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.
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References
Callaway E (2021) Heavily mutated Omicron variant puts scientists on alert. Nature 600:21. https://doi.org/10.1038/d41586-021-03552-w
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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).
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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.
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The treatment was approved by the Institutional Ethics Committee of Beijing Children’s Hospital (Approval No.: IEC-C-006-A04-V.07).
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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
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DOI: https://doi.org/10.1007/s00277-023-05593-9