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MPN-433: Outcomes of COVID-19 in Hematopoietic Stem Cell Transplant Recipients: A Single-Institution, Observational Study
CONTEXT: Hematopoietic stem cell transplant (HSCT) recipients are generally considered high risk for poor outcomes following COVID-19 infection. The CIBMTR observational report published by Sharma et al. found that recipients of allogeneic HSCT who contracted COVID-19 had poor overall survival with...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404081/ http://dx.doi.org/10.1016/S2152-2650(21)01844-9 |
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author | Dwabe, Sami Savitala-Damerla, Lakshmi Ladha, Abdullah Tam, Eric Chaudhary, Preet Yaghmour, George |
author_facet | Dwabe, Sami Savitala-Damerla, Lakshmi Ladha, Abdullah Tam, Eric Chaudhary, Preet Yaghmour, George |
author_sort | Dwabe, Sami |
collection | PubMed |
description | CONTEXT: Hematopoietic stem cell transplant (HSCT) recipients are generally considered high risk for poor outcomes following COVID-19 infection. The CIBMTR observational report published by Sharma et al. found that recipients of allogeneic HSCT who contracted COVID-19 had poor overall survival with a 30-day mortality of 32%. However, there are relatively few other studies that evaluate the effect of COVID-19 on HSCT recipients, especially in the setting of in vivo T-cell depletion protocol. OBJECTIVE: This is a single-institution, retrospective analysis evaluating outcomes of HSCT recipients who were diagnosed with COVID-19 between March 2020 and April 2021. PATIENTS: There were 21 patients at our institution who had undergone HSCT and subsequently contracted COVID-19. Their median age was 53 years at the time of diagnosis. Thirteen of the patients were Hispanic (61.9%). Six of the patients received match-related stem cells (28.6%), 7 received cells from match unrelated donors (33.3%), and 7 received cells from haploidentical donors (33.3%). Fifteen of the patients (71.4%) received myeloablative conditioning regimens, whereas 5 (23.8%) received reduced intensity or non-myeloablative regimens. One patient had received an autologous stem cell transplant. Our most common GVHD prophylaxis regimens were PTCy/Tacro/MMF (12 pts, 57.1%) and Tacro/MTX (6 pts, 28.5%). RESULTS: Our primary endpoint in this retrospective analysis was non-relapse mortality within 60 days of COVID-19 diagnosis. Of the 21 patients with confirmed COVID-19 infection, 1 passed away 20 days after diagnosis, giving us a 4.8% case fatality rate. The median time of COVID-19 diagnosis post-transplant was 469 days. Sixteen of the 21 patients were symptomatic at the time of diagnosis (76.2%). Eight patients received steroids for treatment of COVID-19 (38.1%). Seven of the 21 patients (33.3%) were hospitalized for a median of 7 days (range, 5–17 days), with 2 requiring ICU level of care (9.5%). One patient was intubated and ultimately passed away. CONCLUSION: Our data suggest that our HSCT recipients who contracted COVID-19 have had generally good short-term outcomes. Longer follow-up is required to determine if a COVID-19 diagnosis has any effect on long-term transplant related complications and outcomes in this population. |
format | Online Article Text |
id | pubmed-8404081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84040812021-08-30 MPN-433: Outcomes of COVID-19 in Hematopoietic Stem Cell Transplant Recipients: A Single-Institution, Observational Study Dwabe, Sami Savitala-Damerla, Lakshmi Ladha, Abdullah Tam, Eric Chaudhary, Preet Yaghmour, George Clin Lymphoma Myeloma Leuk Myeloproliferative Neoplasms CONTEXT: Hematopoietic stem cell transplant (HSCT) recipients are generally considered high risk for poor outcomes following COVID-19 infection. The CIBMTR observational report published by Sharma et al. found that recipients of allogeneic HSCT who contracted COVID-19 had poor overall survival with a 30-day mortality of 32%. However, there are relatively few other studies that evaluate the effect of COVID-19 on HSCT recipients, especially in the setting of in vivo T-cell depletion protocol. OBJECTIVE: This is a single-institution, retrospective analysis evaluating outcomes of HSCT recipients who were diagnosed with COVID-19 between March 2020 and April 2021. PATIENTS: There were 21 patients at our institution who had undergone HSCT and subsequently contracted COVID-19. Their median age was 53 years at the time of diagnosis. Thirteen of the patients were Hispanic (61.9%). Six of the patients received match-related stem cells (28.6%), 7 received cells from match unrelated donors (33.3%), and 7 received cells from haploidentical donors (33.3%). Fifteen of the patients (71.4%) received myeloablative conditioning regimens, whereas 5 (23.8%) received reduced intensity or non-myeloablative regimens. One patient had received an autologous stem cell transplant. Our most common GVHD prophylaxis regimens were PTCy/Tacro/MMF (12 pts, 57.1%) and Tacro/MTX (6 pts, 28.5%). RESULTS: Our primary endpoint in this retrospective analysis was non-relapse mortality within 60 days of COVID-19 diagnosis. Of the 21 patients with confirmed COVID-19 infection, 1 passed away 20 days after diagnosis, giving us a 4.8% case fatality rate. The median time of COVID-19 diagnosis post-transplant was 469 days. Sixteen of the 21 patients were symptomatic at the time of diagnosis (76.2%). Eight patients received steroids for treatment of COVID-19 (38.1%). Seven of the 21 patients (33.3%) were hospitalized for a median of 7 days (range, 5–17 days), with 2 requiring ICU level of care (9.5%). One patient was intubated and ultimately passed away. CONCLUSION: Our data suggest that our HSCT recipients who contracted COVID-19 have had generally good short-term outcomes. Longer follow-up is required to determine if a COVID-19 diagnosis has any effect on long-term transplant related complications and outcomes in this population. Elsevier Inc. 2021-09 2021-08-30 /pmc/articles/PMC8404081/ http://dx.doi.org/10.1016/S2152-2650(21)01844-9 Text en Copyright © 2021 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Myeloproliferative Neoplasms Dwabe, Sami Savitala-Damerla, Lakshmi Ladha, Abdullah Tam, Eric Chaudhary, Preet Yaghmour, George MPN-433: Outcomes of COVID-19 in Hematopoietic Stem Cell Transplant Recipients: A Single-Institution, Observational Study |
title | MPN-433: Outcomes of COVID-19 in Hematopoietic Stem Cell Transplant Recipients: A Single-Institution, Observational Study |
title_full | MPN-433: Outcomes of COVID-19 in Hematopoietic Stem Cell Transplant Recipients: A Single-Institution, Observational Study |
title_fullStr | MPN-433: Outcomes of COVID-19 in Hematopoietic Stem Cell Transplant Recipients: A Single-Institution, Observational Study |
title_full_unstemmed | MPN-433: Outcomes of COVID-19 in Hematopoietic Stem Cell Transplant Recipients: A Single-Institution, Observational Study |
title_short | MPN-433: Outcomes of COVID-19 in Hematopoietic Stem Cell Transplant Recipients: A Single-Institution, Observational Study |
title_sort | mpn-433: outcomes of covid-19 in hematopoietic stem cell transplant recipients: a single-institution, observational study |
topic | Myeloproliferative Neoplasms |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404081/ http://dx.doi.org/10.1016/S2152-2650(21)01844-9 |
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