Higher Reported Lung Dose Received During Total Body Irradiation for Allogeneic Hematopoietic Stem Cell Transplantation in Children With Acute Lymphoblastic Leukemia Is Associated With Inferior Survival: A Report from the Children's Oncology Group.
Adolescent
Analysis of Variance
Child
Child, Preschool
Cyclophosphamide
/ administration & dosage
Disease-Free Survival
Dose Fractionation, Radiation
Etoposide
/ administration & dosage
Graft vs Host Disease
/ prevention & control
Hematopoietic Stem Cell Transplantation
/ mortality
Humans
Immunosuppressive Agents
/ administration & dosage
Infant
Lung
/ radiation effects
Patient Positioning
Precursor Cell Lymphoblastic Leukemia-Lymphoma
/ mortality
ROC Curve
Radiation Dosage
Remission Induction
Thiotepa
/ administration & dosage
Transplantation Conditioning
/ methods
Whole-Body Irradiation
/ methods
Young Adult
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 07 2019
01 07 2019
Historique:
received:
20
07
2018
revised:
14
01
2019
accepted:
14
02
2019
pubmed:
27
2
2019
medline:
30
11
2019
entrez:
27
2
2019
Statut:
ppublish
Résumé
To examine the relationship between lung radiation dose and survival outcomes in children undergoing total body irradiation (TBI)-based hematopoietic stem cell transplantation (HSCT) for acute lymphoblastic leukemia on the Children's Oncology Group trial. TBI (1200 or 1320 cGy given twice daily in 6 or 8 fractions) was used as part of 3 HSCT preparative regimens, allowing institutional flexibility regarding TBI techniques, including lung shielding. Lung doses as reported by each participating institution were calculated for different patient setups, with and without shielding, with a variety of dose calculation techniques. The association between lung dose and transplant-related mortality, relapse-free survival, and overall survival (OS) was examined using the Cox proportional hazards regression model controlling for the following variables: TBI dose rate, TBI fields, patient position during TBI, donor type, and pre-HSCT minimal residual disease level. Of a total of 143 eligible patients, 127 had lung doses available for this analysis. The TBI techniques were heterogeneous. The mean lung dose was reported as 904.5 cGy (standard deviation, ±232.3). Patients treated with lateral fields were more likely to receive lung doses ≥800 cGy (P < .001). The influence of lung dose ≥800 cGy on transplant-related mortality was not significant (hazard ratio [HR], 1.78; P = .21). On univariate analysis, lung dose ≥800 cGy was associated with inferior relapse-free survival (HR, 1.76; P = .04) and OS (HR, 1.85; P = .03). In the multivariate analysis, OS maintained statistical significance (HR, 1.85; P = .04). The variability in TBI techniques resulted in uncertainty with reported lung doses. Lateral fields were associated with higher lung dose, and thus they should be avoided. Patients treated with lung dose <800 cGy in this study had better outcomes. This approach is currently being investigated in the Children's Oncology Group AALL1331 study. Additionally, the Imaging and Radiation Oncology Core Group is evaluating effects of TBI techniques on lung doses using a phantom.
Identifiants
pubmed: 30807822
pii: S0360-3016(19)30266-4
doi: 10.1016/j.ijrobp.2019.02.034
pmc: PMC6548591
mid: NIHMS1525832
pii:
doi:
Substances chimiques
Immunosuppressive Agents
0
Etoposide
6PLQ3CP4P3
Cyclophosphamide
8N3DW7272P
Thiotepa
905Z5W3GKH
Types de publication
Clinical Trial, Phase III
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
513-521Subventions
Organisme : NCI NIH HHS
ID : P01 CA214278
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA029511
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL069254
Pays : United States
Organisme : NHLBI NIH HHS
ID : N01HC45220
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098543
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA180803
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States
Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.
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