https://scholars.lib.ntu.edu.tw/handle/123456789/548994
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Kojima T. | en_US |
dc.contributor.author | Shah M.A. | en_US |
dc.contributor.author | Muro K. | en_US |
dc.contributor.author | Francois E. | en_US |
dc.contributor.author | Adenis A. | en_US |
dc.contributor.author | CHIH-HUNG HSU | en_US |
dc.contributor.author | Doi T. | en_US |
dc.contributor.author | Moriwaki T. | en_US |
dc.contributor.author | Kim S.-B. | en_US |
dc.contributor.author | Lee S.-H. | en_US |
dc.contributor.author | Bennouna J. | en_US |
dc.contributor.author | Kato K. | en_US |
dc.contributor.author | Shen L. | en_US |
dc.contributor.author | Enzinger P. | en_US |
dc.contributor.author | Qin S.-K. | en_US |
dc.contributor.author | Ferreira P. | en_US |
dc.contributor.author | Chen J. | en_US |
dc.contributor.author | Girotto G. | en_US |
dc.contributor.author | de la Fouchardiere C. | en_US |
dc.contributor.author | Senellart H. | en_US |
dc.contributor.author | Al-Rajabi R. | en_US |
dc.contributor.author | Lordick F. | en_US |
dc.contributor.author | Wang R. | en_US |
dc.contributor.author | Suryawanshi S. | en_US |
dc.contributor.author | Bhagia P. | en_US |
dc.contributor.author | Peter Kang S. | en_US |
dc.contributor.author | Metges J.-P. | en_US |
dc.contributor.author | KEYNOTE-181 Investigators | en_US |
dc.creator | Kojima T.;Shah M.A.;Muro K.;Francois E.;Adenis A.;Chih-Hung Hsu;Doi T.;Moriwaki T.;Kim S.-B.;Lee S.-H.;Bennouna J.;Kato K.;Shen L.;Enzinger P.;Qin S.-K.;Ferreira P.;Chen J.;Girotto G.;De La Fouchardiere C.;Senellart H.;Al-Rajabi R.;Lordick F.;Wang R.;Suryawanshi S.;Bhagia P.;Peter Kang S.;Metges J.-P.;Keynote-181 Investigators | - |
dc.date.accessioned | 2021-02-19T06:52:26Z | - |
dc.date.available | 2021-02-19T06:52:26Z | - |
dc.date.issued | 2020 | - |
dc.identifier.issn | 0732-183X | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85096380116&doi=10.1200%2fJCO.20.01888&partnerID=40&md5=7746328aaa56c5b138c35f8995d3c9a2 | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/548994 | - |
dc.description.abstract | PURPOSE Patients with advanced esophageal cancer have a poor prognosis and limited treatment options after first-line chemotherapy. PATIENTS AND METHODS In this open-label, phase III study, we randomly assigned (1:1) 628 patients with advanced/metastatic squamous cell carcinoma or adenocarcinoma of the esophagus, that progressed after one prior therapy, to pembrolizumab 200 mg every 3 weeks for up to 2 years or chemotherapy (investigator's choice of paclitaxel, docetaxel, or irinotecan). Primary end points were overall survival (OS) in patients with programmed death ligand-1 (PD-L1) combined positive score (CPS) $ 10, in patients with squamous cell carcinoma, and in all patients (one-sided a 0.9%, 0.8%, and 0.8%, respectively). RESULTS At final analysis, conducted 16 months after the last patient was randomly assigned, OS was prolonged with pembrolizumab versus chemotherapy for patients with CPS $ 10 (median, 9.3 v 6.7 months; hazard ratio [HR], 0.69 [95% CI, 0.52 to 0.93]; P 5.0074). Estimated 12-month OS rate was 43% (95% CI, 33.5% to 52.1%) with pembrolizumab versus 20% (95% CI, 13.5% to 28.3%) with chemotherapy. Median OS was 8.2 months versus 7.1 months (HR, 0.78 [95% CI, 0.63 to 0.96]; P 5.0095) in patients with squamous cell carcinoma and 7.1 months versus 7.1 months (HR, 0.89 [95% CI, 0.75 to 1.05]; P 5.0560) in all patients. Grade 3-5 treatment-related adverse events occurred in 18.2% of patients with pembrolizumab versus 40.9% in those who underwent chemotherapy. CONCLUSION Pembrolizumab prolonged OS versus chemotherapy as second-line therapy for advanced esophageal cancer in patients with PD-L1 CPS $ 10, with fewer treatment-related adverse events. ? 2020 by American Society of Clinical Oncology | - |
dc.publisher | American Society of Clinical Oncology | - |
dc.relation.ispartof | Journal of Clinical Oncology | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | docetaxel; irinotecan; paclitaxel; pembrolizumab; programmed death 1 ligand 1; antineoplastic agent; CD274 protein, human; docetaxel; immunological antineoplastic agent; irinotecan; monoclonal antibody; paclitaxel; pembrolizumab; programmed death 1 ligand 1; adult; advanced cancer; adverse drug reaction; aged; alopecia; anemia; aspiration pneumonia; asthenia; cancer chemotherapy; cancer prognosis; comparative study; Conference Paper; controlled study; decreased appetite; demography; diarrhea; esophageal adenocarcinoma; esophageal squamous cell carcinoma; esophagus cancer; esophagus metastasis; fatigue; female; follow up; hemorrhagic shock; human; hypothyroidism; major clinical study; male; myocarditis; nausea; neutropenia; open study; overall survival; peripheral neuropathy; phase 3 clinical trial; pneumonia; priority journal; progression free survival; protein expression; randomized controlled trial; response evaluation criteria in solid tumors; sensory neuropathy; sepsis; squamous cell carcinoma; treatment response; vomiting; clinical trial; esophagus tumor; immunology; middle aged; multicenter study; pathology; survival rate; very elderly; young adult; Adult; Aged; Aged, 80 and over; Antibodies, Monoclonal, Humanized; Antineoplastic Agents, Immunological; Antineoplastic Combined Chemotherapy Protocols; B7-H1 Antigen; Docetaxel; Esophageal Neoplasms; Esophageal Squamous Cell Carcinoma; Female; Humans; Irinotecan; Male; Middle Aged; Paclitaxel; Progression-Free Survival; Survival Rate; Young Adult | - |
dc.title | Randomized phase III KEYNOTE-181 study of pembrolizumab versus chemotherapy in advanced esophageal cancer | en_US |
dc.type | conference paper | en |
dc.identifier.doi | 10.1200/JCO.20.01888 | - |
dc.identifier.pmid | 33026938 | - |
dc.identifier.scopus | 2-s2.0-85096380116 | - |
dc.relation.pages | 4138-4148 | - |
dc.relation.journalvolume | 38 | - |
dc.relation.journalissue | 35 | - |
item.fulltext | no fulltext | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_5794 | - |
item.grantfulltext | none | - |
item.openairetype | conference paper | - |
crisitem.author.dept | Oncology | - |
crisitem.author.dept | Medical Oncology-NTUCC | - |
crisitem.author.dept | Oncology-NTUH | - |
crisitem.author.dept | Cancer Administration and Coordination Center | - |
crisitem.author.orcid | 0000-0003-0495-973X | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Cancer Center (NTUCC) | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
顯示於: | 腫瘤醫學研究所 |
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