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Rectal NeoplasmsNCT06879197

Clinical Relevance of Major Pathologic Regression for Locally Advanced Rectal Cancer

An observational study of Rectal Neoplasms and Chemotherapy Effect, run by Yanhong Deng.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

We evaluated all related clinical and pathologic data of patients with Locally Advanced Rectal Cancer following Neoadjuvant Chemoradiotherapy, including the pathologic regression grading, and other histopathologic characteristics. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Rectal Neoplasms, Chemotherapy Effect
How many people
1,187 participants
Where
No sites listed yet
Study dates
30 Apr 2016to 30 Mar 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: patients with Locally Advanced Rectal Cancer following Locally Advanced Rectal Cancer

Who may be able to join

  • 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).

Who cannot join

  • Metastatic disease at diagnosis. Incomplete clinical or pathologic records.

About this study

Official title: Clinical Relevance of the Major Pathologic Regression for Locally Advanced Rectal Cancer Following Neoadjuvant Chemoradiotherapy: A Multi-center Study

We evaluated all related clinical and pathologic data of patients with Locally Advanced Rectal Cancer following Neoadjuvant Chemoradiotherapy, including the pathologic regression grading, 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 and (2) comparing different Neoadjuvant Chemoradiotherapy treatments of this uncommon disease through conducting a large, multi-center cohort study.

Read the detailed description

This large-scale, multi-center cohort study aims to investigate the clinical and prognostic implications of histopathologic characteristics in patients with Locally Advanced Rectal Cancer (LARC) following Neoadjuvant Chemoradiotherapy (NCRT). The study will retrospectively and prospectively analyze data from consecutive LARC patients treated at participating institutions between 2016 and 2022.

Study Design and Objectives

Primary Objective:

To evaluate the clinical significance of Major Pathologic Regression (MPR) in LARC patients following NCRT. MPR is defined as ≤10% residual viable tumor within the tumor bed in the pathologic evaluation. The study will correlate MPR status with long-term survival outcomes, including Progression-Free Survival (PFS) and Overall Survival (OS), to determine its validity as a surrogate endpoint for treatment efficacy.

Secondary Objectives:

To compare the efficacy of different NCRT regimens (e.g., fluoropyrimidine-based vs. oxaliplatin-containing protocols) in achieving MPR and improving survival outcomes.

To assess the prognostic value of novel histopathologic parameters, such as tumor necrosis density (NECR-TD), tumor-infiltrating lymphocyte (TLS) density, and TLS-to-necrosis ratio (T/NR), in predicting DFS and OS.

Study Population

Inclusion Criteria:

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).

Exclusion Criteria:

Metastatic disease at diagnosis. Incomplete clinical or pathologic records. Data Collection and Variables

Clinical Data:

Demographics, tumor stage ( ypTNM), NCRT regimen, surgical approach, recurrence, and survival outcomes.

Pathologic Data:

Regression Grading: Residual viable tumor percentage, necrosis extent, and lymph node regression (ypN-Reg+/-).

Quantitative Digital Pathology: AI-driven analysis of WSIs to compute NECR-TD, TLS-TD, and T/NR (Figure 1).

Follow-Up:

PFS and OS will be tracked for a minimum of 3 years post-surgery. Statistical Analysis

Survival Analysis:

Kaplan-Meier curves and Cox proportional hazards models will assess associations between MPR, histopathologic parameters, and survival outcomes.

Comparative Analysis:

Subgroup analyses will compare outcomes across NCRT regimens and LARC subtypes (e.g., mucinous vs. adenocarcinoma).

Machine Learning:

Prognostic models integrating clinical and histopathologic variables will be developed to predict DFS/OS.

Ethical Considerations The Institutional Review Boards (IRBs) of all participating centers have approved the study protocol.

Patient data will be anonymized, and informed consent will be waived for retrospective cohorts but obtained prospectively.

Innovation and Impact

This study addresses critical gaps in the prognostication of LARC by:

Validating MPR as a standardized endpoint for NCRT efficacy. Introducing quantitative, AI-driven histopathologic biomarkers (e.g., T/NR) to refine risk stratification.

Providing evidence for optimizing NCRT regimens based on tumor biology and regression patterns.

Results will be disseminated through peer-reviewed publications and clinical guidelines to improve personalized treatment strategies for LARC.

Medical subject headings
Rectal Neoplasms

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. PFS

    Progression free regression

    Measured: 5 year

  2. OS

    overall survival

    Measured: 5 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Mar 2025
  2. Study start30 Apr 2016
  3. Primary completion30 Dec 2022
  4. Study completion30 Mar 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
1,187 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06879197
Sponsor's protocol ID
GIH-SYSUyip33
Status last verified
Mar 2025
First submitted
11 Mar 2025
Last updated
17 Mar 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Rectal Neoplasms and Chemotherapy Effect, run by Yanhong Deng.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 17 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

PFS (time frame: 5 year). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Mar 2025.

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