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NCT05563922RecruitingPhase 2

Organ Preservation Strategy of Total Neoadjuvant Chemoradiotherapy for Low Rectal Carcinoma

Organ Preservation Strategy of Total Neoadjuvant Chemoradiotherapy for Early Low Rectal Carcinoma: A Prospective, Exploratory Trial

Source: ClinicalTrials.gov · Last updated 3 Oct 2022 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study aims to evaluate the efficacy and safety of an organ-sparing strategy after neoadjuvant chemoradiotherapy followed by transanal endoscopic microsurgery (TEM) or endoscopic local resection for early low rectal cancer(cT 1-3N0M0).Besides, the clinical complete response rate and near-clinical complete response rate, organ preservation rate, local recurrence rate, distant metastasis rate and quality of life (QoL) will also be assessed.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
56 (estimated)
First submitted
4 Sept 2022
Start date
1 Sept 2022
Primary completion date
31 Aug 2025
Lead sponsor
Shanghai Zhongshan Hospital
NCT number
NCT05563922

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 56
  • From 1 Sept 2022 to the primary completion date, 31 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Have received previous treatment (including endoscopic resection, transanal local resection, radiotherapy, chemotherapy, etc.) before enrollment
  • Patients with concurrent colorectal organic diseases
  • Patients with a previous history of colorectal surgery or pelvic radiotherapy that may affect the outcome of this treatment
  • Organ transplantation requires immunosuppressive therapy
  • Serious uncontrolled recurrent infections, or other serious uncontrolled concomitant diseases

Other illness

  • The patient or family members could not understand the conditions and objectives of this study
  • With a history of uncontrolled epilepsy, central nervous system diseases, or mental disorders, their clinical severity may hinder the signing of an informed consent form or affect their compliance with oral medication
  • It is difficult to achieve complete remission base on existing evidence , such as: maximum diameter of cT2/T3 tumor\>4cm; suspicious Lateral lymph nodes (maximum diameter) =5mm; baseline CEA≥100; biopsy pathology contains signet ring cell carcinoma mucinous adenocarcinoma; evaluation team determines whether circumferential constrictive tumor should be included or not when necessary Severe heart disease, such as symptomatic coronary heart disease, New York Cardiology Association (NYHA) grade II or above severe congestive heart failure, or severe arrhythmia requiring pharmacological intervention, or a history of myocardial infarction within the last 12 months

Lab values

  • The baseline blood routine and biochemical indexes of the subject do not meet the following criteria: hemoglobin ≥90g / L; absolute neutrophil count (ANC) ≥1.5\*10\^9 / L; platelet ≥100\*10\^9 / L; ALT and AST≤ 2.5 times normal upper limit; ALP ≤2.5 times normal upper limit; serum total bilirubin \<1.5 times normal upper limit; serum normal creatinine"\<1 time upper limit; and serum albumin ≥30g / L

Other

  • Patients with familial polyposis
  • Pregnant or lactating women

Who the study is looking for

  • Age≥18 years
  • cT1-3N0M0 assessed by CT, MRI and ultrasound colonoscopy
  • Rectal adenocarcinoma confirmed by biopsy pathology and the lower edge of the lesion was within 5cm from the anal edge
  • Patients who have a strong desire to preserve the anus and are willing to accept neoadjuvant treatment, meanwhile is suitable for the implementation of organ preservation strategy after discussion within the multidisciplinary team of the hospital
  • No previous treatment (including endoscopic resection, transanal local resection, radiotherapy, chemotherapy, etc.) before enrollment
  • No contraindications to chemoradiotherapy
  • No other colorectal organic diseases
  • Voluntarily sign the informed consent

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Fudan University Zhongshan Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

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This page is information, not medical advice. Discuss any trial with your doctor.