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Omitting Axillary Dissection in Breast Cancer with Sentinel-Node Metastases

Authors :
de Boniface, Jana
Filtenborg Tvedskov, Tove
Ryden, Lisa
Szulkin, Robert
Reimer, Toralf
Kuehn, Thorsten
Kontos, Michalis
Gentilini, Oreste D.
Olofsson Bagge, Roger
Sund, Malin
Lundstedt, Dan
Appelgren, Matilda
Ahlgren, Johan
Norenstedt, Sophie
Celebioglu, Fuat
Sackey, Helena
Scheel Andersen, Inge
Hoyer, Ute
Nyman, Per F.
Vikhe Patil, Eva
Wieslander, Elinore
Dahl Nissen, Henrik
Alkner, Sara
Andersson, Yvette
Offersen, Birgitte V.
Bergkvist, Leif
Frisell, Jan
Christiansen, Peer
de Boniface, Jana
Filtenborg Tvedskov, Tove
Ryden, Lisa
Szulkin, Robert
Reimer, Toralf
Kuehn, Thorsten
Kontos, Michalis
Gentilini, Oreste D.
Olofsson Bagge, Roger
Sund, Malin
Lundstedt, Dan
Appelgren, Matilda
Ahlgren, Johan
Norenstedt, Sophie
Celebioglu, Fuat
Sackey, Helena
Scheel Andersen, Inge
Hoyer, Ute
Nyman, Per F.
Vikhe Patil, Eva
Wieslander, Elinore
Dahl Nissen, Henrik
Alkner, Sara
Andersson, Yvette
Offersen, Birgitte V.
Bergkvist, Leif
Frisell, Jan
Christiansen, Peer
Publication Year :
2024

Abstract

Background: Trials evaluating the omission of completion axillary-lymph-node dissection in patients with clinically node-negative breast cancer and sentinel-lymph-node metastases have been compromised by limited statistical power, uncertain nodal radiotherapy target volumes, and a scarcity of data on relevant clinical subgroups. Methods: We conducted a noninferiority trial in which patients with clinically node-negative primary T1 to T3 breast cancer (tumor size, T1, ≤ 20 mm; T2, 21 to 50 mm; and T3, >50 mm in the largest dimension) with one or two sentinel-node macrometastases (metastasis size, >2 mm in the largest dimension) were randomly assigned in a 1:1 ratio to completion axillary-lymph-node dissection or its omission (sentinel-node biopsy only). Adjuvant treatment and radiation therapy were used in accordance with national guidelines. The primary end point was overall survival. We report here the per-protocol and modified intention-to-treat analyses of the prespecified secondary end point of recurrence-free survival. To show noninferiority of sentinel-node biopsy only, the upper boundary of the confidence interval for the hazard ratio for recurrence or death had to be below 1.44. Results: Between January 2015 and December 2021, a total of 2766 patients were enrolled across five countries. The per-protocol population included 2540 patients, of whom 1335 were assigned to undergo sentinel-node biopsy only and 1205 to undergo completion axillary-lymph-node dissection (dissection group). Radiation therapy including nodal target volumes was administered to 1192 of 1326 patients (89.9%) in the sentinel-node biopsy-only group and to 1058 of 1197 (88.4%) in the dissection group. The median follow-up was 46.8 months (range, 1.5 to 94.5). Overall, 191 patients had recurrence or died. The estimated 5-year recurrence-free survival was 89.7% (95% confidence interval [CI], 87.5 to 91.9) in the sentinel-node biopsy-only group and 88.7% (95% CI, 86.3 to 91.1) in the dis

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1457643100
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1056.NEJMoa2313487