Abstract

BackgroundIn ALK-positive advanced NSCLC, crizotinib has a high response rate and effectively increases quality of life and survival. CT measurement of the tumor may insufficiently reflect the actual tumor load changes during targeted therapy with crizotinib. We explored whether 18F-FDG PET measured metabolic changes are different from CT based changes and studied the impact of these changes on disease progression.Methods18F-FDG PET/CT was performed prior to and after 6 weeks of crizotinib treatment. Tumor response on CT was classified with RECIST 1.1, while 18F-FDG PET response was assessed according to the 1999 EORTC recommendations and PERCIST criteria. Agreement was assessed using McNemars test. During follow-up, patients received additional PET/CT during crizotinib treatment and second generation ALK inhibition. We assessed whether PET was able to detect progression earlier then CT.ResultsIn this exploratory study 15 patients were analyzed who were treated with crizotinib. There was a good agreement in the applicability of CT and 18F-FDG PET/CT using the EORTC recommendations. During first line crizotinib and subsequent second line ALK inhibitors, PET was able to detect progression earlier then CT in 10/22 (45%) events of progression and in the others disease progression was detected simultaneously.ConclusionIn advanced ALK positive NSCLC PET was able to detect progressive disease earlier than with CT in nearly half of the assessments while both imaging tests performed similar in the others.

Highlights

  • In clinical practice, tumor response measurements are performed using the anatomical CT based RECIST criteria[1]

  • There was a good agreement in the applicability of CT and 18F-FDG PET/CT using the EORTC recommendations

  • In advanced ALK positive NSCLC PET was able to detect progressive disease earlier than with CT in nearly half of the assessments while both imaging tests performed similar in the others

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Summary

Introduction

Tumor response measurements are performed using the anatomical CT based RECIST criteria[1]. It has been recognized that metabolic tumor changes as measured with 18F-FDG PET can be used as an indicator of effectiveness (EORTC recommendations[2], PERCIST[3]). Examples of this principle include imatinib treated gastrointestinal stromal tumors and EGFR-TKI treatment for EGFR mutated advanced NSCLC [4,5,6,7]. ALK positive advanced NSCLC are treated with different ALK inhibitors such as crizotinib, ceritinib and alectinib[8,9,10,11] Whether targeted treatment such as crizotinib induces quick metabolic changes, and whether these metabolic changes are related to lesions size alterations is currently unknown. We explored whether 18F-FDG PET measured metabolic changes are different from CT based changes and studied the impact of these changes on disease progression

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