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推进哥伦比亚的癌症护理:首次全面基因组分析原位实施的结果

Advancing Cancer Care in Colombia: Results of the First In Situ Implementation of Comprehensive Genomic Profiling.

作者信息

López Rivera Juan Javier, Rueda-Gaitán Paula, Rios Pinto Laura Camila, Rodríguez Gutiérrez Diego Alejandro, Gomez-Lopera Natalia, Lamilla Julian, Rojas Aguirre Fabio Andrés, Bernal Vaca Laura, Isaza-Ruget Mario Arturo

机构信息

Laboratorio Clínico Especializado, Clínica Universitaria Colombia, Clínica Colsanitas, Bogotá 111321, Colombia.

Grupo de Genética Médica, Clínica Universitaria Colombia, Clínica Colsanitas, Bogotá 111321, Colombia.

出版信息

J Pers Med. 2024 Sep 14;14(9):975. doi: 10.3390/jpm14090975.

Abstract

BACKGROUND

Comprehensive genomic profiling (CGP) identifies genetic alterations and patterns that are crucial for therapy selection and precise treatment development. In Colombia, limited access to CGP tests underscores the necessity of documenting the prevalence of treatable genetic alterations. This study aimed to describe the somatic genetic profile of specific cancer types in Colombian patients and assess its impact on treatment selection.

METHODS

A retrospective cohort study was conducted at Clínica Colsanitas S.A. from March 2023 to June 2024. Sequencing was performed on the NextSeq2000 platform with the TruSight Oncology 500 (TSO500) assay, which simultaneously evaluates 523 genes for DNA analysis and 55 for RNA; additionally, analyses were performed with the SOPHiA DDM software. The tumor mutational burden (TMB), microsatellite instability (MSI), and programmed cell death ligand 1 (PDL1) were assessed.

RESULTS

Among 111 patients, 103 were evaluated, with gastrointestinal (27.93%), respiratory (13.51%), and central nervous system cancers (10.81%) being the most prevalent. TP53 (37%), KMT2C (28%), and KRAS (21%) were frequent mutations. Actionable findings were detected in 76.7% of cases, notably in digestive (20 patients) and lung cancers (8 patients). MSI was stable at 82.52% and high at 2.91%, whilst TMB was predominantly low (91.26%).

CONCLUSIONS

The test has facilitated access to targeted therapies, improving clinical outcomes in Colombian patients. This profiling test is expected to increase opportunities for personalized medicine in Colombia.

摘要

背景

综合基因组分析(CGP)可识别对治疗选择和精准治疗方案制定至关重要的基因改变和模式。在哥伦比亚,CGP检测的获取机会有限,这凸显了记录可治疗基因改变患病率的必要性。本研究旨在描述哥伦比亚患者特定癌症类型的体细胞基因图谱,并评估其对治疗选择的影响。

方法

于2023年3月至2024年6月在Clínica Colsanitas S.A.进行了一项回顾性队列研究。使用TruSight Oncology 500(TSO500)检测在NextSeq2000平台上进行测序,该检测可同时评估523个用于DNA分析的基因和55个用于RNA的基因;此外,还使用SOPHiA DDM软件进行分析。评估了肿瘤突变负荷(TMB)、微卫星不稳定性(MSI)和程序性细胞死亡配体1(PDL1)。

结果

在111名患者中,对103名进行了评估,其中胃肠道癌(27.93%)、呼吸道癌(13.51%)和中枢神经系统癌(10.81%)最为常见。TP53(37%)、KMT2C(28%)和KRAS(21%)是常见突变。在76.7%的病例中检测到可采取行动的发现,尤其是在消化道癌(20例患者)和肺癌(8例患者)中。MSI稳定的占82.52%,高度不稳定的占2.91%,而TMB主要较低(91.26%)。

结论

该检测有助于获得靶向治疗,改善了哥伦比亚患者的临床结局。预计这种基因图谱检测将增加哥伦比亚个性化医疗的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d266/11433056/cf83cb781097/jpm-14-00975-g001.jpg

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