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Second diagnostic phase - special investigations

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Second diagnostic phase - special investigations

  • tumour markers
    • do not measure tumour markers during diagnosis except for:
      • AFP and hCG in patients with presentations compatible with germ-cell tumours (particularly those with mediastinal and/or retroperitoneal masses and in young men)
      • AFP in patients with presentations compatible with hepatocellular cancer
      • PSA in men with presentations compatible with prostate cancer
      • CA125 in women with presentations compatible with ovarian cancer (including those with inguinal node, chest, pleural, peritoneal or retroperitoneal presentations)
    • carefully interpret the results because of limited test specificity

  • upper and lower gastrointestinal endoscopy
    • do not carry out upper or lower gastrointestinal (GI) endoscopy in patients with metastatic disease of unknown origin (MUO) unless the symptoms, histology or radiology suggest a GI primary tumour

  • mammography
    • do not offer mammography routinely to women presenting with MUO, unless clinical or pathological features are compatible with breast cancer
  • breast magnetic resonance imaging efer patients with adenocarcinoma involving the axillary nodes to a breast cancer MDT for evaluation and treatment. If no breast primary tumour is identified after standard breast investigations, consider dynamic contrast-enhanced breast magnetic resonance imaging (MRI) to identify lesions suitable for targeted biopsy

  • positron emission tomography-computed tomography
    • offer positron emission tomography-computed tomography (18F-FDG PET-CT) to patients with provisional CUP presenting with cervical lymphadenopathy with no primary tumour identified on ear, nose and throat panendoscopy if radical treatment is considered to be an option.
    • consider 18F-FDG PET-CT in patients with provisional cancer with unknonw primary with extra-cervical presentations

  • immunohistochemistry
    • use a panel of antibodies comprising cytokeratin 7 (CK7), CK20, thyroid transcription factor-1 (TTF-1), placental alkaline phosphatase (PLAP), oestrogen receptor (ER; women only) and PSA (men only) in all patients with adenocarcinoma of unknown origin
    • use additional immunohistochemistry to refine the differential diagnosis, guided by the results of the panel of antibodies

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