Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Response-Adapted Omission of Nodal Boost In N3 Breast Cancer After Neoadjuvant Systemic Therapy

18 septembre 2026 mis à jour par: Jinli Ma, Fudan University

Omitting the Boost to Initially Involved But Undissected Nodal Stations That Achieved Clinical Complete Response After Neoadjuvant Systemic Therapy in cN3 Breast Cancer: A Phase III Randomized Study

Background Clinical N3 (cN3) breast cancer represents a high-risk subgroup of locally advanced disease. After neoadjuvant systemic therapy (NST), patients who achieve a clinical complete response (cCR) in initially involved but undissected nodal stations currently receive a boost to these regions as part of standard postoperative radiotherapy. However, whether this boost is necessary in this setting remains unknown, and prospective evidence on the safety of boost omission is lacking.

Objective The REACT-N3 trial aims to evaluate whether omitting the boost to undissected nodal stations that achieve cCR after NST is non-inferior to standard boost in terms of 3-year invasive breast cancer recurrence-free interval (IBCRFI), while reducing toxicity to adjacent organs.

Methods This is an open-label, multicenter, randomized phase 3 trial. Eligible patients are women with cN3 breast cancer who have completed NST, undergone breast/axillary surgery with the internal mammary, supraclavicular, and infraclavicular nodes left undissected, and have no macroscopic residual disease in these stations on post-NST [¹⁸F]FDG PET-CT or other imaging. Participants will be randomized 1:1 to receive either a standard boost (10 Gy in 5 fractions) or no boost to the initially involved but cCR-converted undissected nodal stations. Randomization is stratified by postoperative axillary nodal status (ypN- vs. ypN+), location of the involved nodal station (SCV vs. non-SCV), and molecular subtype (TNBC vs. non-TNBC). The primary endpoint is 3-year IBCRFI. Secondary endpoints include locoregional recurrence-free survival, distant metastasis-free survival, disease-free survival, overall survival, toxicity, and patient-reported outcomes. With a non-inferiority margin of 8%, a one-sided α of 0.05, 80% power, and 10% drop-out rate, a total of 534 patients will be enrolled.

Discussion The REACT-N3 trial will provide high-level evidence on the safety of boost omission in cN3 breast cancer patients with cCR after NST. If non-inferiority is confirmed, this strategy could establish a new, toxicity-sparing standard for regional nodal irradiation in this high-risk population.

Aperçu de l'étude

Statut

Recrutement

Les conditions

Type d'étude

Interventionnel

Inscription (Estimé)

534

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Chine, 200032
        • Recrutement
        • Fudan University Shanghai Cancer Center
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 75 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Female/male, aged 18-75 years.
  • ECOG performance status 0-1.
  • Histologically confirmed unilateral invasive breast cancer.
  • No DM (M0), as confirmed by standard staging.
  • cN3 disease, defined according to AJCC 8th staging system, confirmed by imaging and/or pathology, including any of the following: cN3a: metastasis to ipsilateral ICV nodes, with or without level I/II ALN involvement.

cN3b: metastasis to ipsilateral IMNs with concurrent level I/II ALN involvement.

cN3c: metastasis to ipsilateral SCV nodes, with or without ALN or IMN involvement.

Imaging confirmation is mandatory for all cN3 designations and may be performed using ultrasound, contrast-enhanced CT, MRI, or [18F]FDG PET-CT [16-18]. Across all modalities, abnormal features include, but are not limited to: abnormal enlargement (short-axis ≥5mm), rounded morphology with loss of the normal oval shape, solid appearance with effacement of the fatty hilum and cortical thickening, with or without irregular margins or necrosis. Modality-specific criteria include: heterogeneous enhancement on CT or MRI, or increased FDG uptake (SUVmax > mediastinal blood pool) on PET-CT. Pathological verification by fine-needle aspiration (FNA) or core needle biopsy (CNB) is recommended for SCV and ICV nodes when clinically feasible. If pathological confirmation is not obtained, the cN3 status is based solely on imaging criteria specified above.

  • Completion of NST. Standard-of-care regimens must include at least four cycles of chemotherapy; Anti-HER2 targeted therapy is mandatory for HER2-positive disease, and immunotherapy may be added for eligible triple-negative breast cancer (TNBC). Clinical trial regimens are permitted per protocol, with or without chemotherapy, including novel agents (e.g., antibody-drug conjugates [ADCs], immunotherapies, anti-angiogenics, PARP inhibitors, or other investigational drugs). Both pathways are accepted provided the full protocol-specified course is completed.
  • Underwent breast-conserving surgery (BCS) or mastectomy with levels I-II axillary lymph node dissection (ALND); IMN, SCV, and ICV nodes were left undissected. All surgical margins must be negative.
  • Post-neoadjuvant imaging confirms no macroscopic residual disease in the initially involved but undissected nodal stations. The preferred modality is [18F]FDG PET-CT; ultrasound, contrast-enhanced CT or MRI are acceptable alternatives if PET-CT is unavailable. Imaging may be performed before or after surgery, but must be completed prior to randomization. For all modalities, cCR is defined as the complete disappearance of all previously involved but undissected lymph nodes. In cases where visible nodes persist on imaging, cCR may still be considered if: on PET-CT, no pathologic uptake; on ultrasound, CT, or MRI, nodes have normalized in size and morphology, and no suspicious features are present. Suspicious or equivocal findings require biopsy confirmation of negativity before randomization. All imaging studies must be interpreted by experienced radiologists using standardized criteria.
  • Radiotherapy must start within 12 weeks of last surgery or last adjuvant chemotherapy cycle.
  • Adjuvant systemic therapy per guidelines or trial protocols; investigational regimens require active trial enrollment.
  • Written informed consent obtained.

Exclusion Criteria:

  • Stage IV (metastatic) breast cancer.
  • Prior or synchronous contralateral breast cancer.
  • Macroscopic residual disease in the initially involved but undissected nodal stations (ICV, IMN, or SCV) in cN3 patients, as evidenced by post-neoadjuvant imaging and/or biopsy.
  • Incomplete NST or no definitive breast/ALN surgery.
  • Prior radiotherapy to the breast, CW, or regional nodes.
  • History of other malignancies, except for adequately treated basal cell carcinoma of the skin or cervical carcinoma in situ (disease-free >3 years).
  • Current pregnancy or lactation.
  • Severe uncontrolled comorbidities (e.g., cardiac, hepatic, renal, or infectious) precluding radiotherapy, as judged by the investigator.
  • Known intolerance or contraindication to radiotherapy or to the planned adjuvant systemic therapy (chemotherapy, endocrine therapy, anti HER2 therapy, or immunotherapy).
  • Inability or unwillingness to comply with protocol requirements.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: standard boost

a standard boost of 10Gy was delivered to the initially involved but undissected nodal stations that achieved clinical complete response

a boost dose of 10 Gy in 5 fractions to initially involved but undissected nodal stations that achieved clincial complete response after neoadjuvant systemic therapy

Expérimental: boost omission

no boost was given to the initially involved but undissected nodal stations that achieved clinical complete response after neoadjuvant systemic therapy

no boost to the initially involved but undissected nodal stations that achieved clinical complete response after neoadjuvant systemic therapy

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
3-year invasive breast cancer (IBC) recurrence-free interval (RFI)
Délai: 3-year
3-year

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

12 septembre 2026

Achèvement primaire (Estimé)

12 septembre 2030

Achèvement de l'étude (Estimé)

12 septembre 2033

Dates d'inscription aux études

Première soumission

15 septembre 2026

Première soumission répondant aux critères de contrôle qualité

15 septembre 2026

Première publication (Réel)

21 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

23 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

18 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner