COVID-19 in Pediatric Patients With Acute Lymphoblastic Leukemia or Lymphoma.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
05 Feb 2024
Historique:
medline: 16 2 2024
pubmed: 16 2 2024
entrez: 16 2 2024
Statut: epublish

Résumé

COVID-19 in pediatric patients with acute lymphoblastic leukemia or lymphoma (ALL/LLy) has not been described in detail and may affect chemotherapy administration and long-term outcomes. To describe the clinical presentation of COVID-19 and chemotherapy modifications in pediatric patients with ALL/LLy. This is a retrospective case series of patients at St Jude Children's Research Hospital and its affiliate sites with newly diagnosed ALL/LLy who were treated on the Total XVII protocol (NCT03117751) between March 30, 2020, and June 20, 2022. Participants included patients aged 1 to 18 years who were receiving protocol chemotherapy. Acute symptoms and chemotherapy modifications were evaluated for 60 days after the COVID-19 diagnosis, and viral clearance, adverse events, and second SARS-CoV-2 infections were followed up during the 27-month study period. SARS-CoV-2; all patients were screened at least weekly and at symptom onset and/or after known exposure to SARS-CoV-2. Description of the spectrum of COVID-19 illness and chemotherapy modifications. Of 308 pediatric patients, 110 (36%) developed COVID-19 at a median age of 8.2 (IQR, 5.3-14.5) years. Sixty-eight patients (62%) were male. Most patients were in the continuation/maintenance phase of chemotherapy (101 [92%]). Severe disease was rare (7 [6%]) but was associated with older age, higher white blood cell counts at ALL/LLy diagnosis, lower absolute lymphocyte counts at COVID-19 diagnosis, abnormal chest imaging findings, and SARS-CoV-2 reinfection. Rare but serious thrombotic events included pulmonary embolism and cerebral venous sinus thrombosis (n = 1 for each). No multisystem inflammatory syndrome in children or death was seen. SARS-CoV-2 reinfection occurred in 11 patients (10%) and was associated with older age and with receiving standard or high-risk vs low-risk ALL/LLy therapy. Chemotherapy interruptions occurred in 96 patients (87%) and were longer for patients with severe disease, SARS-CoV-2 reinfection, and/or a COVID-19 diagnosis during the pre-Omicron variant period vs the post-Omicron period (after December 27, 2021). In this case series of COVID-19 in pediatric patients with ALL/LLy, severe COVID-19 was rare, but chemotherapy administration was affected in most patients. Long-term studies are needed to establish the outcomes of COVID-19 in this population.

Identifiants

pubmed: 38363571
pii: 2815232
doi: 10.1001/jamanetworkopen.2023.55727
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2355727

Auteurs

Saman K Hashmi (SK)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
Department of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, Tennessee.

Jessica Bodea (J)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.

Tushar Patni (T)

Department of Biostatistics, St Jude Children's Research Hospital, Memphis, Tennessee.

Savannah Angel (S)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.

Nickhill H Bhakta (NH)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
Department of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, Tennessee.

Sima Jeha (S)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
Department of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, Tennessee.

Seth E Karol (SE)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.

Raul C Ribeiro (RC)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.

Jeffrey E Rubnitz (JE)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.

Joshua Wolf (J)

Department of Infectious Diseases, St Jude Children's Research Hospital, Memphis, Tennessee.

Yimei Li (Y)

Department of Biostatistics, St Jude Children's Research Hospital, Memphis, Tennessee.

Ching-Hon Pui (CH)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
Department of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, Tennessee.

Diego R Hijano (DR)

Department of Infectious Diseases, St Jude Children's Research Hospital, Memphis, Tennessee.

Hiroto Inaba (H)

Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.

Classifications MeSH