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EORTC trial 22922/10925

1996-2004

Eligible: pN0 with centrally/medially tumour or pN+

R to +/- RT to IM-MS, mostly including IC3

Primary endpoint: OS

Secondary endpoints: DFS and BCM

4004 patients, 44% node-negative

Around 25% had mastectomy

Median follow up 10.9 yr