1. Radiotherapy or surgery of the axilla after a positive sentinel node in breast cancer (EORTC 10981-22023 AMAROS): a randomised, multicentre, open-label, phase 3 non-inferiority trial
- Author
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Donker, M., Tienhoven, G. van, Straver, M.E., Meijnen, P., Velde, C.J. van de, Mansel, R.E., Cataliotti, L., Westenberg, A.H., Klinkenbijl, J.H.G., Orzalesi, L., Bouma, W.H., Mijle, H.C. van der, Nieuwenhuijzen, G.A., Veltkamp, S.C., Slaets, L., Duez, N.J., Graaf, P.W. de, Dalen, T. van, Marinelli, A., Rijna, H., Snoj, M., Bundred, N.J., Merkus, J.W.M.J., Belkacemi, Y., Petignat, P., Schinagl, D.A.X., Coens, C., Messina, C.G., Bogaerts, J., Rutgers, E.J., Donker, M., Tienhoven, G. van, Straver, M.E., Meijnen, P., Velde, C.J. van de, Mansel, R.E., Cataliotti, L., Westenberg, A.H., Klinkenbijl, J.H.G., Orzalesi, L., Bouma, W.H., Mijle, H.C. van der, Nieuwenhuijzen, G.A., Veltkamp, S.C., Slaets, L., Duez, N.J., Graaf, P.W. de, Dalen, T. van, Marinelli, A., Rijna, H., Snoj, M., Bundred, N.J., Merkus, J.W.M.J., Belkacemi, Y., Petignat, P., Schinagl, D.A.X., Coens, C., Messina, C.G., Bogaerts, J., and Rutgers, E.J.
- Abstract
Item does not contain fulltext, BACKGROUND: If treatment of the axilla is indicated in patients with breast cancer who have a positive sentinel node, axillary lymph node dissection is the present standard. Although axillary lymph node dissection provides excellent regional control, it is associated with harmful side-effects. We aimed to assess whether axillary radiotherapy provides comparable regional control with fewer side-effects. METHODS: Patients with T1-2 primary breast cancer and no palpable lymphadenopathy were enrolled in the randomised, multicentre, open-label, phase 3 non-inferiority EORTC 10981-22023 AMAROS trial. Patients were randomly assigned (1:1) by a computer-generated allocation schedule to receive either axillary lymph node dissection or axillary radiotherapy in case of a positive sentinel node, stratified by institution. The primary endpoint was non-inferiority of 5-year axillary recurrence, considered to be not more than 4% for the axillary radiotherapy group compared with an expected 2% in the axillary lymph node dissection group. Analyses were by intention to treat and per protocol. The AMAROS trial is registered with ClinicalTrials.gov, number NCT00014612. FINDINGS: Between Feb 19, 2001, and April 29, 2010, 4823 patients were enrolled at 34 centres from nine European countries, of whom 4806 were eligible for randomisation. 2402 patients were randomly assigned to receive axillary lymph node dissection and 2404 to receive axillary radiotherapy. Of the 1425 patients with a positive sentinel node, 744 had been randomly assigned to axillary lymph node dissection and 681 to axillary radiotherapy; these patients constituted the intention-to-treat population. Median follow-up was 6.1 years (IQR 4.1-8.0) for the patients with positive sentinel lymph nodes. In the axillary lymph node dissection group, 220 (33%) of 672 patients who underwent axillary lymph node dissection had additional positive nodes. Axillary recurrence occurred in four of 744 patients in the axillary lymph node di
- Published
- 2014