Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Gynaecological
Poster (digital)
Clinical
SBRT for gynecological oligometastases: mono-institutional report of toxicity and clinical outcomes
Francesco Cuccia, Italy
PO-1353

Abstract

SBRT for gynecological oligometastases: mono-institutional report of toxicity and clinical outcomes
Authors:

Francesco Cuccia1, Edoardo Pastorello1, Claudio Vitale1, Vanessa Figlia1, Niccolò Giaj-Levra1, Luca Nicosia1, Francesco Ricchetti1, Michele Rigo1, Rosario Mazzola1, Marcello Ceccaroni2, Ruggero Ruggieri1, Filippo Alongi1

1IRCCS Sacro Cuore Don Calabria, Advanced Radiation Oncology Department, Negrar di Valpolicella, Italy; 2IRCCS Sacro Cuore Don Calabria, Gynecology Unit, Negrar di Valpolicella, Italy

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Purpose or Objective

Background: The use of stereotactic radiotherapy (SBRT) for oligometastases is supported by several studies, despite being quite unexplored in the setting of gynecological malignancies. This study reports a preliminary evaluation of clinical outcomes in a cohort of 40 patients with oligometastatic gynecological cancers.

Material and Methods

Methods: Radiotherapy was delivered in 3-10 fractions with VMAT-IGRT technique. Toxicity was retrospectively collected according to CTCAE v4.0. Univariate and multivariate analyses were performed for assessing any potential predictive factor for clinical outcomes.

Results

Results: A total of 63 oligometastases were treated from December 2014 to February 2021. Median age was 63 years (range 30-89). Most frequent primary tumors were ovarian cancer in 42.5% and endometrium cancer in 42.5%. With a median follow-up of 27 months (range 6-69), no local failures were observed, our progression-free survival rates were 43.6% and 23% at one and 2 years, respectively. Sixteen patients developed a sequential oligometastatic disease, candidate to a further SBRT course, with a second progression-free survival (PFS2) of 13 months (range 2–27); nonetheless,  this did not lead to a survival advantage, when compared to patients who developed immediate polymetastatic spread (p= 0.47). 1 and 2-year overall survival rates were both 70%, with only one patient dead by disease. No acute or late G≥ 2 adverse events were observed.

Conclusion

Conclusions: SBRT for oligometastatic gynecological malignancies resulted in promising results in terms of clinical outcomes, with excellent local control and no evidence of severe toxicity. Prospective studies to further investigate the role of this option in the management of gynecological malignancies are advocated.