Koyi Hirsh, Johansson Leif, From Jesper, Nyrén Sven
1 Department of Respiratory Medicine, Gävle Hospital; Centre for Research and Development Uppsala University, County Council of Gävleborg; and Karolinska Institutet, Stockholm, Sweden ; 2 Department of Pathology, Skåne University Hospital, Lund, Sweden ; 3 AstraZeneca NordicBaltic, Södertälje, Sweden ; 4 Department of Radiology, Solna, Karolinska University Hospital; and Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
J Thorac Dis. 2015 Dec;7(12):2226-33. doi: 10.3978/j.issn.2072-1439.2015.12.52.
Correct diagnosis and staging are required for optimal treatment choice in lung cancer patients. This retrospective, patient medical records study investigated the clinical practice of lung cancer biopsy procedures and testing in Sweden.
Consecutive patients with a recorded inoperable, malignant tumour of bronchus and lung were retrospectively identified at geographically widespread pulmonology clinics (NCT01139619). Data, including diagnostic sampling methodology [bronchoscopy, biopsy by pulmonologist and computed tomography (CT)-guided biopsy], were collected for patients diagnosed between 1 June 2009-31 May 2010, and analysed using descriptive statistics. A study-predefined algorithm, including six criteria on tumour localization and size, forced expiratory volume in one second (FEV1), blood saturation and risk of bleeding theoretically categorizing patient suitability for CT-guided biopsy, was used.
In total, 132 patients (mean age 68 years, 48% women, 61% adenocarcinoma, 86% current/ former smokers, 96% performance status ≤2, mean FEV1 volume ≥2 L) were included. The majority were examined by >1 diagnostic procedure (29% by CT-guided biopsy). Median overall time from first hospital contact to established diagnosis was 12.0 days (10.0 and 28.0 days for bronchoscopy and CT-guided biopsy, respectively). No major differences in lung function, age, performance status or predefined algorithm criteria were noted for patients examined by CT-guided biopsy versus bronchoscopy or biopsy. Complications were reported for 11 patients, including pneumothorax in six patients. Histopathology was used most frequently to diagnose and subtype (70%), although 66% of patients examined solely by bronchoscopy were diagnosed by cytology. For 26.5% of patients, epidermal growth factor receptor (EGFR) mutation testing was recorded.
No limitations regarding patient suitability or methodological complications were noted in this real-life, observational study. The CT-guided biopsy is a relatively safe and well-established method, and may need to be utilized further to fulfil current and future demands for faster diagnosis and high quality tissue as new tumour markers and targeted therapies become available.
肺癌患者的最佳治疗选择需要正确的诊断和分期。这项回顾性患者病历研究调查了瑞典肺癌活检程序和检测的临床实践。
在地理分布广泛的肺病诊所(NCT01139619)对连续记录的患有不可手术的支气管和肺部恶性肿瘤的患者进行回顾性识别。收集了2009年6月1日至2010年5月31日期间确诊患者的数据,包括诊断采样方法[支气管镜检查、肺科医生活检和计算机断层扫描(CT)引导下活检],并使用描述性统计进行分析。使用了一种研究预定义算法,该算法包括关于肿瘤定位和大小、一秒用力呼气量(FEV1)、血氧饱和度和出血风险的六个标准,理论上对患者进行CT引导下活检的适用性进行分类。
总共纳入了132例患者(平均年龄68岁,48%为女性,61%为腺癌,86%为当前/既往吸烟者,96%的体能状态≤2,平均FEV1容积≥2L)。大多数患者接受了>1种诊断程序(29%接受CT引导下活检)。从首次医院接触到确诊的中位总时间为12.0天(支气管镜检查和CT引导下活检分别为10.0天和28.0天)。接受CT引导下活检与支气管镜检查或活检的患者在肺功能、年龄、体能状态或预定义算法标准方面未发现重大差异。11例患者报告了并发症,包括6例气胸。组织病理学最常用于诊断和亚型分类(70%),尽管仅通过支气管镜检查的患者中有66%通过细胞学诊断。26.5%的患者记录了表皮生长因子受体(EGFR)突变检测。
在这项现实生活中的观察性研究中,未发现患者适用性或方法学并发症方面的限制。CT引导下活检是一种相对安全且成熟的方法,随着新的肿瘤标志物和靶向治疗的出现,可能需要进一步利用以满足当前和未来对更快诊断和高质量组织的需求。