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Clinical Meaningfulness in Alzheimer’s Disease Clinical Trials. A Report from the EU-US CTAD Task Force

  • D. Angioni,
  • J. Cummings,
  • C. J. Lansdall,
  • L. Middleton,
  • C. Sampaio,
  • S. Gauthier,
  • S. Cohen,
  • R. C. Petersen,
  • D. M. Rentz,
  • A. M. Wessels,
  • S. B. Hendrix,
  • F. Jessen,
  • M. C. Carrillo,
  • R. S. Doody,
  • M. Irizarry,
  • J. S. Andrews,
  • B. Vellas,
  • P. Aisen,
  • Sandrine Andrieu,
  • Randall Bateman,
  • Richard Batrla,
  • Joanne Bell,
  • Oskar Bosson,
  • Sasha Bozeat,
  • Dawn Brooks,
  • Samantha Budd Haeberlein,
  • Teresa Buracchio,
  • Min Cho,
  • Matthew Choung,
  • Gavin Cook,
  • Darrin Crisitello,
  • Fernando Dangond,
  • Susan de Santi,
  • Ellen Dennehy,
  • Shobha Dhadda,
  • Harjeet Dhillon,
  • Billy Dunn,
  • Michael Egan,
  • Fiona Elwood,
  • Sven Eriksson,
  • Tom Fagan,
  • Howard Fillit,
  • Per-Ola Freskgard,
  • Diana Gallagher,
  • Gopi Gangi,
  • Carlos Granda,
  • David Greeley,
  • Anna-Kaija Gronblad,
  • Harald Hampel,
  • Paul Hawthorne,
  • David Henley,
  • Joe Herring,
  • Steve Hersch,
  • Bill Holt,
  • Takeshi Iwatsubo,
  • Daryl Jones,
  • Anja Kahl,
  • Gene Kinney,
  • Hartmuth Kolb,
  • Lynn Kramer,
  • Luka Kulic,
  • Sanjay Kumar,
  • Lars Lannfelt,
  • John Lawson,
  • Valérie Legrand,
  • Rachel Lenington,
  • Frank Longo,
  • Brandy Matthews,
  • Donna Masterman,
  • Kristina McLinden,
  • Sarah Mikels,
  • Michael Miller,
  • Mark Mintun,
  • Hans Moebius,
  • Cecilia Monteiro,
  • Mario Morken,
  • Jennifer Murphy,
  • Tomas Odergren,
  • Gunilla Osswald,
  • Laura Parnas,
  • Maria-Magdalena Patru,
  • Charlene Prazma,
  • Rema Raman,
  • Larisa Reyderman,
  • Sharon Rogers,
  • Lise Roman,
  • Gary Romano,
  • Mark Roskey,
  • Ivana Rubino,
  • Laurie Ryan,
  • Stephen Salloway,
  • Rachel Schindler,
  • Lon Schneider,
  • David Scott,
  • John Sims,
  • Daniel Skovronsky,
  • Marion Soto,
  • Reisa Sperling,
  • Lennert Steukers,
  • Erik Stoops,
  • Stephen Strittmatter,
  • Amir Tahami,
  • Gilles Tamagnan,
  • Gilles Tariot,
  • Masoud Toloue,
  • Jacques Touchon,
  • Eugeen Vanmechelen,
  • Len Walt,
  • Mark Weinberg,
  • Michael Weiner,
  • Anne White,
  • Iris Wiesel,
  • David Wilson,
  • Lisa Yarenis,
  • Wagner Zago,
  • Jin Zhou

摘要

Recent positive results of three phase III anti-amyloid monoclonal antibody trials are transforming the landscape of disease-modifying therapeutics for Alzheimer’s disease, following several decades of failures. Indeed, all three trials have met their primary endpoints. However, the absolute size of the benefit measured in these trials has generated a debate on whether the change scores observed on clinical outcome assessments represent a clinically meaningful benefit to patients. An evidence-based conclusion is urgently required to inform decision-making related to the approval, reimbursement, and ultimately, the management of emerging therapies in clinical practice. The EU-US CTAD Task Force met in Boston to address this important question. The current state-of-the-art knowledge for interpreting clinical meaningfulness of AD clinical trial results, including the point of view of patients and study partners on what is clinically meaningful, was discussed and is summarized here. A combination of methodologies to address the challenges emerged. There remain gaps in the understanding of clinical meaningfulness that only long-term longitudinal studies will be able to address.