Proton Beam Therapy for Early Breast Cancer: A Systematic Review and Meta-analysis of Clinical Outcomes.


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:
15 11 2023
Historique:
received: 09 12 2022
revised: 06 02 2023
accepted: 11 02 2023
medline: 23 10 2023
pubmed: 4 3 2023
entrez: 3 3 2023
Statut: ppublish

Résumé

Adjuvant proton beam therapy (PBT) is increasingly available to patients with breast cancer. It achieves better planned dose distributions than standard photon radiation therapy and therefore may reduce the risks. However, clinical evidence is lacking. A systematic review of clinical outcomes from studies of adjuvant PBT for early breast cancer published in 2000 to 2022 was undertaken. Early breast cancer was defined as when all detected invasive cancer cells are in the breast or nearby lymph nodes and can be removed surgically. Adverse outcomes were summarized quantitatively, and the prevalence of the most common ones were estimated using meta-analysis. Thirty-two studies (1452 patients) reported clinical outcomes after adjuvant PBT for early breast cancer. Median follow-up ranged from 2 to 59 months. There were no published randomized trials comparing PBT with photon radiation therapy. Scattering PBT was delivered in 7 studies (258 patients) starting 2003 to 2015 and scanning PBT in 22 studies (1041 patients) starting 2000 to 2019. Two studies (123 patients) starting 2011 used both PBT types. For 1 study (30 patients), PBT type was unspecified. Adverse events were less severe after scanning than after scattering PBT. They also varied by clinical target. For partial breast PBT, 498 adverse events were reported (8 studies, 358 patients). None were categorized as severe after scanning PBT. For whole breast or chest wall ± regional lymph nodes PBT, 1344 adverse events were reported (19 studies, 933 patients). After scanning PBT, 4% (44/1026) of events were severe. The most prevalent severe outcome after scanning PBT was dermatitis, which occurred in 5.7% (95% confidence interval, 4.2-7.6) of patients. Other severe adverse outcomes included infection, pain, and pneumonitis (each ≤1%). Of the 141 reconstruction events reported (13 studies, 459 patients), the most prevalent after scanning PBT was prosthetic implant removal (34/181, 19%). This is a quantitative summary of all published clinical outcomes after adjuvant PBT for early breast cancer. Ongoing randomized trials will provide information on its longer-term safety compared with standard photon radiation therapy.

Identifiants

pubmed: 36868521
pii: S0360-3016(23)00168-2
doi: 10.1016/j.ijrobp.2023.02.023
pmc: PMC7615202
mid: EMS164673
pii:
doi:

Types de publication

Meta-Analysis Systematic Review Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

869-882

Subventions

Organisme : Cancer Research UK
ID : 28284
Pays : United Kingdom
Organisme : Cancer Research UK
ID : A21133
Pays : United Kingdom
Organisme : Department of Health
ID : NIHR300676
Pays : United Kingdom

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Francesca Holt (F)

Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom. Electronic address: francesca.holt@ndph.ox.ac.uk.

Jake Probert (J)

Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.

Sarah C Darby (SC)

Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.

Joanne S Haviland (JS)

Centre for Evaluation and Methods, Wolfson Institute of Population Health, Queen Mary University of London, London, United Kingdom.

Charlotte E Coles (CE)

Department of Oncology, University of Cambridge, Cambridge, United Kingdom.

Anna M Kirby (AM)

Royal Marsden NHS Foundation Trust and Institute of Cancer Research, London, United Kingdom.

Zulian Liu (Z)

Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.

David Dodwell (D)

Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.

Georgios Ntentas (G)

Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom; Department of Medical Physics, Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom.

Frances Duane (F)

St. Luke's Radiation Oncology Network and Trinity St. James's Cancer Institute, Dublin, Ireland.

Carolyn Taylor (C)

Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.

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