Stereotactic Ablative Radiotherapy for Gynecological Oligometastatic and Oligoprogessive Tumors

Elysia K Donovan1, Simon S Lo2, Sushil Beriwal3

  • 1Department of Oncology, Division of Radiation Oncology, Escarpment Cancer Research Institute, McMaster University, Hamilton, Ontario, Canada.

JAMA Oncology
|June 13, 2024
PubMed
Abstract

Insights

Stereotactic ablative radiotherapy (SABR) shows excellent local control for gynecologic cancers with few side effects. This treatment may help delay chemotherapy, reducing its toxicity in select patients.

Area of Science:

  • Gynecologic Oncology
  • Radiation Oncology
  • Medical Physics

Background:

  • The clinical utility of stereotactic ablative radiotherapy (SABR) for gynecologic malignancies remains under investigation.
  • Recent clinical adoption necessitates a clearer definition of SABR's role in managing these cancers.

Purpose of the Study:

  • To assess the outcomes of SABR in patients with gynecologic cancers presenting with oligometastatic or oligoprogressive disease.
  • To evaluate local control, distant recurrence, chemotherapy-free survival (CFS), and overall survival (OS) following SABR.

Main Methods:

  • A retrospective pooled analysis of 215 patients with 320 lesions from 5 institutions in Canada and the US.
  • Data collected from January 2011 to December 2020, analyzed from January to December 2023.
  • Kaplan-Meier methods for survival probabilities and Cox regression for univariable and multivariable analyses.

Main Results:

  • Excellent local control was observed, with 1- and 5-year cumulative incidences of local recurrence at 13.7% and 18.5%, respectively.
  • Five-year distant recurrence was 73.1%, 5-year OS was 33.1%, and median CFS was 21.7 months.
  • Multivariable analysis identified factors like nodal metastasis, lesion size, and biologically effective dose influencing local recurrence, distant progression, OS, and CFS.

Conclusions:

  • SABR demonstrates promising local control and minimal toxicity in a large cohort of gynecologic cancer patients.
  • Durable distant control and improved OS are achievable in select individuals, potentially allowing for chemotherapy delay.
  • Further prospective multicenter trials are essential to identify optimal patient candidates and timing for SABR integration.