Comparing Rituximab and Cyclophosphamide in Induction Therapy for Childhood-Onset ANCA-Associated Vasculitis: An ARChiVe registry-cohort study.


Journal

Arthritis care & research
ISSN: 2151-4658
Titre abrégé: Arthritis Care Res (Hoboken)
Pays: United States
ID NLM: 101518086

Informations de publication

Date de publication:
28 Oct 2024
Historique:
revised: 18 09 2024
received: 05 02 2024
accepted: 22 10 2024
medline: 28 10 2024
pubmed: 28 10 2024
entrez: 28 10 2024
Statut: aheadofprint

Résumé

Granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) are chronic life-threatening vasculitides requiring substantial immunotherapy. Adult trials identified rituximab (RTX) as an alternative to cyclophosphamide (CYC) for remission-induction of GPA/MPA. Disease rarity has limited feasibility of similar trials in pediatrics. We aim to evaluate the relative efficacy and toxicity of CYC and RTX for childhood GPA/MPA through registry-based comparative evaluation. From A Registry of Childhood Vasculitis we identified GPA/MPA patients who received induction with RTX or CYC. Pediatric vasculitis activity score (PVAS) and pediatric vasculitis damage index (pVDI) evaluated disease activity and damage. Descriptive statistics summarized patient characteristics. RTX/CYC comparisons used logistic regression for primary outcomes of post-induction remission (PVAS=0) or low disease activity (PVAS<2). Hospital admission for adverse events and pVDI were compared using logistic regression and ordinal regression, respectively. Among 104 patients, 43% received RTX, 46% CYC, 11% both. Treatment groups did not significantly differ for diagnosis PVAS and onset age. There was no difference in remission between groups (63% overall; OR 1.07, 95% CI: 0.45, 2.52). Hospitalizations occurred in 22% of RTX patients versus 10% on CYC (OR 2.27, 95% CI: 0.73, 7.05). The median 12-month pVDI was one in both groups (OR 0.98, 95% CI 0.43, 2.22). This is the first study comparing CYC and RTX for induction in pediatric GPA/MPA. No significant differences were shown in rates of remission, severe adverse events, or organ damage. Limitations included lack of standardized treatment regimens, retrospectivity, and lack of longitudinal adverse drug-related event data.

Identifiants

pubmed: 39467015
doi: 10.1002/acr.25455
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

This article is protected by copyright. All rights reserved.

Auteurs

Samuel J Gagne (SJ)

Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA.
University of Pittsburgh School of Medicine, Pittsburgh, PA.

Vidya Sivaraman (V)

Nationwide Children's Hospital, Rheumatology, Columbus, OH.
The Ohio State University, Columbus, OH.

Else S Bosman (ES)

British Columbia's Children's Hospital, Vancouver, BC.

Brett Klamer (B)

The Ohio State University School of Biomedical Science, Center for Biostatistics Columbus, OH.

Kimberly A Morishita (KA)

British Columbia's Children's Hospital, Vancouver, BC.

Adam Huber (A)

IWK Health Centre/Dalhousie University, Halifax, NS.

Alvaro Orjuela (A)

Baylor College of Medicine, Houston, TX.
Texas Children's Hospital, Houston, TX.

Barbara Eberhard (B)

Cohen Children's Northwell Health, New Hyde Park, NY.

Charlotte Myrup (C)

Copenhagen University Hospital, Copenhagen, DK.

Dana Gerstbacher (D)

Stanford Children's Hospital, Palo Alto, CA.

Dirk Foell (D)

University of Muenster, Muenster, Germany.

Eslam Al-Abadi (E)

Birmingham Children's Hospital, Birmingham, UK.

Flora McErlane (F)

Great North Children's Hospital, Newcastle Upon Tyne, UK.
Newcastle University Population Health Sciences Institute, Newcastle upon Tyne, UK.

Kathryn Cook (K)

Akron Children's Hospital, Akron, OH.

Linda Wagner-Weiner (L)

The University of Chicago Medical Center, Chicago, IL.

Melissa Elder (M)

University of Florida, Gainesville, FL.

L Nandini Moorthy (LN)

Robert Wood Johnson Medical School, New Brunswick, NJ.

Paul Dancey (P)

Janeway Children's Health and Rehabilitation Centre, St. John's, NL.

Rae Yeung (R)

The Hospital for Sick Children and University of Toronto, Toronto, ON.

Raju Khubchandani (R)

SRCC Childrens Hospital, Mumbai, Mumbai, IN.

Samundeeswari Deepak (S)

Nottingham Children's Hospital, Nottingham, UK.

Sirirat Charuvanij (S)

Riley Hospital for Children at Indiana University Health, Indianapolis, IN.

Stacey Tarvin (S)

Seattle Childrens Hospital, Seattle, WA.

Susan Shenoi (S)

Montefiore Hospital and Medical Center, Bronx, NY.

Tamara Tanner (T)

Siriraj Hospital, Mahidol University, Bangkok, TH.

Kelly Brown (K)

British Columbia's Children's Hospital, Vancouver, BC.

David A Cabral (DA)

British Columbia's Children's Hospital, Vancouver, BC.

Classifications MeSH