
Tarlatamab Continues to Elicit Responses in Patients With SCLC
The bispecific T-cell engager tarlatamab showed continued efficacy and tolerable safety, according to follow-up from the phase 2 DeLLphi-301 study.
Extended follow-up from the phase 2 DeLLphi-301 study (NCT05060016) showed that tarlatamab-dlle (Imdelltra) led to sustained anticancer activity and manageable safety in patients with extended-stage small cell lung cancer previously treated with platinum-based chemotherapy. These data were presented at the 2024 World Conference on Lung Cancer.1,2
At a median follow-up of 13.6 months (range, 0.1-20.9) for efficacy evaluation, the overall response rate (ORR) was 40.4% and the median duration of response was not estimable in patients receiving the 10 mg dose. Responses were ongoing in 47.5% (n = 19) of responders. The median progression-free survival was 4.3 months, and the median overall survival (OS) was 15.2 months. The 6- and 12-month estimated OS rates were 73.4% and 56.7%, respectively.
The study evaluated both 10-mg and 100-mg dose levels, with the 10-mg dose selected as the appropriate choice for subsequent trials.
No new safety signals were identified, and the most common adverse event (AE) was cytokine release syndrome (CRS; 56.8%). Most events were grade 1 or 2, with no grade 4 or 5 events. Only 2.7% of patients discontinued treatment due to treatment-related AEs.
In May 2024, the
Here, the ORR for patients treated with the 10 mg dose of tarlatamab was 40% (97.5% CI, 29%-52%). Fifty-eight percent of patients in the 10-mg group responded to tarlatamab for at least 6 months.4,5 CRS occurred in 49% of patients in the 10 mg group, primarily during the first cycle and mostly grade 1 or 2.





































