From:  Response-adaptive breast cancer care in the grey zones: integrating ER and HER2 targeted PET, FDG PET/CT under immunotherapy, and ctDNA kinetics

 Evidence maturity and clinical readiness of reviewed biomarker applications.

Biomarker domainMore established usePromising but not yet practice-shapingInvestigational/conceptual use
FES PET/CTProblem-solving whole-body ER mapping in selected ER-positive disease when receptor status or disease extent is uncertain.Refining endocrine-treatment selection and biopsy targeting in heterogeneous disease.Routine response-adaptive escalation/de-escalation based on FES patterns alone.
HER2-targeted PETNo broad routine indication; use remains mainly specialised and problem-solving.Detection of suspected HER2 conversion/heterogeneity when biopsy is infeasible or inconclusive.PET-directed anti-HER2 treatment selection without prospective outcome validation.
FDG PET/CT under immunotherapyWhole-body metabolic assessment when conventional imaging is equivocal or bone-dominant disease limits RECIST.Immunotherapy-aware interpretation of atypical response patterns in TNBC.Treatment continuation, discontinuation, or escalation based on a single early PET scan.
FDG PET/CT + ctDNActDNA genotyping in selected metastatic settings; PET for spatial disease assessment.Combined risk stratification and surveillance concepts in trial settings.Routine treatment de-escalation or escalation based only on early combined biomarker kinetics.

ctDNA: circulating tumour DNA; ER: oestrogen receptor; TNBC: triple-negative breast cancer; HER2: human epidermal growth factor receptor 2; PET/CT: positron emission tomography/computed tomography.