Next-generation sequencing in cancer diagnosis and treatment: clinical applications and future directions

被引:3
作者
Ghoreyshi, Nima [1 ]
Heidari, Reza [1 ]
Farhadi, Arezoo [2 ]
Chamanara, Mohsen [3 ,4 ]
Farahani, Nastaran [5 ]
Vahidi, Mahmood [1 ,6 ]
Behroozi, Javad [1 ,7 ]
机构
[1] AJA Univ Med Sci, Canc Epidemiol Res Ctr, Tehran, Iran
[2] Zanjan Univ Med Sci, Sch Med, Dept Genet & Mol Med, Zanjan, Iran
[3] AJA Univ Med Sci, Fac Med, Dept Clin Pharm, Tehran, Iran
[4] AJA Univ Med Sci, Toxicol Res Ctr, Tehran, Iran
[5] Islamic Azad Univ, Fac Life Sci, Dept Genet & Biotechnol, Varamin Pishva Branch, Varamin, Iran
[6] AJA Univ Med Sci, Sch Allied Hlth Med, Dept Med Lab Sci, Tehran, Iran
[7] Tarbiat Modares Univ, Fac Med Sci, Dept Med Genet, Tehran, Iran
关键词
Next-generation sequencing; Cancer diagnosis; Precision oncology; Genomic profiling; Biomarkers; Cancer treatment; ACUTE LYMPHOBLASTIC-LEUKEMIA; MINIMAL RESIDUAL DISEASE; CIRCULATING TUMOR DNA; III COLON-CANCER; LIQUID BIOPSY; BREAST-CANCER; LUNG-CANCER; RISK STRATIFICATION; PRECISION MEDICINE; SOMATIC MUTATIONS;
D O I
10.1007/s12672-025-01816-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Next-generation sequencing (NGS) has emerged as a pivotal technology in the field of oncology, transforming the approach to cancer diagnosis and treatment. This paper provides a comprehensive overview of the integration of NGS into clinical settings, emphasizing its significant contributions to precision medicine. NGS enables detailed genomic profiling of tumors, identifying genetic alterations that drive cancer progression and facilitating personalized treatment plans targeting specific mutations, thereby improving patient outcomes. This capability facilitates the development of personalized treatment plans targeting specific mutations, leading to improved patient outcomes and the potential for better prognosis. The application of NGS extends beyond identifying actionable mutations; it is instrumental in detecting hereditary cancer syndromes, thus aiding in early diagnosis and preventive strategies. Furthermore, NGS plays a crucial role in monitoring minimal residual disease, offering a sensitive method to detect cancer recurrence at an early stage. Its use in guiding immunotherapy by identifying biomarkers that predict response to treatment is also highlighted. Ethical issues related to genetic testing, such as concerns around patient consent and data privacy, are also important considerations that need to be addressed for the broader implementation of NGS. These include the complexities of data interpretation, the need for robust bioinformatics support, cost considerations, and ethical issues related to genetic testing. Addressing these challenges is essential for the widespread adoption of NGS. Looking forward, advancements such as single-cell sequencing and liquid biopsies promise to further enhance the precision of cancer diagnostics and treatment. This review emphasizes the transformative impact of NGS in oncology and advocates for its incorporation into routine clinical practice to promote molecularly driven cancer care.
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页数:20
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