Abstract

ObjectivesConcomitant radiotherapy with immune checkpoint blockade could be synergistic. Out-of-field effects could improve survival by slowing or blocking metastatic spreading. However, not much is known about the optimal size per fraction and inter-fraction time in that new context.MethodsThe new concept of Immunologically Effective Dose (IED) is proposed: it models an intrinsic immunogenicity of radiotherapy schedules, i.e. the fraction of immunogenicity that results from the choice of the dosing regimen. The IED is defined as the single dose, given in infinitely low dose rate, that produces the same amount of abscopal response as the radiation schedule being considered. The IED uses the classic parameters of the BED formula and adds two parameters for immunogenicity that describe the local availability of immune effectors within the tumor micro-environment. Fundamentally, the IED adds a time dimension in the BED formula and describes an intrinsic immunogenicity level for radiotherapy.ResultsThe IED is positively related to the intensity of the out-of-field, radiotherapy-mediated, immune effects described in some preclinical data. Examples of numerical simulations are given for various schedules. A web-based calculator is freely available.ConclusionsOut-of-field effects of radiotherapy with immune checkpoint blockers might be better predicted and eventually, radiotherapy schedules with better local and systemic immunogenicity could be proposed.Advances in knowledgeA model for the intrinsic level of immunogenicity of radiotherapy schedules, referred to as the Immunologically Effective Dose (IED), that is independent of the type of immunotherapy.

Highlights

  • The abscopal effect of radiotherapy describes a rarely observed phenomenon in which one or more metastases located out of the irradiation field regress at some point in time after radiotherapy [1]

  • The Immunologically Effective Dose (IED) is positively related to the intensity of the out-of-field, radiotherapy-mediated, immune effects described in some preclinical data

  • Advances in knowledge: A model for the intrinsic level of immunogenicity of radiotherapy schedules, referred to as the Immunologically Effective Dose (IED), that is independent of the type of immunotherapy

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Summary

Introduction

The abscopal effect of radiotherapy describes a rarely observed phenomenon in which one or more metastases located out of the irradiation field regress at some point in time after radiotherapy [1]. The out-of-field mechanism could initially involve an in-field recruitment of dendritic cells (DC) and other types of Antigen Presenting Cells (APC) in the tumour micro-environment, attracted by radiation-induced inflammation and necrosis These immune effectors have a strong radio-sensitivity: lymphocytes are among the most radiosensitive cells within the body (with doses as low as 0.5 Gy already strongly cytotoxic [5]), while DC and APC may survive higher doses but quickly suffer loss of function [6]. The quantity of tumour antigens could be mainly driven by the size of the dose per fraction and the radio sensitivity of tumour cells: higher doses per fraction could release larger quantities of tumour antigens and produce an increased diversity of epitopes This reasoning, supported by experimental confirmations from the preclinical setup [8] and several clinical reports, has aroused interest in hypo-fractionated schedules for recent clinical trials of radio-immunotherapy [17]

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