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作 者:Dmitri Shek Bo Gao Hema Mahajan Adnan Nagrial Matteo S.Carlino Fabio Luciani Scott A.Read Golo Ahlenstiel
机构地区:[1]Blacktown Clinical School,Western Sydney University,Sydney,NSW 2148,Australia [2]Westmead Institute for Medical Research,Sydney,Nsw 2145,Australia [3]Blacktown Mt Druitt Hospital,Sydney,NSW 2148,Australia [4]Westmead Hospital,Sydney,Nsw 2145,Australia [5]Westmead Clinical School,University of Sydney,Sydney,NSW 2145,Australia [6]Institute of Clinical Pathology and Medical Research,Sydney,NSW 2145,Australia [7]Melanoma Institute Australia,Sydney,NSW 2065,Australia [8]School of Medical Sciences,University of New South Wales,Sydney,NSW 2052,Australia [9]Garvan Institute for Medical Research,Sydney,NSW 2010,Australia
出 处:《Genes & Diseases》2024年第6期28-31,共4页基因与疾病(英文)
基 金:The NCT04631731 is funded by (i)Western Sydney Local Health District Research and Education Grant 2021, (ii)Bristol Myers Squibb (CA209-6KR),and (iii)BGI ANZ Genetic Service Grant 2021.
摘 要:Malignant pleural mesothelioma(MPM)is a rare and aggressive cancer with low survival probability as it is generally diagnosed at later stages.'Using a combination of immune-checkpoint inhibitors(ICls)ipilimumab(IPl)and nivolumab(NivO)as a first-line treatment for unresectable MPM,the CheckMate 743 trial reported higher overall survival and prolonged duration of response compared with traditional chemotherapy.
关 键 词:PLEURAL CHEMOTHERAPY IMMUNE
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