Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 12 min ago
Peer-reviewedCC BYCurrent oncology (Toronto, Ont.)

CBCT-Guided Online Adaptive Ultrahypofractionated Whole-Breast Radiotherapy for Early-Stage Breast Cancer: Dosimetric Outcomes and Acute Toxicity.

4 affiliations
  1. 1Specialty Hospital Radiochirurgia Zagreb, 10431 Sveta Nedelja, Croatia.
  2. 2Department of Physics, Faculty of Science, University of Zagreb, 10000 Zagreb, Croatia.
  3. 3Medical Faculty Osijek, University Josip Juraj Strossmayer in Osijek, 31000 Osijek, Croatia.
  4. 4Medical Faculty, Juraj Dobrila University of Pula, 52100 Pula, Croatia.

Abstract

Ultrahypofractionated whole-breast radiotherapy reduces treatment burden but increases the importance of accurate dose delivery at each fraction. This retrospective single-center study evaluated cone-beam computed tomography-guided online adaptive radiotherapy in 55 patients with early-stage breast cancer treated with 26 or 27 Gy in five fractions. Dosimetric analysis was available for 52 patients and 259 paired scheduled and adapted fractions. Linear mixed-effects models with a patient-specific random intercept were used to account for repeated fractions within individual patients. The adapted plan was selected for 242 out of 260 delivered fractions (93.1%). Mean planning target volume V95% increased from 93.52 ± 2.94% with the scheduled plan to 98.13 ± 1.04% with adaptation (p < 0.001), with reduced interfraction variability. Ipsilateral lung V30% increased modestly from 13.94% to 14.96% (p < 0.001). In left-sided cases, no significant differences were observed for heart V25% (1.400% vs. 1.395%; p = 0.3825) or left anterior descending coronary artery D0.03 cm³ (1.771 vs. 1.873 Gy; p = 0.1390). Acute grade 1 toxicity occurred in five patients (9.1%), with no grade ≥ 2 events. Mean treatment-session duration was 28 min. Online adaptation significantly improved daily target coverage and was technically feasible within a five-fraction whole-breast workflow. Acute toxicity was limited in this cohort, while longer follow-up and cumulative dose analyses are needed to further define its impact on organ-at-risk exposure and clinical outcomes.

Related

  1. Exploratory machine-learning evaluation of clinical and dosimetric features in late prostate radiotherapy toxicity.
    Karl Jordan, Christopher J Talbot, John D Kelleher +2
    Clinical and translational radiation oncologyPeer-reviewedCC BY-NC-NDFull textApplied physics & instrumentationEurope PMC
  2. Hypofractionated and conventionally fractionated radiotherapy for synchronous bilateral breast cancer: clinical and dosimetric outcomes
    Bahar Cepni, Line Hoeltgen, David Neugebauer +11
    Strahlentherapie Und OnkologiePeer-reviewedCC BY 4.0Full textApplied physics & instrumentationPMC
  3. Dosimetric Comparison of Intensity-Modulated Radiotherapy and Four-Field Three-Dimensional Conformal Radiotherapy in the Management of Prostate Cancer: A Retrospective Dual-Centre Analysis
    Alaa AbdAllah, wafaa mohamed, Amani Saber +1
    Minia Journal of Medical ResearchPeer-reviewedCC BYFull textApplied physics & instrumentationDOAJ
  4. Dosimetric and Treatment Delivery Efficiency Comparison of Two Ring-gantry Linear Accelerator Platforms for Liver Stereotactic Body Radiotherapy
    Srikanth Guduru, Rohith Singareddy, N. V. N. Madhusudhana Sresty +2
    Journal of Medical PhysicsPeer-reviewedCC BY-NC-SAFull textApplied physics & instrumentationDOAJ
  5. Optimising electron beam 6 MeV radiotherapy: field-size-dependent dosimetric impact of perforated thermoplastic immobilisation masks.
    Mohammed Rezzoug, Yassine Oulhouq, Omar Hamzaoui +3
    Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation OncologyPeer-reviewedCC BY-NC-NDFull textApplied physics & instrumentationEurope PMC
BibTeX
@article{ursi2026cbctguided,
  title = {{CBCT-Guided Online Adaptive Ultrahypofractionated Whole-Breast Radiotherapy for Early-Stage Breast Cancer: Dosimetric Outcomes and Acute Toxicity.}},
  author = {Giovanni Ursi and Matea Lekić and Hrvoje Kaučić and Aleksandar Kovačević and Domagoj Kosmina and Karla Schwarz and Dragan Schwarz and Damir Vučinić},
  journal = {Current oncology (Toronto, Ont.)},
  year = {2026},
  month = oct,
  doi = {10.3390/curroncol33100634},
  url = {https://europepmc.org/article/MED/42930201},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - CBCT-Guided Online Adaptive Ultrahypofractionated Whole-Breast Radiotherapy for Early-Stage Breast Cancer: Dosimetric Outcomes and Acute Toxicity.
AU  - Giovanni Ursi
AU  - Matea Lekić
AU  - Hrvoje Kaučić
AU  - Aleksandar Kovačević
AU  - Domagoj Kosmina
AU  - Karla Schwarz
AU  - Dragan Schwarz
AU  - Damir Vučinić
PY  - 2026
DA  - 2026/10/20
JO  - Current oncology (Toronto, Ont.)
DO  - 10.3390/curroncol33100634
UR  - https://europepmc.org/article/MED/42930201
AB  - Ultrahypofractionated whole-breast radiotherapy reduces treatment burden but increases the importance of accurate dose delivery at each fraction. This retrospective single-center study evaluated cone-beam computed tomography-guided online adaptive radiotherapy in 55 patients with early-stage breast cancer treated with 26 or 27 Gy in five fractions. Dosimetric analysis was available for 52 patients and 259 paired scheduled and adapted fractions. Linear mixed-effects models with a patient-specific random intercept were used to account for repeated fractions within individual patients. The adapted plan was selected for 242 out of 260 delivered fractions (93.1%). Mean planning target volume V95% increased from 93.52 ± 2.94% with the scheduled plan to 98.13 ± 1.04% with adaptation (p < 0.001), with reduced interfraction variability. Ipsilateral lung V30% increased modestly from 13.94% to 14.96% (p < 0.001). In left-sided cases, no significant differences were observed for heart V25% (1.400% vs. 1.395%; p = 0.3825) or left anterior descending coronary artery D0.03 cm³ (1.771 vs. 1.873 Gy; p = 0.1390). Acute grade 1 toxicity occurred in five patients (9.1%), with no grade ≥ 2 events. Mean treatment-session duration was 28 min. Online adaptation significantly improved daily target coverage and was technically feasible within a five-fraction whole-breast workflow. Acute toxicity was limited in this cohort, while longer follow-up and cumulative dose analyses are needed to further define its impact on organ-at-risk exposure and clinical outcomes.
SN  - 1198-0052
SN  - 1718-7729
ER  -