医学
胰腺癌
内科学
肿瘤科
癌症
胰腺疾病
放射治疗
疾病
梅德林
癌症研究
胰腺导管腺癌
作者
Brian Matthew Wolpin,Wungki Park,Ignacio Garrido‐Laguna,Alexander I. Spira,Alexander Starodub,David Sommerhalder,Salman Rafi Punekar,Minal Barve,Meredith S. Pelster,Benjamin Herzberg,Nilofer Saba Azad,Joel Randolph Hecht,Sai‐Hong Ignatius Ou,Tong Lin,Sumit Kar,Lin Tao,Rashmi Vora,Aparna Hegde,Kyaw Aung,David S. Hong
标识
DOI:10.1056/nejmoa2505783
摘要
BACKGROUND: mutations occur in more than 90% of PDAC tumors. Daraxonrasib (RMC-6236) is an oral RAS(ON) multiselective inhibitor that targets guanosine triphosphate-bound mutant and wild-type RAS. METHODS: -mutated PDAC. RESULTS: G12, G13, or Q61 mutations, 29% (95% CI, 15 to 46) had an objective response. The median duration of response was 8.2 months (95% CI, 3.8 to 8.8), with median values of 8.1 months for progression-free survival and 15.6 months for overall survival. CONCLUSIONS: -mutated PDAC; antitumor activity was also reported. (Funded by Revolution Medicines; RMC-6236-001 ClinicalTrials.gov number, NCT05379985.).
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