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NCT Number: NCT05563922

Organ Preservation Strategy of Total Neoadjuvant Chemoradiotherapy for Low Rectal Carcinoma

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Fudan University Zhongshan Hospital

Shanghai, Shanghai Municipality, 200032, China

Location status: Recruiting

Location contact

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

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

Treatment and study plan

Total Neoadjuvant Chemoradiotherapy

Combination Product

Radiotherapy:45Gy/25F+Boost 50Gy/25F. A total of 45 Gy, 25 fractions of 1.8 Gy, 5 fractions a week

CapOx:

Capecitabine 1000mg / m² po bid (1-14 days, 21 days a cycle) Oxaliplatin 130mg / m2 igtt(Day 1, 21 days a cycle) TEM or endoscopic local resection

Other names: Total Neoadjuvant Treatment

Primary outcomes

  1. Organ preservation rate at 3 years

    Time frame: 3 years

    Patients with a good pathological response(ypT 0-1 without neural vascular invasion)after neoadjuvant treatment followed by transanal endoscopic microsurgery(TEM)or endoscopic local resection will be offered an organ preservation strategy

Secondary outcomes

  1. Clinical complete response rate after neoadjuvant chemoradiotherapy

    Time frame: 18 weeks

    Define as complete withdrawal of rectal cancer after neoadjuvant radiotherapy and chemotherapy, and no distant metastasis in imaging examination, and no tumor residue in imaging examination and endoscopic biopsy

  2. 3-year local recurrence rate

    Time frame: 3 years

    Occurrence of local recurrence in patients with an organ preservation strategy

  3. 3-year distant metastases rate

    Time frame: 3 years

    Occurrence of distant metastases in patients with an organ preservation strategy

  4. 3-year Disease-free survival(DFS)rates

    Time frame: 3 years

    Disease free survival defined as the time from enrollment to the first documented disease progression of local recurrence or distance metastasis or death due to any cause

  5. 3-year overall survival(OS) rates

    Time frame: 3 years

    OS is defined as the time from enrollment to death due to any cause

  6. Quality of life (EORTC-QLQ-C 30, psychological status)

    Time frame: 20 weeks

    Assess QLQ-C30 in patients with an organ preservation strategy

  7. 5-year Disease-free survival(DFS)rates

    Time frame: 5 years

    Disease free survival defined as the time from enrollment to the first documented disease progression of local recurrence or distance metastasis or death due to any cause

  8. 5-year overall survival(OS) rates

    Time frame: 5 years

    OS is defined as the time from enrollment to death due to any cause

Study contacts

Contact information is provided by the study sponsor or research team.

Jian Wang, M.D.

CONTACT

[email protected]

+8613816101686

Sponsors and collaborators

Lead sponsor

Shanghai Zhongshan Hospital

Other

Registry information

Official study title

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

Acronym: OP-TNT

Important dates

Study start
2022
Primary completion
2025
Study completion
2027
First posted
Oct 3, 2022
Registry last updated
Oct 3, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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