Oncology ·
Tarlatamab added to first-line maintenance in ES-SCLC improves overall survival
A Nature Reviews Clinical Oncology article reports results from the phase III DeLLphi-305 trial, in which 563 patients with extensive-stage small-cell lung cancer were randomized after induction therapy. The article describes an overall-survival benefit with tarlatamab added to maintenance durvalumab but provides no numerical results in the available text.
- Phase III trial randomized 563 patients after induction therapy.
- Compared maintenance durvalumab with versus without tarlatamab.
- Review reports overall-survival benefit but gives no numerical estimates.
Patients with extensive-stage small-cell lung cancer (ES-SCLC) often have limited opportunity to receive second-line treatment if their disease progresses rapidly. In the phase III DeLLphi-305 trial, 563 patients whose cancer had not progressed after platinum–etoposide chemotherapy plus durvalumab were randomized 1:1 to maintenance durvalumab with or without tarlatamab. Overall survival, measured from randomization at the start of maintenance, was the primary endpoint.
The Nature Reviews Clinical Oncology article says the addition of tarlatamab, a DLL3 × CD3 bispecific T-cell engager, produced a substantial overall-survival benefit. It notes that trial findings were presented at the ESMO Congress 2026 and published simultaneously in The New England Journal of Medicine. The available text does not report survival estimates, hazard ratios, confidence intervals, or adverse-event data, so the magnitude and safety profile cannot be assessed from this report. These results concern maintenance after the specified induction regimen; the source does not provide enough detail to determine how they should affect treatment decisions.
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Nature Reviews Clinical Oncology: Unprecedented OS with the addition of tarlatamab to first-line maintenance therapy for ES-SCLC ↗This is an automated AI-condensed summary that has not yet been reviewed by an editor. Always consult the full item at the original source.
