Efficacy and Safety of COVID-19 Convalescent Plasma in Hospitalized Patients
Mila B. Ortigoza, Hyunah Yoon, Keith Goldfeld, Andrea B. Troxel, Johanna P. Daily, Yinxiang Wu, Yi Li, Danni Wu, Gia Cobb, Gillian Baptiste, Mary O’Keeffe, Marilou Corpuz, Luis Ostrosky‐Zeichner, Amee Amin, Ioannis M. Zacharioudakis, Dushyantha Jayaweera, Yanyun Wu, Julie V. Philley, Megan Devine, Mahalia S. Desruisseaux, Alessandro D. Santin, Shweta Anjan, Reeba Mathew, Bela Patel, Masayuki Nigo, Rabi Upadhyay, Tania Kupferman, Andrew Dentino, Rahul Nanchal, Christian A. Merlo, David N. Hager, Kartik Chandran, Jonathan R. Lai, Johanna Rivera, Chowdhury R. Bikash, Gorka Lasso, Timothy P. Hilbert, Monika Paroder, Andrea A. Asencio, Mengling Liu, Eva Petkova, Alexander Bragat, Reza Shaker, David D. McPherson, Ralph L. Sacco, Marla J. Keller, Corita R. Grudzen, Judith S. Hochman, Liise-anne Pirofski, Fatema Z Rahman, Adeyinka Ajayi, Sara L. Rodriguez, Ana G Ledesma, Deborah Keeling, Norka Rappoport, Sam F Ebel, Jayne Kim, Michelle Chang, Kevin M. Chan, Payal Patel, Anne Martocci, Shivang R. Dave, Yousef Darwish, Monica R Taveras, Victoria Shoyelu, Patrick Xin, Eduardo Iturrate, Lee C Moldolsky, Brian J Raimondo, Sarah Mendez, Patricia Hughes, Stephanie Sterling, Aaron Lord, Shadi Yaghi, Karen Veloso, Masooma Sheikh, Erica Visconti-Ferrara, Andrew J. Fleming, Heekoung Youn, Baby Jane Fran, Rosario Medina, Renee McKell, Saila Khan, Tanya Hamilton, Carlos J. Sánchez, Nandini H Patel, Levi G. Cleare, Olivia Vergnolle, Antonio Nakouzi, Gregory Quevedo, Robert H. Bortz, Ariel S. Wirchnianski, Catalina Florez, Rachelle Babb, Jennifer Ayala, K. Zoe Tsagaris, Andria James, Isaiah Eke, Aisha Obeidallah, Oana Sandu
Abstract
Importance: There is clinical equipoise for COVID-19 convalescent plasma (CCP) use in patients hospitalized with COVID-19. Objective: To determine the safety and efficacy of CCP compared with placebo in hospitalized patients with COVID-19 receiving noninvasive supplemental oxygen. Design, Setting, and Participants: CONTAIN COVID-19, a randomized, double-blind, placebo-controlled trial of CCP in hospitalized adults with COVID-19, was conducted at 21 US hospitals from April 17, 2020, to March 15, 2021. The trial enrolled 941 participants who were hospitalized for 3 or less days or presented 7 or less days after symptom onset and required noninvasive oxygen supplementation. Interventions: A unit of approximately 250 mL of CCP or equivalent volume of placebo (normal saline). Main Outcomes and Measures: The primary outcome was participant scores on the 11-point World Health Organization (WHO) Ordinal Scale for Clinical Improvement on day 14 after randomization; the secondary outcome was WHO scores determined on day 28. Subgroups were analyzed with respect to age, baseline WHO score, concomitant medications, symptom duration, CCP SARS-CoV-2 titer, baseline SARS-CoV-2 serostatus, and enrollment quarter. Outcomes were analyzed using a bayesian proportional cumulative odds model. Efficacy of CCP was defined as a cumulative adjusted odds ratio (cOR) less than 1 and a clinically meaningful effect as cOR less than 0.8. Results: Of 941 participants randomized (473 to placebo and 468 to CCP), 556 were men (59.1%); median age was 63 years (IQR, 52-73); 373 (39.6%) were Hispanic and 132 (14.0%) were non-Hispanic Black. The cOR for the primary outcome adjusted for site, baseline risk, WHO score, age, sex, and symptom duration was 0.94 (95% credible interval [CrI], 0.75-1.18) with posterior probability (P[cOR<1] = 72%); the cOR for the secondary adjusted outcome was 0.92 (95% CrI, 0.74-1.16; P[cOR<1] = 76%). Exploratory subgroup analyses suggested heterogeneity of treatment effect: at day 28, cORs were 0.72 (95% CrI, 0.46-1.13; P[cOR<1] = 93%) for participants enrolled in April-June 2020 and 0.65 (95% CrI, 0.41 to 1.02; P[cOR<1] = 97%) for those not receiving remdesivir and not receiving corticosteroids at randomization. Median CCP SARS-CoV-2 neutralizing titer used in April to June 2020 was 1:175 (IQR, 76-379). Any adverse events (excluding transfusion reactions) were reported for 39 (8.2%) placebo recipients and 44 (9.4%) CCP recipients (P = .57). Transfusion reactions occurred in 2 (0.4) placebo recipients and 8 (1.7) CCP recipients (P = .06). Conclusions and Relevance: In this trial, CCP did not meet the prespecified primary and secondary outcomes for CCP efficacy. However, high-titer CCP may have benefited participants early in the pandemic when remdesivir and corticosteroids were not in use. Trial Registration: ClinicalTrials.gov Identifier: NCT04364737.