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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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (推定)

480

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

      • Limoges、フランス
        • まだ募集していません
        • University Hospital, Limoges
        • コンタクト:
        • 主任研究者:
          • Jeremie Jacques, Prof.
      • Gdansk、ポーランド、80210
        • 募集
        • University Clinical Centre
        • 主任研究者:
          • Piotr Spychalski, MD, PhD
        • コンタクト:
        • 副調査官:
          • Jaroslaw Kobiela, Prof.
        • 副調査官:
          • Piotr Wysocki, MD, PhD
        • 副調査官:
          • Katarzyna Polomska
      • Warsaw、ポーランド
        • 募集
        • Institute of Oncology in Warsaw
        • コンタクト:
        • 主任研究者:
          • Michal Kaminski, Prof.
        • 副調査官:
          • Nastazja Pilonis, Prof.

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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).

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:積極的な監視
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.
アクティブコンパレータ: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Disease-related treatment failure
時間枠: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
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Disease-free survival
時間枠: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
時間枠:3 and 5 years after randomization
Time from randomization to death from any cause.
3 and 5 years after randomization
Stoma formation rate
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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.

協力者と研究者

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出版物と役立つリンク

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一般刊行物

便利なリンク

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年6月14日

一次修了 (推定)

2037年6月1日

研究の完了 (推定)

2037年6月1日

試験登録日

最初に提出

2026年6月16日

QC基準を満たした最初の提出物

2026年6月20日

最初の投稿 (実際)

2026年6月25日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月25日

QC基準を満たした最後の更新が送信されました

2026年6月20日

最終確認日

2026年6月1日

詳しくは

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医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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