Comment on: Brentuximab vedotin‐related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?-Reference-Cited by-同舟云学术

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Comment on: Brentuximab vedotin‐related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?

Published:2023-06-26 Issue:11 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Marco Carla¹^ORCID,Padró‐Miquel Ariadna²,Domingo‐Domenech Eva³^ORCID,Velasco Roser¹^ORCID

Affiliation:

1. Neuro‐Oncology Unit Department of Neurology Hospital Universitari de Bellvitge ‐ Institut Català d'Oncologia, IDIBELL L'Hospitalet de Llobregat Barcelona Spain

2. Molecular Genetics Unit, Clinical Laboratory, Hospital Universitari de Bellvitge, IDIBELL L'Hospitalet de Llobregat Barcelona Spain

3. Department of Clinical Hematology Institut Català d'Oncologia Hospital Duran I Reynals, IDIBELL, L'Hospitalet de Llobregat Barcelona Spain

Funder

Instituto de Salud Carlos III

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30527

Reference4 articles.

1. Brentuximab vedotin related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?

2. Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter

3. Brentuximab-Induced Peripheral Neurotoxicity: A Multidisciplinary Approach to Manage an Emerging Challenge in Hodgkin Lymphoma Therapy

4. Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline forUGT1A1and Atazanavir Prescribing

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