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 M. Wolpin,Wungki Park,Ignacio Garrido-Laguna,A Spira,Alexander Starodub,David Sommerhalder,Salman R. Punekar,Minal Barve,Meredith Pelster,Benjamin Herzberg,Nilofer S. Azad,J. 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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