Skip to main content

Advertisement

Log in

Clinical characteristics of SARS-CoV-2 Omicron variant infection in children with acute leukemia

  • Original Article
  • Published:
Annals of Hematology Aims and scope Submit manuscript

Abstract

Hematologic diseases and various therapeutic stages can impact the presentation of SARS-CoV-2 Omicron variant infection. This study retrospectively analyzed data on Omicron infection in children with acute leukemia treated at our hospital between January 16, 2023, and February 25, 2023, using questionnaires. The prevalence of Omicron infection in children undergoing consolidation chemotherapy, maintenance chemotherapy, drug withdrawal, and healthy children was 81.8%, 75.2%, 55.2%, and 61.9%, respectively. The observed differences were statistically significant (P < 0.05). During the course of infection, children with leukemia undergoing chemotherapy, including both the consolidation and maintenance chemotherapy groups, exhibited a prolonged time to achieve SARS-CoV-2 negativity compared to the drug withdrawal and healthy groups. However, there was no significant increase in the incidence of symptoms across all body systems, and no children experienced serious sequelae or death. Furthermore, our observations indicated that all manifestations of Omicron infection in children with leukemia after drug withdrawal were not significantly different from those in healthy children. This suggested, to a certain extent, that the immune function of children with leukemia recovers effectively after the cessation of drug treatment. These findings are crucial for guiding clinical management and alleviating concerns about infection for both children with leukemia and their parents.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

Data availability

All data generated or analyzed during this study are available within the article.

References

  1. Callaway E (2021) Heavily mutated Omicron variant puts scientists on alert. Nature 600:21. https://doi.org/10.1038/d41586-021-03552-w

    Article  CAS  PubMed  Google Scholar 

  2. Kohn M, Alsuliman T, Lamure S et al (2022) Characteristics of SARS-CoV-2 infection in lymphoma/chronic lymphocytic leukemia patients during the Omicron outbreak. Leuk Lymphoma 63:2686–2690. https://doi.org/10.1080/10428194.2022.2086249

    Article  CAS  PubMed  Google Scholar 

  3. Qu P, Evans JP, Faraone JN et al (2023) Enhanced neutralization resistance of SARS-CoV-2 Omicron subvariants BQ.1, BQ.1.1, BA.4.6, BF.7, and BA.2.75.2. Cell Host Microbe 31:9-17.e3. https://doi.org/10.1016/j.chom.2022.11.012

    Article  CAS  PubMed  Google Scholar 

  4. Singh J, Anantharaj A, Panwar A et al (2023) BA.1, BA.2 and BA.2.75 variants show comparable replication kinetics, reduced impact on epithelial barrier and elicit cross-neutralizing antibodies. PLoS Pathog 19:e1011196. https://doi.org/10.1371/journal.ppat.1011196

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Barrière J, Zalcman G, Fignon L et al (2022) Omicron variant: a clear and present danger for patients with cancer. Eur J Cancer 165:25–26. https://doi.org/10.1016/j.ejca.2022.01.010

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Fonager J, Bennedbæk M, Bager P et al (2022) Molecular epidemiology of the SARS-CoV-2 variant Omicron BA.2 sub-lineage in Denmark, 29 November 2021 to 2 January 2022. Euro Surveill 27:2200181. https://doi.org/10.2807/1560-7917.ES.2022.27.10.2200181

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Fan Y, Li X, Zhang L et al (2022) SARS-CoV-2 Omicron variant: recent progress and future perspectives. Signal Transduct Target Ther 7:141. https://doi.org/10.1038/s41392-022-00997-x

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Lee M, Quinn R, Pradhan K et al (2022) Impact of COVID-19 on case fatality rate of patients with cancer during the Omicron wave. Cancer Cell 40:343–345. https://doi.org/10.1016/j.ccell.2022.02.012

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Modemann F, Ghandili S, Schmiedel S et al (2022) COVID-19 and adult acute leukemia: our knowledge in progress. Cancers 14:3711. https://doi.org/10.3390/cancers14153711

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Choi S-H, Choi JH, Lee JK et al (2023) Clinical characteristics and outcomes of children with SARS-CoV-2 infection during the Delta and Omicron variant-dominant periods in Korea. J Korean Med Sci 38:e65. https://doi.org/10.3346/jkms.2023.38.e65

    Article  PubMed  PubMed Central  Google Scholar 

  11. Ramasamy C, Mishra AK, John KJ, Lal A (2021) Clinical considerations for critically ill COVID-19 cancer patients: a systematic review. World J Clin Cases 9:8441–8452. https://doi.org/10.12998/wjcc.v9.i28.8441

    Article  PubMed  PubMed Central  Google Scholar 

  12. He W, Chen L, Chen L et al (2020) COVID-19 in persons with haematological cancers. Leukemia 34:1637–1645. https://doi.org/10.1038/s41375-020-0836-7

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Haeusler GM, Ammann RA, Carlesse F et al (2021) SARS-CoV-2 in children with cancer or after haematopoietic stem cell transplant: an analysis of 131 patients. Eur J Cancer 159:78–86. https://doi.org/10.1016/j.ejca.2021.09.027

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Sharma A, Bhatt NS, St Martin A et al (2021) Clinical characteristics and outcomes of COVID-19 in haematopoietic stem-cell transplantation recipients: an observational cohort study. The Lancet Haematology 8:e185–e193. https://doi.org/10.1016/S2352-3026(20)30429-4

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Niemann CU, Da Cunha-Bang C, Helleberg M et al (2022) Patients with CLL have a lower risk of death from COVID-19 in the Omicron era. Blood 140:445–450. https://doi.org/10.1182/blood.2022016147

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Blennow O, Salmanton-García J, Nowak P et al (2022) Outcome of infection with omicron SARS-CoV-2 variant in patients with hematological malignancies: an EPICOVIDEHA survey report. Am J Hematol 97:E312–E317. https://doi.org/10.1002/ajh.26626

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. OnCovid Study Group, Pinato DJ, Patel M et al (2022) Time-dependent COVID-19 mortality in patients with cancer: an updated analysis of the OnCovid registry. JAMA Oncol 8:114–122. https://doi.org/10.1001/jamaoncol.2021.6199

    Article  Google Scholar 

  18. Passamonti F, Cattaneo C, Arcaini L et al (2020) Clinical characteristics and risk factors associated with COVID-19 severity in patients with haematological malignancies in Italy: a retrospective, multicentre, cohort study. The Lancet Haematology 7:e737–e745. https://doi.org/10.1016/S2352-3026(20)30251-9

    Article  PubMed  PubMed Central  Google Scholar 

  19. Haidar G, Mellors JW (2021) Improving the outcomes of immunocompromised patients with coronavirus disease 2019. Clin Infect Dis 73:e1397–e1401. https://doi.org/10.1093/cid/ciab397

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Mair MJ, Mitterer M, Gattinger P et al (2022) Enhanced SARS-CoV-2 breakthrough infections in patients with hematologic and solid cancers due to Omicron. Cancer Cell 40:444–446. https://doi.org/10.1016/j.ccell.2022.04.003

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Suzuki R, Yamasoba D, Kimura I et al (2022) Attenuated fusogenicity and pathogenicity of SARS-CoV-2 Omicron variant. Nature 603:700–705. https://doi.org/10.1038/s41586-022-04462-1

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We sincerely thank the patients who participated in this study, their families who actively cooperated, and the healthcare professionals who treated and cared for the patients in the clinical setting.

Funding

This work was supported by Beijing Natural Science Foundation (No. 7222056), Capital’s Funds for Health Improvement and Research (CFH) (No. 2022–1-2091).

Author information

Authors and Affiliations

Authors

Contributions

Pengli Huang and Henghui Chang collected data and drafted the manuscript. Ruidong Zhang, Ying Wu, and Peijing Qi treated the patients. Yaguang Peng and Xueling Zheng participated in statistical work. Huyong Zheng designed the questionnaires and reviewed the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Huyong Zheng.

Ethics declarations

Ethics approval and consent to participate

The treatment was approved by the Institutional Ethics Committee of Beijing Children’s Hospital (Approval No.: IEC-C-006-A04-V.07).

Competing interests

The authors declare no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Huang, P., Chang, H., Zhang, R. et al. Clinical characteristics of SARS-CoV-2 Omicron variant infection in children with acute leukemia. Ann Hematol 103, 729–736 (2024). https://doi.org/10.1007/s00277-023-05593-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00277-023-05593-9

Keywords

Navigation