Checkpoint inhibitors demonstrate salutary anticancer effects, including long-term remissions. PD-L1 expression/amplification, high mutational burden, and mismatch repair deficiency correlate with response. Champiat et al for the first time described a small subset of patients that could actually have tumor growth accelerated when given PD1/PDL1-targeting agents [1].
Hyperprogression may be defined as accelerated progression outpaces the expected rate of growth induced by the therapies.
Champiat suggests that a subset of patients with disease progression have a course that is more deleterious than they might have had with other therapies, or even in the absence of therapy.
Keywords: immunotherapy
Published on: Mar 15, 2018 Pages: 1-2
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DOI: 10.17352/ijrro.000026
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