tetano
Editor, Senior Moderator
Clin Infect Dis
. 2021 Sep 1;ciab732.
doi: 10.1093/cid/ciab732. Online ahead of print.
Fostamatinib for the treatment of hospitalized adults with COVD-19 A randomized trial
Jeffrey R Strich[SUP] 1 2 [/SUP], Xin Tian[SUP] 3 [/SUP], Mohamed Samour[SUP] 3 [/SUP], Christopher S King[SUP] 4 [/SUP], Oksana Shlobin[SUP] 4 [/SUP], Robert Reger[SUP] 3 [/SUP], Jonathan Cohen[SUP] 5 [/SUP], Kareem Ahmad[SUP] 4 [/SUP], A Whitney Brown[SUP] 4 [/SUP], Vikramjit Khangoora[SUP] 4 [/SUP], Shambhu Aryal[SUP] 4 [/SUP], Yazan Migdady[SUP] 3 [/SUP], Jennifer Jo Kyte[SUP] 3 [/SUP], Jungnam Joo[SUP] 3 [/SUP], Rebecca Hays[SUP] 4 [/SUP], A Claire Collins[SUP] 4 [/SUP], Edwinia Battle[SUP] 4 [/SUP], Janet Valdez[SUP] 2 3 [/SUP], Josef Rivero[SUP] 2 3 [/SUP], Ick-Ko Kim[SUP] 2 3 [/SUP], Julie Erb-Alvarez[SUP] 2 3 [/SUP], Ruba Shalhoub[SUP] 3 [/SUP], Mala Chakraborty[SUP] 3 [/SUP], Susan Wong[SUP] 3 [/SUP], Benjamin Colton[SUP] 6 [/SUP], Marcos J Ramos-Benitez[SUP] 1 7 [/SUP], Seth Warner[SUP] 1 [/SUP], Daniel S Chertow[SUP] 1 2 8 [/SUP], Kenneth N Olivier[SUP] 3 [/SUP], Georg Aue[SUP] 3 [/SUP], Richard T Davey[SUP] 8 [/SUP], Anthony F Suffredini[SUP] 1 [/SUP], Richard W Childs[SUP] 2 3 [/SUP], Steven D Nathan[SUP] 4 [/SUP]
Affiliations
Abstract
Background: Coronavirus Disease 2019 (Covid-19) requiring hospitalization is characterized by robust antibody production, dysregulated immune response and immunothrombosis. Fostamatinib, is a novel spleen tyrosine kinase inhibitor we hypothesize will ameliorate Fc activation and attenuate harmful effects of the anti-COVID-19 immune response.
Methods: We conducted a double-blind, randomized, placebo-controlled trial in hospitalized adults requiring oxygen with Covid-19 where patients receiving standard of care were randomized to receive fostamatinib or placebo. The primary outcome was serious adverse events by day 29.
Results: A total of 59 patients underwent randomization (30 to fostamatinib and 29 to placebo). Serious adverse events occurred in 10.5% of patients in the fostamatinib group compared to 22% in placebo (P = .2). Three deaths occurred by day 29, all receiving placebo. The mean change in ordinal score at day 15 was greater in the fostamatinib group (-3.6 ± 0.3 vs. -2.6 ± 0.4, P = .035) and the median length in the ICU was 3 days in the fostamatinib group vs. 7 days in placebo (P = .07). Differences in clinical improvement were most evident in patients with severe or critical disease (median days on oxygen, 10 vs. 28, P = .027). There were trends towards more rapid reductions in C-reactive protein, D-dimer, fibrinogen and ferritin levels in the fostamatinib group.
Conclusion: For COVID-19 requiring hospitalization, the addition of fostamatinib to standard of care was safe and patients were observed to have improved clinical outcomes compared to placebo. These results warrant further validation in larger confirmatory trials.
Keywords: COVID-19; Immunomodulator; Respiratory failure; SARS-CoV-2.
. 2021 Sep 1;ciab732.
doi: 10.1093/cid/ciab732. Online ahead of print.
Fostamatinib for the treatment of hospitalized adults with COVD-19 A randomized trial
Jeffrey R Strich[SUP] 1 2 [/SUP], Xin Tian[SUP] 3 [/SUP], Mohamed Samour[SUP] 3 [/SUP], Christopher S King[SUP] 4 [/SUP], Oksana Shlobin[SUP] 4 [/SUP], Robert Reger[SUP] 3 [/SUP], Jonathan Cohen[SUP] 5 [/SUP], Kareem Ahmad[SUP] 4 [/SUP], A Whitney Brown[SUP] 4 [/SUP], Vikramjit Khangoora[SUP] 4 [/SUP], Shambhu Aryal[SUP] 4 [/SUP], Yazan Migdady[SUP] 3 [/SUP], Jennifer Jo Kyte[SUP] 3 [/SUP], Jungnam Joo[SUP] 3 [/SUP], Rebecca Hays[SUP] 4 [/SUP], A Claire Collins[SUP] 4 [/SUP], Edwinia Battle[SUP] 4 [/SUP], Janet Valdez[SUP] 2 3 [/SUP], Josef Rivero[SUP] 2 3 [/SUP], Ick-Ko Kim[SUP] 2 3 [/SUP], Julie Erb-Alvarez[SUP] 2 3 [/SUP], Ruba Shalhoub[SUP] 3 [/SUP], Mala Chakraborty[SUP] 3 [/SUP], Susan Wong[SUP] 3 [/SUP], Benjamin Colton[SUP] 6 [/SUP], Marcos J Ramos-Benitez[SUP] 1 7 [/SUP], Seth Warner[SUP] 1 [/SUP], Daniel S Chertow[SUP] 1 2 8 [/SUP], Kenneth N Olivier[SUP] 3 [/SUP], Georg Aue[SUP] 3 [/SUP], Richard T Davey[SUP] 8 [/SUP], Anthony F Suffredini[SUP] 1 [/SUP], Richard W Childs[SUP] 2 3 [/SUP], Steven D Nathan[SUP] 4 [/SUP]
Affiliations
- PMID: 34467402
- DOI: 10.1093/cid/ciab732
Abstract
Background: Coronavirus Disease 2019 (Covid-19) requiring hospitalization is characterized by robust antibody production, dysregulated immune response and immunothrombosis. Fostamatinib, is a novel spleen tyrosine kinase inhibitor we hypothesize will ameliorate Fc activation and attenuate harmful effects of the anti-COVID-19 immune response.
Methods: We conducted a double-blind, randomized, placebo-controlled trial in hospitalized adults requiring oxygen with Covid-19 where patients receiving standard of care were randomized to receive fostamatinib or placebo. The primary outcome was serious adverse events by day 29.
Results: A total of 59 patients underwent randomization (30 to fostamatinib and 29 to placebo). Serious adverse events occurred in 10.5% of patients in the fostamatinib group compared to 22% in placebo (P = .2). Three deaths occurred by day 29, all receiving placebo. The mean change in ordinal score at day 15 was greater in the fostamatinib group (-3.6 ± 0.3 vs. -2.6 ± 0.4, P = .035) and the median length in the ICU was 3 days in the fostamatinib group vs. 7 days in placebo (P = .07). Differences in clinical improvement were most evident in patients with severe or critical disease (median days on oxygen, 10 vs. 28, P = .027). There were trends towards more rapid reductions in C-reactive protein, D-dimer, fibrinogen and ferritin levels in the fostamatinib group.
Conclusion: For COVID-19 requiring hospitalization, the addition of fostamatinib to standard of care was safe and patients were observed to have improved clinical outcomes compared to placebo. These results warrant further validation in larger confirmatory trials.
Keywords: COVID-19; Immunomodulator; Respiratory failure; SARS-CoV-2.