Vienna, Austria

ESTRO 2023

Session Item

Saturday
May 13
16:45 - 17:45
Plenary Hall
Palliation - Oligometastases
Mateusz SpaƂek, Poland;
Vincent Khoo, United Kingdom
1500
Proffered Papers
Clinical
17:15 - 17:25
Should OARs be prioritized in SABR for oligometastases? A secondary analysis of the SABR-5 trial
Reno Eufemon Cereno, Canada
OC-0268

Abstract

Should OARs be prioritized in SABR for oligometastases? A secondary analysis of the SABR-5 trial
Authors:

Reno Eufemon Cereno1, Benjamin Mou1, Sarah Baker2, Nick Chng3, Gregory Arbour4, Alanah Bergman5, Mitchell Liu5, Devin Schellenberg2, Quinn Matthews3, Vicky Huang6, Ante Mestrovic7, Derek Hyde8, Abraham Alexander9, Hannah Carolan5, Fred Hsu10, Siavash Atrchian1, Islam Mohamed1, Angela Lin1, Tanya Berrang9, Andrew Bang5, Will Jiang2, Howard Pai9, Scott Tyldesley5, Robert Olson11

1University of British Columbia / BC Cancer - Kelowna, Radiation Oncology, Vancouver / Kelowna, Canada; 2University of British Columbia / BC Cancer - Surrey, Radiation Oncology, Vancouver / Surrey, Canada; 3BC Cancer - Prince George, Radiation Oncology, Prince George, Canada; 4University of British Columbia, Data Science Institute, Vancouver, Canada; 5University of British Columbia / BC Cancer - Vancouver, Radiation Oncology, Vancouver, Canada; 6BC Cancer - Surrey, Radiation Oncology, Surrey, Canada; 7BC Cancer - Victoria, Radiation Oncology, Victoria, Canada; 8BC Cancer - Kelowna, Radiation Oncology, Kelowna, Canada; 9University of British Columbia / BC Cancer - Victoria, Radiation Oncology, Vancouver / Victoria, Canada; 10University of British Columbia / BC Cancer - Abbotsford, Radiation Oncology, Vancouver / Abbotsford, Canada; 11University of British Columbia / BC Cancer - Prince George, Radiation Oncology, Vancouver / Prince George, Canada

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Purpose or Objective

Despite potential improvement in survival after stereotactic ablative radiotherapy (SABR) for oligometastasis, concerns over its safety remain. To mitigate the risk of toxic effects, target coverage is sacrificed to prioritize organs-at-risk (OAR) during SABR planning. This study evaluated the effect of this practice on dosimetry, local recurrence (LR), and progression-free survival (PFS) in patients treated from a population-based phase II trial.

Material and Methods

The single-arm phase II SABR-5 trial treated patients with up to 5 oligometastases between November 2016 and July 2020. The protocol-specific planning objective was to cover 95% of the planning treatment volume (PTV) with 100% of the prescribed dose, however PTV coverage must be reduced as needed to meet OAR constraints. This trade-off was measured using the coverage compromise index (CCI), computed as minimum dose received by the hottest 99% of the PTV (D99) divided by the prescription dose. Under-coverage was defined as CCI < 0.90. The potential association between CCI and outcomes (LR and PFS) was evaluated.

Results

A total of 549 lesions from 381 patients were assessed. Mean CCI was 0.88 (95% confidence interval [CI], 0.86-0.89), and 196 (36%) lesions were under-covered. The highest mean CCI (0.95; 95% CI, 0.93-0.97) was seen in non-spine bone lesions (n=116), while the lowest mean CCI (0.71; 95% CI, 0.69-0.73) was seen in spine lesions (n=104). On multivariable analysis, CCI < 0.90 did not predict for worse local recurrence or progression-free survival.

Conclusion

Under-coverage of the PTV is not associated with worse local recurrence and progression-free survival rates in this large, population-based phase II trial. Combined with low rates of toxic effects, this study supports the practice of prioritizing OAR constraints during SABR treatment planning for oligometastases.