S_inary The prognostic value of oestrogen receptor (ER) and progesterone receptor (PR) was estimated through a multicentric study of 2257 operable breast cancer patients followed up for a median of 8.5 years. None of the patients had received adjuvant therapy.

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Among well-established prognostic factors in ovarian cancers, CA 125 half-life and nadir concentration bear a strong and independent prognostic value.

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BACKGROUND.Previous reports based on small patient numbers suggested that changes in serum HER‐2/neu levels may predict response or lack of response to trastuzumab‐based therapies in metastatic breast cancer (MBC). The objectives of this study were to pool data from 307 patients with MBC from 7 medical institutions to validate that the serum HER‐2/neu profile predicts patient resistance to trastuzumab and to establish a clinically relevant cutoff.METHODS.This was an international, multicenter, retrospective analysis of individual pooled data from 307 patients with MBC who were treated with first‐line trastuzumab‐based therapy. Serum was collected at baseline and 30 to 120 days after the initiation of trastuzumab therapy. A serum HER‐2/neu decrease ≥20% (receiver operating curve analysis) was defined as a significant HER‐2/neu change.RESULTS.Of the 307 patients with MBC, 191 patients (62%) had a significant decline (>20%) in serum HER‐2/neu and 116 patients (38%) did not. The objective response rate was 57% for patients who achieved this decline in serum HER‐2/neu (>20%) compared with 28% for patients who did not. Patients who achieved this decline in serum HER‐2/neu also had a significantly longer time to disease progression (320 days vs 180 days; P < .0001), longer duration of response (369 days vs 230 days; P = .008), and longer overall survival (898 days vs 593 days; P < .018).CONCLUSIONS.In this pooled analysis of 307 patients with MBC, individuals who did not achieve a significant decline (≥20%) in serum HER‐2/neu levels had decreased benefit from trastuzumab‐based therapy, and these patients should be considered for clinical trials evaluating additional HER‐2/neu‐targeted interventions. Cancer 2008. © 2008 American Cancer Society.