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PIT方案:一项针对恶性胸膜间皮瘤患者在进行有创胸壁干预后对术区进行预防性放疗的III期试验。

Protocol for PIT: a phase III trial of prophylactic irradiation of tracts in patients with malignant pleural mesothelioma following invasive chest wall intervention.

作者信息

Bayman N, Ardron D, Ashcroft L, Baldwin D R, Booton R, Darlison L, Edwards J G, Lang-Lazdunski L, Lester J F, Peake M, Rintoul R C, Snee M, Taylor P, Lunt C, Faivre-Finn C

机构信息

Department of Clinical Oncology, The Christie NHS Foundation Trust, Manchester, UK.

The National Cancer Research Institute (NCRI) Consumer Liaison Group, London, UK.

出版信息

BMJ Open. 2016 Jan 27;6(1):e010589. doi: 10.1136/bmjopen-2015-010589.

Abstract

INTRODUCTION

Histological diagnosis of malignant mesothelioma requires an invasive procedure such as CT-guided needle biopsy, thoracoscopy, video-assisted thorascopic surgery (VATs) or thoracotomy. These invasive procedures encourage tumour cell seeding at the intervention site and patients can develop tumour nodules within the chest wall. In an effort to prevent nodules developing, it has been widespread practice across Europe to irradiate intervention sites postprocedure--a practice known as prophylactic irradiation of tracts (PIT). To date there has not been a suitably powered randomised trial to determine whether PIT is effective at reducing the risk of chest wall nodule development.

METHODS AND ANALYSIS

In this multicentre phase III randomised controlled superiority trial, 374 patients who can receive radiotherapy within 42 days of a chest wall intervention will be randomised to receive PIT or no PIT. Patients will be randomised on a 1:1 basis. Radiotherapy in the PIT arm will be 21 Gy in three fractions. Subsequent chemotherapy is given at the clinicians' discretion. A reduction in the incidence of chest wall nodules from 15% to 5% in favour of radiotherapy 6 months after randomisation would be clinically significant. All patients will be followed up for up to 2 years with monthly telephone contact and at least four outpatient visits in the first year.

ETHICS AND DISSEMINATION

PIT was approved by NRES Committee North West-Greater Manchester West (REC reference 12/NW/0249) and recruitment is currently on-going, the last patient is expected to be randomised by the end of 2015. The analysis of the primary end point, incidence of chest wall nodules 6 months after randomisation, is expected to be published in 2016 in a peer reviewed journal and results will also be presented at scientific meetings and summary results published online. A follow-up analysis is expected to be published in 2018.

TRIAL REGISTRATION NUMBER

ISRCTN04240319; NCT01604005; Pre-results.

摘要

引言

恶性间皮瘤的组织学诊断需要进行侵入性操作,如CT引导下针吸活检、胸腔镜检查、电视辅助胸腔镜手术(VATS)或开胸手术。这些侵入性操作会促使肿瘤细胞在干预部位播散,患者可能会在胸壁出现肿瘤结节。为了防止结节形成,在欧洲,术后对干预部位进行照射已成为普遍做法——这种做法称为术道预防性照射(PIT)。迄今为止,尚未有一项样本量足够的随机试验来确定PIT是否能有效降低胸壁结节形成的风险。

方法与分析

在这项多中心III期随机对照优势试验中,374名在胸壁干预后42天内可接受放疗的患者将被随机分为接受PIT组或不接受PIT组。患者将按1:1的比例随机分组。PIT组的放疗剂量为21 Gy,分三次给予。后续化疗由临床医生酌情决定。随机分组6个月后,胸壁结节发生率从15%降至5%且有利于放疗,这在临床上将具有显著意义。所有患者将接受长达2年的随访,每月通过电话联系,第一年至少进行4次门诊就诊。

伦理与传播

PIT已获得西北大曼彻斯特西部国家研究伦理服务委员会(REC编号12/NW/0249)的批准,目前正在招募患者,预计最后一名患者将在2015年底随机分组。对主要终点(随机分组6个月后胸壁结节的发生率)的分析预计将于2016年发表在同行评审期刊上,结果也将在科学会议上公布,总结结果将在线发表。预计2018年将发表随访分析结果。

试验注册号

ISRCTN04240319;NCT01604005;预结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6369/4735163/958c5ca512a2/bmjopen2015010589f01.jpg

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