Stenzl - Figure 32

Studies of Immune Checkpoint Inhibitors in Selected Populations

FIG. 32:  Several of the newly-available checkpoint inhibitors have been successfully used to treat other tumor types.[21]  Figure 32 shows that immunohistochemistry staining for the presence of a programmed death receptor, either on the tumor cell or on the T-cell, or on both, can predict an outcome.[20]  Unfortunately this does not allow us to say whether these patients should have a checkpoint inhibitor, at least as second-line therapy, because cells that were not stained with any programmed-death receptors in a small percentage of patients were still responding, whereas not all patients in whom the receptor was present responded well to any of the checkpoint inhibitors currently available.  This is a possibility that we must investigate further, meaning we need new ways not only of looking at the receptors, but also of looking at their activity.

References

[20]

Groenendijk FH, de Jong J, Fransen van de Putte EE, et al. ERBB2 mutations characterize a subgroup of muscle-invasive bladder cancers with excellent response to neoadjuvant chemotherapy. Eur Urol. 2016;69:384−8  http://dx.doi.org/10.1016/j.eururo.2015.01.014

[21]

Powles T, Smith K, Stenzl  A, Bedke J. Immune checkpoint inhibition in metastatic urothelial cancer. Eur Urol. Published online April 13, 2017  http://dx.doi.org/10.1016/j.eururo.2017.03.047