Evidence map›Paper›PMID 37266769›Full record

ArticleJournal of clinical immunology2023

Safety and Efficacy of Hizentra® Following Pediatric Hematopoietic Cell Transplant for Treatment of Primary Immunodeficiencies.

Niraj C Patel, Troy Torgerson, Monica S Thakar, M Elizabeth M Younger, Panida Sriaroon, Tamara C Pozos, Rebecca H Buckley, David Morris, Diana Vilkama, Jennifer Heimall

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of clinical immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 71% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 8 institutions in 1 country.

Niraj C PatelDepartment of Pediatrics, Division of Allergy and Immunology, Duke University, Durham, NC, USA. niraj.patel@duke.edu.ORCID http://orcid.org/0000-0002-3657-145X
Troy TorgersonAllen Institute for Immunology, Seattle, WA, USA.
Monica S ThakarClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
M Elizabeth M YoungerDivision of Allergy, Immunology and Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Panida SriaroonDivision of Allergy and Immunology, University of South Florida, Tampa, FL, USA.
Tamara C PozosDepartment of Clinical Immunology, Children's Minnesota, Minneapolis, MN, USA.
Rebecca H BuckleyDepartment of Pediatrics, Division of Allergy and Immunology, Duke University, Durham, NC, USA.
David Morris, Webbwrites, Durham, USA.
Diana VilkamaDepartment of Clinical Immunology, Children's Minnesota, Minneapolis, MN, USA.
Jennifer HeimallDivision of Allergy and Immunology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Children's Minnesota · USDuke University · USAllen Institute for Immunology · USChildren's Hospital of Philadelphia · USJohns Hopkins University · USUniversity of South Florida · USUniversity of Washington · USWebb Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary immunodeficiency disease (PIDD) comprises a group of disorders of immune function. Some of the most severe PIDD can be treated with hematopoietic cell transplant (HCT). Hizentra® is a 20% liquid IgG product approved for subcutaneous administration in adults and children greater than 2 years of age with PIDD-associated antibody deficiency. Limited information is available on the use of Hizentra® in children following HCT for PIDD. A multicenter retrospective chart review demonstrated 37 infants and children (median age 70.1 [range 12.0 to 176.4] months) with PIDD treated by HCT who received Hizentra® infusions over a median duration of 31 (range 4-96) months post-transplant. The most common indication for HCT was IL2RG SCID (n = 16). Thirty-two patients switched from IVIG to SCIG administration, due to one or more of the following reasons: patient/caregiver (n = 17) or physician (n = 12) preference, discontinuation of central venous catheter (n = 16), desire for home infusion (n = 12), improved IgG serum levels following lower levels on IVIG (n = 10), and loss of venous access (n = 8). Serious bacterial infections occurred at a rate of 0.041 per patient-year while on therapy. Weight percentile increased by a mean of 16% during the observation period, with females demonstrating the largest gains. Mild local reactions were observed in 24%; 76% had no local reactions. One serious adverse event (death from sepsis) was reported. Hizentra® was discontinued in 15 (41%) patients, most commonly due to recovery of B cell function (n = 11). These data demonstrate that Hizentra® is a safe and effective option in children who have received HCT for PIDD.

Indexed as

Hematopoietic Stem Cell TransplantationImmunologic Deficiency SyndromesPrimary Immunodeficiency DiseasesAdultChildFemaleHumansImmunoglobulin GImmunoglobulins, IntravenousInfantInfusions, SubcutaneousRetrospective StudiesHizentraImmunoglobulin GImmunoglobulins, IntravenousHematopoietic cell transplantInborn errors of immunityPrimary immunodeficiency diseasesSubcutaneous immunoglobulin

Identifiers

PMID37266769
PMCPMC10499723
OpenAlexW4379094532

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.