Rectal Cancer Stage III Clinical Trial
Official title:
A Clinical Trial of Sentinel Lymph Node Biopsy in Rectal Cancer
NCT number | NCT05830890 |
Other study ID # | SLNB |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 2023 |
Est. completion date | December 2025 |
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.
Status | Not yet recruiting |
Enrollment | 87 |
Est. completion date | December 2025 |
Est. primary completion date | December 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
China | National Cancer Center | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
National Cancer Center, China |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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). |
up to 14 days | |
Primary | 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. |
up to 14 days | |
Secondary | 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. |
up to 14 days | |
Secondary | 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). |
up to 14 days | |
Secondary | 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)? |
up to 14 days |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05495308 -
"Oncologic Results and Risk Factors for Recurrence in Patients With Locally Advanced Rectal Cancer and Pathologic Complete Response After Neoadjuvant Treatment. Results From an Observational Retrospective Multicenter Long-term Follow-up Study".
|
||
Recruiting |
NCT04598984 -
The Role of Serum Adipokines in Predicting Response to Neoadjuvant Therapy in Patients With Rectal Cancer
|
||
Active, not recruiting |
NCT04246684 -
Short RT Versus RCT,Followed by Chemo.and Organ Preservation for Interm and High-risk Rectal Cancer Patients
|
Phase 3 | |
Completed |
NCT05723965 -
Using Artificial Intelligence to Predict Rectal Cancer Outcomes
|
||
Active, not recruiting |
NCT04503694 -
Neoadjuvant Regorafenib in Combination With Nivolumab and Short-course Radiotherapy in Stage II-III Rectal Cancer
|
Phase 2 | |
Completed |
NCT02363374 -
Induction Chemotherapy Before or After Preoperative Chemoradiotherapy and Surgery for Locally Advanced Rectal Cancer
|
Phase 2 | |
Recruiting |
NCT03561142 -
Organ Preservation in Locally Advanced Rectal Cancer by Radiochemotherapy Followed by Consolidation Chemotherapy.
|
Phase 2 | |
Completed |
NCT03602079 -
Study of A166 in Patients With Relapsed/Refractory Cancers Expressing HER2 Antigen or Having Amplified HER2 Gene
|
Phase 1/Phase 2 | |
Recruiting |
NCT05148767 -
UGT1A1-Based Irinotecan Therapy for Locally Advanced Rectal Cancer
|
Phase 4 | |
Recruiting |
NCT06254521 -
The Effects of Neoadjuvant Tislelizumab Combined With Chemotherapy in Locally Advanced MSS Rectal Cancer
|
Phase 2 | |
Completed |
NCT01325649 -
Optimal Surgery and MRI Based Radiochemotherapy in Rectal Carcinoma
|
N/A | |
Recruiting |
NCT04970498 -
Application of MRI in Identifying Myelosuppression Risk of Neoadjuvant Chemoradiotherapy for Rectal Cancer
|
||
Active, not recruiting |
NCT03840239 -
TNT to Increase the Clinical Complete Response Rate for Distal LARC
|
Phase 2 | |
Active, not recruiting |
NCT03391843 -
Neoadjuvant Chemotherapy Combined With Cetuximab for EGFR Wild Type Locally Advanced Rectal Cancer
|
Phase 2 |