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Dose response and architecture in volume staged radiosurgery for large arteriovenous malformations: A multi-institutional study.
Seymour, Zachary A; Chan, Jason W; Sneed, Penny K; Kano, Hideyuki; Lehocky, Craig A; Jacobs, Rachel C; Ye, Hong; Chytka, Tomas; Liscak, Roman; Lee, Cheng-Chia; Yang, Huai-Che; Ding, Dale; Sheehan, Jason; Feliciano, Caleb E; Rodriguez-Mercado, Rafael; Chiang, Veronica L; Hess, Judith A; Sommaruga, Samuel; McShane, Brendan; Lee, John; Vasas, Lucas T; Kaufmann, Anthony M; Grills, Inga; McDermott, Michael W.
Afiliación
  • Seymour ZA; Beaumont Health, Oakland University William Beaumont School of Medicine, Department of Radiation Oncology, United States. Electronic address: Zachary.seymour@beaumont.org.
  • Chan JW; University of California - San Francisco School of Medicine, Department of Radiation Oncology, United States.
  • Sneed PK; University of California - San Francisco School of Medicine, Department of Radiation Oncology, United States.
  • Kano H; University of Pittsburgh, School of Medicine, Department of Neurosurgery, United States.
  • Lehocky CA; University of Pittsburgh, School of Medicine, Department of Neurosurgery, United States.
  • Jacobs RC; University of Pittsburgh, School of Medicine, Department of Neurosurgery, United States.
  • Ye H; Beaumont Health, Department of Radiation Oncology, United States.
  • Chytka T; Na Homolce Hospital, Department of Stereotactic Radioneurosurgery, Prague, Czech Republic.
  • Liscak R; Na Homolce Hospital, Department of Stereotactic Radioneurosurgery, Prague, Czech Republic.
  • Lee CC; Taipei General Hospital, Department of Neurosurgery, Taiwan.
  • Yang HC; Taipei General Hospital, Department of Neurosurgery, Taiwan.
  • Ding D; University of Virginia School of Medicine, Department of Neurosurgery, United States.
  • Sheehan J; University of Virginia School of Medicine, Department of Neurosurgery, United States.
  • Feliciano CE; University of Puerto Rico School of Medicine, Department of Neurosurgery, United States.
  • Rodriguez-Mercado R; University of Puerto Rico School of Medicine, Department of Neurosurgery, United States.
  • Chiang VL; Yale University School of Medicine, Department of Neurosurgery, United States.
  • Hess JA; Yale University School of Medicine, Department of Neurosurgery, United States.
  • Sommaruga S; Yale University School of Medicine, Department of Neurosurgery, United States.
  • McShane B; University of Pennsylvania School of Medicine, Department of Neurosurgery, United States.
  • Lee J; University of Pennsylvania School of Medicine, Department of Neurosurgery, United States.
  • Vasas LT; University of Manitoba School of Medicine, Department of Neurosurgery, Canada.
  • Kaufmann AM; University of Manitoba School of Medicine, Department of Neurosurgery, Canada.
  • Grills I; Beaumont Health, Oakland University William Beaumont School of Medicine, Department of Radiation Oncology, United States.
  • McDermott MW; University of California - San Francisco School of Medicine, Department of Neurosurgery, United States.
Radiother Oncol ; 144: 180-188, 2020 03.
Article en En | MEDLINE | ID: mdl-31835173
ABSTRACT

BACKGROUND:

Optimal treatment paradigm for large arteriovenous malformations (AVMs) is controversial. Volume-staged stereotactic radiosurgery (VS-SRS) provides an effective option for these high-risk lesions, but optimizing treatment for these recalcitrant and rare lesions has proven difficult.

METHODS:

This is a multi-centered retrospective review of patients treated with a planned prospective volume staging approach to stereotactically treat the entire nidus of an AVM with volume stages separated by intervals of 3-6 months. A total of 9 radiosurgical centers treated 257 patients with VS-SRS between 1991 and 2016. We evaluated near complete response (nCR), obliteration, cure, and overall survival.

RESULTS:

With a median age of 33 years old at the time of first SRS volume stage, patients received 2-4 total volume stages and a median follow up of 5.7 years after VS-SRS. The median total AVM nidus volume was 23.25 cc (range 7.7-94.4 cc) with a median margin dose per stage of 17 Gy (range 12-20 Gy). Total AVM volume, margin dose per stage, compact nidus, lack of prior embolization, and lack of thalamic location involvement were all associated with improved outcomes. Dose >/= 17.5 Gy was strongly associated with improved rates of nCR, obliteration, and cure. With dose >/= 17.5 Gy, 5- and 10-year cure rates were 33.7% and 76.8% in evaluable patients compared to 23.7% and 34.7% of patients with 17 Gy and 6.4% and 20.6% with <17 Gy per volume-stage (p = 0.004). Obliteration rates in diffuse nidus architecture with <17 Gy were particularly poor with none achieving obliteration compared to 32.3% with doses >/= 17 Gy at 5 years (p = 0.007). Comparatively, lesions with a compact nidus architecture exhibited obliteration rates at 5 years were 10.7% vs 9.3% vs 26.6% for dose >17 Gy vs 17 Gy vs >/=17.5 Gy.

CONCLUSION:

VS-SRS is an option for upfront treatment of large AVMs. Higher dose was associated with improved rates of nCR, obliteration, and cure suggesting that larger volumetric responses may facilitate salvage therapy and optimize the chance for cure.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Malformaciones Arteriovenosas Intracraneales / Radiocirugia Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Radiother Oncol Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Malformaciones Arteriovenosas Intracraneales / Radiocirugia Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Radiother Oncol Año: 2020 Tipo del documento: Article
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