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Poster Display session

26P - Uterine Sarcoma: A Retrospective Tunisian Study Of 103 Cases

Date

17 Jun 2022

Session

Poster Display session

Topics

Tumour Site

Endometrial Cancer

Presenters

Emna Ouertani

Citation

Annals of Oncology (2022) 33 (suppl_5): S391-S394. 10.1016/annonc/annonc917

Authors

E. Ouertani1, Y. Yahyaoui2, Z. Ghodhbani2, F. Letaief-ksontini2, A. Gabsi2, K. meddeb2, M. Ayadi2, A. Mokrani2, N. Chraiet2, H. Rais2, Y. Zenzri2, H. Ben Mansour2, A. Mezlini2

Author affiliations

  • 1 Hopital Abderrahmen Mami de Pneumo-Phtisiologie, Ariana/TN
  • 2 Salah Azaiez Institute, Tunis/TN

Resources

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Abstract 26P

Background

Uterine sarcomas (US) are rare tumors, representing less than 3% of gynecologic malignancies and between 3% and 7% of uterine malignancies. US are characterized by being aggressive with a high rate of local and metastatic recurrence. Their management is not well codified. The aim of our study was to investigate the epidemiological, clinical, therapeutic, and prognostic characteristics of US.

Methods

This was a monocentric, descriptive, retrospective study that included patients with US treated in Salah Azaiez Tunisian oncological institute between 2000 and 2020.

Results

The study included 103 patients. The average age was 50 years. Menometrorrhagia was the main circumstance of discovery (n=70). In 73.8% of cases, the diagnosis was postoperative. Histological confirmation was done on hysterectomy specimen in 82 patients. The most frequent histological type was leiomyosarcoma in 72.8% of cases. Stage I was the most represented (41.7%). Ninety-seven patients underwent surgery, 87 of them had a total hysterectomy associated with bilateral salpingo-oophorectomy and lymph node dissection. Adjuvant chemotherapy was indicated in 16.5% of cases. Adjuvant pelvic radiotherapy was performed in 35 patients. Thirty-one patients received first-line chemotherapy. The protocol used was the combination of doxorubicin and ifosfamide in 82.3% of cases. Two patients received palliative endocrine therapy after progression to first line. After a median follow-up of 56 months, the overall survival at 2 and 5 years, all stages combined, was 56% and 40%, respectively. For metastatic stages, the overall survival was 36% and 25% at 2 and 3 years, respectively. In multivariate analysis, no prognostic factors were identified. Progression-free survival at 3 and 5 years was 82% and 72%, respectively. In multivariate analysis, only the circumstance of discovery was a prognostic factor impacting progression-free survival (p=0.042).

Conclusions

US is a particular neoplasm. Prospective randomized studies are needed to better codify its management.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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