Evidence map›Paper›PMID 42661232›Full record

ArticleCancer imaging : the official publication of the International Cancer Imaging Society2026

Heterogeneous treatment response in metastatic breast cancer: discordance between FDG-PET and CT classification.

Vilma Landfors Andersson, Kristin Johnson, Ida Skarping

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Article in Cancer imaging : the official publication of the International Cancer Imaging Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Vilma Landfors AnderssonFaculty of Medicine, Lund University, Lund, Sweden.
Kristin JohnsonDepartment of Translational Medicine, Diagnostic Radiology, Lund University, Malmö, Sweden.ORCID https://orcid.org/0000-0002-5099-423X
Ida SkarpingDepartment of Imaging, Physiology, and Nuclear Medicine, Skåne University Hospital, Region Skåne, Sweden. ida.skarping@med.lu.se.ORCID http://orcid.org/0000-0002-1265-8649

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeterogeneous treatment response, characterized by simultaneous regression of some lesions and progression of others within the same patient, is increasingly recognized in metastatic breast cancer (mBC) and may reflect biological heterogeneity. However, this response pattern is not captured by current response assessment frameworks. We aimed to determine the prevalence of heterogeneous treatment response on FDG-PET and mixed response on CT during mBC systemic therapy.

methodsThis retrospective study included 51 female patients with mBC, treated between November 2017 and November 2025, each undergoing ≥ 2 FDG-PET/CT scans. Response was assessed according to RECIST 1.1 (CT) and PERCIST (FDG-PET), with using study‑specific definitions for heterogeneous/mixed response informed by literature.

resultsHeterogeneous metabolic response was observed in 30% of all follow‑up FDG‑PET examinations (40/132). These examinations accounted for 60% (40/67) of the scans classified as progressive metabolic disease (PMD) according to PERCIST. Among CT-examinations, 65 of 141 (46%) follow-up examinations had measurable disease; none of these scans (0/65, 0%) fulfilled the mixed response criteria.

conclusionIn this real-world cohort of mBC undergoing systemic therapy, FDG-PET identified heterogeneous treatment response in a substantial proportion of patients; however, under current PERCIST criteria, these cases were uniformly classified as PMD. In contrast, using RECIST-inspired criteria, CT did not classify any patient as mixed response. These findings suggest that existing frameworks may not fully capture intra-patient response heterogeneity. As heterogeneous response is not an established PERCIST response category, further work is needed to determine how such patterns should be defined and incorporated into future response assessment frameworks. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Breast NeoplasmsPositron Emission Tomography Computed TomographyTomography, X-Ray ComputedAdultAgedAged, 80 and overFemaleFluorodeoxyglucose F18HumansMiddle AgedNeoplasm MetastasisPositron-Emission TomographyRadiopharmaceuticalsRetrospective StudiesTreatment Effect HeterogeneityFluorodeoxyglucose F18RadiopharmaceuticalsCTFDG-PETHeterogeneous responseMetastatic breast cancerTreatment evaluation

Identifiers

PMID42661232
PMCPMC13520370

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.