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Determining Planning Priorities for SABR for Oligometastatic Disease: A Secondary Analysis of the SABR-COMET Phase II Randomized Trial.
Van Oirschot, Matthew; Bergman, Alanah; Verbakel, Wilko F A R; Ward, Lucy; Gagne, Isabelle; Huang, Vicky; Chng, Nick; Houston, Peter; Symes, Kerry; Thomas, Christopher G; Basran, Parminder; Bowes, David; Harrow, Stephen; Olson, Robert; Senan, Suresh; Warner, Andrew; Palma, David A; Gaede, Stewart.
Afiliación
  • Van Oirschot M; London Health Sciences Centre, London, Ontario, Canada.
  • Bergman A; British Columbia Cancer, Vancouver Centre, Vancouver, British Columbia, Canada.
  • Verbakel WFAR; Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Ward L; Nova Scotia Health, Halifax, Nova Scotia, Canada.
  • Gagne I; British Columbia Cancer, Victoria Centre, Victoria, British Columbia, Canada.
  • Huang V; British Columbia Cancer, Surrey Centre, Surrey, British Columbia, Canada.
  • Chng N; British Columbia Cancer, Centre for the North, Prince George, British Columbia, Canada.
  • Houston P; Beatson West of Scotland Cancer Centre, Glasgow, Scotland.
  • Symes K; British Columbia Cancer, Vancouver Centre, Vancouver, British Columbia, Canada.
  • Thomas CG; Nova Scotia Health, Halifax, Nova Scotia, Canada.
  • Basran P; Cornell University, Ithaca, New York.
  • Bowes D; Nova Scotia Health, Halifax, Nova Scotia, Canada.
  • Harrow S; Beatson West of Scotland Cancer Centre, Glasgow, Scotland.
  • Olson R; British Columbia Cancer, Centre for the North, Prince George, British Columbia, Canada.
  • Senan S; Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Warner A; London Health Sciences Centre, London, Ontario, Canada.
  • Palma DA; London Health Sciences Centre, London, Ontario, Canada.
  • Gaede S; London Health Sciences Centre, London, Ontario, Canada. Electronic address: Stewart.Gaede@LHSC.on.ca.
Int J Radiat Oncol Biol Phys ; 114(5): 1016-1021, 2022 12 01.
Article en En | MEDLINE | ID: mdl-35031340
PURPOSE: SABR may improve survival in patients with oligometastases, but for some lesions, safe delivery of SABR may require a reduction in delivered dose or target coverage. This study assessed the association between target coverage compromise and oncologic and survival outcomes. METHODS AND MATERIALS: Patients with a controlled primary malignancy and 1 to 5 oligometastases were randomized (1:2) between standard of care (SOC) treatment and SOC plus SABR. In patients receiving SABR, the target dose coverage was reduced to meet organ at risk (OAR) constraints, if necessary. The D99 value (minimum dose received by the hottest 99% of the planning target volume [PTV]) was used as a measure of PTV coverage for each treatment plan, and the relationship between the coverage compromise index (CCI, defined as D99/prescription dose) and patient outcomes was assessed. RESULTS: Sixty-two patients in the SABR arm had dosimetric information available and a total of 109 lesions were evaluated. The mean CCI per lesion was 0.96 (95% CI, 0.56-1.61). Of the 109 lesions evaluated, 29.4% (n = 32) required coverage compromise (CCI <0.9). Adrenal metastases required coverage compromise in 100% of analyzed lesions (n = 7). CCI was not significantly associated with lesional control, adverse events, overall survival (OS), or progression-free survival (PFS). CONCLUSIONS: Target compromise was required in a substantial minority of cases, but PTV coverage was not associated with OS, progression-free survival, or lesional control. This suggests that OAR constraints used for SABR treatments in the oligometastatic setting should continue to be prioritized during planning.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Radiocirugia Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Int J Radiat Oncol Biol Phys Año: 2022 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Radiocirugia Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Int J Radiat Oncol Biol Phys Año: 2022 Tipo del documento: Article País de afiliación: Canadá