- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04096118
Relationship Between Lymph Node Ratio and Survival Rate in Preoperative Chemoradiation Rectal Cancer Patients
May 7, 2020 updated by: Mahidol University
Colorectal cancer is the most-common cancer of the gastrointestinal tract.
The number of positive lymph nodes and total number of lymph nodes retrieved are important prognostic factors.
In patients who do not receive preoperative chemoradiation, the total number of lymph nodes should be more than 12 nodes to predict accurate staging.
In cases of locally-advanced rectal cancer when patients receive neoadjuvant chemoradiation it is sometimes impossible to retrieve adequate amount of lymph nodes due to the chemoradiation effect.
Therefore, this study was to evaluate and predict survival rates based on positive lymph node ratio.
Study Overview
Status
Completed
Conditions
Detailed Description
The primary endpoint of this study was to assess the lymph node ratio as another predictor for survival rate in preoperative chemoradiation rectal cancer patients.
The other secondary objective was to determine the relationship between total harvested lymph nodes and survival rate in each stage.
This is a retrospective, single-centered study, collecting data of patients from January 2011 to December 2017.
Including a total of 163 patients with rectal cancer who underwent surgery following neoadjuvant chemoradiation.
Using Cox regression and Kaplan-Meier survival analysis to determine whether the lymph node ratio can be used to predict the survival rate and determine the cut-off value to distinguish the prognosis of the disease.
Study Type
Observational
Enrollment (Actual)
160
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Bankok
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Bangkok, Bankok, Thailand, 10400
- Chairat Supsamutchai
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with rectal cancer who underwent curative surgery following neoadjuvant chemoradiation.
Description
Inclusion Criteria:
- Patients with rectal cancer who underwent surgery following neoadjuvant chemoradiation.
- Patients have tissues confirmed by Pathology
- no metastasis before surgery
Exclusion Criteria:
- Distant metastasis during surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Survival rates
Time Frame: 5 year
|
survival rate in preoperative chemoradiation rectal cancer patients.
|
5 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Chairat Supsamutchai, MD, Faculty of Medicine Ramathibodi Hospital, Mahidol University
- Principal Investigator: Tanet Chatmongkonwat, MD, of Medicine Ramathibodi Hospital, Mahidol University.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2018
Primary Completion (Actual)
September 30, 2019
Study Completion (Actual)
October 30, 2019
Study Registration Dates
First Submitted
April 17, 2019
First Submitted That Met QC Criteria
September 17, 2019
First Posted (Actual)
September 19, 2019
Study Record Updates
Last Update Posted (Actual)
May 11, 2020
Last Update Submitted That Met QC Criteria
May 7, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2017/426
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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