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基于(18)F-FDG-PET的策略对优化喉癌放疗后疑似复发病例诊断流程的有效性:RELAPS多中心随机试验

Effectiveness of an (18)F-FDG-PET based strategy to optimize the diagnostic trajectory of suspected recurrent laryngeal carcinoma after radiotherapy: The RELAPS multicenter randomized trial.

作者信息

de Bree Remco, van der Putten Lisa, van Tinteren Harm, Wedman Jan, Oyen Wim J G, Janssen Luuk M, van den Brekel Michiel W M, Comans Emile F I, Pruim Jan, Takes Robert P, Hobbelink Monique G G, Valdés Olmos Renato, van der Laan Bernard F A M, Boers Maarten, Hoekstra Otto S, Leemans C René

机构信息

Department of Otolaryngology - Head and Neck Surgery, VU University Medical Center, Amsterdam, The Netherlands; Department of Head and Neck Surgical Oncology, UMC Utrecht Cancer Center, University Medical Center Utrecht, The Netherlands.

Department of Otolaryngology - Head and Neck Surgery, VU University Medical Center, Amsterdam, The Netherlands.

出版信息

Radiother Oncol. 2016 Feb;118(2):251-6. doi: 10.1016/j.radonc.2015.10.010. Epub 2015 Oct 20.

Abstract

PURPOSE

The purpose of this study is to evaluate the efficacy of (18)F-FDG-PET as first-line diagnostic investigation, prior to performing a direct laryngoscopy with biopsy under general anesthesia, in patients suspected of recurrent laryngeal carcinoma after radiotherapy.

PATIENTS AND METHODS

150 patients suspected of recurrent T2-4 laryngeal carcinoma at least two months after prior (chemo)radiotherapy with curative intent for resectable disease were randomized to direct laryngoscopy (CWU: conventional workup strategy) or to (18)F-FDG-PET only followed by direct laryngoscopy if PET was assessed 'positive' or 'equivocal' (PWU: PET based workup strategy), to compare the effectiveness of these strategies. Primary endpoint was the number of indications for direct laryngoscopies classified as unnecessary based on absence of recurrence, both on direct laryngoscopy and on six month follow up. Safety endpoints comprised resectability of recurrent lesions and completeness of surgical margins following salvage laryngectomy.

RESULTS

Intention-to-treat analyses were performed on all randomized patients (CWU: n=74, PWU: n=76). Tumor recurrence was similar in both groups: 45 patients (30%; 21 CWU, 24 PWU) within six months. In 53 patients in the CWU arm (72%, 95% CI: 60-81) unnecessary direct laryngoscopies were performed compared to 22 in the PWU arm (29%, 95% CI: 19-40) (p<0·0001). The percentage of salvage laryngectomies (resectability) and positive surgical margins were similar between CWU and PWU (81%, 63% respectively, p=0·17, and 29%, 7%, respectively, p=0.20). The prevalence of the combination of local unresectability and positive margins is in the CWU group 24% and in the PWU group 8%. No difference (p=0.32) in disease specific survival between both groups was found.

CONCLUSION

In patients with suspected laryngeal carcinoma after radiotherapy, PET as the first diagnostic procedure can reduce the need for direct laryngoscopy by more than 50% without jeopardizing quality of treatment.

摘要

目的

本研究旨在评估(18)F-FDG-PET作为一线诊断检查的疗效,该检查在对怀疑放疗后复发性喉癌的患者进行全身麻醉下直接喉镜活检之前进行。

患者与方法

150例怀疑在先前旨在治愈可切除疾病的(化疗)放疗后至少两个月出现T2-4复发性喉癌的患者被随机分为直接喉镜检查组(CWU:传统检查策略)或仅接受(18)F-FDG-PET检查组,若PET评估为“阳性”或“可疑”则随后进行直接喉镜检查(PWU:基于PET的检查策略),以比较这些策略的有效性。主要终点是根据直接喉镜检查和六个月随访中无复发情况分类为不必要的直接喉镜检查的指征数量。安全终点包括复发性病变的可切除性和挽救性喉切除术后手术切缘的完整性。

结果

对所有随机分组的患者进行了意向性分析(CWU组:n = 74,PWU组:n = 76)。两组的肿瘤复发情况相似:六个月内有45例患者(30%;CWU组21例,PWU组24例)。CWU组有53例患者(72%,95%CI:60-81)进行了不必要的直接喉镜检查,而PWU组为22例(

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