So BTK inhibitors have a tremendous impact in mantle cell and in the front-line space, there’s a couple of ways in which we’re starting to use them. I think first and foremost, for patients who are older or perhaps not great chemotherapy candidates, we have data to support either monotherapy use of covalent BTK inhibitors or in combination with rituximab. There are some larger trials going on to help us define the benefit of that approach, compared to chemoimmunotherapy in the MANGROVE trial...
So BTK inhibitors have a tremendous impact in mantle cell and in the front-line space, there’s a couple of ways in which we’re starting to use them. I think first and foremost, for patients who are older or perhaps not great chemotherapy candidates, we have data to support either monotherapy use of covalent BTK inhibitors or in combination with rituximab. There are some larger trials going on to help us define the benefit of that approach, compared to chemoimmunotherapy in the MANGROVE trial. And then we can also combine these BTK inhibitors with existing standards of care. So for example, this summer, the ECHO data showed us that combination of acalabrutinib with BR did lead to an improvement in progression-free survival and prolongs that time between start of first treatment and start of next treatment for patients. And then in the younger population, looking at perhaps consolidation with BTK inhibitors rather than, say, autologous transplant, which has been a mainstay. So really, I think across the spectrum, we’re starting to generate data that helps us define that BTK inhibitors are likely to play a big role.