Clinicopathologic Features of a Series of Primary Renal CIC-rearranged Sarcomas With Comprehensive Molecular Analysis

Shamlal Mangray1, David R Kelly2, Sophie LeGuellec3

  • 1Alpert Medical School of Brown University, Rhode Island Hospital, Providence, RI.

Insights

This study details rare kidney sarcomas with CIC rearrangements, often linked to DUX4 or NUTM1 fusions. These aggressive tumors show a tendency for metastasis and poor outcomes, highlighting the need for advanced diagnostic testing.

Area of Science:

  • Oncology
  • Genetics
  • Pathology

Background:

  • CIC-rearranged sarcomas are rare, particularly in visceral organs like the kidney.
  • The CIC-DUX4 fusion is common, but variant fusion partners are increasingly recognized.

Observation:

  • Four primary renal CIC-rearranged sarcomas in females (13-82 years) showed varied histology (round, spindle, rhabdoid cells).
  • Immunohistochemistry revealed diverse WT1, CD99, c-myc, ETV4, and calretinin staining patterns.
  • CIC rearrangement was confirmed by FISH in 3 cases.

Findings:

  • Comprehensive genomic profiling identified CIC-DUX4 fusion in two cases and CIC-NUTM1 fusion in one case.
  • All analyzed tumors exhibited low mutation burden with few genomic alterations in key oncogenic drivers.
  • Immunohistochemistry for DUX4 correlated with CIC-DUX4 fusion status.

Implications:

  • CIC-rearranged sarcomas in the kidney are aggressive, with a propensity for lung metastasis and poor prognosis.
  • The identification of a CIC-NUTM1 fusion highlights emerging variants at visceral sites.
  • Fluorescence in situ hybridization or comprehensive genomic profiling is crucial for accurate diagnosis, especially with variant fusion partners.

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