Department of Pathology, Brigham & Women's Hospital, Boston, MA 02115-6110, USA.
Arch Pathol Lab Med. 2013 Jun;137(6):828-60. doi: 10.5858/arpa.2012-0720-OA. Epub 2013 Apr 3.
To establish evidence-based recommendations for the molecular analysis of lung cancers that are required to guide EGFR- and ALK-directed therapies, addressing which patients and samples should be tested, and when and how testing should be performed.
Three cochairs without conflicts of interest were selected, one from each of the 3 sponsoring professional societies: College of American Pathologists, International Association for the Study of Lung Cancer, and Association for Molecular Pathology. Writing and advisory panels were constituted from additional experts from these societies.
Three unbiased literature searches of electronic databases were performed to capture articles published from January 2004 through February 2012, yielding 1533 articles whose abstracts were screened to identify 521 pertinent articles that were then reviewed in detail for their relevance to the recommendations. Evidence was formally graded for each recommendation.
Initial recommendations were formulated by the cochairs and panel members at a public meeting. Each guideline section was assigned to at least 2 panelists. Drafts were circulated to the writing panel (version 1), advisory panel (version 2), and the public (version 3) before submission (version 4).
The 37 guideline items address 14 subjects, including 15 recommendations (evidence grade A/B). The major recommendations are to use testing for EGFR mutations and ALK fusions to guide patient selection for therapy with an epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) inhibitor, respectively, in all patients with advanced-stage adenocarcinoma, regardless of sex, race, smoking history, or other clinical risk factors, and to prioritize EGFR and ALK testing over other molecular predictive tests. As scientific discoveries and clinical practice outpace the completion of randomized clinical trials, evidence-based guidelines developed by expert practitioners are vital for communicating emerging clinical standards. Already, new treatments targeting genetic alterations in other, less common driver oncogenes are being evaluated in lung cancer, and testing for these may be addressed in future versions of these guidelines.
为指导表皮生长因子受体(EGFR)和间变性淋巴瘤激酶(ALK)靶向治疗,建立肺癌分子分析的循证推荐意见,确定应检测哪些患者和样本,以及何时以及如何进行检测。
从三个发起专业协会(美国病理学家学院、国际肺癌研究协会和分子病理学会)中各选出一名无利益冲突的主席,三人共同担任主席。还从这些协会的其他专家中组建了写作和顾问小组。
对电子数据库进行了三次无偏见的文献检索,以捕获 2004 年 1 月至 2012 年 2 月期间发表的文章,共获得 1533 篇摘要进行筛选,确定了 521 篇相关文章,然后详细审查这些文章与建议的相关性。为每项建议正式分级证据。
主席和小组成员在一次公开会议上制定了初步建议。每个指南部分至少分配给两名小组成员。草案在提交前分发给写作小组(版本 1)、顾问小组(版本 2)和公众(版本 3)(版本 4)。
37 条指南项目涵盖 14 个主题,包括 15 条建议(证据等级 A/B)。主要建议是在所有晚期肺腺癌患者中,无论性别、种族、吸烟史或其他临床危险因素如何,使用 EGFR 突变和 ALK 融合检测分别指导表皮生长因子受体(EGFR)或间变性淋巴瘤激酶(ALK)抑制剂的治疗选择,并将 EGFR 和 ALK 检测优先于其他分子预测性检测。随着科学发现和临床实践的步伐超过随机临床试验的完成,由专家从业者制定的循证指南对于传达新兴临床标准至关重要。针对其他较少见驱动致癌基因的遗传改变的新治疗方法正在肺癌中进行评估,未来版本的这些指南可能会解决这些检测问题。