Use of tocilizumab in kidney transplant recipients with COVID-19

被引:66
|
作者
Perez-Saez, Maria J. [1 ]
Blasco, Miquel [2 ]
Redondo-Pachon, Dolores [1 ]
Ventura-Aguiar, Pedro [2 ]
Bada-Bosch, Teresa [3 ]
Perez-Flores, Isabel [4 ]
Melilli, Edoardo [5 ]
Sanchez-Camara, Luis A. [6 ]
Lopez-Oliva, Maria O. [7 ]
Canal, Cristina [8 ]
Shabaka, Amir [9 ]
Garra-Moncau, Nuria [10 ]
Martin-Moreno, Paloma L. [11 ]
Lopez, Veronica [12 ]
Hernandez-Gallego, Roman [13 ]
Siverio, Orlando [14 ]
Galeano, Cristina [15 ]
Espi-Reig, Jordi [16 ]
Cabezas, Carlos J. [17 ]
Rodrigo, Maria T. [18 ]
Llinas-Mallol, Laura [1 ]
Fernandez-Reyes, Maria J. [19 ]
Cruzado-Vega, Leonidas [20 ]
Perez-Tamajon, Lourdes [21 ]
Santana-Estupinan, Raquel [22 ]
Ruiz-Fuentes, Maria C. [23 ]
Tabernero, Guadalupe [24 ]
Zarraga, Sofia [25 ]
Ruiz, Juan C. [26 ]
Gutierrez-Dalmau, Alex [27 ]
Mazuecos, Auxiliadora [28 ]
Sanchez-Alvarez, Emilio [29 ]
Crespo, Marta [1 ]
Pascual, Julio [1 ]
机构
[1] Hosp del Mar, Inst Mar Med Res, Dept Nephrol, REDinREN RD16 0009 0013, Barcelona, Spain
[2] Inst Biomed Res August Pi i Sunyer, Transplantat Hosp Clin, Dept Nephrol & Kidney, REDinREN RD16 0009 0023, Barcelona, Spain
[3] Hosp Univ 12 Octubre, Dept Nephrol, Madrid, Spain
[4] Hosp Clin San Carlos, Dept Nephrol, Madrid, Spain
[5] Hosp Bellvitge Princeps Espanya, Dept Nephrol, Barcelona, Spain
[6] Hosp Gen Univ Gregorio Maranon, Inst Invest Sanitaria Gregorio Maranon IISGM, Dept Nephrol, Madrid, Spain
[7] Hosp Univ La Paz, Dept Nephrol, Madrid, Spain
[8] Fundacio Puigvert, Res Support Unit, Dept Nephrol, Barcelona, Spain
[9] Hosp Fdn Alcorcon, Dept Nephrol, Madrid, Spain
[10] Fundacio Althaia, Dept Nephrol, Barcelona, Spain
[11] Clin Univ Navarra, Dept Nephrol, IdiSNA, Pamplona, Spain
[12] Univ Malaga, Hosp Reg Univ, Dept Nephrol, IBIMA,REDinREN RD16 0009 0006, Malaga, Spain
[13] Hosp Univ, Dept Nephrol, Badajoz, Spain
[14] Hosp Univ Nuestra Senora de la Candelaria, Dept Nephrol, Tenerife, Spain
[15] Hosp Univ Ramon y Cajal, Inst Ramon y Cajal Invest Sanitaria IRYCIS, Dept Nephrol, Madrid, Spain
[16] Hosp Univ & Politecn La Fe, Dept Nephrol, Valencia, Spain
[17] Complejo Hosp Toledo, Dept Nephrol, Toledo, Spain
[18] Hosp Univ Donostia, Dept Nephrol, Donostia San Sebastian, Spain
[19] Complejo Asistencial Segovia, Dept Nephrol, Segovia, Spain
[20] Hosp Gen Univ, Dept Nephrol, Alicante, Spain
[21] Complejo Hosp Univ Canarias, Dept Nephrol, Tenerife, Spain
[22] Hosp Univ Gran Canaria Doctor Negrin, Dept Nephrol, Las Palmas Gran Canaria, Spain
[23] Hosp Univ Virgen de las Nieves, Dept Nephrol, Granada, Spain
[24] Hosp Univ, Dept Nephrol, IBSAL, Salamanca, Spain
[25] Hosp Cruces, Dept Nephrol, Bilbao, Spain
[26] Univ Cantabria, Hosp Valdecilla, Dept Nephrol, IDIAL, Santander, Spain
[27] Hosp Univ Miguel Servet, Dept Nephrol, Zaragoza, Spain
[28] Hosp Univ Puerta del Mar, Dept Nephrol, Cadiz, Spain
[29] Hosp Univ Cabuenes, Dept Nephrol, Gijon, Spain
关键词
clinical research; practice; infection and infectious agents - viral; kidney transplantation; nephrology; patient survival;
D O I
10.1111/ajt.16192
中图分类号
R61 [外科手术学];
学科分类号
摘要
Acute respiratory distress syndrome associated with coronavirus infection is related to a cytokine storm with large interleukin-6 (IL-6) release. The IL-6-receptor blocker tocilizumab may control the aberrant host immune response in patients with coronavirus disease 2019 (COVID-19) . In this pandemic, kidney transplant (KT) recipients are a high-risk population for severe infection and showed poor outcomes. We present a multicenter cohort study of 80 KT patients with severe COVID-19 treated with tocilizumab during hospital admission. High mortality rate was identified (32.5%), related with older age (hazard ratio [HR] 3.12 for those older than 60 years,P = .039). IL-6 and other inflammatory markers, including lactic acid dehydrogenase, ferritin, and D-dimer increased early after tocilizumab administration and their values were higher in nonsurvivors. Instead, C-reactive protein (CRP) levels decreased after tocilizumab, and this decrease positively correlated with survival (mean 12.3 mg/L in survivors vs. 33 mg/L in nonsurvivors). Each mg/L of CRP soon after tocilizumab increased the risk of death by 1% (HR 1.01 [confidence interval 1.004-1.024],P = .003). Although patients who died presented with worse respiratory situation at admission, this was not significantly different at tocilizumab administration and did not have an impact on outcome in the multivariate analysis. Tocilizumab may be effective in controlling cytokine storm in COVID-19 but randomized trials are needed.
引用
收藏
页码:3182 / 3190
页数:9
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