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Review
. 2021 Jan 5:13:13345-13355.
doi: 10.2147/OTT.S279998. eCollection 2020.

Individualized Management of Blood Concentration in Patients with Gastrointestinal Stromal Tumors

Affiliations
Review

Individualized Management of Blood Concentration in Patients with Gastrointestinal Stromal Tumors

Hao Xu et al. Onco Targets Ther. .

Abstract

Gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumor, and surgical resection is the first choice for the treatment of the disease, but since the advent of tyrosine kinase inhibitors (TKIs) such as imatinib (IM), the prognosis of the disease has undergone revolutionary changes. According to the current version of the guidelines, most GIST patients receive a fixed dose without taking into account their own individual differences, resulting in a wide difference in blood concentration, adverse reactions and prognosis. With more studies on the relationship between blood drug concentrations and prognosis, the concept of individualized therapy has been paid more attention by researchers. Therapeutic drug monitoring (TDM) has also been made available for the research field of GIST targeted therapy. How to reduce the incidence of drug resistance and adverse reactions in patients with GISTs has become the focus of the current research. This article reviews the common monitoring methods and timing of TKIs blood concentration, the reasonable range of blood drug concentration, the toxic or adverse effects caused by high blood drug concentration, some possible factors affecting blood drug concentration and recent research progress, in order to discuss and summarize the treatment strategy of individual blood drug concentration, improve the prognosis of patients and reduce the adverse effects as much as possible.

Keywords: GIST; TDM; imatinib; sunitinib; targeted therapy; therapeutic drug monitoring.

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Conflict of interest statement

The authors report no conflicts of interest for this work and declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

Figure 1
Figure 1
Recommended blood drug monitoring flow chart.

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