Dose Optimization in Oncology Drug Development: The Emerging Role of Pharmacogenomics, Pharmacokinetics, and Pharmacodynamics.

Author: PapachristosApostolos, PatelJai, PatrinosGeorge P, VasileiouMaria

Paper Details 
Original Abstract of the Article :
Drugs' safety and effectiveness are evaluated in randomized, dose-ranging trials in most therapeutic areas. However, this is only sometimes feasible in oncology, and dose-ranging studies are mainly limited to Phase 1 clinical trials. Moreover, although new treatment modalities (e.g., small molecule ...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296931/

データ提供:米国国立医学図書館(NLM)

Dose Optimization in Oncology: A Journey Through the Sands of Precision Medicine

Cancer treatment is a complex and challenging journey, navigating through the vast desert of drug development and personalized medicine. This study delves into the crucial aspect of dose optimization in oncology, emphasizing the need for precision in tailoring treatment regimens to individual patients. It explores the emerging role of pharmacogenomics, pharmacokinetics, and pharmacodynamics in enhancing treatment efficacy and minimizing adverse effects.

The Quest for Optimal Dosing in Oncology

This study sheds light on the limitations of the traditional Maximum Tolerated Dose (MTD) approach in oncology drug development. The emergence of targeted therapies necessitates a more nuanced approach to dose optimization, considering factors like target saturation limits and therapeutic indices. Researchers are increasingly embracing pharmacogenomics, pharmacokinetics, and pharmacodynamics to personalize treatment and achieve optimal outcomes. These tools provide a deeper understanding of how individual variations in drug metabolism and response can impact treatment efficacy and safety.

Navigating the Desert of Personalized Medicine

The integration of pharmacogenomics, pharmacokinetics, and pharmacodynamics into oncology drug development represents a significant step forward in personalized medicine. By understanding individual patient characteristics and tailoring treatment accordingly, we can improve treatment outcomes and minimize adverse effects. This study emphasizes the need for ongoing research and clinical trials to refine these tools and guide us through the desert of personalized medicine, ensuring that patients receive the most effective and safe treatment possible.

Dr. Camel's Conclusion

This study highlights the need for precision in oncology drug development, emphasizing the vital role of dose optimization. By embracing pharmacogenomics, pharmacokinetics, and pharmacodynamics, we can navigate the desert of personalized medicine, finding the optimal path to effective and safe treatment for each patient. As we continue to explore the vast desert of cancer research, these tools will play an increasingly important role in ensuring that patients receive the best possible care.

Date :
  1. Date Completed n.d.
  2. Date Revised 2023-07-01
Further Info :

Pubmed ID

37370844

DOI: Digital Object Identifier

PMC10296931

SNS
PICO Info
in preparation
Languages

English

Positive IndicatorAn AI analysis index that serves as a benchmark for how positive the results of the study are. Note that it is a benchmark and requires careful interpretation and consideration of different perspectives.

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