inhibitors and targeted therapies. In metastatic renal cell carcinoma (mRCC) the median overall survival (mOS) was not reached in patients assessed to have SD post HD IL-2 (Figure 1). The mOS was over 2.5 years in patients with stable disease with metastatic melanoma (mM). The median follow-up for both diseases was 3 years. We further sought to examine whether patients with SD after 1 course, received benefit with additional HD IL-2 treatment. In mRCC patients that did not respond to treatment but continued onto another cycle of HD IL-2, the mOS was not reached and was statistically significant from patients that stopped treatment (p = 0.0269) (Figure 2).
Figure 1
Figure 1

Time Since First Dose of IL-2, Months.

Figure 2
Figure 2

Time Since First Dose of IL-2, Months.


Unlike chemotherapy and targeted therapies, immunotherapeutics have the unique potential to achieve long lasting durable responses in cancer. The continual homeostasis between the immune system and the tumor requires constant immune pressure, and tipping the balance toward the immune system using immunotherapy may be important. Registries such as PROCLAIMSM provide data which may guide the optimal sequencing of therapies and/or prioritization of randomized clinical trials [6].


We conclude that stable disease is durable and should be considered a valuable end point. Consolidation of this response with additional HD IL-2 treatment following SD may be important.

Authors’ Affiliations

Rutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA
Prometheus Laboratory, San Diego, CA, USA
Duke University, Durham, NC, USA
Department of Medicine, University of Southern California, Los Angeles, CA, USA
Prometheus Laboratory, San Diego, CA, USA
Moores Cancer Center, San Diego, CA, USA
Beth Israel Hospital Deaconess Medical Center, Boston, MA, USA


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© Kaufman et al.; licensee BioMed Central Ltd. 2014

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