So for B-cell ALL, we have seen dramatic improvement a lot for the immunotherapy. I think for, for example, Ph+ ALL that we have seen that these patients may not even need intensive chemotherapy to be cured as well too. So I think it will be interesting to look at the CAR T-cell therapy, now we have shown the efficacy and better toxicity profiles in the relapsed/refractory setting. These agents are now moving into the frontline setting in MRD positive settings and hopefully also in consolidation to try to shorten the whole duration of ALL therapy...
So for B-cell ALL, we have seen dramatic improvement a lot for the immunotherapy. I think for, for example, Ph+ ALL that we have seen that these patients may not even need intensive chemotherapy to be cured as well too. So I think it will be interesting to look at the CAR T-cell therapy, now we have shown the efficacy and better toxicity profiles in the relapsed/refractory setting. These agents are now moving into the frontline setting in MRD positive settings and hopefully also in consolidation to try to shorten the whole duration of ALL therapy. So it’s not a novel agent, but another way, a novel way of using that therapy, which is kind of quite interesting. We’re now beginning to see more CAR T-cell therapy targeting T-cells. T-ALL, so CD-7 targeted CAR-T cells, we have seen several data now that’s been presented in a multicenter study that’s going on, so that will be kind of an interesting study as well for ALL patients.