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T2-T3ab期、N0、M0直肠癌的放化疗与局部切除对比全直肠系膜切除术:TAUTEM随机临床试验

Chemoradiotherapy and Local Excision vs Total Mesorectal Excision in T2-T3ab, N0, M0 Rectal Cancer: The TAUTEM Randomized Clinical Trial.

作者信息

Serra-Aracil Xavier, Pericay Carles, Cidoncha Ariadna, Badia-Closa Jesus, Golda Thomas, Kreisler Esther, Hernández Pilar, Targarona Eduardo, Borda-Arrizabalaga Nerea, Reina Angel, Delgado Salvadora, Espín-Bassany Eloy, Caro-Tarrago Aleidis, Gallego-Plazas Javier, Pascual Marta, Álvarez-Laso Carlos, Guadalajara-Labajo Hector, Otero Ana, Biondo Sebastiano

机构信息

Coloproctology Unit, General and Digestive Surgery Service, Parc Tauli University Hospital, Sabadell, Institut d'investigació i innovació Parc Tauli I3PT-CERCA, Department of Surgery, Universitat Autònoma de Barcelona, Sabadell, Spain.

Medical Oncology Department, Mutua de Terrassa University Hospital, Terrassa, Spain.

出版信息

JAMA Surg. 2025 May 28. doi: 10.1001/jamasurg.2025.1398.

Abstract

IMPORTANCE

According to international guidelines, the standard treatment for stage T2-T3ab, N0, M0 rectal cancer is total mesorectal excision (TME), but it is associated with high morbidity and quality of life disorders.

OBJECTIVE

To analyze locoregional recurrence (LR) after a follow-up of 2 years, applying a 1-sided noninferiority margin of 10%, and to assess distant recurrence (DR), overall survival (OS), and disease-free survival (DFS).

DESIGN, SETTING, AND PARTICIPANTS: This was a multicenter, prospective, open-label, noninferiority, phase 3 randomized clinical trial comparing TME (TME group) with chemoradiotherapy followed by local excision with transanal endoscopic microsurgery (CRT-TEM group). This study involved 17 hospitals in Spain. Eligibility criteria included patients with rectal adenocarcinoma located lower than 10 cm from the anal verge; stage T2-T3ab N0, M0; tumor size less than or equal to 4 cm in diameter; and American Society of Anesthesiologists stage III or less with no metastasis. Sample size was calculated with a 1-sided significance level of 2.5% and a power of 80%, assuming a nonrecurrence rate of 95% in each arm and a possible loss of 15%. Randomization was performed with a 1:1 allocation ratio. Data were analyzed from July 2010 to October 2021.

INTERVENTIONS

The 2 treatment groups were CRT-TEM and TME.

MAIN OUTCOMES AND MEASURES

The main study outcome was LR.

RESULTS

From July 2010 to October 2021, 173 patients (median [IQR] age, 67 [59-75] years; 116 male [67.1%]) were included (CRT-TEM, n = 86; TME, n = 87). In the 5-year modified intention-to-treat analysis, LR was 6.2% (5 of 81 patients) in the TME group and 7.4% (6 of 81 patients) in the CRT-TEM group (difference, -1.23%; 95% CI, 6.51% to -8.98%). DR was 17.3% (14 of 81 patients) in the TME group and 12.3% (10 of 81 patients) in the CRT-TEM group (difference, 4.94%; 95% CI, 15.85% to -5.98%). OS was 85.2% (69 of 81 patients) in the TME group and 82.7% (67 of 81 patients) in the CRT-TEM group (difference, 2.47%; 95% CI, 0.38%-1.78%). DFS in both groups was 88.9% (72 of 81), with a 95% CI of 9.68 to -9.68.

CONCLUSIONS AND RELEVANCE

Results of this randomized clinical trial reveal that CRT-TEM achieved noninferior results compared with standard TME treatment in terms of LR and similar results in terms of DR, OS, and DFS. CRT-TEM appears to be a suitable treatment option for patients with T2-T3ab, N0, M0 rectal cancer.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT01308190.

摘要

重要性

根据国际指南,T2-T3ab期、N0、M0期直肠癌的标准治疗方法是全直肠系膜切除术(TME),但该手术具有高发病率和生活质量障碍的问题。

目的

在2年的随访后分析局部区域复发(LR)情况,采用单侧非劣效性界值为10%,并评估远处复发(DR)、总生存期(OS)和无病生存期(DFS)。

设计、地点和参与者:这是一项多中心、前瞻性、开放标签、非劣效性3期随机临床试验,比较TME(TME组)与放化疗后经肛门内镜显微手术进行局部切除(CRT-TEM组)。本研究涉及西班牙的17家医院。纳入标准包括距肛缘低于10 cm的直肠腺癌患者;T2-T3ab期、N0、M0期;肿瘤直径小于或等于4 cm;美国麻醉医师协会分级为III级或更低且无转移。样本量计算采用单侧显著性水平2.5%和检验效能80%,假设每组无复发率为95%且可能有15%的失访率。随机分组按1:1分配比例进行。对2010年7月至2021年10月的数据进行分析。

干预措施

两个治疗组分别为CRT-TEM组和TME组。

主要结局和测量指标

主要研究结局为LR。

结果

2010年7月至2021年10月,共纳入173例患者(年龄中位数[四分位间距]为67[59-75]岁;男性116例[67.1%])(CRT-TEM组,n = 86;TME组,n = 87)。在5年修正意向性分析中,TME组LR为6.2%(81例患者中的5例),CRT-TEM组为7.4%(81例患者中的6例)(差异为-1.23%;95%CI为6.51%至-8.98%)。TME组DR为17.3%(81例患者中的14例),CRT-TEM组为12.3%(81例患者中的10例)(差异为4.94%;95%CI为15.85%至-5.98%)。TME组OS为85.2%(81例患者中的69例),CRT-TEM组为82.7%(81例患者中的67例)(差异为2.47%;95%CI为0.38%-1.78%)。两组DFS均为88.9%(81例中的72例),95%CI为9.68至-9.68。

结论和相关性

这项随机临床试验的结果显示,在LR方面,CRT-TEM与标准TME治疗相比取得了非劣效结果,在DR、OS和DFS方面取得了相似结果。CRT-TEM似乎是T2-T3ab期、N0、M0期直肠癌患者的一种合适治疗选择。

试验注册

ClinicalTrials.gov标识符:NCT01308190。

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