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

 Practical decision pathway for response-adaptive biomarker use.

Clinical questionMost relevant toolPossible actionCaution/evidence status
Is ER expression still functionally present across disease sites?FES PET/CT, alongside pathology and standard imagingSupport endocrine-based strategy discussion or identify discordant lesion for biopsy.Most useful when linked to a specific endocrine decision; not a universal biopsy replacement.
Is HER2 expression heterogeneous or converted when tissue is inaccessible?HER2-targeted PET where availablePrioritise biopsy site or support multidisciplinary treatment discussion.Exploratory/problem-solving; outcome benefit of PET-directed therapy remains unproven.
Is apparent early progression during ICI therapy true progression?FDG PET/CT interpreted with immunotherapy-aware criteriaCorrelate clinically; consider confirmation imaging in stable patients before changing therapy.TNBC-specific validation is limited; inflammatory uptake can mislead.
Is early response sufficient to consider adaptation?FDG PET/CT plus serial ctDNA in predefined protocolsEscalation or surveillance adaptation only within trials or highly selected MDT contexts.De-escalation is highest risk and requires prospective outcome validation.

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