J Hoffend1, C Sachpekidis2,3, A Dimitrakopoulou-Strauss2. 1. Onkologische Diagnostik/PET-CT, Zentralinstitut für diagnostische und interventionelle Radiologie, Klinikum der Stadt Ludwigshafen am Rhein gGmbH, Bremserstraße 79, 67063, Ludwigshafen, Deutschland. hoffendj@klilu.de. 2. Klinische Kooperationseinheit Nuklearmedizin, Forschungsschwerpunkt Bildgebung und Radiologie, Deutsches Krebsforschungszentrum Heidelberg, Heidelberg, Deutschland. 3. Abteilung Radiologie, Forschungsschwerpunkt Bildgebung und Radiologie, Deutsches Krebsforschungszentrum Heidelberg, Heidelberg, Deutschland.
Abstract
CLINICAL/METHODICAL ISSUE: Established criteria to categorize metabolic tumor response to cytotoxic chemotherapies may not be suited to capture the effects of therapy with immune checkpoint inhibitors (ICI) or with kinase inhibitors (KI), such as BRAF or MEK inhibitors. NUCLEAR MEDICINE STANDARD METHODS: To assess the metabolic response to cytotoxic chemotherapy by positron emission tomography (PET) with 18F-fluorodeoxyglucose (FDG), the criteria of the European Organization for Research and Treatment of Cancer (EORTC) and the positron emission tomography response criteria in solid tumors (PERCIST) were conceived. The salient features of both criteria are detailed in a comparative way. PERFORMANCE AND ACHIEVEMENTS: To date only retrospective data exist for the evaluation of therapies with either ICI or KI. They show that response to ICI cannot be reliably determined using the established criteria. Employing the EORTC criteria the responses to KI can be adequately ascertained so that the metabolic tumor response in FDG-PET is regarded as a surrogate marker for the efficacy of these drugs. PRACTICAL RECOMMENDATIONS: Tumor response to therapy with ICI cannot at present be assessed with FDG-PET. Responses to BRAF and MEK inhibitors are, however, assessable using the criteria that were originally developed to evaluate responses to cytotoxic chemotherapy.
CLINICAL/METHODICAL ISSUE: Established criteria to categorize metabolic tumor response to cytotoxic chemotherapies may not be suited to capture the effects of therapy with immune checkpoint inhibitors (ICI) or with kinase inhibitors (KI), such as BRAF or MEK inhibitors. NUCLEAR MEDICINE STANDARD METHODS: To assess the metabolic response to cytotoxic chemotherapy by positron emission tomography (PET) with 18F-fluorodeoxyglucose (FDG), the criteria of the European Organization for Research and Treatment of Cancer (EORTC) and the positron emission tomography response criteria in solid tumors (PERCIST) were conceived. The salient features of both criteria are detailed in a comparative way. PERFORMANCE AND ACHIEVEMENTS: To date only retrospective data exist for the evaluation of therapies with either ICI or KI. They show that response to ICI cannot be reliably determined using the established criteria. Employing the EORTC criteria the responses to KI can be adequately ascertained so that the metabolic tumor response in FDG-PET is regarded as a surrogate marker for the efficacy of these drugs. PRACTICAL RECOMMENDATIONS: Tumor response to therapy with ICI cannot at present be assessed with FDG-PET. Responses to BRAF and MEK inhibitors are, however, assessable using the criteria that were originally developed to evaluate responses to cytotoxic chemotherapy.
Authors: Françoise Kraeber-Bodéré; Thomas Carlier; Valérie Meresse Naegelen; Eliezer Shochat; Jean Lumbroso; Carlos Trampal; James Nagarajah; Sue Chua; Florent Hugonnet; Marcel Stokkel; Fergus Gleeson; Jean Tessier Journal: J Nucl Med Date: 2012-11-09 Impact factor: 10.057
Authors: H Young; R Baum; U Cremerius; K Herholz; O Hoekstra; A A Lammertsma; J Pruim; P Price Journal: Eur J Cancer Date: 1999-12 Impact factor: 9.162
Authors: Antoni Ribas; Matthias R Benz; Martin S Allen-Auerbach; Caius Radu; Bartosz Chmielowski; Elizabeth Seja; John L Williams; Jesus Gomez-Navarro; Timothy McCarthy; Johannes Czernin Journal: J Nucl Med Date: 2010-02-11 Impact factor: 10.057
Authors: Jedd D Wolchok; Axel Hoos; Steven O'Day; Jeffrey S Weber; Omid Hamid; Celeste Lebbé; Michele Maio; Michael Binder; Oliver Bohnsack; Geoffrey Nichol; Rachel Humphrey; F Stephen Hodi Journal: Clin Cancer Res Date: 2009-11-24 Impact factor: 12.531
Authors: Benjamin Y Kong; Alexander M Menzies; Catherine A B Saunders; Elizabeth Liniker; Sangeetha Ramanujam; Alex Guminski; Richard F Kefford; Georgina V Long; Matteo S Carlino Journal: Pigment Cell Melanoma Res Date: 2016-08-04 Impact factor: 4.693