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

Published:2021-11-12 Issue: Volume: Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Diebert Nicole¹,Baker Katherine²,Fernández Karen S.³^ORCID

Affiliation:

1. Department of Pharmacy Cancer and Blood Disorders Center, Valley Children's Hospital Madera California USA

2. Hematology/Oncology, Cancer and Blood Disorders Center, Valley Children's Hospital Madera California USA

3. Pediatric Hematology/Oncology, Cancer and Blood Disorders Center, Valley Children's Hospital Madera California USA

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29444

Reference5 articles.

1. Brentuximab vedotin: axonal microtubule’s Apollyon

2. Effects of UGT1A1 genotype on the pharmacokinetics, pharmacodynamics, and toxicities of belinostat administered by 48‐hour continuous infusion in patients with cancer

3. UGT1A1 Guided Cancer Therapy: Review of the Evidence and Considerations for Clinical Implementation

4. UGT1A1 polymorphisms in cancer: impact on irinotecan treatment

5. Novel genetic and epigenetic factors of importance for inter-individual differences in drug disposition, response and toxicity

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1. Comment on: Brentuximab vedotin‐related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?;Pediatric Blood & Cancer;2023-06-26

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