J 2021

Successful early treatment combining remdesivir with high-titer convalescent plasma among COVID-19-infected hematological patients

WEINBERGEROVÁ, Barbora, Jiří MAYER, Tomáš KABUT, Štěpán HRABOVSKÝ, Jiřina PROCHÁZKOVÁ et. al.

Basic information

Original name

Successful early treatment combining remdesivir with high-titer convalescent plasma among COVID-19-infected hematological patients

Authors

WEINBERGEROVÁ, Barbora (203 Czech Republic, guarantor, belonging to the institution), Jiří MAYER (203 Czech Republic, belonging to the institution), Tomáš KABUT (203 Czech Republic, belonging to the institution), Štěpán HRABOVSKÝ (203 Czech Republic, belonging to the institution), Jiřina PROCHÁZKOVÁ (203 Czech Republic), Zdeněk KRÁL (203 Czech Republic, belonging to the institution), Vladimír HEROUT (203 Czech Republic, belonging to the institution), Rita PACASOVÁ (203 Czech Republic, belonging to the institution), Lenka ZDRAŽILOVÁ DUBSKÁ (203 Czech Republic), Petr HUSA (203 Czech Republic, belonging to the institution), Petr BEDNAR (203 Czech Republic), Daniel RUZEK (203 Czech Republic) and Martina LENGEROVÁ (203 Czech Republic, belonging to the institution)

Edition

Hematological Oncology, MALDEN, USA, WILEY-BLACKWELL, 2021, 0278-0232

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30205 Hematology

Country of publisher

United States of America

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 4.850

RIV identification code

RIV/00216224:14110/21:00123269

Organization unit

Faculty of Medicine

UT WoS

000685941400001

Keywords in English

COVID-19; remdesivir; hematological patients

Tags

International impact, Reviewed
Změněno: 15/12/2021 09:14, Mgr. Tereza Miškechová

Abstract

V originále

Immunocompromised patients with hematological malignancies are at high risk for a severe course of COVID-19 (Coronavirus Disease 2019) with a deadly outcome.1, 2 With remdesivir use, several randomized trials have recorded abbreviated recovery periods, lower mortality, and positive consequences of early treatment initiation.3, 4 Based on randomized trial results, the FDA has approved remdesivir for the treatment of COVID-19. Regarding convalescent plasma (CP), evidence from recently published large trials implies that early administration of high-titer CP is most efficacious.5 However, no published studies assessing the effect of remdesivir or CP in COVID-19 have included a substantial proportion of hematooncology patients, and available data are limited to case reports.6, 7 In view of this dearth of data, we decided to analyze the efficacy of early combination therapy of remdesivir and high-titer CP among hematological patients. This treatment strategy was implemented after observing several grim COVID-19 outcomes among these patients.