Two enemies, one fight: An update of oral cancer in patients with Fanconi anemia

Cancer. 2019 Nov 15;125(22):3936-3946. doi: 10.1002/cncr.32435. Epub 2019 Aug 7.

Abstract

Fanconi anemia (FA) is a rare inherited genetic condition that may lead to bone marrow failure, leukemia, and/or solid tumors. It is caused by the loss of function of at least 1 gene of the FA/BRCA pathway, which is necessary for DNA repair. Patients with FA have a 200-fold to 1000-fold risk of developing head and neck cancer, mainly oral squamous cell carcinoma (OSCC), and of doing so at a much younger age than individuals within the general population. Also, patients who have FA with OSCC have poor overall survival rates, reinforcing the necessity to detect OSCC early. The scope of the current review is to provide an update on OSCC in patients with FA.

Keywords: Fanconi anemia; cancer screening; oral cancer; squamous cell carcinoma.

Publication types

  • Review

MeSH terms

  • Combined Modality Therapy
  • Disease Management
  • Disease Susceptibility
  • Fanconi Anemia / complications*
  • Fanconi Anemia / diagnosis
  • Fanconi Anemia / epidemiology*
  • Fanconi Anemia / etiology
  • Genetic Predisposition to Disease
  • Humans
  • Mouth Neoplasms / diagnosis
  • Mouth Neoplasms / epidemiology*
  • Mouth Neoplasms / etiology*
  • Mouth Neoplasms / therapy
  • Risk Factors
  • Treatment Outcome