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在不明原发癌的诊断和治疗中应用即时检测基因组分析的可行性。

Feasibility of Point-of-Care Genomic Profiling in the Diagnosis and Treatment of Cancer of Unknown Primary.

机构信息

Medical Oncology Training Program, Department of Medicine, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Department of Laboratory Medicine, William Osler Health System, Brampton, ON, Canada.

出版信息

Oncologist. 2023 Jun 2;28(6):474-478. doi: 10.1093/oncolo/oyad054.

Abstract

INTRODUCTION

Cancer of unknown primary remains a challenging clinical entity. Despite receiving empiric chemotherapy, median overall survival is approximately 6-12 months. Site-specific therapy based on molecular characterization has been shown to improve outcomes; however, feasibility outside of clinical trials, especially in community centers, is lacking. This study explores the application of rapid next-generation sequencing in defining cancer of unknown primary and to identify therapeutic biomarkers.

METHODS

A retrospective chart review was performed by identifying pathological samples designated cancer of unknown primary. Next-generation sequencing testing was based on an automated workflow utilizing the Genexus integrated sequencer, validated for clinical use. Genomic profiling was further integrated within a routine immunohistochemistry service, with results reported directly by anatomic pathologists.

RESULTS

Between October 2020 and October 2021, 578 solid tumor samples underwent genomic profiling. Among this cohort, 40 were selected based on an initial diagnosis of cancer of unknown primary. The median (range) age at diagnosis was 70 (42-85) and 23 (57%) were female. Genomic data were used to support a site-specific diagnosis in 6 patients (15%). Median turnaround time was 3 business days (IQR: 1-5). Most common alterations identified were KRAS (35%), CDKN2A (15%), TP53 (15%), and ERBB2 (12%). Actionable molecular targeted therapies were identified in 23 (57%) patients, including alterations in BRAF, CDKN2A, ERBB2, FGFR2, IDH1, and KRAS. Immunotherapy-sensitizing mismatch repair deficiency was identified in 1 patient.

CONCLUSION

This study supports the adoption of rapid next-generation sequencing among patients with cancer of unknown primary. We also demonstrate the feasibility of integration of genomic profiling with diagnostic histopathology and immunohistochemistry in a community practice setting. Diagnostic algorithms incorporating genomic profiling to better define cancer of unknown primary should be considered for future study.

摘要

介绍

不明原发灶癌仍然是一种具有挑战性的临床实体。尽管接受了经验性化疗,中位总生存期仍约为 6-12 个月。基于分子特征的靶向治疗已被证明可以改善预后;然而,临床试验以外的可行性,尤其是在社区中心,仍然缺乏。本研究探讨了快速下一代测序在确定不明原发灶癌中的应用,并确定治疗生物标志物。

方法

通过确定指定为不明原发灶癌的病理样本,进行回顾性图表审查。下一代测序测试基于使用 Genexus 集成测序仪的自动化工作流程,该流程已通过临床验证。基因组分析进一步整合到常规免疫组织化学服务中,由解剖病理学家直接报告结果。

结果

在 2020 年 10 月至 2021 年 10 月期间,578 个实体瘤样本进行了基因组分析。在该队列中,根据最初诊断为不明原发灶癌,选择了 40 个样本。诊断时的中位(范围)年龄为 70 岁(42-85 岁),23 名(57%)为女性。基因组数据用于支持 6 名患者(15%)的特定部位诊断。中位周转时间为 3 个工作日(IQR:1-5)。最常见的改变是 KRAS(35%)、CDKN2A(15%)、TP53(15%)和 ERBB2(12%)。在 23 名(57%)患者中确定了可采取的分子靶向治疗,包括 BRAF、CDKN2A、ERBB2、FGFR2、IDH1 和 KRAS 的改变。在 1 名患者中发现了免疫治疗致敏的错配修复缺陷。

结论

本研究支持在不明原发灶癌患者中采用快速下一代测序。我们还证明了在社区实践环境中,将基因组分析与诊断组织病理学和免疫组织化学相结合的可行性。应考虑纳入基因组分析的诊断算法,以更好地确定不明原发灶癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3208/10243757/8fd153466f77/oyad054_fig1.jpg

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