<sup>18</sup> F-Fluorodeoxyglucose Positron Emission Tomography for Estimating Outcomes After Initial Treatment for Metastatic Breast Cancer
Importance: Optimizing treatment decisions in metastatic breast cancer (MBC) can alleviate patients' burden and improve quality of life. Whether 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) can be used to better estimate outcomes is unknown. Objective: To evaluate clinical utility of early metabolic change on FDG-PET for improving outcome estimation compared with standard diagnostic evaluation in patients with newly diagnosed MBC. Design, Setting, and Participants: The multicenter IMPACT-MBC clinical cohort trial enrolled patients with nonrapidly progressive, newly diagnosed MBC from August 2013 to May 2018, before initiation of first-line systemic therapy. Baseline assessment included metastasis biopsy procedure and FDG-PET and CT imaging. Early FDG-PET was performed after 2 weeks of treatment, and CT response evaluation after 8 weeks. Clinical utility was defined as the ability of early FDG-PET to estimate progressive disease (PD) on CT, progression-free survival (PFS), and overall survival (OS). Data were analyzed from October 19, 2025, to February 13, 2026. Intervention: Early FDG-PET or standard-of-care (SOC) biopsy-based treatment. Main Outcomes and Measures: Clinical utility of molecular imaging to improve outcome estimation of standard diagnostics defined as the capacity to identify poor patient outcomes. Measures were PD at 8 weeks, PFS, and OS. Results: The analysis included 200 patients (median [range] age, 61 [32-84] years; 198 females [99%] and 2 males [1%]). Non-PD on early FDG-PET had a negative predictive value (NPV) of 94.7% (95% CI, 89.5%-97.4%) for non-PD on 8-week CT. This was similar in all MBC subtypes and bone-only disease. Patients with SOC treatment and non-PD on early FDG-PET (n = 133) had a median PFS of 19.4 (95% CI, 15.2-22.8) months and OS of 39.4 (95% CI, 33.7-48.3) months compared to 4.1 (95% CI, 3.3-15.5) months and 18.5 (95% 3 CI, 7.0-33.0) months, respectively (P < .001 for both). Patients with non-PD on 8-week CT but with PD on early FDG-PET had a median (IQR) PFS and OS of 9.5 (4.1-18.1) and 19.4 (8.7-33.0) months compared to 22.3 (15.3-96.1) months and 40.1 (23.4-72.7) months without PD. Conclusions and Relevance: In this clinical cohort trial of patients with nonrapidly progressive, newly diagnosed MBC before initiation of first-line systemic therapy, early FDG-PET after only 2 weeks of treatment identified patients with MBC with distinct long-term outcomes. Incorporating early FDG-PET can improve outcome estimation of standard CT assessment. Trial Registration: ClinicalTrials.gov Identifier: NCT01957332.
Authors
- Wim J.G. Oyen (ORCID: https://orcid.org/0000-0001-8235-7078)
- Sophie L. Gerritse (ORCID: https://orcid.org/0000-0002-6287-4016)
- Albert D. Windhorst (ORCID: https://orcid.org/0000-0002-1250-7656)
- Ellis Barbé
- Daniëlle J. Vugts (ORCID: https://orcid.org/0000-0001-7068-8152)
- Bert van der Vegt (ORCID: https://orcid.org/0000-0002-2613-1506)
- Otto C. Boerman (ORCID: https://orcid.org/0000-0001-6832-101X)
- Wim Mali
- Jelle Overbosch
- Erik van Helden
- Evelien J. M. Kuip (ORCID: https://orcid.org/0000-0002-9114-643X)
- Jorianne Boers (ORCID: https://orcid.org/0000-0002-1143-4432)
- Monique D. Dorrius (ORCID: https://orcid.org/0000-0001-9825-6001)
- Gonda de Jonge
- Harm van Tinteren (ORCID: https://orcid.org/0000-0002-4626-8702)
- Sigrid Stroobants (ORCID: https://orcid.org/0000-0002-6450-9944)
- Jasper JL van Geel
- Bertha Eisses (ORCID: https://orcid.org/0000-0002-9288-0353)
- Özgül Ekmekçioğlu (ORCID: https://orcid.org/0000-0002-3313-8087)
- Frederike Bensch (ORCID: https://orcid.org/0000-0001-8648-0612)
- Mieke C. Zwager (ORCID: https://orcid.org/0000-0002-4470-7628)
- Eline Boon (ORCID: https://orcid.org/0000-0002-9768-2911)
- Marcel Janssen (ORCID: https://orcid.org/0000-0002-5754-6050)
- Adrienne H. Brouwers (ORCID: https://orcid.org/0000-0003-2698-1516)
- Jasper Emmering
- Erik Buskens (ORCID: https://orcid.org/0000-0002-6463-1106)
- Katja van Rij
- Carolina P. Schröder (ORCID: https://orcid.org/0000-0001-7537-489X)
- Anne I.J. Arens (ORCID: https://orcid.org/0000-0001-7066-5372)
- Ton Velleman (ORCID: https://orcid.org/0000-0002-5731-7258)
- Jaco Kraan (ORCID: https://orcid.org/0000-0001-7445-7984)
- Lindsay Angus (ORCID: https://orcid.org/0000-0002-7928-1102)
- Sarah R. Verhoeff (ORCID: https://orcid.org/0000-0003-4679-8938)
- Suzanne van Es
- Schuuring
- Jolien Tol
- Astrid van der Veldt
- Harry Hendrikse
- Carla van Herpen
- Winette van der Graaf
- Marc Huisman
- John Martens
- Guus van Dongen
- Otto Hoekstra
- Eric Visser
- Rudy Dierckx
- Henk Verheul
- Theo Kok
- Peter Bult
- Geke Hospers
- Anita Siewerts
- Elisabeth G. E. de Vries
- Stefan Sleijffer
- Karl Moons
- Annemarie Jorritsma
- Ronald Boellaard
- Marjolijn N. Lub-de Hooge
- Agnes Jager
- Sjoerd G. Elias
- C. Willemien Menke-van der Houven van Oord
- Martijn Dekker
- Shekar Mahesh
- Daniela E. Oprea-Lager
- Andor W. J. M. Glaudemans
- Thomas Kwee
- Jeroen Janssen
- Lioe-Fee de Geus-Oei
Institutions
- University Medical Center Groningen (NL)
- Humanitas University (IT)
- Radboud University Nijmegen (NL)
- University of Groningen (NL)
- Breast Cancer Research Foundation (US)
- Erasmus MC (NL)
- Radboud University Medical Center (NL)
- University Medical Center Utrecht (NL)
- Maasstad Ziekenhuis (NL)
- Oncode Institute (NL)
- Metastatic Breast Cancer Network (US)
- Erasmus MC Cancer Institute (NL)
- Amsterdam University Medical Centers (NL)
- Rijnstate Hospital (NL)
- Erasmus University Rotterdam (NL)
Publication Details
- Journal
- JAMA Oncology
- Published
- 2026-04-16
- DOI
- https://doi.org/10.1001/jamaoncol.2026.0767
- Primary Topic
- Medical Imaging Techniques and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00