Molecular profiling of breast and lung cancer in women with HIV reveals high tumor mutational burden

Carolina Caro-Vegas, Catalina Ramirez, Justin Landis, Adaora A. Adimora, Howard Strickler, Audrey L. French, Igho Ofotokun, Margaret Fischl, Eric C. Seaberg, Chia Ching J. Wang, Amanda B. Spence, Dirk P. Dittmer

Research output: Contribution to journalArticlepeer-review

Abstract

Objective: This study compared the mutation profile and tumor mutational burden (TMB) in women with HIV (WWH) diagnosed with lung adenocarcinoma (n = 8) or breast ductal neoplasm (n = 13) who were enrolled into the Women's Interagency HIV Study (WIHS). Design: Previous studies tended to focus on single institutions based on sample availability. This study is based on a representative, multicenter cohort that represents the racial and ethnic composition of women with HIV in the United States Methods: The study sequenced the complete human exome of n = 26 cancer samples from HIV-positive women, using Ion torrent next-generation sequencing. The study cohort was compared with a HIV-negative cohort obtained from the Genomic Data Commons Data Portal of the NCI. Results: There were no differences in known cancer mutations between breast cancer and lung cancer that developed in WWH and those that developed in HIV-negative (HIV-) women; however, WWH presented a significantly higher TMB in comparison to HIV- patients. Seventy-five percent of lung cancers and 61% of breast cancers were defined as TMB-high (more than 10 mutation/mb of DNA). Conclusion: This study affirms the recommendation that WWH be included in clinical trials of novel treatments for these cancers. Although these data are preliminary, the high TMB in WLHV suggests, paradoxically, that this immune challenged population may benefit greatly from immune checkpoint inhibitor therapies.

Original languageEnglish (US)
Pages (from-to)567-571
Number of pages5
JournalAIDS
Volume36
Issue number4
DOIs
StatePublished - Mar 15 2022
Externally publishedYes

Keywords

  • Breast
  • Exome
  • High-throughput nucleotide sequencing
  • Lung
  • Mutation
  • Women

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Infectious Diseases

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