4.4 Article

Clinical characteristics and outcomes of COVID-19 in haematopoietic stem-cell transplantation recipients: an observational cohort study

期刊

LANCET HAEMATOLOGY
卷 8, 期 3, 页码 E185-E193

出版社

ELSEVIER SCI LTD
DOI: 10.1016/S2352-3026(20)30429-4

关键词

-

资金

  1. NCI [U24CA076518]
  2. National Heart, Lung and Blood Institute (NHLBI)
  3. National Institute of Allergy and Infectious Diseases
  4. NHLBI [U24HL138660, OT3HL147741, U01HL128568]
  5. NCI
  6. Health Resources and Services Administration (HRSA) [HHSH250201700006C, HHSH250201700007C]
  7. Office of Naval Research [N00014-18-1-2850, N00014-18-1-2888, N00014-20-1-2705]
  8. NIH [P01CA111412, R01CA152108, R01CA215134, R01CA218285, R01CA231141, R01AI128775, R01HL126589, R01HL129472, R01HL130388, R01HL131731, U01AI069197, U01AI126612]
  9. Be the Match Foundation
  10. Boston Children's Hospital
  11. Dana Farber
  12. St Baldrick's Foundation
  13. Stanford University
  14. Medical College of Wisconsin the National Marrow Donor Program
  15. AbbVie
  16. Actinium Pharmaceuticals
  17. Adaptive Biotechnologies
  18. Adienne SA
  19. Allovir
  20. Amgen
  21. Angiocrine Bioscience
  22. Astellas Pharma US
  23. AstraZeneca
  24. Atara Biotherapeutics
  25. Bluebird bio
  26. Bristol Myers Squibb
  27. Celgene
  28. CSL Behring
  29. CytoSen Therapeutics
  30. Daiichi Sankyo
  31. Gamida-Cell
  32. Genentech
  33. HistoGenetics
  34. Incyte Corporation
  35. Janssen Biotech
  36. Jazz Pharmaceuticals
  37. Johnson Johnson
  38. Kiadis Pharma
  39. Kite (a Gilead Company)
  40. Kyowa Kirin
  41. Legend Biotech
  42. Magenta Therapeutics
  43. Mallinckrodt
  44. Merck Company
  45. Merck Sharp Dohme
  46. Millennium
  47. Takeda Oncology
  48. Miltenyi Biotec
  49. Novartis
  50. Omeros
  51. Oncoimmune
  52. Orca Biosystems
  53. Pfizer
  54. Pharmacyclics
  55. Sanofi Genzyme
  56. Shire
  57. Sobi
  58. Stemcyte
  59. Takeda
  60. Terumo
  61. Viracor Eurofins
  62. Vor Bio Pharma
  63. Xenikos

向作者/读者索取更多资源

This study examined the characteristics and outcomes of HSCT recipients after developing COVID-19. It found that recipients of autologous and allogeneic HSCT who develop COVID-19 have poor overall survival rates. Factors such as age, sex, and time since transplantation were associated with higher risk of mortality in HSCT recipients.
Background Haematopoietic stem-cell transplantation (HSCT) recipients are considered at high risk of poor outcomes after COVID-19 on the basis of their immunosuppressed status, but data from large studies in HSCT recipients are lacking. This study describes the characteristics and outcomes of HSCT recipients after developing COVID-19. Methods In response to the pandemic, the Center for International Blood and Marrow Transplant Research (CIBMTR) implemented a special form for COVID-19-related data capture on March 27, 2020. All patients-irrespective of age, diagnosis, donor type, graft source, or conditioning regimens-were included in the analysis with data cutoff of Aug 12, 2020. The main outcome was overall survival 30 days after a COVID-19 diagnosis. Overall survival probabilities were calculated using Kaplan-Meier estimator. Factors associated with mortality after COVID-19 diagnosis were examined using Cox proportional hazard models. Findings 318 HSCT recipients diagnosed with COVID-19 were reported to the CIBMTR. The median time from HSCT to COVID-19 diagnosis was 17 months (IQR 8-46) for allogeneic HSCT recipients and 23 months (8-51) for autologous HSCT recipients. The median follow-up of survivors was 21 days (IQR 8-41) for allogeneic HSCT recipients and 25 days (12-35) for autologous HSCT recipients. 34 (18%) of 184 allogeneic HSCT recipients were receiving immunosuppression within 6 months of COVID-19 diagnosis. Disease severity was mild in 155 (49%) of 318 patients, while severe disease requiring mechanical ventilation occurred in 45 (14%) of 318 patients-ie, 28 (15%) of 184 allogeneic HSCT recipients and 17 (13%) of 134 autologous HSCT recipients. At 30 days after the diagnosis of COVID-19, overall survival was 68% (95% CI 58-77) for recipients of allogeneic HSCT and 67% (55-78) for recipients of autologous HSCT. Age 50 years or older (hazard ratio 2.53, 95% CI 1.16-5.52; p=0.020); male sex (3.53; 1.44-8.67; p=0.006), and development of COVID-19 within 12 months of transplantation (2.67, 1.33-5.36; p=0.005) were associated with a higher risk of mortality among allogeneic HSCT recipients, and a disease indication of lymphoma was associated with a higher risk of mortality compared with plasma cell disorder or myeloma (2.41, [1.08-5.38]; p=0.033) in autologous HSCT recipients. Interpretation Recipients of autologous and allogeneic HSCT who develop COVID-19 have poor overall survival. These data emphasise the need for stringent surveillance and aggressive treatment measures in HSCT recipients who develop COVID-19. Copyright (C) 2021 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据