Impact of Imaging-Guided Localization on Performance of Tailored Axillary Surgery in Patients with Clinically Node-Positive Breast Cancer: Prospective Cohort Study Within TAXIS (OPBC-03, SAKK 23/16, IBCSG 57-18, ABCSG-53, GBG 101).
Обработка статьи · этапы, ошибки и управление
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Weber Walter P, Heidinger Martin, Hayoz Stefanie, Matrai Zoltan, Tausch Christoph, Henke Guido, Zwahlen Daniel R, Gruber Günther, Zimmermann Frank, Montagna Giacomo, Andreozzi Mariacarla, Goldschmidt Maite, Schulz Alexandra, Mueller Andreas, Ackerknecht Markus, Tampaki Ekaterini Christina, Bjelic-Radisic Vesna, Kurzeder Christian, Sávolt Ákos, Smanykó Viktor, Hagen Daniela, Müller Dieter J, Gnant Michael, Loibl Sibylle, Fitzal Florian, Markellou Pagona, Bekes Inga, Egle Daniel, Heil Jörg, Knauer Michael
Аннотация
PATIENTS AND METHODS: This was a prospective observational cohort study preplanned in the randomized phase-III OPBC-03/TAXIS trial. IGL was performed at the surgeon's discretion for targeted removal of LNs during TAS. Immediate back-up axillary lymph node dissection (ALND) followed TAS according to TAXIS randomization.
RESULTS: Five-hundred patients were included from 44 breast centers in six countries, 151 (30.2%) of whom underwent NACT. IGL was performed in 84.4% of all patients, with significant variation by country (77.6-100%, p < 0.001). No difference in the median number of removed (5 vs. 4, p = 0.3) and positive (2 vs. 2, p = 0.6) LNs by use of IGL was noted. The number of LNs removed during TAS with IGL remained stable over time (p = 0.8), but decreased significantly without IGL, from six (IQR 4-6) in 2019 to four (IQR 3-4) in 2022 (p = 0.015). An ALND was performed in 249 patients, removing another 12 (IQR 9-17) LNs, in which a median number of 1 (IQR 0-4) was positive. There was no significant difference in residual nodal disease after TAS with or without IGL (68.0% vs. 57.6%, p = 0.2).
CONCLUSIONS: IGL did not significantly change either the performance of TAS or the volume of residual nodal tumor burden.
TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03513614.