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NCT Number: NCT06146946

Safety of Mid and Low Rectal Cancer Surgery Without Dissection of the No.253 Lymph Node (S-M-O-O-T-H)

The goal of this clinical trial is to learn about whether it is safe to omit dissection of the No.253 lymph nodes in mid and low rectal cancer surgery. The main question it aims to answer is that if it is possible to achieve the same long-term survival with and without the dissection of the No.253 lymph node in mid and low rectal cancer surgery. Participants will underwent laparoscopic rectal radical resection with or without the dissection of the No.253 lymph node.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Beijing Cancer Hospital, Beijing, Beijing Municipality, China

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About this study

The No.253 lymph node, as the third station in the inferior mesenteric artery lymphatic system, plays a significant role in the lymphatic circulation of the descending colon, sigmoid colon, and rectum. They act as the last barrier for tumor metastasis from the regional to distant areas. However, there is still controversy regarding whether rectal cancer patients universally require dissection of the No.253 lymph node. The rate of metastasis to the No.253 lymph node in rectal cancer patients is extremely low, and dissection may not bring survival benefits. Additionally, postoperative urinary and sexual functions may be impaired due to damage to the sympathetic nerves. However, current prospective randomized controlled trials on the safety of omitting the dissection of the No.253 lymph node have small sample sizes and lack sufficient test power. Further confirmation is needed from large-sample prospective randomized controlled studies. Based on this, the investigator plans to collaborate with Peking Union Medical College Hospital, China-Japan Friendship Hospital, Chinese People's Liberation Army General Hospital, Shanghai Ruijin Hospital, Fudan Cancer Hospital, and West China Hospital of Sichuan University, totaling eight medical centers, to conduct a prospective randomized controlled study. This study aims to confirm the safety of mid and low rectal surgery without dissection of the No.253 lymph node, providing high-level evidence-based medical evidence for the implementation of this surgical technique.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patient age between 18-75 years.
  • Colonic biopsy pathology confirms adenocarcinoma.
  • At initial treatment, colonoscopy and imaging diagnose the tumor's lower edge as less than or equal to 7cm from the anus.
  • At initial treatment, imaging diagnoses the tumor T stage as less than or equal to 3.
  • At initial treatment, imaging diagnoses no enlarged lymph nodes at the root of the inferior mesenteric artery.
  • At initial treatment, imaging diagnoses the number of mesenteric metastatic lymph nodes as less than or equal to three.
  • Strong willingness for surgery and signed informed consent.

Exclusion criteria

  • Previous history of malignant colorectal tumors.
  • Colonic biopsy pathology reveals mucinous adenocarcinoma or signet ring cell carcinoma.
  • Imaging diagnosis of distant metastasis.
  • Patients who have undergone multiple abdominal-pelvic surgeries or have extensive abdominal adhesions.
  • Patients with complications such as intestinal obstruction, intestinal perforation, or intestinal bleeding requiring emergency surgery.
  • Extensive lesions not amenable to R0 resection.
  • Diagnosed with other malignancies within the past five years.
  • ASA (American Society of Anesthesiologists) classification ≥ IV and/or ECOG (Eastern Cooperative Oncology Group) performance status score ≥ 2.
  • Patients with severe liver, kidney, cardiac, pulmonary, coagulation dysfunctions, or serious underlying diseases that cannot tolerate surgery.
  • History of severe mental illness.
  • Pregnant or breastfeeding women.

Treatment and study plan

Dissection of the No.253 lymph node

Procedure

The range of the No.253 lymph node is as follows: medially, it extends from the root of the inferior mesenteric artery to the starting section of the left colonic artery; caudally, from the starting point of the left colonic artery to the intersection with the inferior mesenteric vein; laterally, it is bordered by the outer margin of the inferior mesenteric vein; and cranially, from the horizontal section of the duodenum to the beginning of the jejunum. In the controlled group, the surgery is performed with dissection of the No.253 lymph node.

Omitting the dissection of the No.253 lymph node

Procedure

In the experimental group, the surgery is performed without dissection of the No.253 lymph node.

Primary outcomes

  1. 3-year disease free survival rate

    Time frame: 3 years after surgery

    Disease free survival refers to the length of time after primary treatment during which a patient survives without any signs or symptoms of the cancer.

Secondary outcomes

  1. Number of harvested lymph nodes

    Time frame: About 10 days after surgery

    Total number of lymph nodes dissected in the pathology report

  2. Incidence of postoperative complications

    Time frame: 30 days after surgery

    The proportion of short-term complications occurring within 30 days post-surgery

  3. Intraoperative blood loss

    Time frame: Intraoperative

    Total blood loss during the surgery

  4. Operative duration

    Time frame: Intraoperative

    total time spent performing a surgical procedure. This time is typically measured from the moment the surgery begins (marked by the initial incision) to its conclusion (marked by the closure of the surgical wound)

  5. Postoperative urination and sexual function

    Time frame: 1 year after surgery

    Three months, six months, and one year postoperatively, evaluate patients' urinary and sexual functions using scales.

  6. 3-year local recurrence rate

    Time frame: 3 years after surgery

    Local recurrence refers to the return of cancer in the same area where it originally developed, typically after treatment has been completed.

  7. 3-year overall survival rate

    Time frame: 3 years after surgery

    Overall survival refers to the length of time from the primary treatment that patients are still alive.

Study contacts

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

Mingguang Zhang, Dr.

CONTACT

[email protected]

+8613261967603

Qian Liu, Dr.

CONTACT

[email protected]

13601008906

Sponsors and collaborators

Lead sponsor

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Other

Collaborators

  • China-Japan Friendship Hospital
  • Chinese PLA General Hospital
  • Fudan University
  • Peking Union Medical College Hospital
  • Peking University Cancer Hospital & Institute
  • Ruijin Hospital
  • West China Hospital

Registry information

Official study title

Safety of Mid and Low Rectal Cancer Surgery Without Dissection of the No.253 Lymph Node, a Prospective, Multicenter, Non-inferior Randomized Controlled Trial

Important dates

Study start
2023
Primary completion
2026
Study completion
2029
First posted
Nov 27, 2023
Registry last updated
Mar 26, 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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