Cancer of unknown primary

BMJ. 2020 Dec 7:371:m4050. doi: 10.1136/bmj.m4050.

Abstract

Cancers of unknown primary (CUPs) are histologically confirmed, metastatic malignancies with a primary tumor site that is unidentifiable on the basis of standard evaluation and imaging studies. CUP comprises 2-5% of all diagnosed cancers worldwide and is characterized by early and aggressive metastasis. Current standard evaluation of CUP requires histopathologic evaluation and identification of favorable risk subtypes that can be more definitively treated or have superior outcomes. Current standard treatment of the unfavorable risk subtype requires assessment of prognosis and consideration of empiric chemotherapy. The use of molecular tissue of origin tests to identify the likely primary tumor site has been extensively studied, and here we review the rationale and the evidence for and against the use of such tests in the assessment of CUPs. The expanding use of next generation sequencing in advanced cancers offers the potential to identify a subgroup of patients who have actionable genomic aberrations and may allow for further personalization of therapy.

Publication types

  • Review

MeSH terms

  • Anaplastic Lymphoma Kinase / genetics
  • Antineoplastic Agents / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Biomarkers, Tumor / metabolism*
  • Biopsy
  • Circulating Tumor DNA / genetics
  • Gene Expression Profiling*
  • Genes, erbB-1
  • Genes, erbB-2
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • Lymph Nodes / pathology
  • Mammography
  • Molecular Diagnostic Techniques*
  • Molecular Targeted Therapy
  • Mutation
  • Neoplasms, Unknown Primary / diagnosis*
  • Neoplasms, Unknown Primary / drug therapy
  • Neoplasms, Unknown Primary / epidemiology
  • Neoplasms, Unknown Primary / genetics
  • Occult Blood
  • Physical Examination
  • Physical Functional Performance
  • Positron Emission Tomography Computed Tomography
  • Proto-Oncogene Proteins B-raf / genetics
  • Real-Time Polymerase Chain Reaction
  • Risk Assessment
  • Tomography, X-Ray Computed

Substances

  • Antineoplastic Agents
  • Biomarkers, Tumor
  • Circulating Tumor DNA
  • Anaplastic Lymphoma Kinase
  • Proto-Oncogene Proteins B-raf