Data from Early [18F]FDG PET/CT Response after a Single Dose of Anti-EGFR Therapy as a Predictive Biomarker for Treatment Benefit in Patients with Advanced Colorectal Cancer

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Authors: Sophie L. Gerritse, Erik Jacobus Van Helden, Anne I.J. Arens, Ronald Boellaard, Tineke E. Buffart, Mariëtte Labots, Lindsay Angus, Elisabeth G. E. de Vries, Derk Jan A. de Groot, Hans F. M. Pruijt, Rutger H.T. Koornstra, Otto S. Hoekstra
+4 more Gerben J.C. Zwezerijnen, Elske C. Gootjes, Henk M.W. Verheul, C. Willemien Menke‐van der Houven van Oordt
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Abstract

AbstractPurpose: Anti-EGFR mAb therapy improves the clinical outcome of patients with metastatic colorectal cancer (mCRC). This study assessed the predictive value of early [18F]fluorodeoxyglucose ([18F]FDG) PET/CT after one anti-EGFR mAb treatment in patients with mCRC. Patients and Methods: The multicenter IMPACT-CRC study (NCT02117466) prospectively included patients with mCRC receiving second- or third-line anti-EGFR mAb monotherapy. Clinical benefit (complete/partial response or stable disease per RECIST version 1.1) was determined with CT at 8 weeks. [18F]FDG PET/CT scans were performed at baseline and before the second treatment cycle (2 weeks). Total lesion glycolysis (TLG) change was evaluated as a predictive biomarker for clinical benefit using a predetermined data-driven threshold. Results: In patients with RAS/BRAF wild-type left-sided mCRC, the clinical benefit rate was 92% (31% partial response, 61% stable disease), with a median progression-free survival of 5.7 months (95% CI, 5.2–10). Seventy-five patients, including those with right-sided mCRC, were eligible for metabolic response analysis. Patients with clinical benefit (n = 57) showed a mean decrease in sum TLG of 58% (SD = 19%), compared with 1.9% (SD = 36%) in those without clinical benefit (n = 18; P = 0.003). A threshold of

Fields of Study & Subjects

Colorectal Cancer Treatments and Studies Radiomics and Machine Learning in Medical Imaging Medical Imaging Techniques and Applications

Publication details

Publication date
6 January 2026