Sequencing of a central nervous system tumor demonstrates cancer transmission in an organ transplant

Life Sci Alliance. 2021 Jul 22;4(9):e202000941. doi: 10.26508/lsa.202000941. Print 2021 Sep.

Abstract

Four organ transplant recipients from an organ donor diagnosed with anaplastic pleomorphic xanthoastrocytoma developed fatal malignancies for which the origin could not be confirmed by standard methods. We identified the somatic mutational profiles of the neoplasms using next-generation sequencing technologies and tracked the relationship between the different samples. The data were consistent with the presence of an aggressive clonal entity in the donor and the subsequent proliferation of descendent tumors in each recipient. Deleterious mutations in BRAF, PIK3CA, SDHC, DDR2, and FANCD2, and a chromosomal deletion spanning the CDKN2A/B genes, were shared between the recipients' lesions. In addition to demonstrating that DNA sequencing tracked a donor/recipient cancer transmission, this study established that the genetic profile of a donor tumor and its potential aggressive phenotype could have been determined before transplantation was considered. As the genetic correlates of tumor invasion and metastases become better known, adding genetic profiling by DNA sequencing to the data considered for transplant safety should be considered.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Biomarkers, Tumor / genetics*
  • Biopsy
  • Central Nervous System Neoplasms / etiology*
  • Central Nervous System Neoplasms / mortality
  • Central Nervous System Neoplasms / pathology*
  • DNA Mutational Analysis
  • Exome Sequencing
  • Female
  • Humans
  • INDEL Mutation
  • Male
  • Middle Aged
  • Mutation
  • Organ Transplantation / adverse effects*
  • Organ Transplantation / methods
  • Prognosis
  • Sequence Analysis, DNA* / methods
  • Tissue Donors
  • Transplant Recipients
  • Transplants / pathology*
  • Young Adult

Substances

  • Biomarkers, Tumor