Organs at Risk Considerations for Thoracic Stereotactic Body Radiation Therapy: What Is Safe for Lung Parenchyma?
Carcinoma, Non-Small-Cell Lung
/ diagnostic imaging
Humans
Lung
/ diagnostic imaging
Lung Neoplasms
/ diagnostic imaging
Models, Biological
Models, Theoretical
Organs at Risk
/ radiation effects
Pulmonary Fibrosis
/ etiology
Radiation Pneumonitis
/ etiology
Radiation Tolerance
Radiosurgery
/ adverse effects
Radiotherapy Dosage
Re-Irradiation
Risk Factors
Tumor Burden
Journal
International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616
Informations de publication
Date de publication:
01 05 2021
01 05 2021
Historique:
received:
09
11
2018
revised:
09
11
2018
accepted:
14
11
2018
pubmed:
30
11
2018
medline:
5
8
2021
entrez:
30
11
2018
Statut:
ppublish
Résumé
Stereotactic body radiation therapy (SBRT) has become the standard of care for inoperable early-stage non-small cell lung cancer and is often used for recurrent lung cancer and pulmonary metastases. Radiation-induced lung toxicity (RILT), including radiation pneumonitis and pulmonary fibrosis, is a major concern for which it is important to understand dosimetric and clinical predictors. This study was undertaken through the American Association of Physicists in Medicine's Working Group on Biological Effects of Stereotactic Body Radiotherapy. Data from studies of lung SBRT published through the summer of 2016 that provided detailed information about RILT were analyzed. Ninety-seven studies were ultimately considered. Definitions of the risk organ and complication endpoints as well as dose-volume information presented varied among studies. The risk of RILT, including radiation pneumonitis and pulmonary fibrosis, was reported to be associated with the size and location of the tumor. Patients with interstitial lung disease appear to be especially susceptible to severe RILT. A variety of dosimetric parameters were reported to be associated with RILT. There was no apparent threshold "tolerance dose-volume" level. However, most studies noted safe treatment with a rate of symptomatic RILT of <10% to 15% after lung SBRT with a mean lung dose (MLD) of the combined lungs ≤8 Gy in 3 to 5 fractions and the percent of total lung volume receiving more than 20 Gy (V To allow more rigorous analysis of this complication, future studies should standardize reporting by including standardized endpoint and volume definitions and providing dose-volume information for all patients, with and without RILT.
Identifiants
pubmed: 30496880
pii: S0360-3016(18)34014-8
doi: 10.1016/j.ijrobp.2018.11.028
pmc: PMC9454379
mid: NIHMS1830323
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
172-187Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA129182
Pays : United States
Informations de copyright
Copyright © 2018 Elsevier Inc. All rights reserved.
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