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Enregistrement W4411288900 · doi:10.1158/1557-3265.sabcs24-p3-12-26

Abstract P3-12-26: Partial breast re-irradiation using ultra hypofractionation: A Phase 2 multi- institutional study

2025· article· en· W4411288900 sur OpenAlexaboutno aff
Danielle Rodin, Fadwa Abdel Rahman, Michelle Audoin, Aisling Barry, Jean‐Marc Bourque, Keelan Byrne, Michelle M. Chan, Hanbo Chen, Eileen P. Connolly, Marc David, Jane De Rocchis, Frances Duane, Elizabeth E. Evans, Naamit K. Gerber, Guilherme Rocha Melo Gondim, Revathy Krishnamurthy, Zhihui Liu, Valérie Théberge, Timothy J. Whelan, Michael A. Yassa, Eileen Rakovitch, Anne Koch

Notice bibliographique

RevueClinical Cancer Research · 2025
Typearticle
Langueen
DomaineMedicine
ThématiqueCancer Risks and Factors
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésMedicinePhase (matter)IrradiationOncologyChemistryPhysics

Résumé

récupéré en direct d'OpenAlex

Abstract Background: Most patients with breast cancer are treated with breast conserving surgery (BCS) followed by adjuvant radiation (RT) to reduce the risk of recurrence in the same breast (local recurrence (LR)) and to maximize long-term breast preservation. Although these treatments are quite effective, a growing number of individuals who receive them are at risk of LR or develop a second primary breast cancer, which is traditionally treated with mastectomy. However, mastectomy has been associated with deleterious effects on quality of life. Advances in screening now allow many LRs to be detected as localized, small tumours amenable to further BCS. BCS followed by reirradiation with partial breast irradiation (rPBI) has recently been found to be a safe treatment option in women with prior breast RT, but the optimal fractionation is unknown. For women with early-stage breast cancer receiving upfront treatment, a shorter 1-week course of breast RT (ultra-hypofractionation) has been found to be equivalent to longer fractionation schedules. However, this data cannot be directly applied to LR due to the higher cumulative RT doses and to tissue changes from previous treatment. The safety and efficacy of ultra-hypofractionated rPBI for LR are the focus of the proposed study. We hypothesize that ultra-hypofractionated rPBI following BCS for LR or new primary breast cancer in the previously irradiated breast will be associated with acceptable toxicity at 1 year (<13% grade >3 toxicity). Methods: This study is a phase II, prospective, multi-center, international trial of ultra-hypofractionated rPBI following repeat BCS for LR or new primary breast cancer in the previously irradiated breast. rPBI will be delivered at a dose of 26 Gy in 5 daily fractions over a period of 1-week (excluding weekends and statutory holidays). Boost RT is not permitted. The primary endpoint is the risk of grade >3 adverse events (AEs) occurring at 1-year from rPBI completion (CTCAE v5.0). Secondary endpoints include local, regional and distant recurrence, invasive breast cancer-free survival, mastectomy-free survival, overall survival, financial toxicity, and patient-reported satisfaction. To achieve 80% power with a Type I error rate of 0.05 and 3% lost to follow up or unevaluable, 171 patients will be accrued. Eligible patients are status post BCS for ductal carcinoma in situ or invasive cancer <3 cm in greatest diameter (invasive and non-invasive components) with negative margins (no tumor on ink) who are clinically node negative and who completed treatment >5 years earlier for breast cancer in the ipsilateral breast treated with BCS and adjuvant whole or partial breast RT. Patients with grade >2 late skin toxicity from prior radiation are excluded, as are those with T4 or multicentric disease or the presence of an extensive intraductal component. Final eligibility is determined at the time of RT planning based on ability to clearly define the surgical cavity. The RT planning target volume must be <50% of the whole breast. The study is open to accrual 7 sites in Canada, the US, and Jordan, with an additional 9 international centers in the process of opening; 17 patients have been enrolled and treated as of 10-07-2024. Patients will be followed for a total of 5 years. Clinical trial information: NCT05592938. Supported by the Canadian Cancer Society and the Princess Margaret Cancer Foundation. Citation Format: Danielle Rodin, Fadwa Abdel Rahman, Michelle Audoin, Aisling Barry, Jean-Marc Bourque, Keelan Byrne, Michelle Chan, Hanbo Chen, Eileen Connolly, Marc David, Jane De Rocchis, Frances Duane, Elizabeth Evans, Naamit Gerber, Guilherme Gondim, Revathy Krishnamurthy, Zhihui Liu, Tom Purdie, Valerie Theberge, Timothy Whelan, Martina Wood, Michael Yassa, Eileen Rakovitch, Anne Koch. Partial breast re-irradiation using ultra hypofractionation: A Phase 2 multi- institutional study [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2024; 2024 Dec 10-13; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2025;31(12 Suppl):Abstract nr P3-12-26.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction distillée sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.

score de la tête « metaresearch » (Codex)0,002
score de la tête « metaresearch » (Gemma)0,001
Version: codex-gemma-dda1882f352aStatut de validation: machine_predicted_unvalidated
Catégories candidatesCharge utile insuffisante (le modèle a refusé de juger)
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Observationnel · Signal consensuel: Observationnel
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,262
Score d'incertitude au seuil1,000

Scores Codex et Gemma par catégorie

CatégorieCodexGemma
Métarecherche0,0020,001
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0000,001
Études des sciences et des technologies0,0000,000
Communication savante0,0000,000
Science ouverte0,0000,000
Intégrité de la recherche0,0000,001
Charge utile insuffisante (le modèle a refusé de juger)0,0010,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,494
Tête enseignante GPT0,631
Écart entre enseignants0,137 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.

Devis d'étudeObservationnel
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations0
Publié2025
Routes d'admission1
Résumé présentoui

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