Antibody treatment relies on the specific binding of monoclonal antibody with the antigen on cell surface. To better classify the population that response to the treatment, co-develop diagnostic antibody along with the therapeutic partner is routine. Usually the two antibodies for these two aims are separately developed. Examples are PD-1 inhibitor Opdivo and keytruda and their corresponding diagnostic reagents. My confusion is why not directly use the therapeutic antibody as the diagnose tool to evaluate the potential responding in patient sample. If cells can be detected, that means they have a greater chance to be targeted in the treatment.