The Goldilocks Window of Personalized Chemotherapy: Getting the Immune Response Just Right

Cancer Res. 2019 Oct 15;79(20):5302-5315. doi: 10.1158/0008-5472.CAN-18-3712. Epub 2019 Aug 6.

Abstract

The immune system is a robust and often untapped accomplice of many standard cancer therapies. A majority of tumors exist in a state of immune tolerance where the patient's immune system has become insensitive to the cancer cells. Because of its lymphodepleting effects, chemotherapy has the potential to break this tolerance. To investigate this, we created a mathematical modeling framework of tumor-immune dynamics. Our results suggest that optimal chemotherapy scheduling must balance two opposing objectives: maximizing tumor reduction while preserving patient immune function. Successful treatment requires therapy to operate in a "Goldilocks Window" where patient immune health is not overly compromised. By keeping therapy "just right," we show that the synergistic effects of immune activation and chemotherapy can maximize tumor reduction and control. SIGNIFICANCE: To maximize the synergy between chemotherapy and antitumor immune response, lymphodepleting therapy must be balanced in a "Goldilocks Window" of optimal dosing.Graphical Abstract: http://cancerres.aacrjournals.org/content/canres/79/20/5302/F1.large.jpg.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / pharmacology
  • Cancer Vaccines / administration & dosage
  • Cancer Vaccines / therapeutic use*
  • Cytotoxicity, Immunologic
  • Dose-Response Relationship, Drug
  • Dose-Response Relationship, Immunologic
  • Drug Administration Schedule
  • Humans
  • Immune System / drug effects*
  • Immunologic Memory
  • Immunotherapy* / adverse effects
  • Immunotherapy* / methods
  • Lymphocyte Depletion
  • Models, Immunological*
  • Neoplasms / drug therapy
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Neutropenia / chemically induced
  • Neutropenia / immunology
  • Precision Medicine*
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / immunology
  • Tumor Escape
  • Tumor Microenvironment / immunology

Substances

  • Antineoplastic Agents
  • Cancer Vaccines