{"description":"Eligible patients who had received the protocol treatments and who were evaluable for adverse event assessment were included in the adverse event summaries. Any CTCAE 3.0 event of Grade 3 (serious), Grade 4 (life threatening) or Grade 5 (fatal) which were deemed to be related to protocol treatment are included.","eventGroups":[{"description":"Patients receive oral anastrozole once daily on days 1-28","id":"EG000","otherNumAffected":309,"otherNumAtRisk":337,"seriousNumAffected":21,"seriousNumAtRisk":337,"title":"Anastrozole"},{"description":"Patients receive oral anastrozole as in arm I. 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