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|Molecular Profile||Indication/Tumor Type||Response Type||Therapy Name||Approval Status||Evidence Type||Efficacy Evidence||References|
|Unknown unknown||nasopharynx carcinoma||not applicable||Camrelizumab||Phase I||Actionable||In a Phase I trial, Camrelizumab (SHR-1210) treatment was well tolerated in patients with refractory nasopharyngeal carcinoma, and demonstrated preliminary efficacy with an overall response rate of 34% (31/91, 2 complete responses and 29 partial responses) and a disease control rate of 59% (54/91, stable disease or better) (PMID: 30213452; NCT02721589).||30213452|
|Unknown unknown||nasopharynx carcinoma||not applicable||Camrelizumab||Phase I||Actionable||In a Phase I trial, Camrelizumab (SHR-1210) demonstrated safety and preliminary anti-tumor activity, resulted in partial response in 33.3% (1/3) of patients with nasopharynx cancer (J Clin Onc. 2017 35:15_suppl, e15572-e15572; NCT02742935).||detail...|
|PubMed Id||Reference Title||Details|
|Phase I study of the anti-PD-1 antibody SHR-1210 in patients with advanced solid tumors.||Full reference...|
|(30213452)||Camrelizumab (SHR-1210) alone or in combination with gemcitabine plus cisplatin for nasopharyngeal carcinoma: results from two single-arm, phase 1 trials.||Full reference...|