Cardiac-Sparing Whole Lung IMRT in Patients With Pediatric Tumors and Lung Metastasis: Final Report of a Prospective Multicenter Clinical Trial.


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 01 2019
Historique:
received: 05 04 2018
revised: 13 08 2018
accepted: 23 08 2018
pubmed: 1 9 2018
medline: 10 7 2019
entrez: 1 9 2018
Statut: ppublish

Résumé

A prospective clinical trial was conducted for patients undergoing cardiac sparing (CS) whole lung irradiation (WLI) using intensity modulated radiation therapy (IMRT). The 3 trial aims were (1) to demonstrate the feasibility of CS IMRT with real-time central quality control; (2) to determine the dosimetric advantages of WLI using IMRT compared with standard anteroposterior (AP) techniques; and (3) to determine acute tolerance and short-term efficacy after a protocol-mandated minimum 2-year follow-up for all patients. All patients underwent a 3-dimensional chest computed tomography scan and a contrast-enhanced 4-dimensional (4D) gated chest computed tomography scan using a standard gating device. The clinical target volume was the entire bilateral 3-dimensional lung volume, and the internal target volume was the 4D minimum intensity projection of both lungs. The internal target volume was expanded by 1 cm to get the planning target volume. All target volumes, cardiac contours, and treatment plans were centrally reviewed before treatment. The different cardiac volumes receiving percentages of prescribed radiation therapy (RT) doses on AP and IMRT WLI plans were estimated and compared. The target 20 patients were accrued in 2 years. Median RT dose was 15 Gy. Real-time central quality assurance review and plan preapproval were obtained for all patients. WLI using IMRT was feasible in all patients. Compared with standard AP WLI, CS IMRT resulted in a statistically significant reduction in radiation doses to the whole heart, atria, ventricles, and coronaries. One child developed cardiac dysfunction and pulmonary restrictive disease 5.5 years after CS IMRT (15 Gy) and doxorubicin (375 mg/m We have demonstrated the feasibility of WLI using CS IMRT and confirmed the previously reported advantages of IMRT, including superior cardiac protection and superior dose coverage of 4D lung volumes. Further studies are required to establish the efficacy and safety of this irradiation technique.

Identifiants

pubmed: 30170102
pii: S0360-3016(18)33640-X
doi: 10.1016/j.ijrobp.2018.08.034
pmc: PMC6391051
mid: NIHMS1516208
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

28-37

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA159547
Pays : United States

Informations de copyright

Copyright © 2018. Published by Elsevier Inc.

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Auteurs

John A Kalapurakal (JA)

Radiation Oncology, Northwestern University, Chicago, Illinois. Electronic address: j-kalapurakal@northwestern.edu.

Mahesh Gopalakrishnan (M)

Radiation Oncology, Northwestern University, Chicago, Illinois.

David O Walterhouse (DO)

Pediatric Oncology and Medical Imaging, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.

Cynthia K Rigsby (CK)

Pediatric Oncology and Medical Imaging, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.

Alfred Rademaker (A)

Radiation Oncology, Northwestern University, Chicago, Illinois.

Irene Helenowski (I)

Radiation Oncology, Northwestern University, Chicago, Illinois.

Sandy Kessel (S)

Imaging and Radiation Oncology Core, Providence, Rhode Island.

Karen Morano (K)

Imaging and Radiation Oncology Core, Providence, Rhode Island.

Fran Laurie (F)

Imaging and Radiation Oncology Core, Providence, Rhode Island.

Ken Ulin (K)

Imaging and Radiation Oncology Core, Providence, Rhode Island.

Natia Esiashvili (N)

Radiation Oncology, Emory University, Atlanta, Georgia.

Howard Katzenstein (H)

Pediatric Oncology, Nemours Children's Clinic, Jacksonville, Florida.

Karen Marcus (K)

Radiation Oncology, Harvard University, Boston, Massachusetts.

David S Followill (DS)

Imaging and Radiation Oncology Core, Houston, Texas.

Suzanne L Wolden (SL)

Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, New York.

Anita Mahajan (A)

Radiation Oncology, MD Anderson Cancer Center, Houston, Texas.

Thomas J Fitzgerald (TJ)

Imaging and Radiation Oncology Core, Providence, Rhode Island.

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Classifications MeSH