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. 2022 Jul 13;41(8):e341–e342. doi: 10.1097/INF.0000000000003552

A Single-center Experience in Treating Young Children at High Risk For Severe COVID-19 With Sotrovimab

Giulia Pruccoli 1,, Nicoletta Bertorello 2, Elisa Funiciello 3, Federica Mignone 4, Erika Silvestro 4, Carlo Scolfaro 4, Silvia Garazzino 4
PMCID: PMC9281427  PMID: 35421051

To the Editors:

In Italy, the B.1.1.529 (Omicron) variant of concern (VOC) of Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is now dominant1 and sotrovimab is thought to retain activity against it.2,3

To the best of our knowledge, there are few data on its use in children less than 12 years old and weighing less than 40 kg.4 European Medicine Agency (EMA) and Italian Medicine Agency (AIFA) both authorized sotrovimab for treating COVID-19 in adults and adolescents (from 12 years of age and weighing at least 40 kilograms) who do not require supplemental oxygen and who are at increased risk of the disease becoming severe.

We describe a series of 5 children less than 12 years old, treated with sotrovimab in the Department of Pediatric and Public Health Sciences, Infectious Diseases Unit, Regina Margherita Children’s Hospital, Turin. All 5 patients were admitted for reasons other than COVID-19 and tested positive for SARS-CoV-2 infection. They were hospitalized to ensure clinical observation because they all fulfilled the criteria for high risk of progression to severe COVID-19 (Table 1) and they all met AIFA’s indications for treatment with sotrovimab, with the exception of age and weight.5 None of them had received vaccination for SARS-CoV-2 (4 out 5 were less than 5 years old). As required by the hospital’s policy, off-label monoclonal antibodies (mAb) use for age and weight was prescribed after Hospital Drug Committee approval and once we obtained the informed parental consent.

TABLE 1.

Demographic and COVID-19 Related Symptoms in Our Pediatric Patients

Subjects Age Weight Sex Ethnicity Comorbidity First positive test for SARS-CoV-2 COVID-19 related symptoms Sotrovimab infusion
Patient 1 2 months 5.5 kg F Caucasian ALL at onset 27 January 2022 Fatigue 29 January 2022
Patient 2 1 year 12.5 kg M African Mucopolysaccharidosis type I, sleep apnea syndrome with nocturnal NIV, AHSCT complicated with reactivation of CMV and EBV infection, immunosuppressive treatment with anti–B lymphocyte monoclonal antibodies (rituximab) 2 January 2022 Rhinitis, sore throat 8 January 2022
Patient 3 1 year 10 kg F African Embryonal rhabdomyosarcoma and neutropenia (ongoing chemotherapeutic agents) 27 January 2022 Fever 29 January 2022
Patient 4 2 years 14 kg M Caucasian ALL (ongoing chemotherapeutic agents) 27 January 2022 Fever 29 January 2022
Patient 5 8 years 18 kg M Hispanic Chronic pulmonary graft versus host disease after AHSCT in ALL 1 January 2022 Headache, rhinitis 8 January 2022

AHSCT indicates allogeneic hematopoietic stem cell transplant; ALL, acute lymphoblastic leukemia; CMV, cytomegalovirus; EBV, epstein barr virus; F, female; M, male; NIV, noninvasive ventilation.

Since pediatric clinical trials on SARS-CoV-2 treatment with sotrovimab are lacking in children, there are no formal guidelines and recommendations about the dosage in patients younger than 12 years of age and weighing less than 40 kg. Considering that the recommended dose in adults and adolescents (weighing at least 40 kg) is a single 500 mg intravenous administration,3 we established a dose based on anthropometric values of 12.5 mg/kg for our patients.

There were no significant adverse events and reactions that required the cessation of infusion. None of the treated patients required either intensive care admission or oxygen supplementation, except for 1, who presented pulmonary worsening the day after Sotrovimab infusion and recovered with a short course of steroids.

Among the first 2 patients treated, none was readmitted for reasons related to COVID-19 or Multisystem Inflammatory Syndrome in children (MIS-C) within 30 days of follow-up. Of the other 3, 1 was discharged the day after sotrovimab infusion and another 5 days later; the last is still hospitalized for reasons other than COVID-19. These 3 children did not develop COVID-19 related symptoms at the 7-day follow-up.

In conclusion, the administration of sotrovimab in the initial phase of SARS-CoV-2 infection might be considered also in young children with risk factors for severe COVID-19.

Although our data are limited, this report provides preliminary information on the use, weight-based dosage and tolerability of sotrovimab in young children at high risk for unfavourable and complicated COVID-19 evolution.

Footnotes

The authors have no funding or conflicts of interest to disclose.

All authors have participated in the drafting or revising of the correspondence, and have approved the correspondence as submitted.

Contributor Information

Nicoletta Bertorello, Email: nbertorello@cittadellasalute.to.it.

Elisa Funiciello, Email: elisa.funiciello91@gmail.com.

Federica Mignone, Email: fede_by@hotmail.com.

Erika Silvestro, Email: silvestro.er@gmail.com.

Carlo Scolfaro, Email: carloscolfaro@yahoo.it.

REFERENCES


Articles from The Pediatric Infectious Disease Journal are provided here courtesy of Wolters Kluwer Health

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