Paper Details 
Original Abstract of the Article :
Label="BACKGROUND" NlmCategory="BACKGROUND">Fluoropyrimidine drugs (such as 5-fluorouracil and capecitabine) are used to treat different types of cancer. However, these drugs may cause severe toxicity in about 10% to 40% of patients. A deficiency in the dihydropyrimidine dehydrogenase (DPD) enzyme, ...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382304/

データ提供:米国国立医学図書館(NLM)

DPYD Genotyping: A Tool for Personalized Fluoropyrimidine Therapy

Fluoropyrimidine drugs, like 5-fluorouracil and capecitabine, are widely used in cancer treatment. However, these medications can cause severe toxicity in some patients. This study examines the role of DPYD genotyping, a genetic test that identifies variants associated with DPD deficiency, in predicting and mitigating the risk of fluoropyrimidine-related toxicity. The researchers conducted a health technology assessment to evaluate the clinical validity, utility, and cost-effectiveness of DPYD genotyping.

DPYD Genotyping: A Guidepost for Personalized Cancer Treatment

The study highlights the potential of DPYD genotyping to personalize fluoropyrimidine therapy. By identifying patients at higher risk of toxicity, DPYD genotyping can guide treatment decisions, allowing for dose adjustments or alternative therapies. It's like having a map of the desert, highlighting areas of potential danger and guiding travelers to safer routes.

Empowering Personalized Cancer Care

DPYD genotyping has the potential to improve the safety and effectiveness of fluoropyrimidine therapy by allowing for personalized treatment strategies. This approach, like a well-stocked oasis, provides the resources and knowledge needed to navigate the complexities of cancer treatment, ensuring a smoother and safer journey for patients.

Dr.Camel's Conclusion

This study emphasizes the importance of personalized medicine in cancer treatment. DPYD genotyping, like a compass guiding a traveler through the desert, can help clinicians personalize fluoropyrimidine therapy, minimizing the risk of toxicity and optimizing treatment outcomes.

Date :
  1. Date Completed 2021-10-28
  2. Date Revised 2022-05-31
Further Info :

Pubmed ID

34484488

DOI: Digital Object Identifier

PMC8382304

Related Literature

SNS
PICO Info
in preparation
Languages

English

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