Acute Promyelocytic Leukemia With Torque Teno Mini Virus::RARA Fusion: An Approach to Screening and Diagnosis

Harrison K Tsai1, Mark F Sabbagh2, Meagan Montesion3

  • 1Department of Pathology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Pathology, Brigham & Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Insights

Acute promyelocytic leukemia (APL) can involve the torque teno mini virus (TTMV) RARA fusion gene. This rare entity is often missed by standard tests but can be detected using next-generation sequencing (NGS) with custom bioinformatics.

Area of Science:

  • Hematology
  • Oncology
  • Molecular Diagnostics

Background:

  • Acute promyelocytic leukemia (APL) typically involves RARA translocations with over 15 known partner genes.
  • Recent literature has identified torque teno mini virus (TTMV) as a rare RARA partner in APL.
  • This TTMV::RARA fusion is likely underdiagnosed due to limited familiarity, detection challenges with routine methods, and bioinformatics hurdles.

Purpose of the Study:

  • To describe a clinicopathologic approach for diagnosing APL with TTMV::RARA.
  • To provide tools for screening and diagnosing this rare leukemia using next-generation sequencing (NGS).
  • To report the identification and characteristics of APL with TTMV::RARA.

Main Methods:

  • Development of a clinicopathologic strategy for APL diagnosis.
  • Utilizing existing DNA- or RNA-based NGS assays with custom informatics for fusion detection.
  • Screening large datasets of hematopoietic malignancies for TTMV::RARA rearrangements.

Main Results:

  • Identified 4 cases of APL with TTMV::RARA, all lacking other known drivers.
  • One case was identified prospectively, and three retrospectively, including two from large-scale data screening.
  • Cases presented as myeloid sarcoma or leukemia, with variable responses to chemotherapy but potential remission with all-trans retinoic acid and stem cell transplant.

Conclusions:

  • APL with TTMV::RARA is a rare leukemia with a high treatment failure rate.
  • Diagnosis should be considered in APL-like leukemias lacking detectable RARA fusions or other drivers.
  • NGS with custom bioinformatics is crucial for accurate diagnosis and classification, potentially guiding treatment with all-trans retinoic acid.