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Poster Display session

75P - Review of the systemic treatment of leiomyosarcomas in a Spanish reference center in the last 10 years

Date

15 Mar 2024

Session

Poster Display session

Presenters

Javier Martinez Trufero

Citation

Annals of Oncology (2024) 9 (suppl_2): 1-32. 10.1016/esmoop/esmoop102441

Authors

S.E. Campos Ramirez1, S.E. Ruffini Egea2, M.L. Monreal Cepero2, P.G. Mugarza2, S. Barriendos Sanz2, P. Trincado Cobos2, F. Mocha Campillo2, N. Pascual de La Fuente2, J. Martinez Trufero3, M.P. Felices Lobera4

Author affiliations

  • 1 Medical Oncology, Hospital Universitario Miguel Servet, 50009 - Zaragoza/ES
  • 2 Medical Oncology, HospItal Universitario Miguel Servet, 50009 - Zaragoza/ES
  • 3 Dept. Medical Oncology, Hospital Miguel Servet, 50009 - Zaragoza/ES
  • 4 Medical Oncology Dept., Hospital General San Jorge, 22004 - Huesca/ES

Resources

This content is available to ESMO members and event participants.

Abstract 75P

Background

Leiomyosarcomas (LMS) belong to the group of soft tissue sarcomas (STS) and are one of the most common subtypes, along with liposarcoma (LPS). In the initial stages the gold standard treatment is based on surgery, while the role of chemotherapy (CT) is reserved for advanced stages, although its use has also been studied in the adjuvant and neoadjuvant context, with not enough evidence to support its use in these context. First-line treatment include doxorubicin in monotherapy or in association with other active agents such as gemcitabine, dacarbazine and trabectedin. Other molecules can be used for further lines such as hormone treatment, pazopanib and others.

Methods

We conducted a retrospective, longitudinal and observational study. We reviewed a total of 50 patients with LMS who have received treatment with CT either in the context of adjuvant or metastatic disease. The data was analyzed using the free statistics software Jamovi, using non-parametrical tests for variable associations and frequency measurements for descriptive analysis.

Results

Regarding adjuvant treatment, a total of 26 cases were analyzed, and the relapse rate was 57.6%. Not affected surgical margins was the only factor associated with better OS (50 vs 23 months, p value= 0.005) and RFS (12 vs 3, p value= 0.039). Of the 34 patients with metastatic disease analyzed. Main findings of different regimens and agents of RR, median OF and median PFS are shown in the table. Table: 75P

Chemotherapy OR (%) p value median OS (months) p value median PFS (months) p value
First line: Adriamicine vs gemcitabine 86 vs 50 0.07 36 vs 16 0.55 6 vs 4 0.96
Second line: Gemcitabine vs trabectedin 66 vs 57 1.00 11 vs 9 0.66 9 vs 5 0.1
Subsequent lines: Gemcitabine Trabectedine Pazopanib 66 33.3 50 - - - 9 6.5 4 - - - 6.5 3.5 3 - - -

Conclusions

The only factor that was associated with better RFS and OS in patients who received adjuvant treatment with CT was the presence of free surgical margins. First-line treatment with CT in patients with metastatic disease with regimens based on doxorubicin showed more activity compared with others such as gemcitabine, trabectedin, but no statistically significant differences were found. We consider that any of these three agents can be used for patients with metastatic disease.

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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