3.9 Article

Use of amantadine in the evaluation of response to chemotherapy in lung cancer: a pilot study

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FUTURE SCIENCE OA
卷 7, 期 4, 页码 -

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FUTURE SCI LTD
DOI: 10.2144/fsoa-2020-0176

关键词

acetylated amantadine; amantadine; biomarker; lung cancer; response to treatment

资金

  1. Biomark Diagnostics Inc. (BC, Canada)
  2. MaundersMcNeil Foundation (AB, Canada)
  3. University of Manitoba

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The study aims to assess tumor response to therapy by monitoring changes in plasma acetylamantadine concentrations. Results showed a reduction of approximately 32% in responders and an increase of approximately 34% in nonresponders at the 4-hour collection point. Larger-scale studies are needed, but the test could potentially provide an effective tool for assessing treatment response and improving patient management.
Aim: The assessment of tumor response to therapy is of critical importance as it permits for a prospective end point evaluation and provides a guide to clinicians for making future treatment decisions. However, current practices in early evaluation of chemotherapy are insufficient. Amantadine is a substrate for SSAT-1. The present pilot study tests the hypothesis that SSAT-1 activity within the tumor, as measured by plasma acetylamantadine concentrations, can be used to monitor patient response to therapy. Results: In cases with evidence of disease response, there was a reduction in the plasma acetylamantadine concentration at 4 h by approximately 32%. There was a mean increase of approximately 34% at the 4 h collection in the nonresponders. Conclusion: Although large-scale studies are required these findings suggest that the amantadine test could allow for determination of the efficacy of therapeutic interventions earlier, providing an effective test to assess response to treatment and for better management of patients. Lay abstract Aim: It is very important to get early information on the effectiveness of tumor treatment such that clinicians have a better understanding and decide on the next treatment regimen. Current methods are not sufficient to assess whether chemotherapy is effective early during a treatment cycle. We have previously used the presence of the acetylated metabolite of the drug amantadine in urine of patients diagnosed with lung cancer as a biomarker for disease. In the present study, our goal was to test the hypothesis that tumor responsiveness to therapy could be assessed by monitoring changes in the levels of the acetylated form of amantadine in the blood during the course of treatment. Results: In 70% of the patients we were able to relate disease progression or remission/stability to the levels of the acetylated form of amantadine in the blood. Conclusion: Although a larger study with a greater number of patients is required, our test could be used as a simple and effective tool to assess response to treatment and to better tailor treatment of the patient as well as reduce side effects and costs.

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