Risk of radiation-induced second malignant neoplasms from photon and proton radiotherapy in paediatric abdominal neuroblastoma.

Abdominal neuroblastoma Childhood cancer Intensity modulated arc therapy (IMAT) Paediatric Pencil beam scanning Proton therapy Second malignant neoplasm

Journal

Physics and imaging in radiation oncology
ISSN: 2405-6316
Titre abrégé: Phys Imaging Radiat Oncol
Pays: Netherlands
ID NLM: 101704276

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 25 02 2021
revised: 28 05 2021
accepted: 18 06 2021
entrez: 26 7 2021
pubmed: 27 7 2021
medline: 27 7 2021
Statut: epublish

Résumé

State-of-the-art radiotherapy modalities have the potential of reducing late effects of treatment in childhood cancer survivors. Our aim was to investigate the carcinogenic risk associated with 3D conformal (photon) radiation (3D-CRT), intensity modulated arc therapy (IMAT) and pencil beam scanning proton therapy (PBS-PT) in the treatment of paediatric abdominal neuroblastoma. The risk of radiation-induced second malignant neoplasm (SMN) was estimated using the concept of organ equivalent dose (OED) for eleven organs (lungs, rectum, colon, stomach, small intestine, liver, bladder, skin, central nervous system (CNS), bone, and soft tissues). The risk ratio (RR) between radiotherapy modalities and lifetime absolute risks (LAR) were reported for twenty abdominal neuroblastoma patients (median, 4y; range, 1-9y) historically treated with 3D-CRT that were also retrospectively replanned for IMAT and PBS-PT. The risk of SMN due to primary radiation was reduced in PBS-PT against 3D-CRT and IMAT for most patients and organs. The RR across all organs ranged from 0.38 ± 0.22 (bladder) to 0.98 ± 0.04 (CNS) between PBS-PT and IMAT, and 0.12 ± 0.06 (rectum and bladder) to 1.06 ± 0.43 (bone) between PBS-PT and 3D-CRT. The LAR for most organs was within 0.01-1% (except the colon) with a cumulative risk of 21 ± 13%, 35 ± 14% and 35 ± 16% for PBS-PT, IMAT and 3D-CRT, respectively. PBS-PT was associated with the lowest risk of radiation-induced SMN compared to IMAT and 3D-CRT in abdominal neuroblastoma treatment. Other clinical endpoints and plan robustness should also be considered for optimal plan selection.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
State-of-the-art radiotherapy modalities have the potential of reducing late effects of treatment in childhood cancer survivors. Our aim was to investigate the carcinogenic risk associated with 3D conformal (photon) radiation (3D-CRT), intensity modulated arc therapy (IMAT) and pencil beam scanning proton therapy (PBS-PT) in the treatment of paediatric abdominal neuroblastoma.
MATERIALS AND METHODS METHODS
The risk of radiation-induced second malignant neoplasm (SMN) was estimated using the concept of organ equivalent dose (OED) for eleven organs (lungs, rectum, colon, stomach, small intestine, liver, bladder, skin, central nervous system (CNS), bone, and soft tissues). The risk ratio (RR) between radiotherapy modalities and lifetime absolute risks (LAR) were reported for twenty abdominal neuroblastoma patients (median, 4y; range, 1-9y) historically treated with 3D-CRT that were also retrospectively replanned for IMAT and PBS-PT.
RESULTS RESULTS
The risk of SMN due to primary radiation was reduced in PBS-PT against 3D-CRT and IMAT for most patients and organs. The RR across all organs ranged from 0.38 ± 0.22 (bladder) to 0.98 ± 0.04 (CNS) between PBS-PT and IMAT, and 0.12 ± 0.06 (rectum and bladder) to 1.06 ± 0.43 (bone) between PBS-PT and 3D-CRT. The LAR for most organs was within 0.01-1% (except the colon) with a cumulative risk of 21 ± 13%, 35 ± 14% and 35 ± 16% for PBS-PT, IMAT and 3D-CRT, respectively.
CONCLUSIONS CONCLUSIONS
PBS-PT was associated with the lowest risk of radiation-induced SMN compared to IMAT and 3D-CRT in abdominal neuroblastoma treatment. Other clinical endpoints and plan robustness should also be considered for optimal plan selection.

Identifiants

pubmed: 34307918
doi: 10.1016/j.phro.2021.06.003
pii: S2405-6316(21)00033-6
pmc: PMC8295851
doi:

Types de publication

Journal Article

Langues

eng

Pagination

45-52

Informations de copyright

© 2021 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Sophie Taylor (S)

Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, London, UK.

Pei Lim (P)

Department of Oncology, University College London Hospitals NHS Foundation Trust, London, UK.

Reem Ahmad (R)

Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, London, UK.

Ammar Alhadi (A)

Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, London, UK.

William Harris (W)

Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, London, UK.

Vasilis Rompokos (V)

Radiotherapy Physics Services, University College London Hospitals NHS Foundation Trust, London, UK.

Derek D'Souza (D)

Radiotherapy Physics Services, University College London Hospitals NHS Foundation Trust, London, UK.

Mark Gaze (M)

Department of Oncology, University College London Hospitals NHS Foundation Trust, London, UK.

Jennifer Gains (J)

Department of Oncology, University College London Hospitals NHS Foundation Trust, London, UK.

Catarina Veiga (C)

Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, London, UK.

Classifications MeSH