Margin-Free Fractionated Stereotactic Radiation Therapy for Pediatric Brain Tumors.


Journal

Practical radiation oncology
ISSN: 1879-8519
Titre abrégé: Pract Radiat Oncol
Pays: United States
ID NLM: 101558279

Informations de publication

Date de publication:
Historique:
received: 07 11 2019
revised: 14 02 2020
accepted: 09 03 2020
pubmed: 20 5 2020
medline: 24 8 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

Conventional radiation therapy (RT) to pediatric brain tumors exposes a large volume of normal brain to unwarranted radiation causing late toxicity. We hypothesized that in well demarcated pediatric tumors lacking microscopic extensions, fractionated stereotactic RT (SRT), without target volume expansions, can reduce high dose normal tissue irradiation without affecting local control. Between 2008 and 2017, 52 pediatric patients with brain tumors were treated using the CyberKnife (CK) with SRT in 180 to 200 cGy per fraction. Thirty representative cases were retrospectively planned for intensity modulated RT (IMRT) with 4-mm PTV expansion. We calculated the volume of normal tissue within the high or intermediate dose region adjacent to the target. Plan quality and radiation dose-volume dosimetry parameters were compared between CK and IMRT plans. We also reported overall survival, progression-free survival (PFS), and local control. Tumors included low-grade gliomas (n = 28), craniopharyngiomas (n = 16), and ependymomas (n = 8). The volumes of normal tissue receiving high (≥80% of prescription dose or ≥40 Gy) or intermediate (80% > dose ≥50% of the prescription dose or 40 Gy > dose ≥25 Gy) dose were significantly smaller with CK versus IMRT plans (P < .0001 for all comparisons). With a median follow-up of 3.7 years (range, 0.1-9.0), 3-year local control was 92% for all patients. Eight failures occurred: 1 craniopharyngioma (marginal), 2 ependymomas (both in-field), and 5 low-grade gliomas (2 in-field, 1 marginal, and 2 distant). Fractionated SRT using CK without target volume expansion appears to reduce the volume of irradiated tissue without majorly compromising local control in pediatric demarcated brain tumors. These results are hypothesis generating and should be tested and validated in prospective studies.

Identifiants

pubmed: 32428764
pii: S1879-8500(20)30110-7
doi: 10.1016/j.prro.2020.03.013
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e485-e494

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

Osama Mohamad (O)

University of Texas-Southwestern, Department of Radiation Oncology, Dallas, Texas; Department of Radiation Oncology, University of California, San Francisco, San Francisco, California.

Zabi Wardak (Z)

University of Texas-Southwestern, Department of Radiation Oncology, Dallas, Texas.

Daniel C Bowers (DC)

Department of Pediatrics, University of Texas-Southwestern, Dallas, Texas.

Anh H Le (AH)

University of Texas-Southwestern, Department of Radiation Oncology, Dallas, Texas.

Tu Dan (T)

University of Texas-Southwestern, Department of Radiation Oncology, Dallas, Texas.

Ramzi Abdulrahman (R)

University of Texas-Southwestern, Department of Radiation Oncology, Dallas, Texas.

Lynn Gargan (L)

Department of Pediatric Neurosurgery, Children's Medical Center, Dallas, Texas.

Laura Klesse (L)

Department of Pediatrics, University of Texas-Southwestern, Dallas, Texas.

Bradley Weprin (B)

Department of Pediatric Neurosurgery, Children's Medical Center, Dallas, Texas.

Dale Swift (D)

Department of Pediatric Neurosurgery, Children's Medical Center, Dallas, Texas.

Angela Price (A)

Department of Pediatric Neurosurgery, Children's Medical Center, Dallas, Texas.

Chuxiong Ding (C)

University of Texas-Southwestern, Department of Radiation Oncology, Dallas, Texas.

Strahinja Stojadinovic (S)

University of Texas-Southwestern, Department of Radiation Oncology, Dallas, Texas.

Frederick Sklar (F)

Department of Pediatric Neurosurgery, Children's Medical Center, Dallas, Texas.

Bruno Braga (B)

Department of Pediatric Neurosurgery, Children's Medical Center, Dallas, Texas.

Robert Timmerman (R)

University of Texas-Southwestern, Department of Radiation Oncology, Dallas, Texas. Electronic address: Robert.Timmerman@UTSouthwestern.edu.

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Classifications MeSH