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tarlatamab–durvalumab therapy shows 21.1-month OS

, 5 items in Neuroscience and AI, 3 min read

In this digest (5 items)

tarlatamab–durvalumab maintenance therapy achieved a median overall survival of 21.1 months in a prespecified interim analysis of a phase 3 trial. Durvalumab alone resulted in a median overall survival of 12.7 months. The data are from the DeLLphi-305 trial presented at ESMO 26.

Key points

  • Median overall survival: 21.1 months with tarlatamab–durvalumab maintenance.

  • Median overall survival: 12.7 months with durvalumab alone.

Sources

Ultra Mobility Vehicle robot adds jumps, wheelies

Ultra Mobility Vehicle bicycle robot adds jumps, wheelies and other athletic moves using its own inertia and momentum. It can also perform track stands and other athletic moves.

Key points

  • Feature: leverages its own inertia and momentum to perform jumps

  • Capability: can do track stands, wheelies and other athletic moves

Sources

Hafnium oxide interface stabilization – Erratum replaces July 2026 Expression of Concern

Hafnium oxide interface stabilization for efficient, photothermally stable perovskite solar cells receives an Erratum. The Erratum replaces the July 2026 Editorial Expression of Concern for the February 2026 research article.

Key points

  • Erratum published by Science

  • Replaces July 2026 Editorial Expression of Concern for the February 2026 article

Sources

Osimertinib–Savolitinib phase 3 SAFFRON trial in advanced NSCLC

Osimertinib–Savolitinib in Advanced NSCLC after Progression during EGFR-TKI Therapy is a phase 3 SAFFRON trial. The trial evaluates the drug combination for patients whose disease progressed on EGFR-TKI therapy.

Key points

  • Phase 3 SAFFRON trial

  • Osimertinib–Savolitinib combination for advanced NSCLC after EGFR-TKI progression

Sources

Stem cell transplant immune suppression analysis shows opposing effects

Stem cell transplant recipients analysis shows immune suppression with cyclophosphamide or tacrolimus shapes T cell reconstitution. The two drugs have opposite impacts on graft-versus-host disease risk and infection risk.

Key points

  • Cyclophosphamide shapes T cell reconstitution and affects GVHD risk.

  • Tacrolimus shapes T cell reconstitution and affects infection risk.

Sources