欧洲学术中心针对上消化道癌症实施精准医疗的当前做法和挑战:EORTC 调查

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摘要

背景精准肿瘤学在管理胃肠道癌症患者方面的发展势头日益强劲。材料与方法来自欧洲 41 家机构的 45 名肿瘤学专家完成了由欧洲癌症研究和治疗组织(EORTC)胃肠道癌症工作组个性化医学工作组设计的调查,提供了有关胃肠道癌症患者的分子检测、时机、靶向治疗的可用性、资金来源以及分子肿瘤委员会(MTB)的使用情况。结果大多数中心都对人类表皮生长因子受体 2(HER2,100%)、程序性死亡配体 1(PD-L1,89%)和 DNA 错配修复(MMR,91%)进行了常规检测。肿瘤组织上的综合基因面板经常被使用,尤其是在胆道癌中,几乎所有中心都将其纳入了常规实践。血液测序的应用越来越广泛,半数中心在循环肿瘤DNA分析中采用了综合基因检测。76%的中心定期进行MTB,主要采用基于ESMO分子靶点临床可操作性量表(ESCAT)的组织分子改变建议。然而,将基因组信息转化为处方治疗的工作仍然有限,大多数中心报告的综合基因检测后分子分层治疗决策的比例为 25%。尽管分子检测已被广泛采用并实施了 MTB,但仍需进一步努力将个性化医疗优化整合到临床实践中。
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Current practices and challenges in implementing precision medicine for upper gastrointestinal cancers in European academic centers: an EORTC survey

Background

Precision oncology is gaining momentum in managing patients with gastrointestinal cancers. This study examines the implementation of personalized medicine technologies in upper gastrointestinal (UGI) oncology across European academic centers.

Material and methods

Forty-five oncology specialists from 41 European institutions completed a survey designed by the Personalized Medicine Task Force of the European Organization of Research and Treatment of Cancer (EORTC) Gastrointestinal Tract Cancer Working Group, providing insights into molecular testing, timing, availability of targeted therapies, funding sources, and utilization of molecular tumor boards (MTBs) for patients with UGI cancers. Frequencies and percentages were calculated.

Results

Routine testing for human epidermal growth factor receptor 2 (HER2, 100%), programmed death-ligand 1 (PD-L1, 89%), and DNA mismatch repair (MMR, 91%) is implemented in most centers. Comprehensive gene panels on tumor tissue are frequently utilized, especially in biliary tract cancer, with almost all centers incorporating them into routine practice. Blood-based sequencing is increasingly employed, and half of centers carry out comprehensive gene panels for circulating tumor DNA analyses. MTBs are regularly held in 76% of centers, predominantly utilizing ESMO Scale for Clinical Actionability of molecular Targets (ESCAT)-based recommendations for tissue molecular alterations. The translation of genomic information into prescribed treatments remains limited, however, with the majority of centers reporting ∼25% of molecularly stratified treatment decisions following comprehensive genetic testing.

Conclusion

This survey provides important insights into current personalized medicine practice in European academic clinical centers for UGI oncology. Despite widespread adoption of molecular testing and implementation of MTBs, further efforts are needed to optimize the integration of personalized medicine into clinical practice.

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