So you know that the FL1 trial did demonstrate an improvement over R-squared in the global population of the trial with a reduced hazard ratio of 0.21. So the basic idea of the subgroup analysis was to see whether this would hold in low and high risk patients. So when you look at the age of the patients, the comorbidity burden, the size of the tumor, the number of lines, the POD24 events or not, the FLIPI score at baseline, what you can see is that all those subgroups of analysis, they achieve the very same hazard ratio of Epco plus R-squared compared to R-squared...
So you know that the FL1 trial did demonstrate an improvement over R-squared in the global population of the trial with a reduced hazard ratio of 0.21. So the basic idea of the subgroup analysis was to see whether this would hold in low and high risk patients. So when you look at the age of the patients, the comorbidity burden, the size of the tumor, the number of lines, the POD24 events or not, the FLIPI score at baseline, what you can see is that all those subgroups of analysis, they achieve the very same hazard ratio of Epco plus R-squared compared to R-squared. So the main takeaway was that all the subgroups are having benefit from this new combination in regard to R-squared. And we did have a quick look to the toxicity rates too. And what was quite striking is that no matter how much comorbidity you had on the NHL5 score, the patients did the same in terms of adverse events. So all in all, a pretty all comer combination.
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