Hyperprogressive Disease Is a New Pattern of Progression in Cancer Patients Treated by Anti-PD-1/PD-L1
By S. Champiat, L. Dercle, S. Ammari, C. Massard, A. Hollebecque, S. Postel-Vinay, N. Chaput, A. Eggermont, A. Marabelle, J. Soria and 1 more. Clinical Cancer Research, 2016
1,067 citations recorded by the source corpus.
Subfields: Oncology, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/f44acb172a9e3e4ca933b99bf9e2870d79e3f138
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Citations in the corpus
- The Society for Immunotherapy of Cancer consensus statement on immunotherapy for the treatment of squamous cell carcinoma of the head and neck (HNSCC) (2019, background): “” Alternatively, other accepted definitions of hyperprogression found in the literature include: a “RECIST progression at the first evaluation and as a ≥2fold increase of the tumor growth rate between the reference and the experimental periods” [90], “time-to-”
- Molecular Determinants of Response to Anti-Programmed Cell Death (PD)-1 and Anti-Programmed Death-Ligand 1 (PD-L1) Blockade in Patients With Non-Small-Cell Lung Cancer Profiled With Targeted Next-Generation Sequencing. (2018, background): “of patients 240 759 Median age, years (range) 66 (22-92) 66 (22-93) .”
- Development of PD-1 and PD-L1 inhibitors as a form of cancer immunotherapy: a comprehensive review of registration trials and future considerations (2018, background): “In addition, one study was among the first to describe the existence of a subset of patients (9%) experiencing hyperprogressive disease defined as RECIST progression at first evaluation characterized by a ≥ 2-fold increase in tumor growth rate in response to anti-PD-1/PD-L1 therapy [70].”
- PD-1+ regulatory T cells amplified by PD-1 blockade promote hyperprogression of cancer (2019, background): “HPD was defined as previously reported (6): time-to-treatment failure <2 mo, >50% increase in tumor burden compared with pretreatment imaging, and >twofold increase in progression speed.”
- Hyper-progressors after Immunotherapy: Analysis of Genomic Alterations Associated with Accelerated Growth Rate (2017, background): “Champiat and colleagues (9) demonstrated that 9% of patients (12/131) showed a 2fold increase in tumor burden when compared with preimmunotherapy imaging.”