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临床试验/NCT07695519
NCT07695519尚未招募不适用

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

Fondazione Policlinico Universitario Agostino Gemelli IRCCS1 个研究点 分布在 1 个国家目标入组 196 人开始时间: 2026年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
196
试验地点
1
主要终点
3-year Disease-Free Survival (DFS)

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 years or older.
  • Good performance status (Eastern Cooperative Oncology Group [ECOG] performance status 0 or 1).
  • 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).
  • 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
  • v) Positive lateral or vertical resection margin (tumor within 1 mm of the surgical margin) or non-assessable resection margin.
  • No lymph node or distant metastases confirmed by computed tomography of the chest, abdomen, and pelvis (clinical N0, M0 disease).
  • Radiotherapy or chemoradiotherapy initiated within 12 weeks after local endoscopic or surgical resection.
  • No previous rectal resection (other than local excision) or pelvic irradiation for any malignancy.
  • Adequate organ function as assessed by the treating physician.
  • 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.
  • Candidate for adjuvant chemoradiotherapy according to routine clinical practice.
  • Written informed consent provided.

排除标准

  • Synchronous or metachronous malignancy diagnosed within the previous 5 years.
  • Infection requiring systemic treatment.
  • Requirement for continuous systemic treatment with corticosteroids or immunosuppressive agents.
  • 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.
  • Squamous cell carcinoma, neuroendocrine neoplasm, or mixed neuroendocrine-non-neuroendocrine neoplasm histology.

结局指标

主要结局

3-year Disease-Free Survival (DFS)

时间窗: 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.

次要结局

  • Disease-free survival at 1 year(1 year)
  • Disease-free survival at 5 years(5 years)
  • Local recurrence-free survival at 1 year(1 year)
  • Local recurrence-free survival at 3 years(3 years)
  • Local recurrence-free survival at 5 years(5 years)
  • Overall survival at 1 year(1 year)
  • Overall survival at 3 years(3 years)
  • Overall survival at 5 years(5 years)
  • Colostomy-free survival at 1 year(1 year)
  • Colostomy-free survival at 3 years(3 years)
  • Quality of life assessed by EORTC QLQ-C30 Global Health Status/Quality of Life score at 1 year(1 year)
  • Colorectal cancer-specific quality of life assessed by EORTC QLQ-CR29 at 1 year(1 year)
  • Quality of life assessed by EORTC QLQ-C30 Global Health Status/Quality of Life score at 3 years(3 years)
  • Colorectal cancer-specific quality of life assessed by EORTC QLQ-CR29 at 3 years(3 years)
  • Acute toxicity within 6 months from treatment(Within 6 months from the end of treatment)
  • Late toxicity at 2 years after the end of treatment(2 years after the end of treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

CHILOIRO GIUDITTA

Principal Investigator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

研究点 (1)

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