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Active Surveillance vs Adjuvant Chemoradiotherapy for Locally Resected Intermediate-Risk T1 Rectal Cancer (T-REX)

2026年6月20日 更新者:Michał F.Kaminski、Medical University of Gdansk

Active Surveillance vs Adjuvant Chemoradiotherapy for Locally Resected Intermediate-Risk T1 Rectal Cancer: Multicentre Randomised Controlled Trial

The goal of this clinical trial is to learn if close follow-up alone (active surveillance) works as well as radiation combined with chemotherapy (chemoradiotherapy) after removing early rectal cancer in adults. The main questions it aims to answer are:

  1. Does active surveillance cause fewer serious adverse events than chemoradiotherapy within 3 years? Serious adverse events include a permanent or temporary ostomy (a surgical opening in the belly to pass stool), major bowel problems, or severe treatment-related complications.
  2. Is active surveillance as safe as chemoradiotherapy in preventing cancer from coming back or spreading within 3 years?

Researchers will compare active surveillance to chemoradiotherapy to see if surveillance causes fewer serious adverse events while keeping cancer outcomes comparable.

To join this study, participants must be adults who had an early-stage rectal cancer (T1) removed by an endoscopic procedure, and whose removed tumor showed certain features that raise the risk of cancer cells remaining nearby.

Participants will be randomly placed in one of two groups:

  1. Active surveillance group: Participants will have regular checkups, blood tests, flexible camera exams of the bowel (rectoscopy), scans of the pelvis and abdomen, and colonoscopy on a set schedule for 5 years. If cancer comes back, doctors will propose further treatment options.
  2. Chemoradiotherapy group: Participants will receive radiation to the pelvis along with a chemotherapy pill (capecitabine) or an intravenous (IV) chemotherapy drug (5-FU) for about 5 weeks. After treatment, they will have regular checkups and scans for 5 years.

研究概览

详细说明

The current standard treatment for T1 rectal cancer (T1N0M0) is local excision by endoscopic submucosal dissection (ESD) or intermuscular dissection (IMD) performed endoscopically or via transanal minimally invasive surgery (TAMIS). More than half of the patients treated with ESD or IMD require secondary treatment due to unfavourable histopathological features in the resected specimen. Lesions can be classified as intermediate-risk if the specimen presents at least one of the following features: poor differentiation (grade 3), lymphovascular invasion, high-grade tumour budding (grade 2-3), or deep submucosal invasion (sm2-sm3).

Secondary treatment can be performed either by total mesorectal excision (TME) or adjuvant chemoradiotherapy. The latest evidence suggests that chemoradiotherapy may offer a superior risk-benefit ratio compared to completion TME. Still, chemoradiotherapy remains associated with a substantial risk of major low anterior resection syndrome (LARS); the risk is reduced but still reported at approximately 25-33%. Given a 15-20% risk of lymph node involvement in the intermediate-risk group, chemoradiotherapy might be overtreatment for the majority of these patients. Active surveillance can reduce treatment-related morbidity, but it is associated with higher local recurrence rates. Available cohort data suggest that most recurrences are detected early during structured surveillance and are salvageable with curative-intent surgery, resulting in oncological outcomes similar to those achieved with adjuvant chemoradiotherapy. However, no randomised trial has directly compared these two strategies in this population.

研究类型

介入性

注册 (估计的)

480

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

      • Limoges、法国
        • 尚未招聘
        • University Hospital, Limoges
        • 接触:
        • 首席研究员:
          • Jeremie Jacques, Prof.
      • Gdansk、波兰、80210
        • 招聘中
        • University Clinical Centre
        • 首席研究员:
          • Piotr Spychalski, MD, PhD
        • 接触:
        • 副研究员:
          • Jaroslaw Kobiela, Prof.
        • 副研究员:
          • Piotr Wysocki, MD, PhD
        • 副研究员:
          • Katarzyna Polomska
      • Warsaw、波兰
        • 招聘中
        • Institute of Oncology in Warsaw
        • 接触:
        • 首席研究员:
          • Michal Kaminski, Prof.
        • 副研究员:
          • Nastazja Pilonis, Prof.

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Pathologically confirmed rectal cancer located extraperitoneally.
  2. Complete tumour resection (R0) by means of ESD or IMD (endoscopic or TAMIS).
  3. Pathological report indicative of:

    - pT1 with at least 1 of the following features: poor histological differentiation (grade 3), vascular invasion, lymphatic invasion, high tumour budding (grade 2-3), sm2 or sm3 invasion.

  4. Endoscopic images or video of the tumour before local excision.
  5. Maximum cancer diameter ≤ 30 mm based on the pathological assessment.
  6. cN0 stage based on pelvic MRI; lymph nodes smaller than 10 mm will be considered as benign, independent of morphologic features. Staging must be performed within 6 weeks before randomisation.

    - If enlarged lymph nodes are present on MRI performed after ESD/IMD (raising the possibility of reactive inflammatory change), fine needle aspiration (FNA) will be undertaken, and patients with negative FNA cytology will remain eligible.

  7. Adequate distant staging (thoracic and abdominal CT) without signs of distant metastasis (cM0).
  8. Have undergone a high-quality full colonoscopy:

    • Boston Bowel Preparation Scale score equal or greater than 2 in all colonic segments.
    • Documented caecal intubation.
    • All polyps ≥20 mm in diameter other than the index lesion must be completely removed and assessed pathologically.
  9. Expected survival time of more than 12 months from randomisation.
  10. At least 18 years old at the time of informed consent.
  11. Eastern Cooperative Oncology Group performance status (ECOG PS) 0, 1 or 2.
  12. Adequate hematologic function, based upon meeting the following laboratory criteria within 7 days before randomisation:

    • Absolute neutrophil count (ANC) ≥ 1.5 × 10^9/L.
    • Haemoglobin (Hb) ≥ 8.0 g/dL (red blood cell transfusions are allowed to reach the target level).
    • Platelet count ≥ 75 × 10^9/L.
  13. Adequate liver function, based upon meeting the following criteria within 7 days before randomisation:

    • Serum albumin ≥ 3.0 g/dL.
    • Total bilirubin (in serum) ≤ 2.0 mg/dL.
    • Aspartate aminotransferase (AST) ≤ 3 × the upper limit of normal (ULN).
    • Alanine aminotransferase (ALT) ≤ 3× ULN.
    • Alkaline phosphatase (ALP) ≤ 3 × ULN.
  14. Adequate coagulation defined by International Normalized Ratio (INR) ≤ 2.0 within 7 days before randomisation.
  15. Adequate renal function, based upon meeting the following laboratory criteria within 7 days before randomisation:

    • Serum creatinine clearance ≥ 50 mL/min calculated using the Cockcroft-Gault formula.
    • Absence of significant proteinuria. If the subject is found to have dipstick test indicative of proteinuria equal or larger than 2+, or lab urinalysis for protein is greater than or equal to 1 g/L, the subject must demonstrate urine protein < 1 g/24 h to be eligible.
  16. Recovery from prior treatment-related toxicities to < Grade 2 severity per CTCAE v6.0, unless the adverse events are clinically nonsignificant and/or stable on supportive therapy.
  17. Sexually active fertile subjects and their partners must agree to use medically accepted methods of contraception (e.g., barrier methods, including male condom, female condom, or diaphragm with spermicidal gel) during the study treatment. This does not apply to postmenopausal women (amenorrhoeic for at least 12 consecutive months), women aged above 55, or surgically sterilized patients (men and women).
  18. Female participants of childbearing potential must not be lactating or pregnant, with a negative beta-human chorionic gonadotropin (beta-hCG) test (blood or urine) at screening and before the first dose of the study treatment.

    Females of childbearing potential are defined as premenopausal females capable of becoming pregnant (i.e., females who have had any evidence of menses in the past 12 months, except for those who had prior hysterectomy). However, women who have been amenorrhoeic for 12 or more months are still considered to be of childbearing potential if the amenorrhea is possibly due to prior chemotherapy, antioestrogens, ovarian suppression, low body weight, or other reasons.

  19. Written informed consent to participate in the study provided before randomisation.
  20. Capability of understanding and complying with the protocol requirements.
  21. Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial.
  22. Eligibility for thoracic, abdominal and pelvic CT and MRI.

Exclusion Criteria:

  1. Suspicion of distant metastases on computed tomography of the abdomen or thorax or lymph node involvement (lymph nodes >9mm in short axis); In case of isolated enlarged nodes biopsy will be required before exclusion.
  2. Mesorectal tumour involvement on pelvic MRI.
  3. Synchronous colorectal cancer in screening colonoscopy.
  4. Known genetic cancer syndrome, including, but not limited to adenomatous or serrated polyposis syndrome; Lynch or Lynch-like syndrome.
  5. Known inflammatory bowel disease.
  6. Previously identified allergy or hypersensitivity to 5-FU or capecitabine.
  7. Known or suspected dihydropyridine dehydrogenase (DPD) deficiency.
  8. Prior receipt of pelvic radiation.
  9. Other contraindications to pelvic irradiation.
  10. Serious illness other than cancer that would preclude safe participation in the study
  11. Uncontrolled and significant condition, including, but not limited to, the following conditions:

    • Heart failure NYHA II or above.
    • Major cardiac arrhythmia.
    • Myocardial infarction within 6 months before randomisation.
    • Unstable angina pectoris.
    • Stroke (including transient ischemic attack, TIA) within 6 months before randomisation.
    • Thromboembolism within 3 months before randomisation.
    • History of hypertensive crisis.
  12. Gastrointestinal disorders associated with a high risk of perforation or fistula formation.
  13. Gastrointestinal bleeding event within 28 days of randomisation.
  14. Major surgery performed within 4 weeks prior to randomisation or scheduled for surgery during the study period. Complete healing from major surgery must have occurred 1 month before randomisation. Complete healing from minor surgery must have occurred at least 7 days before randomisation.
  15. Serious non-healing wound or bone fracture.
  16. Malabsorption syndrome.
  17. Pregnancy or lactation.
  18. Mismatch repair deficiency (dMMR) or microsatellite instability-high (MSI-H).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:主动监控
Active surveillance includes physical examination, and carcinoembryonic antigen (CEA) testing every 3 months during years 1-2 and every 6 months during years 3-5. Rectoscopy is performed every 3 months during years 1-2 and every 6 months during years 3-5. Pelvic MRI is performed every 6 months for 5 years. Thoracic and abdominal CT scans are performed annually for 5 years. Colonoscopy is performed at 1 year after local excision and subsequently according to findings. Recurrences are managed according to multidisciplinary team recommendations.
有源比较器:Adjuvant chemoradiotherapy
Adjuvant long-course pelvic chemoradiotherapy will be initiated within 12 weeks after local excision. Radiotherapy consists of 45 Gy delivered in 25 fractions of 1.8 Gy once daily, 5 days per week, over approximately 5 weeks. Concurrent chemotherapy consists of either oral capecitabine 825 mg/m² twice daily on radiotherapy days or continuous intravenous 5-fluorouracil 225 mg/m²/day throughout radiotherapy. After treatment, follow-up includes history, physical examination, CEA testing, and flexible sigmoidoscopy every 6 months for 5 years; pelvic MRI every 6 months during the first 3 years; annual thoracic and abdominal CT for 5 years; pelvic CT after discontinuation of MRI surveillance; and colonoscopy at 1 year and thereafter according to findings.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Disease-related treatment failure
大体时间:3 years from randomisation

Time from randomisation to the first occurrence of:

  1. Cancer specific death.
  2. Non-salvageable locoregional recurrence.
  3. Distant metastases.
3 years from randomisation
Composite severe treatment-related adverse event
大体时间:3 years from randomisation

Occurrence of any of the following:

  1. Stoma (permanent or temporary).
  2. Major LARS (score ≥30).
  3. CTCAE grade ≥3 toxicity.
  4. Clavien-Dindo ≥3b complications.
3 years from randomisation

次要结果测量

结果测量
措施说明
大体时间
Disease-free survival
大体时间:3 and 5 years after randomization
Time from randomisation to first event: death (any cause), distant metastases, or locoregional recurrence
3 and 5 years after randomization
Overall Survival
大体时间:3 and 5 years after randomization
Time from randomization to death from any cause.
3 and 5 years after randomization
Stoma formation rate
大体时间:12 months, 3 years, and 5 years after randomization
Proportion of patients with a colostomy or ileostomy (permanent or temporary) present at assessment. Stoma rates will be evaluated at predefined follow-up intervals.
12 months, 3 years, and 5 years after randomization
Incidence of Major Low Anterior Resection Syndrome (LARS)
大体时间:12 months, 3 years, and 5 years after treatment
Proportion of patients with a LARS Questionnaire score of 30 points or greater, indicating major low anterior resection syndrome.
12 months, 3 years, and 5 years after treatment
Grade 3 or Higher Treatment-Related Toxicity
大体时间:From treatment initiation through 12 months after completion of chemoradiotherapy.
Incidence of adverse events of grade 3 or higher according to Common Terminology Criteria for Adverse Events (CTCAE) version 6.0 occurring during treatment and follow-up.
From treatment initiation through 12 months after completion of chemoradiotherapy.
Locoregional Recurrence Rate
大体时间:5 years after randomization.
Proportion of patients with radiologically or histologically confirmed recurrence within the pelvis or mesorectum.
5 years after randomization.
Salvageability of Locoregional Recurrence
大体时间:At the time of recurrence detection, up to 5 years after randomization
Proportion of detected locoregional recurrences amenable to curative-intent salvage therapy.
At the time of recurrence detection, up to 5 years after randomization
Duration of Hospital Stay After Primary Treatment
大体时间:From the day of randomization untill 5 years from randomization.
Total cumulative length of hospitalization following the randomized treatment strategy, measured in calendar days.
From the day of randomization untill 5 years from randomization.
Distant Recurrence Rate
大体时间:3 years and 5 years after randomization.
Proportion of patients with radiologically or histologically confirmed distant metastatic disease outside the locoregional area.
3 years and 5 years after randomization.
Health-Related Quality of Life (EORTC QLQ-C30)
大体时间:Baseline, 12 months, 3 years, and 5 years after randomization
Health-related quality of life assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30 (EORTC QLQ-C30).
Baseline, 12 months, 3 years, and 5 years after randomization
Healthcare Resource Utilization Costs per Patient
大体时间:Up to 5 years after randomization.
Direct healthcare resource utilization costs including treatment, procedures, imaging, hospitalization, surveillance, and management of recurrence and complications measured as a total per patient in euro (€).
Up to 5 years after randomization.
Cost-Effectiveness
大体时间:3 years and 5 years after randomization
Incremental cost-effectiveness expressed as cost per quality-adjusted life-year (QALY) gained and cost per disease-free survival year gained.
3 years and 5 years after randomization
Ostomy-Free Survival
大体时间:3 years and 5 years after randomization.
Time from randomization to permanent ostomy formation or death, with estimation of the proportion of patients alive without a permanent ostomy.
3 years and 5 years after randomization.
Health-Related Quality of Life (EORTC QLQ-CR29)
大体时间:Baseline, 12 months, 3 years, and 5 years after randomization.
Health-related quality of life assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Colorectal Cancer Module (EORTC QLQ-CR29).
Baseline, 12 months, 3 years, and 5 years after randomization.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

有用的网址

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年6月14日

初级完成 (估计的)

2037年6月1日

研究完成 (估计的)

2037年6月1日

研究注册日期

首次提交

2026年6月16日

首先提交符合 QC 标准的

2026年6月20日

首次发布 (实际的)

2026年6月25日

研究记录更新

最后更新发布 (实际的)

2026年6月25日

上次提交的符合 QC 标准的更新

2026年6月20日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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