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One-year follow-up of the CAPSID randomized trial for high-dose convalescent plasma in severe COVID-19 patients

Authors :
Korper, Sixten
Gruner, Beate
Zickler, Daniel
Wiesmann, Thomas
Wuchter, Patrick
Blasczyk, Rainer
Zacharowski, Kai
Spieth, Peter
Tonn, Torsten
Rosenberger, Peter
Paul, Gregor
Pilch, Jan
Schwable, Joachim
Bakchoul, Tamam
Thiele, Thomas
Knorlein, Julian
Dollinger, Matthias M.
Krebs, Jorg
Bentz, Martin
Corman, Victor M.
Kilalic, Dzenan
Schmidtke-Schrezenmeier, Gerlinde
Lepper, Philipp M.
Ernst, Lucas
Wulf, Hinnerk
Ulrich, Alexandra
Weiss, Manfred
Kruse, Jan Matthias
Burkhardt, Thomas
Muller, Rebecca
Kluter, Harald
Schmidt, Michael
Jahrsdorfer, Bernd
Lotfi, Ramin
Rojewski, Markus
Appl, Thomas
Mayer, Benjamin
Schnecko, Philipp
Seifried, Erhard
Schrezenmeier, Hubert
Source :
Journal of Clinical Investigation. December 15, 2022, Vol. 132 Issue 24
Publication Year :
2022

Abstract

Introduction The use of COVID-19 convalescent plasma (CCP) from patients recovered from a SARS-CoV-2 infection was evaluated in many randomized trials during the pandemic (1-21). The trials were heterogeneous in [...]<br />BACKGROUND. Results of many randomized trials on COVID-19 convalescent plasma (CCP) have been reported, but information on long-term outcome after CCP treatment is limited. The objectives of this extended observation of the randomized CAPSID trial are to assess long-term outcome and disease burden in patients initially treated with or without CCP. METHODS. Of 105 randomized patients, 50 participated in the extended observation. Quality of life (QoL) was assessed by questionnaires and a structured interview. CCP donors (n = 113) with asymptomatic to moderate COVID-19 were included as a reference group. RESULTS. The median follow-up of patients was 396 days, and the estimated 1-year survival was 78.7% in the CCP group and 60.2% in the control (P = 0.08). The subgroup treated with a higher cumulative amount of neutralizing antibodies showed a better 1-year survival compared with the control group (91.5% versus 60.2%, P = 0.01). Medical events and QoL assessments showed a consistent trend for better results in the CCP group without reaching statistical significance. There was no difference in the increase in neutralizing antibodies after vaccination between the CCP and control groups. CONCLUSION. The trial demonstrated a trend toward better outcome in the CCP group without reaching statistical significance. A predefined subgroup analysis showed a significantly better outcome (long-term survival, time to discharge from ICU, and time to hospital discharge) among those who received a higher amount of neutralizing antibodies compared with the control group. A substantial long-term disease burden remains after severe COVID-19. TRIAL REGISTRATION. EudraCT 2020-001310-38 and ClinicalTrials.gov NCT04433910. FUNDING. Bundesministerium fur Gesundheit (German Federal Ministry of Health).

Details

Language :
English
ISSN :
00219738
Volume :
132
Issue :
24
Database :
Gale General OneFile
Journal :
Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
edsgcl.732737544
Full Text :
https://doi.org/10.1172/JCI163657