Modulation of monocyte functions by muramyl tripeptide phosphatidylethanolamine in a phase II study in patients with metastatic melanoma

J Natl Cancer Inst. 1992 May 6;84(9):694-9. doi: 10.1093/jnci/84.9.694.

Abstract

Background: Muramyl tripeptide phosphatidylethanolamine (MTP-PE) is a synthetic analogue of muramyl dipeptide (MDP), a component of bacterial cell walls that has potent in vitro monocyte-activating properties. We conducted a phase II clinical trial of MTP-PE in 30 patients with metastatic melanoma.

Purpose: Our purpose was to define a clinical response rate for this agent in patients with advanced melanoma and to evaluate the agent's immunomodulatory properties.

Methods: Patients were randomly assigned to 1- or 4-mg dose levels of MTP-PE and received the drug intravenously once a week for 12-24 weeks. Immunological monitoring consisted of measurement of plasma tumor necrosis factor-alpha (TNF-alpha), neopterin, interleukin-1-beta, interleukin-6 (IL-6), and beta 2-microglobulin levels; phenotyping analysis of expression of human HLA-DR, CD-14 on mononuclear cells; and measurement of in vitro monocyte cytotoxicity against SKMel28 targets cells.

Results: MTP-PE was well tolerated; fever and chills were the major toxic effects. Plasma TNF-alpha levels increased 16-fold 2 hours after the first MTP-PE treatment. Increases in TNF-alpha levels after MTP-PE administration continued through week 12, but changes were of a lower magnitude after week 1. Plasma neopterin levels were significantly increased 24 hours after treatment at weeks 1, 6, and 12. A marked increase in IL-6 and a modest rise in beta 2-microglobulin levels were also seen at week 1. No significant changes from baseline IL-1 beta were observed. In the cytotoxicity assay, monocyte cytotoxic activity was significantly increased at weeks 4 and 6. Surface immuno-phenotyping revealed a consistent transient reduction in the number of circulating monocytes 2 hours after MTP-PE was administered. In addition, we observed a down-regulation (i.e., a decrease) in the expression of Leu M3 and HLA-DR on monocytes, 2 hours after MTP-PE treatment, followed by a recovery 24 hours after treatment. No objective clinical responses were seen in this advanced disease population.

Conclusions: We conclude that MTP-PE has pleiotropic and potentially beneficial biologic effects and that further clinical investigations of MTP-PE are justified.

Implications: In view of the clear immunomodulatory actions seen in our study and in earlier clinical trials, we believe that MTP-PE deserves further study in the adjuvant setting.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetylmuramyl-Alanyl-Isoglutamine / analogs & derivatives*
  • Acetylmuramyl-Alanyl-Isoglutamine / therapeutic use
  • Adjuvants, Immunologic / therapeutic use*
  • Biopterins / analogs & derivatives
  • Biopterins / blood
  • Cytotoxicity, Immunologic
  • Drug Evaluation
  • Humans
  • Interleukin-1 / blood
  • Interleukin-6 / blood
  • Leukocyte Count
  • Melanoma / therapy*
  • Monocytes / immunology*
  • Neoplasm Metastasis
  • Neopterin
  • Phosphatidylethanolamines / therapeutic use*
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism
  • beta 2-Microglobulin / metabolism

Substances

  • Adjuvants, Immunologic
  • Interleukin-1
  • Interleukin-6
  • Phosphatidylethanolamines
  • Tumor Necrosis Factor-alpha
  • beta 2-Microglobulin
  • mifamurtide
  • Biopterins
  • Acetylmuramyl-Alanyl-Isoglutamine
  • Neopterin