
DELLPHI-304
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An interview with Professor Chen Xiao focuses on the mechanism, efficacy, and safety of tarlatamab in second-line small cell lung cancer. Its DLL3/CD3 bispecific T-cell engager (TCE) mechanism bypasses MHC-I restriction. In DeLLphi-304, median OS rose from 8.3 months with chemotherapy to 13.6 months, ORR from 20% to 35%, and the risk of death fell by 40%; the Chinese bridging study DeLLphi-307 showed an ORR of 39%.
Excerpted from mp.weixin.qq.com
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- mp.weixin.qq.comProfessor Chen Xiao Interprets Tarlatamab Second-Line Small Cell Lung Cancer Data and Safety Management
An interview with Professor Chen Xiao focuses on the mechanism, efficacy, and safety of tarlatamab in second-line small cell lung cancer. Its DLL3/CD3 bispecific T-cell engager (TCE) mechanism bypasses MHC-I restriction. In DeLLphi-304, median OS rose from 8.3 months with chemotherapy to 13.6 months, ORR from 20% to 35%, and the risk of death fell by 40%; the Chinese bridging study DeLLphi-307 showed an ORR of 39%.
- mp.weixin.qq.comProfessor Yin Xiaojian discusses tarlatamab in small cell lung cancer: clinical use, access and future development
Professor Yin Xiaojian discusses tarlatamab's clinical use after its approval in China, covering second-line efficacy in SCLC, safety management, payment access and earlier-line exploration. DeLLphi-304 showed tarlatamab extended median OS in second-line patients from 8.3 months with chemotherapy to 13.6 months, reducing death risk by 40% (HR=0.60). The drug received third-line and second-line approvals in April and May 2026, and Fujian's Huiminbao 2026 included it in its high-cost drug reimbursement list.
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