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Poster Display session

17P - Gynaecologic carcinosarcomas (GCS)’s chemotherapy landscape: A retrospective analysis from Hospital Clinico San Carlos (HCSC), academic, referral centre for rare gynaecological malignancies in Madrid (Spain)

Date

15 Mar 2024

Session

Poster Display session

Presenters

Beatriz Diez

Citation

Annals of Oncology (2024) 9 (suppl_2): 1-3. 10.1016/esmoop/esmoop102408

Authors

B.G. Diez1, A. Casado Herraez2, A. Manzano Fernández2, P. Coronado3, J. Garcia Santos3, M. Ramirez3, M. Bellon3, R. Sanchez Del Hoyo4, A. Pascual5, C. Diaz Del Arco5, N. Sanmamed6, E. Cerezo6, R. Mendez7, M. Muñoz7, J.M. Espejo7, A. Nava7, C. Rodriguez8, A. Ortega8, G. Marquina2

Author affiliations

  • 1 Medical Oncology, Hospital Clinico Universitario San Carlos, 28040 - Madrid/ES
  • 2 Medical Oncology, Hospital Clinico Universitario San Carlos, IdISCC, UCM, 28040 - Madrid/ES
  • 3 Gynaecology Oncology, Hospital Clinico Universitario San Carlos, IdISCC, UCM, 28040 - Madrid/ES
  • 4 Research Methodological Support Unit And Preventive, Hospital Clinico Universitario San Carlos, IdISCC, UCM, 28040 - Madrid/ES
  • 5 Pathology, Hospital Clinico Universitario San Carlos, IdISCC, UCM, 28040 - Madrid/ES
  • 6 Radiotherapy, Hospital Clinico Universitario San Carlos, IdISCC, UCM, 28040 - Madrid/ES
  • 7 Radiology, Hospital Clinico Universitario San Carlos, IdISCC, UCM, 28040 - Madrid/ES
  • 8 Nuclear Medicine, Hospital Clinico Universitario San Carlos, IdISCC, UCM, 28040 - Madrid/ES

Resources

This content is available to ESMO members and event participants.

Abstract 17P

Background

Gynaecologic carcinosarcomas (GCS) are rare cancers with poor prognosis. From 2003 onwards, GCS are no longer considered sarcomas but epithelial carcinomas, thus shifting the chemotherapy used in their multidisciplinary management. We aim to analyse the chemotherapy regimens used in GCS at our institution and patient’s outcomes.

Methods

Retrospective analysis of 57 GCS patients (pts) treated in HCSC from 1995-2003 and 2003-2022.

Results

Median age at diagnosis: 65 years (range 30-90); ECOG 0 63%. Primary disease: uterus 80.7%, ovary 17.5% or vaginal stump 1.8%. FIGO 2018 staging at diagnosis: I 40.4%, II 14%, III 22.8% and IV 22.8%. Carboplatin (C) and paclitaxel (T) were used initially in 50% of pts (57% adjuvant, 14.2% neoadjuvant and 19% fist line), from 2003, and as a retreatment (monotherapy, CT, or in combination with epirubicin, pegylated liposomal doxorubicin, bevacizumab, gemcitabine or ifosfamide) 10 times. Other drugs used as first strategy were anthracyclines, ifosfamide, cisplatin, cyclophosphamide, gemcitabine, docetaxel and in following lines dacarbazine, etoposide, bevacizumab, methotrexate, trabectedin, megestrol, niraparib and dostarlimab (Table). 11 pts relapsed after a complete response: local 45.5%, lymph node 18.1%, peritoneal 36.4%, visceral 18.2%, lung 10%. After a median follow-up of 20,67 months, median overall survival (mOS) 25.23 months (95% CI, 9-41.5 months) and median progression free survival (mPFS) 16.03 months (95% IC, 7-25 months). Pts treated from 2003 have better mOS than those treated before 2003 (40.5 vs. 9.7 months, p 0.034).

Table: 17P

Intention of initial chemotherapy treatment in the two cohorts regarding FIGO 2018 staging and outcomes

FIGO 2018 stage No treatment Adjuvant Neoadjuvant First line Total pts
Diagnosed <2003 I-III 2 3 5
Response 2 PD 3 CR (2 maintained, 1 relapsed)
IV 2 2 4
Response NE 2 PD
Diagnosed >2003 I-III 9 26 2 2 39
Response 4 CR (2 maintained, 2 relapsed) 3 PD 2 NE 22 CR (16 maintained, 6 relapsed) 4 PD 2 RC (2 relapsed) 2 PD
IV 2 1 6 9
Response 2 PD 1 PD 1 CR (maintained) 5 PD

Conclusions

We have used different chemotherapy regimens in GCS, more liberal use of adjuvant therapy, being CT the main regimen from 2003 onwards concurring with mOS improvement.

Clinical trial identification

Editorial acknowledgement

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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