Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

E-Poster Display

1638P - Are all leiomyosarcomas created equal? Clinical characteristics and experience of a single reference centre

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Sarcoma

Presenters

Raul Teres Lleida

Citation

Annals of Oncology (2020) 31 (suppl_4): S914-S933. 10.1016/annonc/annonc288

Authors

R. Teres Lleida1, B. Martin Cullell2, M. Borrell Puy3, A. Bujosa Rodríguez4, P.G. Gallardo Melo5, C. Molto Valiente6, M. Riudavets Melia6, M. Aguado Sorolla1, A. Piedra Cascon1, J..C. Tapia7, J. Gavira Diaz8, R. Orellana Fernandez9, S. Bague Rosell9, A. Gallardo Alcañiz9, A. Lopez-Pousa10, P. Cerda Serda1, A. Sebio Garcia6

Author affiliations

  • 1 Dept. Medical Oncology, Hospital de la Santa Creu i Sant Pau - Consultes Externes, 08041 - Barcelona/ES
  • 2 Oncology, Hospital de Sant Pau, Barcelona/ES
  • 3 Dept. Medical Oncology, Hospital de la Santa Creu i Sant Pau, 8041 - Barcelona/ES
  • 4 Dept. Oncology, Hospital de la Santa Creu i Sant Pau, 8041 - Barcelona/ES
  • 5 Oncology, Hospital de la Santa Creu i Sant Pau, 08025 - Barcelona/ES
  • 6 Dept. Medical Oncology, Hospital de la Santa Creu i Sant Pau, 08041 - Barcelona/ES
  • 7 Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, 08041 - Barcelona/ES
  • 8 Medical Oncology, Hospital de la Santa Creu i Sant Pau, 08041 - Barcelona/ES
  • 9 Dept. Pathology, Hospital de la Santa Creu i Sant Pau, 08041 - Barcelona/ES
  • 10 Medical Oncology, Hospital Sant Pau, Barcelona/ES

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 1638P

Background

Leiomyosarcomas (LMS) are soft tissue sarcomas that derive from smooth muscle and can arise anywhere in the body. The aim of our study was to describe clinical and pathological characteristics and outcomes of patients with LMS diagnosed in our institution from 2001 to 2019.

Methods

A total of 106 patients with LMS were analysed. Clinical and pathological data were collected retrospectively from patients’ electronic board system and statistically analysed. This study was approved by the hospital ethics committee.

Results

The most frequent locations were extremities (29.2%), uterus (22.6%) and retroperitoneum (RP) (19.8%). Most LMS were high grade (6.7% G1, 36% G2, 57.3% G3). Median overall survival (mOS) was 65.4 months (m) for G3 and was not achieved for G2 localized LMS. At diagnoses, most patients had localized disease (68.3%). 43.5% of uterine leiomyosarcomas (uLMS) had metastasis at diagnose compared to 38.8% of LMS located in the extremity, 30% of RP and 27.8% of LMS in other locations (p=0.095). As expected, cutaneous LMS did not develop metastatic disease. Most of localized LMS (82.1%) were > 5cm at diagnosis (median size 9.5cm). For patients with tumours <5cm mOS was 55m compared to 28.4m for >5cm (p=0.03). 80 patients (75%) underwent surgery, including 16.1% of patients with metastatic disease. Perioperative radiotherapy was administered to 42.5% of the patients and 34% received perioperative chemotherapy (CT). A total of 58.8% of patients who underwent radical surgery relapsed. Risk of relapse was higher for uLMS compared to the rest of locations (0% for cutaneous, 50% for extremities, 92.8% for uLMS, 72.2% for RP and 54.5% for other locations LMS) (p=0.007). mOS was 53.6m for uLMS, 90.5m for RP, 53.9m for extremities and 65.4m for other locations (p>0.05). OS for patients with metastatic disease at diagnose was 18.6m for extremities, 13.5m for RP, 10.9m for other locations and 10m for uLMS (p>0.05). The median CT lines was 2 (range 0 – 7). For all locations, the most frequent first line CT was anthracycline-based.

Conclusions

In our series, size and grade are prognostic factors. uLMS had the worse prognosis presenting more frequently with metastatic disease at diagnose and showing a higher risk of relapse after radical surgery.

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.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.