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Premenopausal patients. In Table 8, it can be seen that there were no strong relationships between on-treatment Ki67 and ER or PgR levels in premenopausal patients in ADAPT, so these levels therefore cannot be recommended to reduce the number of patients who could be spared an on-treatment biopsy, even considering baseline Ki67. Enhanced monitoring when on-treatment biopsy for Ki67 is unavailable. Reliability of Ki67 analysis. Centres wishing to apply on-treatment Ki67 should confirm that their Ki67 analysis is operating to similar levels and should contact the authorship to access material if needed to do so. 75618, cerca de 1,7 do resultado da arrecadação bruta dos concursos de prognósticos e da loteria federal vão para gif sundsvall o COB. Consistency of scores is markedly enhanced by adherence to the methodology for “global scoring” which was validated and endorsed by the KiBCWG 20 and is advocated here. Using this method, the median baseline Ki67 in ER + HER2- tumors in the whole POETIC trial (ie., not just the case-control series described here) was 14.3% ( n = 3452). In ADAPT, median baseline Ki67 was 20% for both pre- and postmenopausal patients ( n = 1954 and 2730, respectively). The median baseline Ki67 in ADAPT was expected to be higher than in POETIC since eligibility for ADAPT was confined to those that were candidates for (neo)adjuvant chemotherapy by conventional prognostic criteria. Clinical factors such as tumor size and nodal status do not impact on response to NeoET but do relate to the overall prognosis of patients.

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