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NCT06854107Completed

Intratumoral and Peritumoral Habitat Radiomics of MRI Predict Pathologic Complete Response to Neoadjuvant Chemoimmunotherapy in Oral Squamous Cell Carcinoma

Source: ClinicalTrials.gov · Last updated 6 Mar 2025

Brief summary (registry, in English)

Background:Neoadjuvant chemoimmunotherapy (NACI) shows promise in oral squamous cell carcinoma (OSCC), but reliable noninvasive biomarkers for predicting pathologic complete response (pCR) remain scarce. Radiomics integrating intratumoral and peritumoral heterogeneity across multi-sequence MRI may offer novel insights into treatment response evaluation. Methods: The data of 212 patients with OSCC after NACI were retrospectively collected and analyzed. Among these patients, 56 (26.4%) achieved pCR after NACI. Intratumoral and peritumoral habitat imaging (HI) was achieved using the K-means clustering algorithm applied to T1-weighted imaging (T1WI), axial T2-weighted imaging with fat suppression (T2WI), and contrast-enhanced T1-weighted imaging with fat suppression (T1C). Moreover, intratumoral and peritumoral HI models were constructed and compared using the receiver operating characteristic (ROC) curve. Five-fold cross-validation was performed to mitigate model overfitting.

Status (registry)
Completed
Study type
Observational
Enrollment
225 (actual)
First submitted
25 Feb 2025
Start date
1 Dec 2023
Primary completion date
1 Dec 2023
Lead sponsor
Zilong Yuan
NCT number
NCT06854107

What you commit to

  • Study type: Observational
  • Participants enrolled: 225
  • From 1 Dec 2023 to the primary completion date, 1 Dec 2023
  • 1 site in 1 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

  • Absence of clinical data and postoperative pathological results;
  • MRI image artifacts significantly affecting image quality.

Who the study is looking for

  • Histopathologically confirmed OSCC at the initial diagnosis;
  • No treatment received prior to the first MRI examination;
  • Receipt of NACI;
  • Underwent MRI examination after NACI;
  • Underwent surgical intervention.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hubei Cancer Hospitla
Coordinator of this site? Confirm its status
WuhanChinaUnknown status

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