Convalescent plasma treatment of B-cell depleted patients with COVID-19: systematic review and individual participant data meta-analysis
Zaremba, S.; Focosi, D.; Pruter, W. W.; Franchini, M.; Collantes Hoyos, D. B.; Cruciani, M.; Miller, A. J.; Ripoll, J. G.; Casadevall, A.; Tulledge-Scheitel, S. M.; Rufer, N.; Hueso, T.; Juskewitch, J. E.; van Buskirk, C. M.; Ioannou, P.; Lanza, F.; Razonable, R. R.; Magyari, F.; Pinczes, L. I.; Ganesh, R.; Denkinger, C. M.; Hurt, R. T.; Janssen, M.; Stubbs, J. R.; Muller-Tidow, C.; Winters, J. L.; Holm, K.; Parikh, S. A.; Simeunovic, G.; Kay, N. E.; Rijnders, B.; Wright, S. R.; Issa, N.; Chaussade, H.; Carter, R. E.; Schroeder, D. R.; Senefeld, J. W.; Joyner, M. J.
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BackgroundCOVID-19 convalescent plasma (CCP) is obtained from people recently recovered from COVID-19 and contains viral-neutralizing antibodies. Because such treatment is safe and effective against SARS-CoV-2, the US Food and Drug Administration (FDA) has recently authorized the use of CCP for COVID-19 patients with immunodeficiencies. Currently available CCP is a "hybrid" product with antibodies from individuals who had both infection and vaccination (vaccine-boosted CCP). In this context, there is growing interest in CCP treatment outcomes in specific groups of immunocompromised patients. Specifically, B-cell depleted patients are at risk of not producing antibodies after either infection or vaccination. Hence, B-cell depleted patients are conceivably among those who would benefit the most from CCP. We thus conducted a systematic review and individual patient data meta-analysis to assess characteristics associated with 60-day survival in B-cell depleted patients transfused with CCP. MethodsThe last search was April 2nd, 2024, and included all studies using CCP in B-cell depleted patients. Whenever not available in the publication, we requested individual participant data from corresponding authors of eligible studies. Risk of bias was assessed using Joanna Briggs Institute Critical Appraisal Tools. Data were analyzed using conditional logistic regression. ResultsWe describe individual patient data extracted from 85 studies and synthesized into a cohort of 570 patients. The overall 60-day survival rate was 86.5%. Of patients with information available, 70.1% achieved SARS-CoV-2 clearance, and 64.3% had clinical improvement within 5 days of CCP transfusion. After controlling for age, sex, calendar year of infection and World Health Organization (WHO) disease severity, we found a significant association between 60-day survival and days since last anti-CD20 dose (OR=1.16 per 10-day increase; 95% CI 1.04 to 1.29; p=0.007) and transfusion of vaccine-boosted CCP (OR=9.49; 95% CI 2.01 to 44.82; p=0.005), but not with concomitant remdesivir treatment (OR=1.31; 95% CI 0.66 to 2.61; p=0.440). DiscussionOur study is limited to individual participant data analysis, with a majority of the studies included being case series and case reports. Overall survival in our cohort of B-cell depleted patients was consistent with prior meta-analysis of randomized controlled trials on survival of immunocompromised patient transfused with CCP ([~]84%). A novel finding from this analysis is that vaccine-boosted CCP with a presumably higher content of neutralizing antibodies is associated with a high survival benefit. RegistrationThe protocol for this systematic review and individual participant data meta-analysis was registered with PROSPERO (CRD42024516513) on March 1st, 2024.
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