The Impact of Cytotoxic T-lymphocyte Antigen-4 Genetic Polymorphisms on the Effectiveness of Ipilimumab and Patients’ Outcome in Melanoma

M. Omer, Peter S Kanjo, Abuzar Elkhazeen, Amin S Osman
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Abstract

Precision medicine is shaping the way medicine is being practiced, pharmacogenomics is the centerpiece of precision medicine. As in several fields, researchers are investigating the role of pharmacogenomic tests in the treatment of melanoma. One of these efforts is the ongoing preclinical and clinical trials investigating the impact of the genetic polymorphism of cytotoxic T-lymphocyte antigen-4 on drugs used in melanoma treatment. This paper reviews ipilimumab as a promising treatment for melanoma and how pharmacogenomic tests can substantially impact utilizing this drug in the treatment plan, whether as a solo treatment or in conjugation with other therapies. In this review, various databases and electronic libraries were utilized to search for and review different journal articles and papers about pharmacogenomic tests for ipilimumab. Although some results showed a minimal effect, most of the results revealed that pharmacogenomic tests for ipilimumab could play a crucial role in patients’ outcomes. Further clinical trials are, however, needed on a larger scale to adopt this therapy in practice.
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细胞毒性t淋巴细胞抗原-4基因多态性对伊匹单抗疗效和黑色素瘤患者预后的影响
精准医学正在塑造医学实践的方式,药物基因组学是精准医学的核心。与其他领域一样,研究人员正在研究药物基因组学测试在黑色素瘤治疗中的作用。这些努力之一是正在进行的临床前和临床试验,研究细胞毒性t淋巴细胞抗原-4的遗传多态性对黑色素瘤治疗药物的影响。本文回顾了ipilimumab作为黑色素瘤的一种有前景的治疗方法,以及药物基因组学测试如何在治疗计划中实质性地影响这种药物的利用,无论是作为单独治疗还是与其他治疗结合。在这篇综述中,我们利用各种数据库和电子图书馆来检索和回顾关于易普利姆单抗药物基因组学测试的不同期刊文章和论文。尽管一些结果显示影响很小,但大多数结果表明,易普利姆单抗的药物基因组学测试可能在患者预后中发挥关键作用。然而,为了在实践中采用这种疗法,还需要进一步的大规模临床试验。
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