Subgroup analyses of progression-free survival showed that, regardless of subgroup, individuals in the olaparib group experienced a lower threat of progression than those in the placebo group . No predictive elements were identified . A complete response to the ultimate platinum-based therapy before research entry was a significant prognostic factor for longer progression-free survival, irrespective of study group . The secondary end point of time to progression according to the RECIST guidelines or CA-125 level, whichever showed earlier progression, was also significantly much longer in the olaparib group than in the placebo group . At study entry, 40 percent of the overall study population experienced measurable disease and could be assessed for an objective response regarding to RECIST recommendations; the response price was 12 percent in the olaparib group, in comparison with 4 percent in the placebo group .Come and join us right now.
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