Abstract
Leiomyosarcoma is a rare and aggressive malignant smooth muscle tumor with limited treatment options and poor outcomes. Large-scale molecular characterization is needed to better understand tumor biology and support precision oncology, as prior studies have been limited by small cohort sizes, single-institution data, and restricted gene panels. This study aimed to characterize clinicogenomic features of leiomyosarcoma using the AACR Project GENIE 19.0 public dataset.
We analyzed 1,017 tumor samples from 957 patients, evaluating demographic patterns, somatic mutation frequencies, copy number alterations, and genomic co-occurrence and exclusivity across primary and metastatic disease sites.
Females comprised 65.7% of cases and White patients 61.4%. The most frequently altered genes were
(50.3%),
(17.9%), and
(15.9%), followed by
, and
. Recurrent copy number alterations included
homozygous deletion (24.4%),
amplification (18.4%), and
homozygous deletion (15.5%). Significant co-occurrence was observed among
, and
alterations (q<0.05). Most genomic alterations were driven by primary tumors, whereas metastatic samples showed enrichment of
and
alterations.
These findings highlight recurrent alterations in
, and
and suggest potential roles for
and
in leiomyosrcoma metastatic disease that warrant further investigation.