Factors associated with response to high-dose interleukin-2 in patients with metastatic melanoma

J Clin Oncol. 2001 Aug 1;19(15):3477-82. doi: 10.1200/JCO.2001.19.15.3477.

Abstract

Purpose: The present study attempted to identify characteristics that correlated with clinical response to interleukin (IL)-2 therapy in patients with metastatic melanoma.

Patients and methods: We retrospectively evaluated laboratory and clinical characteristics of 374 consecutive patients with metastatic melanoma treated with high-dose intravenous bolus IL-2 (720,000 IU/kg) from July 1, 1988, to December 31, 1999, at the Surgery Branch of the National Cancer Institute.

Results: The overall objective response rate was 15.5%. Pretreatment parameters such as patient demographics, laboratory values, and prior therapy did not correlate with response; however, 53.6% of patients with only subcutaneous and/or cutaneous metastases responded, compared with 12.4% of patients with disease at other sites (P2 =.000001). During therapy, patients who were responders tended to have received more doses during course 1 (16.2 +/- 0.3 doses v 14.5 +/- 0.2 doses; P2 =.0095); however, when limited to patients who were able to complete both cycles of course 1, there was no statistically significant difference (P2 =.27). Responders had a higher maximum lymphocyte count immediately after therapy compared with nonresponders (P2 =.0026). The development of abnormal thyroid function tests and vitiligo after therapy was associated with response (thyroid-stimulating hormone, P2 =.01; free T4, P2 =.0049; vitiligo, P2 < 10(-6)), although thyroid dysfunction may have been related more to the length of IL-2 therapy than to response.

Conclusion: The presence of metastases only to subcutaneous and/or cutaneous sites, lymphocytosis immediately after treatment, and long-term immunologic side effects, especially vitiligo, were associated with antitumor response to IL-2 therapy.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Injections, Intravenous
  • Interleukin-2 / adverse effects
  • Interleukin-2 / therapeutic use*
  • Lymphocytosis / chemically induced
  • Male
  • Melanoma / blood
  • Melanoma / drug therapy*
  • Melanoma / secondary
  • Middle Aged
  • Recombinant Proteins / therapeutic use
  • Retrospective Studies
  • Skin Neoplasms / drug therapy
  • Skin Neoplasms / secondary
  • Thyrotropin / blood
  • Thyroxine / blood
  • Treatment Outcome

Substances

  • Interleukin-2
  • Recombinant Proteins
  • Thyrotropin
  • Thyroxine