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Pegloticase response

MedGen UID:
1236000
Concept ID:
CN575653
Sign or Symptom
Synonym: Krystexxa response
Drug:
Pegloticase
MedGen UID:
390050
Concept ID:
C2350656
Amino Acid, Peptide, or Protein
A recombinant modified mammalian urate oxidase (uricase) conjugated to monomethoxypolyethylene glycol (mPEG), that can be used to lower serum uric acid. Upon intravenous infusion, pegloticase catalyzes the oxidation of uric acid to allantoin, thereby lowering serum uric acid. Allantoin is an inert and water-soluble purine metabolite; it is readily eliminated, primarily by renal excretion. [from NCI]
 
Gene (location): G6PD (Xq28)

Definition

Pegloticase is used to treat the high levels of uric acid associated with refractory gout. The use of pegloticase is reserved for individuals with symptomatic, chronic gout who have not responded to, or are unable to take, conventional gout treatments. Pegloticase is given once every 2 weeks as an intravenous infusion, and is given in a healthcare setting that is prepared to manage infusion reactions and anaphylaxis. Pegloticase is a pegylated urate oxidase – a modified version of the enzyme that catalyzes the oxidation of uric acid to 5-hydroxyisourate and hydrogen peroxide in most mammalian species. However, urate oxidase is not active in humans due to an inactivating mutation in the gene. Subsequent hydrolysis and decarboxylation of 5-hydroxyisourate leads to the formation of a more soluble metabolite (allantoin), which is then excreted by the kidneys. Red blood cells that lack the glucose-6-phosphate dehydrogenase (G6PD) enzyme are sensitive to oxidative damage caused by agents like hydrogen peroxide. Once exposed, the red blood cells become rigid, trapped, and are rapidly broken down (hemolysis). This can lead to a deficiency of mature red blood cells (hemolytic anemia) and the production of red blood cells with abnormally high levels of methemoglobin (methemoglobinemia). Approximately 400 million people worldwide have G6PD deficiency. Most of these individuals are asymptomatic. However, they are at risk of life-threating hemolytic reactions and methemoglobinemia if given oxidizing drugs such as pegloticase. Pegloticase is contraindicated in individuals with G6PD deficiency. The FDA-approved label states that individuals at higher risk for G6PD deficiency should be screened before starting pegloticase therapy, with specific examples including individuals of African, Mediterranean (including Southern European and Middle Eastern), and South Asian ancestry. Importantly, approximately 12% of African-Americans have G6PD deficiency. [from Medical Genetics Summaries]

Professional guidelines

PubMed

Pillinger MH, Mandell BF
Semin Arthritis Rheum 2020 Jun;50(3S):S24-S30. doi: 10.1016/j.semarthrit.2020.04.010. PMID: 32620199
Hamburger M, Baraf HS, Adamson TC 3rd, Basile J, Bass L, Cole B, Doghramji PP, Guadagnoli GA, Hamburger F, Harford R, Lieberman JA 3rd, Mandel DR, Mandelbrot DA, McClain BP, Mizuno E, Morton AH, Mount DB, Pope RS, Rosenthal KG, Setoodeh K, Skosey JL, Edwards NL
Phys Sportsmed 2011 Nov;39(4):98-123. doi: 10.3810/psm.2011.11.1946. PMID: 22293773
Lyseng-Williamson KA
Drugs 2011 Nov 12;71(16):2179-92. doi: 10.2165/11202830-000000000-00000. PMID: 22035516

Curated

Gammal et al, Expanded Clinical Pharmacogenetics Implementation Consortium Guideline for Medication Use in the Context of G6PD Genotype. 2 Sept 2022. Clin Pharmacol Ther.

DailyMed Drug Label, KRYSTEXXA- pegloticase injection, 2021

Recent clinical studies

Etiology

Albert J, Broadwell A, Padnick-Silver L, Marder B, LaMoreaux B
Medicine (Baltimore) 2024 Mar 8;103(10):e37424. doi: 10.1097/MD.0000000000037424. PMID: 38457582Free PMC Article
Botson JK, Saag K, Peterson J, Parikh N, Ong S, La D, LoCicero K, Obermeyer K, Xin Y, Chamberlain J, LaMoreaux B, Verma S, Sainati S, Grewal S, Majjhoo A, Tesser JRP, Weinblatt ME
Arthritis Rheumatol 2023 Feb;75(2):293-304. Epub 2022 Dec 16 doi: 10.1002/art.42335. PMID: 36099211Free PMC Article
Bessen SY, Bessen MY, Yung CM
Semin Arthritis Rheum 2019 Aug;49(1):56-61. Epub 2018 Dec 4 doi: 10.1016/j.semarthrit.2018.11.006. PMID: 30583886

Therapy

Albert J, Broadwell A, Padnick-Silver L, Marder B, LaMoreaux B
Medicine (Baltimore) 2024 Mar 8;103(10):e37424. doi: 10.1097/MD.0000000000037424. PMID: 38457582Free PMC Article
Botson JK, Saag K, Peterson J, Parikh N, Ong S, La D, LoCicero K, Obermeyer K, Xin Y, Chamberlain J, LaMoreaux B, Verma S, Sainati S, Grewal S, Majjhoo A, Tesser JRP, Weinblatt ME
Arthritis Rheumatol 2023 Feb;75(2):293-304. Epub 2022 Dec 16 doi: 10.1002/art.42335. PMID: 36099211Free PMC Article
Botson JK, Peterson J
J Clin Rheumatol 2022 Jan 1;28(1):e129-e134. doi: 10.1097/RHU.0000000000001639. PMID: 33044389Free PMC Article
Keenan RT, Botson JK, Masri KR, Padnick-Silver L, LaMoreaux B, Albert JA, Pillinger MH
Semin Arthritis Rheum 2021 Apr;51(2):347-352. Epub 2021 Jan 27 doi: 10.1016/j.semarthrit.2021.01.005. PMID: 33601190
Bessen SY, Bessen MY, Yung CM
Semin Arthritis Rheum 2019 Aug;49(1):56-61. Epub 2018 Dec 4 doi: 10.1016/j.semarthrit.2018.11.006. PMID: 30583886

Prognosis

Botson JK, Peterson J
J Clin Rheumatol 2022 Jan 1;28(1):e129-e134. doi: 10.1097/RHU.0000000000001639. PMID: 33044389Free PMC Article

Clinical prediction guides

Botson JK, Peterson J
J Clin Rheumatol 2022 Jan 1;28(1):e129-e134. doi: 10.1097/RHU.0000000000001639. PMID: 33044389Free PMC Article

Recent systematic reviews

Keenan RT, Botson JK, Masri KR, Padnick-Silver L, LaMoreaux B, Albert JA, Pillinger MH
Semin Arthritis Rheum 2021 Apr;51(2):347-352. Epub 2021 Jan 27 doi: 10.1016/j.semarthrit.2021.01.005. PMID: 33601190

Therapeutic recommendations

From Medical Genetics Summaries

This section contains excerpted 1 information on gene-based dosing recommendations. Neither this section nor other parts of this review contain the complete recommendations from the sources.

2020 Statement from the US Food and Drug Administration (FDA):

Contraindications: Glucose-6-phosphate dehydrogenase (G6PD) deficiency

[...]

Life threatening hemolytic reactions and methemoglobinemia have been reported with pegloticase in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency. Because of the risk of hemolysis and methemoglobinemia, do not administer pegloticase to patients with G6PD deficiency. Screen patients at risk for G6PD deficiency prior to starting pegloticase. For example, patients of African, Mediterranean (including Southern European and Middle Eastern), and Southern Asian ancestry are at increased risk for G6PD deficiency.

Please review the complete therapeutic recommendations that are located here: (1).

1 The FDA labels specific drug formulations. We have substituted the generic names for any drug labels in this excerpt. The FDA may not have labeled all formulations containing the generic drug.

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

    • PubMed
      See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Curated

    • CPIC, 2022
      Gammal et al, Expanded Clinical Pharmacogenetics Implementation Consortium Guideline for Medication Use in the Context of G6PD Genotype. 2 Sept 2022. Clin Pharmacol Ther.
    • DailyMed Drug Label, 2021
      DailyMed Drug Label, KRYSTEXXA- pegloticase injection, 2021

    Consumer resources

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