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基于肿瘤长度和正电子发射断层扫描-计算机断层扫描标准化摄取值评估食管癌的治疗反应和复发情况。

Assessment of treatment response and recurrence in esophageal carcinoma based on tumor length and standardized uptake value on positron emission tomography-computed tomography.

作者信息

Roedl Johannes B, Harisinghani Mukesh G, Colen Rivka R, Fischman Alan J, Blake Michael A, Mathisen Douglas J, Mueller Peter R

机构信息

Division of Abdominal and Interventional Radiology, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Ann Thorac Surg. 2008 Oct;86(4):1131-8. doi: 10.1016/j.athoracsur.2008.05.019.

Abstract

BACKGROUND

Previous studies demonstrated that a decrease of the standardized uptake value between pretreatment and posttreatment positron emission tomography (PET) scans can predict histopathologic treatment response in patients with esophageal cancer.

METHODS

Forty-seven patients who underwent PET-computed tomography (CT) scans before (scan 1) and after (scan 2) neoadjuvant chemoradiotherapy and during the follow-up period after surgery (scan 3) were included in this study. It was evaluated whether decrease of metabolic tumor length between scan 1 and scan 2 can predict histopathologic response to treatment. Moreover, the value of PET-CT was compared with PET in the assessment of tumor recurrence based on a visual analysis of scan 3. Reference standards for treatment response and recurrence were histopathology results.

RESULTS

The reduction of tumor length between before and after chemoradiotherapy scans (between scan 1 and scan 2) was a better predictor of histopathologic response and of time to recurrence than the decrease in standardized uptake value. The most accurate differentiation was achieved when using a cut-off value of 33% reduction of the initial tumor length. Using this threshold to define metabolic response, the sensitivity was 91% (19 of 21) and the specificity was 92% (24 of 26) for predicting histopathologic treatment response. Based on a visual analysis, PET-CT was more accurate than PET in the differentiation of tumor recurrence from posttreatment tissue changes. Integrated PET-CT achieved a sensitivity of 91% (48 of 53) and a specificity of 81% (30 of 37) in identifying sites of tumor recurrence, compared with 83% (44 of 53) and 65% (24 of 37) with PET.

CONCLUSIONS

Decrease of tumor length was shown to be a better predictor of treatment response and disease-free survival than decrease of standardized uptake value. Furthermore, PET-CT is more accurate in the evaluation of recurrence than PET.

摘要

背景

既往研究表明,治疗前与治疗后正电子发射断层扫描(PET)的标准化摄取值降低可预测食管癌患者的组织病理学治疗反应。

方法

本研究纳入了47例在新辅助放化疗前(扫描1)、后(扫描2)以及术后随访期间(扫描3)接受PET计算机断层扫描(CT)的患者。评估扫描1和扫描2之间代谢肿瘤长度的降低是否可预测治疗的组织病理学反应。此外,基于对扫描3的视觉分析,将PET-CT与PET在评估肿瘤复发方面的价值进行比较。治疗反应和复发的参考标准为组织病理学结果。

结果

放化疗前后扫描(扫描1和扫描2之间)肿瘤长度的减少比标准化摄取值的降低更能预测组织病理学反应和复发时间。当使用初始肿瘤长度减少33%的临界值时,区分最为准确。使用该阈值定义代谢反应,预测组织病理学治疗反应的敏感性为91%(21例中的19例),特异性为92%(26例中的24例)。基于视觉分析,在区分肿瘤复发与治疗后组织变化方面,PET-CT比PET更准确。在识别肿瘤复发部位方面,PET-CT的敏感性为91%(53例中的48例),特异性为81%(37例中的30例),而PET的敏感性为83%(53例中的44例),特异性为65%(37例中的24例)。

结论

肿瘤长度的减少比标准化摄取值的降低更能预测治疗反应和无病生存期。此外,在评估复发方面,PET-CT比PET更准确。

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