New lymph node map could sharpen colon cancer prognosis
NCT ID NCT07380464
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study analyzed data from 1,500 colon cancer patients to see if a new way of classifying lymph node involvement—based on both the number and location of affected nodes and tumor deposits—can better predict survival than the current standard system. Researchers collected medical records and follow-up information to compare the two approaches. The goal is to improve how doctors estimate a patient's outlook after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a more accurate staging system for colon cancer, helping doctors better predict patient outcomes.
- What could go wrong
- This is an observational study analyzing existing data, so it cannot prove that the new system improves survival. The results may not change current practice without further validation.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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1,500 people
The number who actually took part.
- Started
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Mar 2010
- Finished
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Jul 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This study enrolled a total of 1,500 participants between January 2010 and December 2022. Inclusion criteria were defined as follows: (1) a confirmed diagnosis of primary colon adenocarcinoma via auxiliary examination or pathology; (2) absence of distant metastasis (M0) verified by preoperative imaging or intraoperative findings; (3) initial radical colectomy; and (4) complete documentation of lymph node counts across three stations. Patients were excluded if they had received any form of neoadjuvant therapy (including chemotherapy, radiotherapy, immunotherapy, or targeted therapy) prior to surgery. Additionally, cases were excluded if intraoperative or postoperative pathology revealed non-malignant tumors (including carcinoma in Tis) or if patients presented with multiple primary cancers or concurrent malignancies in other sites.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Definite diagnosis of primary colon adenocarcinoma via auxiliary examination or pathology. * No distant metastasis (M0) confirmed by preoperative imaging or intraoperative findings. * No prior neoadjuvant therapy (including chemotherapy, radiotherapy, immunotherapy, or targeted therapy). * Underwent initial radical resection for colon cancer. * Available data on lymph node counts for all three stations. Exclusion Criteria: * Intraoperative or postoperative pathology confirming non-malignant tumors (including carcinoma in Tis). * Multiple primary cancers or concurrent malignancies in other sites.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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