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Sentinel Lymph Node Biopsy in Rectal Cancer

Primary Purpose

Rectal Cancer Stage III, Rectal Cancer Stage IV

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Sentinel lymph node biopsy
Indocyanine green solution
fluorescence laparoscope
pathological examination
rapid frozen pathological examination
total mesorectal excision
Sponsored by
National Cancer Center, China
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Rectal Cancer Stage III focused on measuring Laparoscope, Rectal cancer, Indocyanine green, Sentinel lymph node, lymph node dissection

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Aged 18 to 75 years old. Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-1. Newly diagnosed patients with confirmed rectal cancer by histopathology. Preoperative clinical staging by imaging examination is T3-4. Preoperative colonoscopy shows the distance from the tumor's lower edge to the anus is less than 10cm. No previous chemotherapy or radiotherapy. Preoperative imaging examination (pelvic enhanced MRI) shows lateral lymph nodes with a maximum short diameter of ≥5mm and <10mm. Women of childbearing age must take effective contraceptive measures. Able to understand the study and sign the informed consent form. Exclusion Criteria: Complete intestinal obstruction. Active hepatitis and peripheral neuropathy (such as peripheral neuritis, pseudomeningitis, motor neuritis, sensory disturbances, etc.). Pregnant or lactating women; women of childbearing potential who have not taken sufficient contraceptive measures. History of other tumors or previous chemotherapy or radiotherapy. Alcoholism or drug addiction. Significant organ dysfunction or other significant diseases, including clinically relevant coronary artery disease, cardiovascular disease, or myocardial infarction within 12 months before enrollment; severe neurological or psychiatric history; severe infection; active disseminated intravascular coagulation. Hypoproteinemia. Preprandial blood glucose control exceeds 11.2mmol/L in the week before surgery. BMI>28 kg/m^2. Poor compliance, and failure to comply with the study protocol. Subject withdrawal from the study

Sites / Locations

  • National Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Sentinel Lymph Node Biopsy

Arm Description

The fluorescence laparoscope was used to visualize and locate the sentinel lymph node, which was then removed.

Outcomes

Primary Outcome Measures

False negative rate
The false negative rate of predicting lateral lymph node metastasis status using rapid frozen pathology results of lateral sentinel lymph nodes in mid-to-low rectal cancer. Namely, the false negative rate= total false negative cases/(total false negative cases+total true positive cases).
Accuracy
The accuracy of predicting lateral lymph node metastasis status using rapid frozen pathology results of lateral sentinel lymph nodes in mid-to-low rectal cancer. Namely, the accuracy = (total true negative cases+total true positive cases)/total number of cases.

Secondary Outcome Measures

Detection rate
The detection rate of lateral sentinel lymph nodes in middle and low rectal cancer. Namely, the detection rate = (total true positive cases+total false positive cases)/total number of cases.
Specificity
The specificity of predicting lateral lymph node metastasis status using rapid frozen pathology results of lateral sentinel lymph nodes in mid-to-low rectal cancer. Namely, the specificity = total true negative cases/(total true negative cases+total false positive cases).
Sensitivity
The Sensitivity of predicting lateral lymph node metastasis status using rapid frozen pathology results of lateral sentinel lymph nodes in mid-to-low rectal cancer. Namely, the sensitivity= total true positive cases/(total true positive cases+total false negative cases)。

Full Information

First Posted
March 15, 2023
Last Updated
April 26, 2023
Sponsor
National Cancer Center, China
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1. Study Identification

Unique Protocol Identification Number
NCT05830890
Brief Title
Sentinel Lymph Node Biopsy in Rectal Cancer
Official Title
A Clinical Trial of Sentinel Lymph Node Biopsy in Rectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
May 2023 (Anticipated)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Cancer Center, China

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Rectal cancer is one of the most common malignant tumors, with 9% to 23% of patients experiencing pelvic sidewall lymph node metastasis. According to the current Chinese guidelines for diagnosing and treating colorectal cancer, pelvic sidewall lymph node dissection is recommended for patients who have experienced or are suspected of having lateral lymph node metastasis. Lateral lymph node dissection can result in longer operation times, increased bleeding, and complications such as urinary and sexual dysfunction after surgery. Currently, the presence of metastasis is primarily determined by the size and enhancement characteristics of lateral lymph nodes observed through imaging studies. However, the pathological lymph node metastasis rate of specimens collected after lateral lymph node dissection based on current imaging criteria is only 20.5%. Therefore, a pressing clinical challenge is accurately determining the presence of lateral lymph node metastasis and avoiding unnecessary lateral lymph node dissection in patients who have not experienced lateral lymph node metastasis. Sentinel lymph node biopsy has been widely used in clinical practice. It has replaced traditional lymph node dissection in some breast cancer and melanoma patients, reducing surgical risks and complications and improving patients' quality of life. This study aims to use indocyanine green as a tracer for fluorescence-guided laparoscopic navigation to locate the lateral sentinel lymph nodes of rectal cancer in the pelvic cavity. By studying the accuracy, specificity, and false-negative rate of predicting lateral lymph node status using the sentinel lymph node, we can further clarify the clinical significance of the lateral sentinel lymph node.
Detailed Description
This study is a prospective single-arm clinical study. 87 patients with middle and low rectal cancer are planned to be included in the study. After general anesthesia during the operation, indocyanine green is injected around the tumor through the anus. After the sentinel lymph nodes are developed and located by fluorescent laparoscopy, they are removed and sent to rapid frozen pathological examination, and then the lateral lymph nodes are cleaned. Through pathological examination and statistical analysis of the fluorescent stained lateral sentinel lymph nodes and all the cleaned lateral lymph nodes, To evaluate the clinical significance of lateral sentinel lymph nodes located by this technique in predicting the status of lateral lymph nodes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer Stage III, Rectal Cancer Stage IV
Keywords
Laparoscope, Rectal cancer, Indocyanine green, Sentinel lymph node, lymph node dissection

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
87 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sentinel Lymph Node Biopsy
Arm Type
Experimental
Arm Description
The fluorescence laparoscope was used to visualize and locate the sentinel lymph node, which was then removed.
Intervention Type
Procedure
Intervention Name(s)
Sentinel lymph node biopsy
Other Intervention Name(s)
Lateral lymph nodes dissection
Intervention Description
After the total mesorectal excision, the indocyanine green was injected around the tumor via the anus. The fluorescence laparoscope was used to visualize and locate the sentinel lymph node, which was then removed and sent for rapid frozen pathological examination. Subsequently, a lateral lymph node dissection was performed.
Intervention Type
Drug
Intervention Name(s)
Indocyanine green solution
Other Intervention Name(s)
Indocyanine green fluorescence imaging
Intervention Description
Indocyanine green was injected around the tumor via the anus to visualize the sentinel lymph nodes under the fluorescence laparoscope.
Intervention Type
Device
Intervention Name(s)
fluorescence laparoscope
Intervention Description
The fluorescence laparoscope was used to visualize and locate the sentinel lymph node.
Intervention Type
Diagnostic Test
Intervention Name(s)
pathological examination
Intervention Description
The surgical specimens and sentinel lymph nodes were routinely examined for pathology.
Intervention Type
Diagnostic Test
Intervention Name(s)
rapid frozen pathological examination
Intervention Description
The lateral green fluorescence imaging sentinel lymph nodes found during surgery was sent to make cryosections. And then a pathologist makes a rapid diagnosis under a microscope。
Intervention Type
Procedure
Intervention Name(s)
total mesorectal excision
Other Intervention Name(s)
TME
Intervention Description
Sharply dissect the vascular interface between the pelvic fascia parietal layer and the visceral layer around the mesentery under direct vision to ensure that the rectal mesentery of the resected specimen is intact and tearless. For medium and low rectal cancer: the distal intestinal tube of the tumor should be resected ≥ 2 cm. TME or mesenteric distal resection margin ≥ 5 cm away from the tumor.
Primary Outcome Measure Information:
Title
False negative rate
Description
The false negative rate of predicting lateral lymph node metastasis status using rapid frozen pathology results of lateral sentinel lymph nodes in mid-to-low rectal cancer. Namely, the false negative rate= total false negative cases/(total false negative cases+total true positive cases).
Time Frame
up to 14 days
Title
Accuracy
Description
The accuracy of predicting lateral lymph node metastasis status using rapid frozen pathology results of lateral sentinel lymph nodes in mid-to-low rectal cancer. Namely, the accuracy = (total true negative cases+total true positive cases)/total number of cases.
Time Frame
up to 14 days
Secondary Outcome Measure Information:
Title
Detection rate
Description
The detection rate of lateral sentinel lymph nodes in middle and low rectal cancer. Namely, the detection rate = (total true positive cases+total false positive cases)/total number of cases.
Time Frame
up to 14 days
Title
Specificity
Description
The specificity of predicting lateral lymph node metastasis status using rapid frozen pathology results of lateral sentinel lymph nodes in mid-to-low rectal cancer. Namely, the specificity = total true negative cases/(total true negative cases+total false positive cases).
Time Frame
up to 14 days
Title
Sensitivity
Description
The Sensitivity of predicting lateral lymph node metastasis status using rapid frozen pathology results of lateral sentinel lymph nodes in mid-to-low rectal cancer. Namely, the sensitivity= total true positive cases/(total true positive cases+total false negative cases)。
Time Frame
up to 14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18 to 75 years old. Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-1. Newly diagnosed patients with confirmed rectal cancer by histopathology. Preoperative clinical staging by imaging examination is T3-4. Preoperative colonoscopy shows the distance from the tumor's lower edge to the anus is less than 10cm. No previous chemotherapy or radiotherapy. Preoperative imaging examination (pelvic enhanced MRI) shows lateral lymph nodes with a maximum short diameter of ≥5mm and <10mm. Women of childbearing age must take effective contraceptive measures. Able to understand the study and sign the informed consent form. Exclusion Criteria: Complete intestinal obstruction. Active hepatitis and peripheral neuropathy (such as peripheral neuritis, pseudomeningitis, motor neuritis, sensory disturbances, etc.). Pregnant or lactating women; women of childbearing potential who have not taken sufficient contraceptive measures. History of other tumors or previous chemotherapy or radiotherapy. Alcoholism or drug addiction. Significant organ dysfunction or other significant diseases, including clinically relevant coronary artery disease, cardiovascular disease, or myocardial infarction within 12 months before enrollment; severe neurological or psychiatric history; severe infection; active disseminated intravascular coagulation. Hypoproteinemia. Preprandial blood glucose control exceeds 11.2mmol/L in the week before surgery. BMI>28 kg/m^2. Poor compliance, and failure to comply with the study protocol. Subject withdrawal from the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yueyang Zhang, M.D.
Phone
+8613552910035
Email
yyzhang0129@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Zheng Xu, M.D.
Phone
+8613141127297
Email
840677252@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Haitao Zhou, M.D.
Organizational Affiliation
National Cancer Center, China
Official's Role
Study Chair
Facility Information:
Facility Name
National Cancer Center
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100000
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Haitao Zhou, M.D.
Phone
+8613381167333
Email
zhouhaitao01745@163.com
First Name & Middle Initial & Last Name & Degree
Yueyang Zhang, M.D.
Phone
+8613552910035
Email
yyzhang0129@163.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Participants' data are only allowed to be used for the analysis of this study and are not authorized to be shared with other researchers.

Learn more about this trial

Sentinel Lymph Node Biopsy in Rectal Cancer

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