Association of Rituximab Use With Adverse Events in Children, Adolescents, and Young Adults

Autor: Pavlos Msaouel, Joseph Lubega, Eyal Muscal, Timothy Lotze, Lisa R. Forbes, Martha Barrow, Kristen Curry, Carl E. Allen, Poyyapakkam Srivaths, Casey L. McAtee, Kristen Underbrink, M. Brooke Bernhardt
Rok vydání: 2021
Předmět:
Male
Nephrotic Syndrome
Time Factors
Lymphoma
Long Term Adverse Effects
Pediatrics
Severity of Illness Index
Cohort Studies
Agammaglobulinemia
Interquartile range
Odds Ratio
Lupus Erythematosus
Systemic
Young adult
Child
Original Investigation
B-Lymphocytes
Incidence (epidemiology)
Leukoencephalopathy
Progressive Multifocal
Immunoglobulins
Intravenous
General Medicine
Online Only
Child
Preschool
Encephalitis
Female
Rituximab
medicine.drug
medicine.medical_specialty
Multiple Sclerosis
Neutropenia
Adolescent
Infections
Young Adult
Autoimmune Diseases of the Nervous System
Internal medicine
medicine
Humans
Immunologic Factors
Lymphocyte Count
Adverse effect
Anaphylaxis
Survival analysis
Proportional Hazards Models
Purpura
Thrombocytopenic
Idiopathic
business.industry
Research
Infant
Retrospective cohort study
medicine.disease
Injection Site Reaction
business
Zdroj: JAMA Network Open
ISSN: 2574-3805
Popis: Key Points Question Is the use of rituximab for young people associated with short- or long-term adverse events? Findings This cohort study identified 468 patients younger than 21 years receiving rituximab for more than 25 indications, among whom infectious and noninfectious adverse events were common. The majority of these events were mild, but a small population experienced prolonged immune suppression and severe infections following even single courses of rituximab. Meaning Findings suggest that rituximab appears to be well tolerated among young people, but the observed frequent infections and prolonged recovery of B lymphocyte numbers highlight the need for better strategies to mitigate infection risk in this population.
Importance Rituximab is among the most frequently used immunotherapies in pediatrics. Few studies have reported long-term adverse events associated with its use for children. Objective To describe the use of rituximab and to assess whether its use is associated with short- or long-term adverse events, infections, or time to immune reconstitution in a diverse group of young people. Design, Setting, and Participants This retrospective cohort study included 468 patients aged younger than 21 years who received rituximab for diverse indications between October 1, 2010, and December 31, 2017, at Texas Children’s Hospital, a large pediatric referral hospital. Patterns of adverse events, infections, and immune recovery are described. Data analyses were conducted from December 2019 to June 2020. Exposure One or more doses of rituximab. Main Outcomes and Measures Adverse drug events (eg, anaphylaxis), incidence of mild and severe infections, and time to recovery of B lymphocyte subset counts and immunoglobulin levels. Survival models and logistic regression analyses and were used to identify associated risk factors of infectious and noninfectious adverse drug events. Results We identified 468 patients receiving at least 1 dose of rituximab. The total follow-up time was 11 713 person-months. Of the 468 patients, 293 (62.6%) were female, the median (interquartile range) age at receipt of dose was 14.3 (9.9-16.8) years, and 209 (44.7%) were self-reported White Hispanic. Adverse events associated with rituximab infusion occurred in 72 patients (15.4%), and anaphylaxis occurred in 17 patients (3.6%). Long-term adverse events, such as prolonged neutropenia and leukoencephalopathy, were absent. Infections occurred in 224 patients (47.9%); 84 patients (17.9%) had severe infections, and 3 patients (0.6%) had lethal infections. Concurrent use of intravenous chemotherapy, treatment of systemic lupus erythematosus, neutropenia, and use of intravenous immunoglobulin were associated with increased risk of infection. Among 135 patients (28.8%) followed up to B cell count recovery, CD19+ or CD20+ cell numbers normalized in a median of 9.0 months (interquartile range, 5.9-14.4 months) following rituximab use; 48 of 95 patients (51%) evaluated beyond a year had low-for-age B cell counts. Recovery of CD27+ memory B cell number occurred in a median of 15.7 months (interquartile range, 6.0-22.7 months). Among patients with normal baseline values, low immunoglobulin G (IgG) levels developed in 67 of 289 patients (23.2%) and low IgM levels in 118 of 255 patients (40.8%); of these patients evaluated beyond 12 months from rituximab, 16 of 117 (13.7%) had persistently low IgG and 37 (33.9%) of 109 had persistently low IgM. Conclusions and Relevance Rituximab is well tolerated among young people and is associated with few serious adverse events, but infections are common, corresponding to a prolonged period of B cell count recovery often lasting for longer than a year. Further examination of strategies to prevent infections following rituximab should be pursued.
This cohort study conducted at a large pediatric referral hospital assesses whether the use of rituximab for many diverse indications is associated with short- or long-term adverse events among patients younger than 21 years.
Databáze: OpenAIRE
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