Genetic convergence of rare lymphomas.

Published

Journal Article (Review)

PURPOSE OF REVIEW: We review the genetic foundations of different rare lymphomas to examine their shared origins. These data indicate the potential application of genomics to improve the diagnosis and treatment of these rare diseases. RECENT FINDINGS: Next generation sequencing technologies have provided an important window into the genetic underpinnings of lymphomas. A growing body of evidence indicates that although some genetic alterations are specific to certain diseases, others are shared across different lymphomas. Many such genetic events have already demonstrated clinical utility, such as BRAF V600E that confers sensitivity to vemurafenib in patients with hairy cell leukemia. SUMMARY: The rareness of many lymphoma subtypes makes the conduct of clinical trials and recruitment of significant numbers of patients impractical. However, a knowledge of the shared genetic origins of these rare lymphomas has the potential to inform 'basket' clinical trials in which multiple lymphoma subtypes are included. These trials would include patients based on the presence of alterations in targetable driver genes. Such approaches would be greatly strengthened by a systematic assessment of significant patient numbers from each subtype using next generation sequencing.

Full Text

Duke Authors

Cited Authors

  • Shingleton, JR; Dave, SS

Published Date

  • July 2018

Published In

Volume / Issue

  • 25 / 4

Start / End Page

  • 307 - 314

PubMed ID

  • 29702524

Pubmed Central ID

  • 29702524

Electronic International Standard Serial Number (EISSN)

  • 1531-7048

Digital Object Identifier (DOI)

  • 10.1097/MOH.0000000000000435

Language

  • eng

Conference Location

  • United States