Multi-parametric MRI and Dual-energy CT in Patients of Gastric Cancer

Sponsor
The First Affiliated Hospital with Nanjing Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05508126
Collaborator
(none)
222
1
62
3.6

Study Details

Study Description

Brief Summary

Accurate preoperative staging of gastric cancer is of major importance for guiding therapeutic decision-making, preventing both under- and over-treatment. The purpose of this study is to investigate the diagnostic performance of the Multi-parametric magnetic resonance imaging (mpMRI) and dual-energy computed tomography (DECT) in gastric cancer.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: DECT examination
  • Diagnostic Test: mpMRI examination

Detailed Description

Gastric cancer is the leading cause of cancer-related death worldwide. The therapeutic approach to gastric cancer is strongly dependent on preoperative stage. The crucial role of gastric cancer imaging lies in implementing individualized treatment regimens according to various stages of tumor.

CT scanning has been recommended as the first-line image modality for preoperative evaluation of gastric cancer by the 8th AJCC staging manual. However, for traditional CT, the accuracy of staging is highly variable and the sensitivity of early gastric cancer detection is relatively low. Recently, DECT has been increasingly used in clinical practice due to its powerful post-processing technique. A recent small sample study showed that monoenergetic images at 40 KeV improved lesion depiction and higher T stage accuracy for gastric cancer. Therefore, this study chose DECT instead of traditional CT to explore the diagnostic performance in preoperative staging.

Historically, the role of MRI in gastric cancer has been limited, and the guidelines have not yet recommended MRI as a first-line examination scheme. But with the continuous technical improvements for abdominal imaging (e.g. breath-hold sequences and high Resolution diffusion-weighted imaging (DWI), free-breathing dynamic contrast-enhanced (DCE) sequence), mpMRI has become a promising imaging technology. In addition, given the advantages of non-radiation, non-invasiveness, and excellent soft tissue contrast, mpMRI may be more suitable for neoadjuvant therapy patients who require multiple evaluations.

Patients with gastric cancer confirmed by endoscopic biopsy will be prospectively included in this study. Patients undergo both mpMRI and DECT at baseline to stage the primary tumor, regional lymph nodes, and to rule out distant sites of disease. The interval between mpMRI and DECT examinations should not exceed 7 days. All patients will be treated according to standard practice in our institution. Patients receiving neoadjuvant chemotherapy will undergo mpMRI and DECT scan again for restaging. The postoperative pathology results of these two examination methods were prospectively collected, and their efficacy was calculated according to the reference standard. After completion of study intervention, patients are followed up periodically.

Study Design

Study Type:
Observational
Anticipated Enrollment :
222 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Diagnostic Accuracy of Multi-parametric MRI and Dual-energy CT in Gastric Cancer: a Paired Validating Confirmatory Study
Actual Study Start Date :
Nov 1, 2021
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Primary staging group I

All patients will be treated according to standard practice. Patients in group I are patients that will be stratified for radical gastrectomy or endoscopic resection. Group I will undergo only a primary staging. All patients will take DECT and mpMRI examination within 1 week before surgery.

Diagnostic Test: DECT examination
DECT examinations will be performed using a 192-slice CT scanner (SOMATOM, Force, Siemens, Forchheim, Germany).

Diagnostic Test: mpMRI examination
The examinations were conducted on a 3-T MR scanner (MAGNETOM Skyra; Siemens Healthcare, Erlangen, Germany).

Restaging group II

Patients in group II are patients that will be stratified for neoadjuvant chemotherapy. Group II will undergo a primary staging (DECT and mpMRI) and 1-2 times restaging (DECT and mpMRI).

Diagnostic Test: DECT examination
DECT examinations will be performed using a 192-slice CT scanner (SOMATOM, Force, Siemens, Forchheim, Germany).

Diagnostic Test: mpMRI examination
The examinations were conducted on a 3-T MR scanner (MAGNETOM Skyra; Siemens Healthcare, Erlangen, Germany).

Outcome Measures

Primary Outcome Measures

  1. Diagnostic performance of DECT and mpMRI in tumor staging assessment [2 years]

    Accuracy for both imaging techniques in the prediction of tumor staging.

  2. Diagnostic performance of DECT and mpMRI in tumor restaging assessment [2 years]

    Accuracy for both imaging techniques in the prediction of tumor restaging.

Secondary Outcome Measures

  1. The kappa value [2 years]

    Inter-rater reliability of the DECT and mpMRI in tumor assessment

  2. Predictive value of DECT and mpMRI after the neoadjuvant treatment for pathologic response [4 years]

    Pathological tumour regression grading (Mandard criterion): from 1 to 5 grading.

  3. Disease free survival (DFS) [4 years]

    Survival analysis: Radiologic data predicting DFS.

  4. Overall survival (OS) [5 years]

    Survival analysis: Radiologic data predicting OS.

  5. Likert scales 1-5 [6 months]

    Qualitative image analysis of mpMRI in a supine and prone position

  6. The signal-to-noise Ratio (SNR) [6 months]

    Quantitative image analysis of mpMRI in a supine and prone position.

  7. Contrast-to-noise Ratio (CNR) [6 months]

    Quantitative image analysis of mpMRI in a supine and prone position.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Consecutive patients with preoperative pathologically confirmed GC by endoscopy and preoperative imaging data (DECT/mpMRI) were included.

  • No contraindications for CT/MRI examination

  • Written informed consent

Exclusion Criteria:
  • Patients with a history of previous therapy.

  • Patients with recurrent gastric cancer

  • Patients with a history of severe allergy to contrast agents

  • Patients with imaging artefacts affect the evaluation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Yu-Dong Zhang Nanjing China 210029

Sponsors and Collaborators

  • The First Affiliated Hospital with Nanjing Medical University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
The First Affiliated Hospital with Nanjing Medical University
ClinicalTrials.gov Identifier:
NCT05508126
Other Study ID Numbers:
  • 2021-SR-475
First Posted:
Aug 19, 2022
Last Update Posted:
Aug 19, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The First Affiliated Hospital with Nanjing Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 19, 2022