de Fonseka Duneesha, Underwood Wendy, Stadon Louise, Rahman Najib, Edey Anthony, Rogers Chris, Maskell Nick A
Academic Respiratory Unit, University of Bristol, Bristol, UK.
Clinical Trials and Evaluation Unit, University of Bristol, Bristol, UK.
BMJ Open Respir Res. 2018 Feb 19;5(1):e000270. doi: 10.1136/bmjresp-2017-000270. eCollection 2018.
Pleural malignancy, particularly malignant pleural mesothelioma (MPM) is increasing in incidence due to the long latency period from exposure to asbestos to development of the disease. MPM can be challenging to diagnose. For patients presenting without a pleural effusion, CT-guided biopsy remains the primary choice of biopsy, but the diagnostic sensitivity of this investigation is 70%-75%. Therefore, a proportion of patients will go on to require further biopsies. If the first biopsy is non-diagnostic, the chances of further non-diagnostic biopsies are high in MPM.
Target is a multicentre randomised controlled trial, aiming to recruit 78 patients over a 30-month period, from 10 centres in the UK. Patients will be randomised to either the standard arm which is a second CT-guided biopsy, or the interventional arm, a positron emission tomography-CT scan followed by a targeted CT-guided biopsy. Patients will be followed up for 12 months (patients recruited in the last 6 months of recruitment will have 6 months of follow-up). MPM biomarker mesothelin will be checked at baseline, 6 month and 12 month follow-up appointments where patients are able to attend these appointments.
Ethical approval for this trial was granted by the South West-Exeter research and ethics committee (reference number 15/SW/0156). Results of the trial will be published in a peer-reviewed journal and presented at an international conference.
ISRCTN 14024829; Pre-results.
由于从接触石棉到发病存在较长的潜伏期,胸膜恶性肿瘤,尤其是恶性胸膜间皮瘤(MPM)的发病率正在上升。MPM的诊断可能具有挑战性。对于没有胸腔积液的患者,CT引导下活检仍然是活检的主要选择,但这项检查的诊断敏感性为70%-75%。因此,一部分患者将需要进一步活检。如果首次活检未能确诊,MPM患者再次活检仍无法确诊的可能性很高。
“靶向”是一项多中心随机对照试验,旨在在30个月内从英国的10个中心招募78名患者。患者将被随机分为标准组(即第二次CT引导下活检)或干预组(正电子发射断层扫描-CT扫描,然后进行靶向CT引导下活检)。患者将接受12个月的随访(在招募的最后6个月招募的患者将有6个月的随访)。MPM生物标志物间皮素将在基线、6个月和12个月的随访预约时检查,前提是患者能够参加这些预约。
该试验已获得西南埃克塞特研究与伦理委员会的伦理批准(参考编号15/SW/0156)。试验结果将发表在同行评审期刊上,并在国际会议上展示。
ISRCTN 14024829;预结果。