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NCT Number: NCT06823297

Can Neoadjuvant Chemoradiotherapy be Ommited in Mid-rectal Cancer

This project aims to compare the oncological and functional outcomes of patients with mid-rectal cancer who have a low risk of local recurrence (without MRF involvement) and who either receive or do not receive neoadjuvant chemoradiotherapy (nCRT).

Main Question:

H0: In mid-rectal cancer patients without MRF involvement (cT2N+ and cT3Nx), there is no difference in 3-year disease-free survival between direct TME and TME after nCRT.

H1: In mid-rectal cancer patients without MRF involvement (cT2N+ and cT3Nx), direct TME is associated with worse 3-year disease-free survival compared to TME after nCRT.

Participants already taking both interventions as part of their regular medical care for rectal cancer will be recruited in a prospective database for 5 years.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Baskent University, Ankara, Turkey (Türkiye)

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About this study

Neoadjuvant chemoradiotherapy (nCRT) followed by total mesorectal excision (TME) is the standard treatment for patients with locally advanced rectal cancer. This approach has been shown to improve local control and reduce recurrence rates. However, there is no clear evidence showing the advantage of neoadjuvant CRT in high and middle rectal tumors without involvement of mesorectal fascia (MRF). The MERCURY study demonstrated that preoperative MRI-predicted positive CRM is an independent factor for local recurrence. Following this study, the selective use of nCRT in patients at high risk of local recurrence has been proposed.

The ESMO guidelines indicate that T3a/b rectal tumors located above the levator muscles, without involvement of the circumferential resection margin (CRM) or extramural venous invasion (EMVI), are associated with a very low risk of local recurrence. Consequently, they suggest that upfront TME may be an appropriate treatment option for this subgroup of patients. This recommendation remains unchanged in the presence of lymph node involvement within the same group. For clinically staged cT3a/b mid- or high-rectal tumors with clear CRM and no evidence of EMVI, the routine use of nCRT remains a subject of debate. If the surgeon consistently performs high-quality total mesorectal excision (TME), upfront surgery may be a suitable treatment option for this subgroup of patients.

In line with these recommendations, some surgeons perform upfront TME for patients with T2-3 node-positive mid-rectal cancer in the absence of MRF involvement. However, in these cases, the common approach is to administer neoadjuvant chemoradiotherapy. This study seeks to observe whether upfront TME achieves similar 3-year disease-free survival compared to the standard approach of nCRT followed by TME in patients with cT2N+ and cT3Nx mid-rectal cancer without mesorectal fascia involvement.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Pathologically confirmed rectal cancer
  • Rectal cancer within 6-12 cm from anal verge confirmed by sigmoidoscopy or located between the anorectal junction and peritoneal reflection identified by MRI
  • Clinical local staging performed by MRI
  • cT2N+, cT3N0 and cT3N+ tumors
  • Patients without mesorectal fascia involvement assessed by MRI (≤1 mm)
  • Patients without pathological (short axis ≥7 mm) lateral (extramesorectal) lymph nodes on MRI
  • Patients without EMVI on MRI

Exclusion criteria

  • cT4 tumors
  • Stage IV disease
  • Patients with MSI (+) in TME pathology
  • PAtients who received neoadjuvant immunotherapy
  • Emergency surgery
  • Clinical obstruction
  • Previous pelvic radiotherapy
  • Patients treated without a multidisciplinary council decision
  • Inflammatory bowel diseases (Crohn's disease, Ulcerative colitis)
  • Familial adenomatous polyposis (FAP), attenuated FAP, and other polyposis syndromes
  • Hereditary non-polyposis colorectal cancer (Lynch syndrome)
  • Synchronous colon tumors

Treatment and study plan

Total mesorectal excision

Other

Direct surgery without receiving neoadjuvant chemoradiotherapy

Neoadjuvant Chemotherapy followed by total mesorectal excision

Other

Neoadjuvant chemoradiotherapy treatment regimens (including conventional chemoradiotherapy/radiotherapy/chemotherapy regimens or total neoadjuvant chemoradiotherapy regimens) before surgery

Primary outcomes

  1. Disease-free survival (DFS)

    Time frame: 3 years

    The proportion of patients who remain free of disease recurrence (local or distant) three years after surgical intervention. DFS will be assessed through clinical evaluations, imaging studies, and pathology reports at regular follow-up intervals.

Secondary outcomes

  1. Overall Survival

    Time frame: 3 and 5 years

    The proportion of patients alive at 3 and 5 years post-treatment, regardless of disease status.

  2. Local Recurrence Rate

    Time frame: 3 years and 5 years

    The percentage of patients experiencing tumor recurrence at the primary site (anastomosis or pelvis) within 3 and 5 years.

  3. Colorectal Cancer Specific Quality of Life

    Time frame: Baseline, 1 year, 3 years and 5 years

    Patient-reported outcomes assessed using the New Cleveland Clinic Colorectal Cancer Quality of Life Questionnaire

  4. Bowel Dysfunction Related Quality of Life

    Time frame: Baseline, 1 year, 3 years and 5 years

    Patient-reported outcomes assessed using the low-anterior resection syndrome (LARS) score.

Study contacts

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

Cigdem N Arslan, Prof.

CONTACT

[email protected]

+905421454435

Feza Karakayali, Prof.

CONTACT

[email protected]

+905421454435

Sponsors and collaborators

Lead sponsor

Turkish Society of Colon and Rectal Surgery

Other

Collaborators

  • Acibadem Kent Hospital
  • Baskent University
  • Dokuz Eylul University
  • Halic University
  • Istanbul Health and Technology University

Registry information

Official study title

Can Neoadjuvant Chemoradiotherapy be Omitted in cT2N+ and cT3 Mid-rectal Cancer: A Prospective, Observational Cohort Study

Acronym: CANO

Important dates

Study start
2025
Primary completion
2030
Study completion
2035
First posted
Feb 12, 2025
Registry last updated
Jun 27, 2025

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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