Tarlatamab in Small-Cell Lung Cancer after Platinum-Based Chemotherapy

铂金 化疗 医学 癌症 肺癌 肿瘤科 内科学 生物 生物化学 催化作用
作者
Giannis Mountzios,Longhua Sun,Byoung Chul Cho,Umut Demırcı,Sofia Baka,Mahmut Gümüş,Antonio Lugini,Bo Zhu,Yan Yu,Ippokratis Korantzis,Ji‐Youn Han,Tudor‐Eliade Ciuleanu,Myung‐Ju Ahn,Pedro Rocha,Julien Mazières,Sally C. M. Lau,Martin Schüler,Fiona Blackhall,Tatsuya Yoshida,Taofeek K. Owonikoko
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
被引量:26
标识
DOI:10.1056/nejmoa2502099
摘要

Tarlatamab, a bispecific delta-like ligand 3-directed T-cell engager immunotherapy, received accelerated approval for the treatment of patients with previously treated small-cell lung cancer. Whether tarlatamab is more effective than chemotherapy in the treatment of patients whose small-cell lung cancer has progressed during or after initial platinum-based chemotherapy is not known. We conducted a multinational, phase 3, open-label trial to compare tarlatamab with chemotherapy as second-line treatment in patients with small-cell lung cancer whose disease had progressed during or after platinum-based chemotherapy. Patients were randomly assigned to receive tarlatamab or chemotherapy (topotecan, lurbinectedin, or amrubicin). The primary end point was overall survival. Key secondary end points were investigator-assessed progression-free survival and patient-reported outcomes. Results of the prespecified interim analysis (data-cutoff date, January 29, 2025) are reported. A total of 509 patients were randomly assigned to receive tarlatamab (254 patients) or chemotherapy (255 patients). Treatment with tarlatamab resulted in significantly longer overall survival than chemotherapy (median, 13.6 months [95% confidence interval {CI}, 11.1 to not reached] vs. 8.3 months [95% CI, 7.0 to 10.2]; stratified hazard ratio for death, 0.60; 95% CI, 0.47 to 0.77; P<0.001). Tarlatamab treatment also had a significant benefit with respect to progression-free survival and cancer-related dyspnea and cough as compared with chemotherapy. The incidence of adverse events of grade 3 or higher was lower with tarlatamab than with chemotherapy (54% vs. 80%), as was the incidence of adverse events resulting in treatment discontinuation (5% vs. 12%). Treatment with tarlatamab led to longer overall survival than chemotherapy among patients with small-cell lung cancer whose disease had progressed during or after platinum-based chemotherapy. (Funded by Amgen; DeLLphi-304 ClinicalTrials.gov number, NCT05740566.).
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