Fact CheckerSign in

NCT06883084Enrolling by invitation

Clinical Relevance of Pathologic Regression IN Lymph Node for Locally Advanced Rectal Cancer

Clinical Relevance of the Pathologic Regression in Lymph Node for Locally Advanced Rectal Cancer Following Neoadjuvant Chemoradiotherapy: A Multi-center Study

Source: ClinicalTrials.gov · Last updated 19 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

We evaluated all related clinical and pathologic data of patients with Locally Advanced Rectal Cancer following Neoadjuvant Chemoradiotherapy, including the pathologic regression grading in the primary tumor site and lymph node, and other histopathologic characteristics. Finally, the present study was aimed at (1) clarifying the clinical significance of the Major Pathologic Regression for Locally Advanced Rectal Cancer following Locally Advanced Rectal Cancer in the primary tumor site and lymph node, and (2) comparing different Neoadjuvant Chemoradiotherapy treatments of this uncommon disease through conducting a large, multi-center cohort study.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
1080 (estimated)
First submitted
12 Mar 2025
Start date
30 Jan 2014
Primary completion date
30 Dec 2025
Lead sponsor
Yanhong Deng
NCT number
NCT06883084

What you commit to

  • Study type: Observational
  • Planned participants: 1080
  • From 30 Jan 2014 to the primary completion date, 30 Dec 2025
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • \- distant Metastatic disease at diagnosis. Incomplete clinical or pathologic records.

Who the study is looking for

  • \- Adults (≥18 years) diagnosed with locally advanced rectal adenocarcinoma (clinical stage II-III).
  • Completion of NCRT followed by curative-intent surgery. Availability of pre- and post-treatment histopathologic data, including standardized regression grading and digitized whole-slide images (WSIs).

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.