We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Adverse prognostic impact of the loss of STAG2 protein expression in patients with newly diagnosed localised Ewing sarcoma: A report from the Children's Oncology Group.
- Authors
Shulman, David S.; Chen, Sonja; Hall, David; Nag, Anwesha; Thorner, Aaron R.; Lessnick, Stephen L.; Stegmaier, Kimberly; Janeway, Katherine A.; DuBois, Steven G.; Krailo, Mark D.; Barkauskas, Donald A.; Church, Alanna J.; Crompton, Brian D.
- Abstract
<bold>Background: </bold>Ewing sarcoma (EWS) is an aggressive sarcoma with no validated molecular biomarkers. We aimed to determine the frequency of STAG2 protein loss by immunohistochemistry (IHC) and whether loss of expression is associated with outcome.<bold>Methods: </bold>We performed a retrospective cohort study of patients with EWS enrolled to Children's Oncology Group studies. We obtained unstained slides from 235 patients and DNA for sequencing from 75 patients. STAG2 expression was tested for association with clinical features and survival was estimated using Kaplan-Meier methods with log-rank tests.<bold>Results: </bold>In total, 155 cases passed quality control for STAG2 IHC. STAG2 expression in 20/155 cases could not be categorised with the limited available tissue, leaving 135 patients with definitive STAG2 IHC. In localised and metastatic disease, STAG2 was lost in 29/108 and 6/27 cases, respectively. Among patients with IHC and sequencing, 0/17 STAG2 expressing cases had STAG2 mutations, and 2/7 cases with STAG2 loss had STAG2 mutations. Among patients with localised disease, 5-year event-free survival was 54% (95% CI 34-70%) and 75% (95% CI 63-84%) for patients with STAG2 loss vs. expression (P = 0.0034).<bold>Conclusion: </bold>STAG2 loss of expression is identified in a population of patients without identifiable STAG2 mutations and carries a poor prognosis.
- Publication
British Journal of Cancer, 2022, Vol 127, Issue 12, p2220
- ISSN
0007-0920
- Publication type
journal article
- DOI
10.1038/s41416-022-01977-2