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Sustained improvements in patient-reported outcomes after long-term sutimlimab in patients with cold agglutinin disease: results from the CADENZA study open-label extension.
Röth, Alexander; Broome, Catherine M; Barcellini, Wilma; Jilma, Bernd; Hill, Quentin A; Cella, David; Anderson Tvedt, Tor Henrik; Yamaguchi, Masaki; Murakhovskaya, Irina; Lee, Michelle; Shafer, Frank; Wardecki, Marek; Jayawardene, Deepthi; Yoo, Ronnie; Msihid, Jerome; Weitz, Ilene C.
Afiliação
  • Röth A; Department of Hematology and Stem Cell Transplantation, West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Broome CM; Division of Hematology, MedStar Georgetown University Hospital, Washington, DC, USA.
  • Barcellini W; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Jilma B; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Hill QA; Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Cella D; Department of Medical Social Sciences, Center for Patient-Centered Outcomes, Institute for Public Health and Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Anderson Tvedt TH; Section for Hematology, Department of Medicine, Haukeland University Hospital, Bergen, Norway.
  • Yamaguchi M; Ishikawa Prefectural Central Hospital, Japan.
  • Murakhovskaya I; Department of Hematology and Oncology, Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, USA.
  • Lee M; Sanofi, Bridgewater, NJ, USA.
  • Shafer F; Sanofi, Bridgewater, NJ, USA.
  • Wardecki M; Sanofi, Warsaw, Poland.
  • Jayawardene D; Sanofi, Cambridge, MA, USA.
  • Yoo R; Sanofi, Cambridge, MA, USA.
  • Msihid J; Sanofi, Gentilly, France.
  • Weitz IC; Keck School of Medicine of USC, Los Angeles, CA, USA.
EClinicalMedicine ; 74: 102732, 2024 Aug.
Article em En | MEDLINE | ID: mdl-39114274
ABSTRACT

Background:

Cold agglutinin disease (CAD) is a rare subtype of autoimmune haemolytic anaemia characterised by classical complement pathway-mediated haemolysis, fatigue, and poor quality of life (QoL). Sutimlimab, a C1s inhibitor, rapidly halted haemolysis, and improved patient-reported outcomes (PROs) in patients with CAD in two phase 3 trials (CARDINAL and CADENZA). Here we report PROs from the CADENZA open-label extension (Part B).

Methods:

The first patient was enrolled in CADENZA (NCT03347422) in March 2018 (Part A) and the last patient completed the study in December 2021 (Part B). All patients who completed the 26-week Part A were eligible to receive biweekly doses of sutimlimab in Part B for up to 1 year after the last patient completed Part A. PROs were assessed throughout Part B, until the last on-treatment visit with available assessment (LV), and after a 9-week washout.

Findings:

In total, 32/39 patients completed Part B; median Part B treatment duration 99 weeks. Patients switching from placebo to sutimlimab in Part B experienced rapid improvement in Functional Assessment of Chronic Illness Therapy (FACIT)-Fatigue score and other PROs. Sustained, clinically important improvements in FACIT-Fatigue were observed throughout Part B in patients who switched to sutimlimab and those continuing sutimlimab treatment (combined-group mean [SE] change from baseline at LV 8.8 [2.1]). Similarly, the combined-group mean [SE] change for 12-Item Short Form Health Survey physical (4.9 [1.7]) and mental (4.0 [1.8]) component scores exceeded clinically important changes from baseline at LV. EuroQol visual analogue scale showed consistent and sustained increases from baseline with sutimlimab treatment. Following a 9-week washout, all PROs approached baseline values.

Interpretation:

Continued inhibition of the classical complement pathway with sutimlimab results in meaningful long-term improvements in PROs (fatigue and QoL) in patients with CAD.

Funding:

Sanofi.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article