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Infections in children following chimeric antigen receptor T-cell therapy for B-cell acute lymphoblastic leukemia.
Diamond, Yonatan; Gilsenan, Maddie; Wang, Stacie Shiqi; Hanna, Diane; Conyers, Rachel; Cole, Theresa; Hughes, David; Fleming, Jacqueline; Meyran, Deborah; Toro, Claudia; Malalasekera, Vajiranee; Khaw, Seong Lin; Haeusler, Gabrielle M.
Afiliação
  • Diamond Y; Kids Cancer Centre, Sydney Children's Hospital, Randwick, New South Wales, Australia.
  • Gilsenan M; Children's Cancer Centre, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Wang SS; Children's Cancer Centre, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Hanna D; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Conyers R; Children's Cancer Centre, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Cole T; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Hughes D; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.
  • Fleming J; Children's Cancer Centre, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Meyran D; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Toro C; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.
  • Malalasekera V; Children's Cancer Centre, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Khaw SL; Children's Cancer Centre, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Haeusler GM; Children's Cancer Centre, Royal Children's Hospital, Parkville, Victoria, Australia.
Transpl Infect Dis ; 25(6): e14202, 2023 Dec.
Article em En | MEDLINE | ID: mdl-38041799
ABSTRACT

BACKGROUND:

CD19-directed chimeric antigen receptor T-cell (CAR-T) therapy is transforming care for pediatric patients with relapsed or refractory B-cell acute lymphoblastic leukemia (B-ALL). There are limited pediatric-specific data concerning the infection risks associated with CD19 CAR-T therapy and the adequacy of current antimicrobial prophylaxis guidelines for these patients.

METHODS:

We describe the antimicrobial prophylaxis used and the types of infectious occurring in the first 100 days following CAR-T therapy for relapsed or refractory B-cell ALL in children and adolescents (≤18 years) at our centre.

RESULTS:

Twenty-seven patients received their first CAR-T infusion (CTI) during the study period. Almost all patients (96%) had a comprehensive Infectious Diseases review prior to CTI, which informed a personalised prophylaxis or fever/sepsis plan in six (22%). Overall, six (22%) patients had one or more infections during the study period including five (19%, 0.9 per 100 days-at-risk) from days 0-30 and three (n = 20, 15%, 0.6 per 100 days-at-risk) from days 31-100. Bacterial blood stream infections were the most common type of infection encountered during both time periods, and one patient had probable pulmonary aspergillosis. There were no infection-related deaths.

CONCLUSION:

Our study contributes important information on the spectrum of infections encountered in pediatric patients with B-ALL post CAR-T therapy. Overall, the burden of infectious complications post CAR-T therapy in our cohort is lower than previously reported in the literature. Results suggest that our prophylaxis recommendations are effective in this population.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Linfoma de Burkitt / Sepse / Leucemia-Linfoma Linfoblástico de Células Precursoras / Receptores de Antígenos Quiméricos / Anti-Infecciosos Limite: Adolescent / Child / Humans Idioma: En Revista: Transpl Infect Dis Assunto da revista: TRANSPLANTE Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Linfoma de Burkitt / Sepse / Leucemia-Linfoma Linfoblástico de Células Precursoras / Receptores de Antígenos Quiméricos / Anti-Infecciosos Limite: Adolescent / Child / Humans Idioma: En Revista: Transpl Infect Dis Assunto da revista: TRANSPLANTE Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália