Evidence map›Paper›PMID 34430209›Full record

ArticleMolecular genetics and metabolism reports2021

Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics.

Darius Adams, Hans C Andersson, Heather Bausell, Kea Crivelly, Caroline Eggerding, Melissa Lah, Joshua Lilienstein, Kristin Lindstrom, Markey McNutt, Joseph W Ray and 8 more

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Article
  4. Article
  5. Escherichia coli in the production of biopharmaceuticals.Biotechnology and applied biochemistry · 2025
    Review
  6. Lessons learned from 5 years of pegvaliase in US clinics: A case series.Molecular genetics and metabolism reports · 2025
    Article
  7. Article
  8. Article
  9. Article
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

18 authors at 15 institutions in 1 country.

Darius AdamsAtlantic Health Morristown Medical Center, Morristown, NJ, USA.
Hans C AnderssonHayward Genetics Center, Tulane University Medical School, New Orleans, LA, USA.
Heather BausellAnn & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Kea CrivellyHayward Genetics Center, Tulane University Medical School, New Orleans, LA, USA.
Caroline EggerdingCooper University Health Care, Camden, NJ, USA.
Melissa LahIndiana University School of Medicine, Indianapolis, IN, USA.
Joshua LiliensteinBioMarin Pharmaceutical Inc., Novato, CA, USA.
Kristin LindstromPhoenix Children's Hospital, Phoenix, AZ, USA.
Markey McNuttUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.
Joseph W RayUniversity of Texas Medical Branch, Galveston, TX, USA.
Heather SaavedraThe University of Texas Health Science Center at Houston - McGovern Medical School, Houston, TX, USA.
Stephanie SacharowBoston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Danielle StarinRare Disease Institute, Children's National, Washington, DC, USA.
Jennifer Tiffany-AmaroSt. Christopher's Hospital for Children, Philadelphia, PA, USA.
Janet ThomasUniversity of Colorado School of Medicine, Aurora, CO, USA.
Erika VuckoAnn & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Leah B WessenbergOHSU Doernbecher Children's Hospital, Portland, OR, USA.
Kaleigh WhitehallBioMarin Pharmaceutical Inc., Novato, CA, USA.
BioMarin (United States) · USLurie Children's Hospital · USTulane University · USChildren's National · USCooper University Health Care · USDoernbecher Children's Hospital · USHarvard University · USIndiana University – Purdue University Indianapolis · USMorristown Medical Center · USPhoenix Children's Hospital · USSt. Christopher's Hospital for Children · USThe University of Texas Health Science Center at Houston · USThe University of Texas Medical Branch at Galveston · USThe University of Texas Southwestern Medical Center · USUniversity of Colorado Denver · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo present a case series that illustrates real-world use of pegvaliase based on the initial experiences of US healthcare providers.

methodsSixteen healthcare providers from 14 centers across the US with substantial clinical experience in treating patients with phenylketonuria (PKU) with pegvaliase in the two-plus years since FDA approval (May 2018) provided cases that exemplified important lessons from their initial experiences treating patients with pegvaliase. Key lessons from each case and takeaway points were discussed in both live and virtual meetings.

resultsFifteen cases of adults with PKU (eight males, seven females), representing a spectrum of age (18 to 53 years), previous PKU care, comorbidities, and socioeconomic situations were reviewed and discussed. Full extended case reports are included in the Supplement. The cases showed that treating patients with a daily injectable can be challenging due to a patient's financial problems, treatment challenges, and neuropsychological and psychiatric comorbidities, which can be identified before starting pegvaliase, but do not prohibit successful treatment. The authors agreed that patient education on adverse events (AEs), time to efficacy, dietary changes, and food preparation is an ongoing process that should start prior to initiating pegvaliase treatment. Treatment goals and planned dietary changes once efficacy is reached should be defined prior to treatment initiation and re-evaluated throughout the course of therapy. Each patient's titration schedule and dietary adjustments are unique, depending on occurrence of AEs and individual goals of treatment. Despite the AE profile of pegvaliase, all but two patients remained motivated to continue treatment and achieved efficacy (except one patient in whom titration was still ongoing). AEs occurring early in the treatment pathway may require prolongation of the titration phase and/or concomitant medication use, but do not seem indicative of future tolerability or eventual efficacy. Close follow-up of patients during titration and maintenance to help with dietary changes is important.

conclusionThis case series provides real-world experience on the use of pegvaliase. Until data from registries and independent research become available, the data presented herein can support appropriate management of patients receiving pegvaliase in clinical practice.

Indexed as

ACMG, American College of Medical Genetics and GenomicsAdverse eventsAEs, adverse eventsBH4, tetrahydrobiopterinCase seriesHCP, healthcare providerI/T/M, induction, titration, and maintenancePAH, phenylalanine hydroxylasePegvaliasePEGylated phenylalanine ammonia lyasePhenylketonuriaPhe, phenylalaninePKU dietPKU, phenylketonuria

Identifiers

PMID34430209
PMCPMC8369061
OpenAlexW3193570833

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.