이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

SCARLET - Italian proSpeCtionAl obseRvationaL multicEntre Study on Treatment for recTal pT1 Cancer (SCARLET)

2026년 7월 8일 업데이트: CHILOIRO GIUDITTA, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
The purpose of this prospective, observational, multicenter study is to evaluate the impact of adjuvant radiotherapy or chemoradiotherapy on disease-free survival (DFS) in patients with pathological T1 (pT1) rectal cancer presenting with at least one high-risk histological factor, such as deep submucosal invasion, poor differentiation, tumor budding, lymphovascular invasion, or positive resection margins, after local surgical or endoscopic excision, including Endoscopic Submucosal Dissection (ESD), Transanal Minimally Invasive Surgery (TAMIS), or Transanal Endoscopic Microsurgery (TEM). The study focuses on a specific patient population that has refused standard radical surgery with Total Mesorectal Excision (TME) because of its potential impact on quality of life and postoperative morbidity. The primary objective is to assess whether organ-preserving local treatment strategies can provide an effective alternative by evaluating long-term oncologic outcomes, quality of life, and colostomy-free survival.

연구 개요

상태

아직 모집하지 않음

정황

상세 설명

Background To date, the therapeutic management of patients with pathological T1 (pT1) rectal cancer after local surgical or endoscopic excision remains a subject of ongoing debate. Although traditional radical surgery has demonstrated proven advantages, discussion persists regarding the adequacy of less invasive techniques for specific subgroups of patients, particularly those with a low risk of disease progression. In these cases, local excision options through endoscopic or surgical interventions, including Endoscopic Submucosal Dissection (ESD), Transanal Minimally Invasive Surgery (TAMIS), and Transanal Endoscopic Microsurgery (TEM), may represent a valid curative approach. These techniques, which generally carry a low risk of lymph node metastasis, offer important advantages in terms of organ preservation and reduction of postoperative complications, including anorectal, urinary, and sexual dysfunction, which may significantly impair quality of life.

Rationale The choice of a conservative approach must be carefully evaluated, especially when post-excision histopathological analysis reveals high-risk features. These include deep submucosal invasion greater than 1 mm, poor tumor differentiation, tumor budding, lymphovascular invasion, or positive or close resection margins. In these situations, radical surgery with Total Mesorectal Excision (TME) is considered the standard treatment strategy for reducing the risk of local and nodal recurrence, although available evidence is largely derived from retrospective studies. Because TME may substantially affect quality of life and functional outcomes, treatment decisions should be discussed within a multidisciplinary team. National and international guidelines suggest that patients with pT1 rectal cancer who present high-risk features and are either unwilling or unsuitable to undergo radical surgery may be considered for alternative organ-preserving strategies, including adjuvant radiotherapy or chemoradiotherapy.

Study Objective This prospective, observational, multicenter study aims to evaluate the impact of adjuvant radiotherapy or chemoradiotherapy on Disease-Free Survival (DFS) in patients with pT1 rectal cancer presenting at least one high-risk histopathological feature who have undergone local excision and declined treatment with TME. The study will also assess long-term oncologic outcomes, organ preservation, and quality of life in this patient population.

연구 유형

관찰

등록 (추정된)

196

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

샘플링 방법

비확률 샘플

연구 인구

dult patients with high-risk pathological T1 (pT1) rectal cancer who have undergone local endoscopic resection using Endoscopic Submucosal Dissection (ESD) or local surgical resection using Transanal Endoscopic Microsurgery (TEM) or Transanal Minimally Invasive Surgery (TAMIS). The study population specifically includes patients who have declined standard treatment with Total Mesorectal Excision (TME) and who subsequently receive adjuvant radiotherapy or chemoradiotherapy according to routine clinical practice following multidisciplinary team evaluation.

설명

Inclusion Criteria:

  1. Age 18 years or older.
  2. Good performance status (Eastern Cooperative Oncology Group [ECOG] performance status 0 or 1).
  3. Primary tumor of the distal rectum (clinical T1) amenable to local endoscopic resection using Endoscopic Submucosal Dissection (ESD) or local surgical resection using Transanal Endoscopic Microsurgery (TEM) or Transanal Minimally Invasive Surgery (TAMIS).
  4. High-risk pathological T1 rectal cancer meeting at least one of the following conditions:

    i) Poorly differentiated adenocarcinoma, mucinous adenocarcinoma, or signet ring cell carcinoma.

    ii) Pathological submucosal invasion greater than 1000 micrometers. iii) Positive lymphatic invasion or positive venous invasion confirmed by immunohistochemistry.

    iv) Tumor budding grade 2 or 3. v) Positive lateral or vertical resection margin (tumor within 1 mm of the surgical margin) or non-assessable resection margin.

  5. No lymph node or distant metastases confirmed by computed tomography of the chest, abdomen, and pelvis (clinical N0, M0 disease).
  6. Radiotherapy or chemoradiotherapy initiated within 12 weeks after local endoscopic or surgical resection.
  7. No previous rectal resection (other than local excision) or pelvic irradiation for any malignancy.
  8. Adequate organ function as assessed by the treating physician.
  9. The treating surgeons have explained to the patient that the current standard of care is Total Mesorectal Excision (TME) with D2 lymph node dissection and the patient has declined this treatment.
  10. Candidate for adjuvant chemoradiotherapy according to routine clinical practice.
  11. Written informed consent provided.

Exclusion Criteria:

  1. Synchronous or metachronous malignancy diagnosed within the previous 5 years.
  2. Infection requiring systemic treatment.
  3. Requirement for continuous systemic treatment with corticosteroids or immunosuppressive agents.
  4. Diagnosis of a hereditary colorectal cancer syndrome, including familial adenomatous polyposis or Lynch syndrome, or diagnosis of inflammatory bowel disease, including ulcerative colitis or Crohn disease.
  5. Squamous cell carcinoma, neuroendocrine neoplasm, or mixed neuroendocrine-non-neuroendocrine neoplasm histology.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
3-year Disease-Free Survival (DFS)
기간: 3-years
Percentage of patients who remain alive and free from rectal cancer recurrence (local, nodal, or distant metastases) at three years from the start of follow-up.
3-years

2차 결과 측정

결과 측정
측정값 설명
기간
Disease-free survival at 1 year
기간: 1 year
Percentage of patients alive and free from rectal cancer recurrence (local, nodal, or distant metastases) at 1 year from follow-up.
1 year
Disease-free survival at 5 years
기간: 5 years
Percentage of patients alive and free from rectal cancer recurrence (local, nodal, or distant metastases) at 5 years from follow-up.
5 years
Local recurrence-free survival at 1 year
기간: 1 year
Time from the end of treatment to the documentation of local disease recurrence at 1 year.
1 year
Local recurrence-free survival at 3 years
기간: 3 years
Time from the end of treatment to the documentation of local disease recurrence at 3 years.
3 years
Local recurrence-free survival at 5 years
기간: 5 years
Time from the end of treatment to the documentation of local disease recurrence at 5 years.
5 years
Overall survival at 1 year
기간: 1 year
Percentage of patients alive at 1 year from the start of follow-up.
1 year
Overall survival at 3 years
기간: 3 years
Percentage of patients alive at 3 years from the start of follow-up.
3 years
Overall survival at 5 years
기간: 5 years
Percentage of patients alive at 5 years from the start of follow-up.
5 years
Colostomy-free survival at 1 year
기간: 1 year
Percentage of patients alive without the need for a temporary or permanent stoma/colostomy at 1 year.
1 year
Colostomy-free survival at 3 years
기간: 3 years
Percentage of patients alive without the need for a temporary or permanent stoma/colostomy at 3 years.
3 years
Quality of life assessed by EORTC QLQ-C30 Global Health Status/Quality of Life score at 1 year
기간: 1 year
Patient-reported quality of life assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30). The Global Health Status/Quality of Life score ranges from 0 to 100 after linear transformation. Higher scores indicate better quality of life.
1 year
Colorectal cancer-specific quality of life assessed by EORTC QLQ-CR29 at 1 year
기간: 1 year
Patient-reported colorectal cancer-specific quality of life assessed using the European Organisation for Research and Treatment of Cancer Colorectal Cancer Questionnaire (EORTC QLQ-CR29). Questionnaire scores are transformed to a 0-100 scale. For functional scales, higher scores indicate better functioning; for symptom scales, higher scores indicate greater symptom burden. Individual QLQ-CR29 scale scores will be analyzed separately.
1 year
Quality of life assessed by EORTC QLQ-C30 Global Health Status/Quality of Life score at 3 years
기간: 3 years
Patient-reported quality of life assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30). The Global Health Status/Quality of Life score ranges from 0 to 100 after linear transformation. Higher scores indicate better quality of life.
3 years
Colorectal cancer-specific quality of life assessed by EORTC QLQ-CR29 at 3 years
기간: 3 years
Patient-reported colorectal cancer-specific quality of life assessed using the European Organisation for Research and Treatment of Cancer Colorectal Cancer Questionnaire (EORTC QLQ-CR29). Questionnaire scores are transformed to a 0-100 scale. For functional scales, higher scores indicate better functioning; for symptom scales, higher scores indicate greater symptom burden. Individual QLQ-CR29 scale scores will be analyzed separately.
3 years
Acute toxicity within 6 months from treatment
기간: Within 6 months from the end of treatment
Incidence and severity of acute adverse events (genitourinary, gastrointestinal, and hematologic) scored according to CTCAE version 5.0.
Within 6 months from the end of treatment
Late toxicity at 2 years after the end of treatment
기간: 2 years after the end of treatment
Incidence and severity of long-term treatment-related toxicities scored according to CTCAE version 5.0.
2 years after the end of treatment

기타 결과 측정

결과 측정
측정값 설명
기간
Nodal Recurrence Rate
기간: Up to 5 years after completion of adjuvant treatment.
ercentage of patients who develop regional lymph node recurrence during the follow-up period, as assessed by imaging modalities.
Up to 5 years after completion of adjuvant treatment.
Distant Metastases Rate
기간: Up to 5 years after completion of adjuvant treatment.
Percentage of patients who develop distant organ metastases (outside the pelvis) during the follow-up period, confirmed by contrast-enhanced chest-abdomen-pelvis CT scan.
Up to 5 years after completion of adjuvant treatment.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Giuditta Chiloiro, MD, PhD, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Università Cattolica del Sacro Cuore, Roma, Italy

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 9월 1일

기본 완료 (추정된)

2029년 9월 1일

연구 완료 (추정된)

2031년 9월 1일

연구 등록 날짜

최초 제출

2026년 7월 1일

QC 기준을 충족하는 최초 제출

2026년 7월 8일

처음 게시됨 (실제)

2026년 7월 10일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 10일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 8일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 27321

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .