Expert recommendations for biomarker evaluation of advanced non-small cell lung cancer in Thailand.

IF 3.5 2区 医学 Q2 ONCOLOGY
Translational lung cancer research Pub Date : 2025-07-31 Epub Date: 2025-07-28 DOI:10.21037/tlcr-2025-201
Shanop Shuangshoti, Naiyarat Prasongsook, Lucksamon Thamlikitkul, Thanyanan Reungwetwattana, Naravat Poungvarin, Artit Jinawath, Chinachote Teerapakpinyo, Songkhun Vinyuvat, Virote Sriuranpong
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引用次数: 0

Abstract

Background: Growing understanding of the heterogenous molecular profiles of non-small cell lung cancer (NSCLC) has led to changes in the treatment landscape of advanced NSCLC towards precision medicine to target actionable gene alterations. Practical barriers, such as lack of awareness/understanding of biomarkers, suboptimal quality or sample management, inappropriate use of biomarker testing results, limited patient access to biomarker tests and targeted treatments, and reimbursement/payment challenges, hinder the wider adoption of guideline-recommended biomarker testing. Limited reimbursement of targeted therapies is a key consideration for Thai oncologists when making a treatment choice for their patients with advanced NSCLC in Thailand. We aim to assess the current state of biomarker testing and treatment for advanced NSCLC in Thailand and provide recommendations to facilitate timely access to appropriate therapies, enhance patient quality of life, and optimize the use of Thailand's existing healthcare schemes.

Methods: The expert panel comprising one clinical pathologist, three anatomic pathologists, one molecular geneticist, and four medical oncologists convened to review recent literature, discuss current clinical practice, and prioritize essential topics for biomarker assessment and management of advanced NSCLC in Thailand. Following the meeting, further discussions on these prioritized topics were conducted via email, and the recommendations were developed.

Results: Our recommendations include adopting an exclusionary strategy for biomarker testing, emphasizing the role of a multidisciplinary team (MDT) in managing patients with advanced NSCLC, and underscoring the importance of laboratory accreditation and external quality assurance programs. Additionally, we highlight the need for high-quality data on the local impact of novel treatments to assist policymakers in making these therapies accessible to suitable patients.

Conclusions: By proposing practical strategies tailored to our local healthcare setting, such as exclusionary biomarker testing approach, MDT involvement, and robust quality assurance measures, we provide a roadmap for improving the diagnosis and treatment of advanced NSCLC.

泰国晚期非小细胞肺癌生物标志物评估专家建议。
背景:对非小细胞肺癌(NSCLC)异质性分子谱的理解不断加深,导致晚期NSCLC的治疗领域发生了变化,朝着靶向可操作基因改变的精准医学方向发展。缺乏对生物标志物的认识/理解、质量或样品管理欠佳、生物标志物检测结果使用不当、患者获得生物标志物检测和靶向治疗的机会有限以及报销/支付方面的挑战等实际障碍阻碍了指南推荐的生物标志物检测的广泛采用。靶向治疗的有限报销是泰国肿瘤学家在为晚期非小细胞肺癌患者选择治疗方案时的一个关键考虑因素。我们的目标是评估泰国晚期NSCLC生物标志物检测和治疗的现状,并提供建议,以促进及时获得适当的治疗,提高患者的生活质量,并优化泰国现有医疗保健计划的使用。方法:由一名临床病理学家、三名解剖病理学家、一名分子遗传学家和四名医学肿瘤学家组成的专家小组回顾了最近的文献,讨论了当前的临床实践,并优先考虑了泰国晚期NSCLC生物标志物评估和管理的基本主题。会议结束后,通过电子邮件就这些优先议题进行了进一步讨论,并提出了建议。结果:我们的建议包括采用生物标志物检测的排他性策略,强调多学科团队(MDT)在管理晚期非小细胞肺癌患者中的作用,并强调实验室认证和外部质量保证计划的重要性。此外,我们强调需要关于新疗法在当地影响的高质量数据,以帮助政策制定者使这些疗法适用于合适的患者。结论:通过提出适合我们当地医疗环境的实用策略,如排他性生物标志物检测方法、MDT参与和强有力的质量保证措施,我们为改善晚期NSCLC的诊断和治疗提供了路线图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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