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PR050/#373  Clinicopathologic and genomic analysis of uterine serous carcinomas arising from endometrial hyperplasia
  1. Tiffany Sia1,
  2. Douglas Allison2,
  3. Arrnaud Da Cruz Paula3,
  4. Edaise Da Silva2,
  5. Qiqi Ye2,
  6. Pier Selenica2,
  7. Fresia Pareja Zea2,
  8. Hunter Green2,
  9. Nadeem Abu-Rustum1,
  10. Britta Weigelt2 and
  11. Lora Ellenson2
  1. 1Memorial Sloan Kettering Cancer Center, Gynecology Service, Department of Surgery, New York, USA
  2. 2Memorial Sloan Kettering Cancer Center, Pathology, New York, USA
  3. 3i3S Instituto de Investigação e Inovação em Saúde, Pathology, Porto, Portugal


Introduction Uterine serous carcinoma (USC) typically arises from atrophic endometrium but may be associated with hyperplasia in 5–10% of cases. We sought to identify USC with concurrent hyperplasia and define if i) they are molecularly related, and ii) USC associated with hyperplasia are genetically distinct from those without.

Methods Patients diagnosed with USC and hyperplasia on hysterectomy specimen between 1/2014 – 2/2021 were identified. Slides were reviewed by two gynecologic pathologists. Hyperplasia and carcinoma were microdissected separately and subjected to tumor-normal panel sequencing. Results were compared to atrophy-associated USC.

Results Of 291 USCs with clinical sequencing and slides available for review, 10 cases were identified (3%), and eight cases with sufficient tissue were included. Recurrently mutated genes included TP53 (100%), PIK3CA (50%), PPP2R1A (50%), ARID1A (38%), and PTEN (25%). In seven patients (87.5%), USC and hyperplasia were clonally related and shared multiple mutations, including TP53 in 4 (57%) cases. In one clonally related case, USC and TP53 wild-type hyperplasia shared 1 of 11 mutations (PIK3CA hotspot mutation) while being distinct at the copy number level. In the last case, USC and hyperplasia were unrelated at the genetic level, and the hyperplasia was TP53 wild-type. The prevalence of ARID1A mutations was higher in hyperplasia-associated USC compared to atrophy-associated USC (43% vs. 0%, p=0.02).

Conclusion/Implications Hyperplasia and USC were clonally related in most cases, commonly harboring TP53 hotspot mutations in both components. ARID1A mutations were more prevalent in hyperplasia- compared to atrophy-associated USC. These results suggest a novel origin of tumorigenesis in this rare subset of endometrial cancers.

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