2016
DOI: 10.1200/jco.2016.34.15_suppl.3060
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A first-in-human phase I study of the anti-PD-1 antibody PDR001 in patients with advanced solid tumors.

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Cited by 11 publications
(7 citation statements)
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“…Spartalizumab (PDR001), which was evaluated in a multicenter phase II trial with including 116 patients with various NETs reported a radiographic response rate of 7.4% for well-differentiated NETs and 0% for gastrointestinal neuroendocrine tumors (GI NET). The stable disease rate in almost 2/3 of patients with both well-differentiated NET and GI NET, was quite promising though [ 73 , 74 ].…”
Section: Resultsmentioning
confidence: 99%
“…Spartalizumab (PDR001), which was evaluated in a multicenter phase II trial with including 116 patients with various NETs reported a radiographic response rate of 7.4% for well-differentiated NETs and 0% for gastrointestinal neuroendocrine tumors (GI NET). The stable disease rate in almost 2/3 of patients with both well-differentiated NET and GI NET, was quite promising though [ 73 , 74 ].…”
Section: Resultsmentioning
confidence: 99%
“…While XmAb18087 has shown potent anti-tumor activity in both in vitro and in vivo studies, 70 the PDR001 has, in a previous phase 1 study on patients with advanced solid tumors, shown that the medication is well tolerated and has a sound safety profile. 71…”
Section: Discussionmentioning
confidence: 99%
“…While XmAb18087 has shown potent anti-tumor activity in both in vitro and in vivo studies, 70 the PDR001 has, in a previous phase 1 study on patients with advanced solid tumors, shown that the medication is well tolerated and has a sound safety profile. 71 The Intuvax trial is the only non-monoclonal antibody trial. Intuvax activates the immune system when administered intratumorally and has previously been used in the treatment of renal and hepatic malignancies with promising results.…”
Section: Immunotherapymentioning
confidence: 99%
“…is may lead to approval of drugs that were effective in specific subtypes, but not robust to overcome progression in all 4 CMS subtypes [42]. A handful of clinical trials targeting the CRC CMS4 subtype with novel immunotherapies including anti-PD-1 mAB spartalizumab [85], dual PD-1/TGFB engineered mAB-fusion protein M7824 [86], and a dendritic cell vaccine (AVEVAC) [87] have already begun in the US and EU. Similar subtyping advances in pancreatic [41], gastric [22], and liver cancers leveraging data accumulated from large-scale multicenter projects including the Cancer Genome Atlas (TCGA), International Cancer Genome Consortium (ICGC), and others hold similar potential.…”
Section: Tme Biomarker Concepts and Personalized Medicinementioning
confidence: 99%