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COVID-19 infection in patients undergoing allogeneic hematopoietic stem cell transplantation

https://doi.org/10.35754/0234-5730-2024-69-1-8-19

Abstract

Introduction. The COVID-19 pandemic has changed the conditions for providing medical care to hematological patients, including those who underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT).

Objective: to analyze the course of the new coronavirus infection COVID-19 in patients who have undergone allo-HSCT. Materials and methods. The retrospective study included 87 patients who developed COVID-19 after allo-HSCT in the period from March 2020 to January 2022. In most cases, transplants were performed in patients with acute leukemia (77 %) using peripheral hematopoietic stem cells (52 %) or bone marrow (48 %) after conditioning in a reduced intensity mode (75 %). COVID-19 infection was considered confi rmed when SARS-CoV-2 RNA was detected by PCR in a smear from the oropharyngeal/nasopharyngeal mucosa.

Results. In 71 (81.6 %) patients, COVID-19 was established a year after performing allo-HSCT, in 16 (18.4 %) patients — during the fi rst year after allo-HSCT. The median age at the time of the development of a new coronavirus infection was 42 years. At the time of the COVID-19 debut, 39 (45 %) patients received immunosuppressive therapy (IST). Performing IST at the time of diagnosis of COVID-19 had a negative effect on overall survival (p = 0.0001). A total of 7 (9 %) patients suffered from the disease asymptomatically, 39 (45 %) — in mild form, 23 (26 %) — in moderate, 10 (11 %) — in severe and 8 (9 %) — in critical form. TCR-αβ/CD19+ graft depletion was associated with a milder course of COVID-19 infection in patients after allo-HSCT (p = 0.06). Hospitalization in a 24-hour hospital was required in 24 (27 %) cases.

Conclusion. Overall survival was comparable in the general group of patients with allo-HSCT compared with healthy individuals with COVID-19, due to a suffi cient degree of immune system reconstruction, as well as a small volume of the study group. The factors that increased the risk of an adverse outcome were age and male gender.

 
 
 

About the Authors

D. A. Mironova
National Medical Research Center for Hematology
Russian Federation

Daria A. Mironova, hematologist of Department of Hemoblastosis Chemotherapy and Bone Marrow and Hematopoietic Stem Cell Transplantation

125167, Moscow



V. A. Vasilyeva
National Medical Research Center for Hematology
Russian Federation

Vera A. Vasilyeva, Cand. Sci. (Med.), head of the Day Hospital of Immunochemotherapy after Bone Marrow and Hematopoietic Stem Cell Transplantation, hematologist

125167, Moscow



M. Yu. Drokov
National Medical Research Center for Hematology
Russian Federation

Mikhail Yu. Drokov, Cand. Sci. (Med.), head of hemoblastosis chemotherapy, hematopoietic depression and bone marrow transplantation research sector

125167, Moscow



Yu.  A. Chabaeva
National Medical Research Center for Hematology
Russian Federation

Yuliya A. Chabaeva, Cand. Sci. (Tech.), deputy Head of the information and analytical Department

125167, Moscow



L. A. Kuzmina
National Medical Research Center for Hematology
Russian Federation

Larisa A. Kuzmina, Cand. Sci. (Med.), head of Department of Hemoblastosis Chemotherapy and Bone Marrow and Hematopoietic Stem Cell Transplantation

125167, Moscow



E. N. Parovichnikova
National Medical Research Center for Hematology
Russian Federation

Elena N. Parovichnikova, Dr. Sci. (Med.), CEO 

125167, Moscow



References

1. Chan J.F.W., Yuan S., Kok K.H., et al. A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster. Lancet. 2020; 395(10223): 514. DOI: 10.1016/S01406736(20)30154-9.

2. Huang J., Lin H., Wu Y., et al. COVID-19 in posttransplant patients—report of 2 cases. Am J Transplant. 2020; 20(7): 1879–81. DOI: 10.1111/AJT.15896.

3. Matsuda S., Koyasu S. Mechanisms of action of cyclosporine. Immunopharmacology. 2000; 47(2–3): 119–25. DOI: 10.1016/S0162-3109(00)00192-2.

4. McMurray R.W., Harisdangkul V. Mycophenolate Mofetil: Selective T Cell Inhibition. Am J Med Sci. 2002; 323(4): 194–6. DOI: 10.1097/00000441200204000-00005.

5. Knight S.R., Morris P.J. Does the evidence support the use of mycophenolate mofetil therapeutic drug monitoring in clinical practice? A systematic review. Transplantation. 2008; 85(12): 1675–85. DOI: 10.1097/TP.0B013E3181744199.

6. Spratt J.S., Hoag M.G. Incidence of multiple primary cancers per man-year of follow up: 20-year review from the Ellis Fischel State Cancer Hospital. Ann Surg. 1966; 164(5): 775–84. DOI: 10.1097/00000658-196611000-00001.

7. Onaka T., Iwai F., Kato-Ogura A., et al. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection after allogeneic stem cell transplantation. Clin case reports. 2020; 8(9): 1791–2. DOI: 10.1002/CCR3.2984.

8. Oltolini C., Guidetti A., Ripa M., et al. Coronavirus Disease 2019 in Recipient of Allogeneic Hematopoietic Stem Cell Transplantation: Life-threating Features Within the Early Post-engraftment Phase. HemaSphere. 2020; 4(4): 4. DOI: 10.1097/HS9.0000000000000448.

9. Dellière S., Dudoignon E., Fodil S., et al. Risk factors associated with COVID-19-associated pulmonary aspergillosis in ICU patients: a French multicentric retrospective cohort. Clin Microbiol Infect. 2020; 27(5): 790.e1–e5. DOI: 10.1016/J.CMI.2020.12.005.

10. Doná D., Torres Canizales J., Benetti E., et al. Pediatric transplantation in Europe during the COVID-19 pandemic: Early impact on activity and healthcare. Clin Transplant. 2020; 34(10). e14063 DOI: 10.1111/CTR.14063.

11. Lee L.Y.W., Cazier J.B., Starkey T., et al. COVID-19 prevalence and mortality in patients with cancer and the effect of primary tumour subtype and patient demographics: a prospective cohort study. Lancet Oncol. 2020; 21(10): 1309–16. DOI: 10.1016/S1470-2045(20)30442-3.

12. Passamonti F., Salvini M., Grossi P.A., et al. Clinical characteristics and risk factors associated with COVID-19 severity in patients with haematological malignancies in Italy: a retrospective, multicentre, cohort study. Artic Lancet Haematol. 2020; 7: 737–82. DOI: 10.1016/S2352-3026(20)30251-9.

13. Gavrilina O.A., Zakurdaeva K.A., Vasileva A.N., et al. Final Results of CHRONOS19 Observational Study in Patients with Hematologic Disease and COVID-19 in Russia. Blood. 2021; 138(Supplement 1): 4994. DOI: 10.1182/BLOOD-2021-152735.

14. Siniaev A.A., Popova M.O., Rogacheva Y.A., et al. Journey of a hematopoietic stem cell transplantation center through COVID-19 pandemic: one-year experience. Cell Ther Transplant. 2021; 10(3-4): 30-37. DOI: 10.18620/ctt-18668836-2021-10-3-4-30-37.

15. Daudt L.E., Corso M.C.M., Kerbauy M.N., et al. COVID-19 in HSCT recipients: a collaborative study of the Brazilian Society of Marrow Transplantation (SBTMO). Bone Marrow Transplant 2022; 57(3): 453–9. DOI: 10.1038/s41409-021-01561-x.

16. Ljungman P., Mikulska M., de la Camara R., et al. The challenge of COVID-19 and hematopoietic cell transplantation; EBMT recommendations for management of hematopoietic cell transplant recipients, their donors, and patients undergoing CAR T-cell therapy. Bone Marrow Transplant. 2020; 55(11): 2071. DOI: 10.1038/S41409-020-0919-0.

17. NIH. COVID-19 Treatment Guidelines Panel. Coronavirus Disease 2019 (COVID-19) Treatment Guidelines. National Institutes of Health. Available at https://www.covid19treatmentguidelines.nih.gov/. Accessed [31.03.2022].

18. Xu Z., Huang X. COVID-19 & Allogeneic Transplant: Activity and Preventive Measures for Best Outcomes in China. Adv cell gene Ther. 2020; 3(4): e94. DOI: 10.1002/ACG2.94.

19. Ayoub H.H., Mumtaz G.R., Seedat S., et al. Estimates of global SARS-CoV-2 infection exposure, infection morbidity, and infection mortality rates in 2020. Glob Epidemiol. 2021; 3: 100068. DOI: 10.1016/j.gloepi.2021.100068.

20. Ljungman P., de la Camara R., Mikulska M., et al. COVID-19 and stem cell transplantation; results from an EBMT and GETH multicenter prospective survey. Leukemia. 2021; 35(10): 2885–94. DOI: 10.1038/S41375-021-01302-5.

21. Schmidt-Hieber M., Schwarck S., Stroux A., et al. Immune reconstitution and cytomegalovirus infection after allogeneic stem cell transplantation: the important impact of in vivo T cell depletion. Int J Hematol. 2010; 91(5): 877–85. DOI: 10.1007/S12185-010-0597-6.

22. Popova N. Reconstitution of memory T-cell subpopulations in acute leukemia patients after allogeneic hematopoietic stem cell transplantation. PhD Thesis. Moscow, 2020. (In Russian).

23. Cordonnier C., Einarsdottir S., Cesaro S., et al. Vaccination of haemopoietic stem cell transplant recipients: guidelines of the 2017 European Conference on Infections in Leukaemia (ECIL 7). Lancet Infect Dis. 2019; 19(6): e200–12. DOI: 10.1016/S1473-3099(18)30600-5.

24. NCCN National Comprehensive Cancer Network. Prevention and treatment of Cancer-Related Infections (Version 1.2021). https://www.nccn.org/guidelines/guidelines-detail?category=3&id=1457. 02.03.2022.

25. Khawaja F., Chemaly R.F., Dadwal S., et al. ASH-ASTCT COVID-19 Vaccination for HCT and CAR T cell recipients. https://www.hematology.org/covid-19/ash-astct-covid-19-vaccination-for-hct-and-car-t-cell-recipients.

26. COVID-19 vaccines. Version 8, January 3, 2022. https://www.ebmt.org/sites/default/files/2022-01/COVID%20vaccines%20version%208.3%20-%202022-01-03.pdf

27. Logunov D.Y., Dolzhikova I. V., Shcheblyakov D. V., et al. Safety and effi cacy of an rAd26 and rAd5 vector-based heterologous prime-boost COVID-19 vaccine: an interim analysis of a randomised controlled phase 3 trial in Russia. Lancet. 2021; 397(10275): 671. DOI: 10.1016/S0140-6736(21)00234-8.

28. Гаврилина О.А., Васильева А.Н. Вакцинация от COVID-19 гематологических больных: обзор клинических рекомендаций. Гематология и трансфузиология. 2021; 66(3): 458–70. DOI: 10.35754/0234-5730-2021-66-3458-470.

29. Piñana J.L., López-Corral L., Martino R., et al. SARS-CoV-2-reactive antibody detection after SARS-CoV-2 vaccination in hematopoietic stem cell transplant recipients: Prospective survey from the Spanish Hematopoietic Stem Cell Transplantation and Cell Therapy Group. Am J Hematol. 2022; 97(1): 30–42. DOI: 10.1002/AJH.26385.

30. Ali H., Ngo D., Aribi A., et al. Safety and Tolerability of SARS-CoV2 Emergency-Use Authorized Vaccines for Allogeneic Hematopoietic Stem Cell Transplant Recipients. Transplant Cell Ther. 2021; 27(11): 938.e1–e6. DOI: 10.1016/J.JTCT.2021.07.008.

31. Bergman P., Blennow O., Hansson L., et al. Safety and effi cacy of the mRNA BNT162b2 vaccine against SARS-CoV-2 in fi ve groups of immunocompromised patients and healthy controls in a prospective open-label clinical trial. EBioMedicine. 2021; 74:103705. DOI: 10.1016/J.EBIOM.2021.103705.

32. Shah G.L., DeWolf S., Lee Y.J., et al. Favorable outcomes of COVID-19 in recipients of hematopoietic cell transplantation. J Clin Invest. 2020; 130(12): 6656. DOI: 10.1172/JCI141777.


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For citations:


Mironova D.A., Vasilyeva V.A., Drokov M.Yu., Chabaeva Yu.A., Kuzmina L.A., Parovichnikova E.N. COVID-19 infection in patients undergoing allogeneic hematopoietic stem cell transplantation. Russian journal of hematology and transfusiology. 2024;69(1):8-19. (In Russ.) https://doi.org/10.35754/0234-5730-2024-69-1-8-19

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ISSN 0234-5730 (Print)
ISSN 2411-3042 (Online)