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放疗前PET/CT上18F-FDG高摄取区域可确定非小细胞肺癌放化疗后局部复发的优先部位。

Areas of high 18F-FDG uptake on preradiotherapy PET/CT identify preferential sites of local relapse after chemoradiotherapy for non-small cell lung cancer.

作者信息

Calais Jérémie, Thureau Sébastien, Dubray Bernard, Modzelewski Romain, Thiberville Luc, Gardin Isabelle, Vera Pierre

机构信息

Nuclear Medicine Department, Henri Becquerel Cancer Center and Rouen University Hospital, Rouen, France QuantIF-LITIS (EA [Equipe d'Accueil] 4108-FR CNRS [Fédération de Recherche-Centre National pour la Recherche Scientifique] 3638), Faculty of Medicine, University of Rouen, Rouen, France.

Nuclear Medicine Department, Henri Becquerel Cancer Center and Rouen University Hospital, Rouen, France QuantIF-LITIS (EA [Equipe d'Accueil] 4108-FR CNRS [Fédération de Recherche-Centre National pour la Recherche Scientifique] 3638), Faculty of Medicine, University of Rouen, Rouen, France Department of Radiotherapy and Medical Physics, Henri Becquerel Cancer Centre and Rouen University Hospital, Rouen, France; and.

出版信息

J Nucl Med. 2015 Feb;56(2):196-203. doi: 10.2967/jnumed.114.144253. Epub 2015 Jan 8.

Abstract

UNLABELLED

The high rates of failure in the radiotherapy target volume suggest that patients with stage II or III non-small cell lung cancer (NSCLC) should receive an increased total dose of radiotherapy. Areas of high (18)F-FDG uptake on preradiotherapy (18)F-FDG PET/CT have been reported to identify intratumor subvolumes at high risk of relapse after radiotherapy. We wanted to confirm these observations on a cohort of patients included in 3 sequential prospective studies. Our aim was to assess an appropriate threshold (percentage of maximum standardized uptake value [SUVmax]) to delineate subvolumes on staging (18)F-FDG PET/CT scans assuming that a smaller target volume would facilitate isotoxic radiotherapy dose escalation.

METHODS

Thirty-nine patients with inoperable stage II or III NSCLC, treated with chemoradiation or with radiotherapy alone, were extracted from 3 prospective studies (ClinicalTrials.gov identifiers NCT01261585, NCT01261598, and RECF0645). All patients underwent (18)F-FDG PET/CT at initial staging, before radiotherapy, during radiotherapy, and during systematic follow-up in a single institution. All (18)F-FDG PET/CT acquisitions were coregistered on the initial scan. Various subvolumes in the initial acquisition (30%, 40%, 50%, 60%, 70%, 80%, and 90% SUVmax thresholds) and in the 3 subsequent acquisitions (40% and 90% SUVmax thresholds) were pasted on the initial scan and compared.

RESULTS

Seventeen patients had a local relapse. The SUVmax measured during radiotherapy was significantly higher in locally relapsed tumors than in locally controlled tumors (mean, 6.8 vs. 4.6; P = 0.02). The subvolumes delineated on initial PET/CT scans with 70%-90% SUVmax thresholds were in good agreement with the recurrent volume at a 40% SUVmax threshold (common volume/baseline volume, 0.60-0.80). The subvolumes delineated on initial PET/CT scans with 30%-60% SUVmax thresholds were in good to excellent agreement with the core volume of the relapse (90% SUVmax threshold) (common volume/recurrent volume and overlap fraction indices, 0.60-0.93). The agreement was moderate (>0.51) when a 70% SUVmax threshold was used to delineate on initial PET/CT scans.

CONCLUSION

High (18)F-FDG uptake areas on pretreatment PET/CT scans identify tumor subvolumes at greater risk of relapse in patients with NSCLC treated by concomitant chemoradiation. We propose a 70% SUVmax threshold to delineate areas of high (18)F-FDG uptake on initial PET/CT scans as the target volumes for potential radiotherapy dose escalation.

摘要

未标注

放射治疗靶区的高失败率表明,II期或III期非小细胞肺癌(NSCLC)患者应接受更高的放射治疗总剂量。据报道,放疗前(18)F-FDG PET/CT上高(18)F-FDG摄取区域可识别放疗后复发风险高的肿瘤内亚体积。我们想在3项连续的前瞻性研究纳入的一组患者中证实这些观察结果。我们的目的是评估一个合适的阈值(最大标准化摄取值[SUVmax]的百分比),以便在分期(18)F-FDG PET/CT扫描上勾勒亚体积,假设较小的靶区体积将有助于等毒性放疗剂量增加。

方法

从3项前瞻性研究(ClinicalTrials.gov标识符NCT01261585、NCT01261598和RECF0645)中提取39例无法手术的II期或III期NSCLC患者,这些患者接受了放化疗或单纯放疗。所有患者在初始分期、放疗前、放疗期间以及在单一机构进行系统随访期间均接受了(18)F-FDG PET/CT检查。所有(18)F-FDG PET/CT采集均与初始扫描进行配准。将初始采集(30%、40%、50%、60%、70%、80%和90% SUVmax阈值)以及随后3次采集(40%和90% SUVmax阈值)中的各种亚体积粘贴到初始扫描上并进行比较。

结果

17例患者出现局部复发。局部复发肿瘤放疗期间测得的SUVmax显著高于局部控制肿瘤(平均值分别为6.8和4.6;P = 0.02)。初始PET/CT扫描上以70%-90% SUVmax阈值勾勒的亚体积与40% SUVmax阈值时的复发体积高度一致(共同体积/基线体积,0.60-0.80)。初始PET/CT扫描上以30%-60% SUVmax阈值勾勒的亚体积与复发核心体积(90% SUVmax阈值)高度一致(共同体积/复发体积和重叠分数指数,0.60-0.93)。当使用70% SUVmax阈值在初始PET/CT扫描上进行勾勒时,一致性为中等(>0.51)。

结论

治疗前PET/CT扫描上高(18)F-FDG摄取区域可识别接受同步放化疗的NSCLC患者中复发风险更高的肿瘤亚体积。我们建议使用70% SUVmax阈值在初始PET/CT扫描上勾勒高(18)F-FDG摄取区域,作为潜在放疗剂量增加的靶区体积。

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