Clinical progress of B7-H3 targeted antibody drug conjugate ifinatamab deruxtecan for small-cell lung cancer

被引:0
作者
Wespiser, Mylene [1 ]
Gille, Romane [1 ]
Perol, Maurice [1 ]
机构
[1] Ctr Leon Berard, Dept Med Oncol, 28 Rue Laennec, F-69008 Lyon, France
关键词
Antibody drug conjugate; B7-H3; clinical trial; small cell lung cancer; tumor immunity; PHASE-III TRIAL; OPEN-LABEL; 2ND-LINE TREATMENT; SUBGROUP ANALYSIS; I-DXD; TOPOTECAN; CHEMOTHERAPY; RECURRENT; SCLC; LURBINECTEDIN;
D O I
10.1080/13543784.2025.2512566
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionSmall cell lung cancer is an aggressive malignancy with limited treatment options and poor prognosis, particularly at extensive stage. While first-line platinum-etoposide chemotherapy combined with anti-PD-L1 therapy improves survival, most patients relapse, highlighting the need for novel therapies.Areas coveredB7-Homolog3 (B7-H3), an immune checkpoint molecule overexpressed in SCLC, has emerged as a promising therapeutic target. Ifinatamab deruxtecan (I-DXd) is an antibody-drug conjugate targeting B7-H3, delivering a topoisomerase I inhibitor. Early clinical trials (IDeate-PanTumor01 and IDeate-Lung01) have demonstrated encouraging results in pretreated ES-SCLC. In the 12 mg/kg cohort of IDeate-Lung01, I-DXd achieved an objective response rate of 54.8%, median progression-free survival of 5.5 months, and median overall survival of 11.8 months. Notably, it showed intracranial activity with a central nervous system-confirmed response rate of 37.8%.Expert opinionI-DXd is currently being evaluated in the phase III IDeate-Lung02 trial. Its promising efficacy, manageable safety profile, and potential in combination strategies position it as a key candidate for future SCLC treatment.
引用
收藏
页码:463 / 471
页数:9
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