- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05709769
Radiomics-based Malnutrition for Cervical Cancer.
Development and Validation of a CT-Based Radiomics Nomogram for the Prediction of Postoperative Malnutrition in Stage IB1-IIA2 Cervical Cancer (Nutrition Helper-1).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Cervical cancer is still a significant health problem worldwide. Based on the pathological findings after surgery, patients with intermediate or high risk factors for recurrence are recommended to receive adjuvant pelvic RT and/or platinum (cisplatin or carboplatin) based CRT to reduce the risk of tumor recurrence. However, around 30% of individuals with CC will still eventually develop tumor relapse, necessitating the investigation of better supportive care, like nutritional support, to improve therapeutic tolerance and reduce toxic reactions in these patients. In this respect, how to early identification of malnutrition by PG-SGA tool is crucial.
Meanwhile, CT-based radiomics approaches have been successfully applied to generate imaging biomarkers as decision support tools for clinical practice. In our recently accepted research (not yet publish on line, abstract available at https://www.frontiersin.org/articles/10.3389/fnut.2023.1113588/abstract), we firstly analyzed the radiomics features of psoas extracted at the level of L3 and then, developed a nomogram prediction model for patients with FIGO stage IB1-IIA2 CC who received postoperative RT/CRT. Our results demonstrated that this nomogram prediction model showed promising ability for detecting malnutrition based on their PG-SGA scores. The aim of the current study is designed to verify the prediction accuracy of the developed radiomics-based nomogram prospectively.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Hong'en Xu, M.D.
- Phone Number: +86-571-85893638
- Email: xuhongenzpph@sina.com
Study Contact Backup
- Name: Huafeng Shou, M.D.
- Phone Number: +86-571-85893385
- Email: hfshou@126.com
Study Locations
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Zhejiang
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Hangzhou, Zhejiang, China, 310000
- Recruiting
- Zhejiang Provincial People's Hospital
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Contact:
- Yongshi Jia, M.D.
- Email: jiayongshi@medmail.com.cn
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients received pelvic lymphadenectomy and radical hysterectomy, and pathological diagnosis of CC;
- Patients had stage IB1-IIA2 CC based on the 2014 FIGO staging system for cervical cancer;
- Patients received postoperative RT/CRT within one week after admission at the ZJPPH;
- Patients must have Eastern Cooperative Oncology Group performance status 0-2;
- No treatments prior to radical surgery;
- Normal marrow function and the blood tests must be collected within 7 days from enrollment with a hemoglobin of ≥ 80g/L (can be transfused with red blood cells pre-study), an white blood cell (WBC) counts of ≥ 3.0×109/L,a neutrophil count of ≥ 2.0×109/L, , a platelet count of ≥100×109/L, a total bilirubin (TBil) of ≤ 1.0 upper normal limitation (UNL), a creatinine (Cr) of ≤ 1.0 UNL, alanine aminotransferase (ALAT) and aspartate aminotransferase (ASAT) of ≤ 2.5 UNL, Alkaline phosphatase (AKP) ≤5.0 UNL. and no major electrocardiogram abnormalities.
- Patient does not have a known allergy to platinum (cisplatin or carboplatin) or compounds of similar biologic composition.
- Patients must be with good compliance and agree to accept nutritional therapy;
- Informed consent signed. -
Exclusion Criteria:
- Poor image quality or visible artifacts around the L3 psoas;
- Prior treatments of chemotherapy or irradiation;
- Poor bone marrow, liver and kidney functions, which would make chemotherapy or radiotherapy intolerable;
- Participating in other clinical trials;
- Pregnancy, breast feeding, or not adopting birth control;
- Clinically significant and uncontrolled major medical conditions including but not limited to: active uncontrolled infection, symptomatic congestive heart failure, Unstable angina pectoris or cardiac arrhythmia, psychiatric illness/ social situation that would limit compliance with study requirements; any medical condition, which in the opinion of the study investigator places the subject at an unacceptably high risk for toxicities;
- The subject has had another active malignancy within the past five years;
- Poor image quality or visible artifacts around the L3 psoas. -
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Training Group
A primary cohort of eligible patients from the cancer center of Zhejiang Provincial People's Hospital is used for developing the radiomics-based nomogram prediction model.
In the training cohort, a sample size of 88 was required to accept the hypothesis that the prediction accuracy of the radiomics-based nomogram model was greater than 45% with 90% power and to reject the hypothesis that the prediction accuracy rate was less than 30% with an α error of 5%.
Initially, we planned to enroll 77 patients in the first stage.
If 27 or more prediction accuracy rates were observed, we planned to continue to the second stage for a total of 88 patients for the analysis.
Considering some deviant cases, the preplanned accrual number was set to 100 patients in the training cohort.
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There are no interventions.
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Validation Group
An independent cohort of eligible patients is used for external validation.
we are planning to enroll an additional 50 patients to further validate this radiomics-based nomogram prediction model.
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There are no interventions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Construction and Validation
Time Frame: 06/30/2023-10/31/2026
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Construction and validation of a radiomics-based nomogram for the prediction of malnutrition based on the PG-SGA scores in cervical cancer patients who underwent postoperative radiotherapy/chemoradiotherapy.
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06/30/2023-10/31/2026
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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GLIM criteria
Time Frame: 02/01/2023-10/31/2026
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Predict malnutrition assessed by the new Global Leadership Initiative on Malnutrition (GLIM) criteria.
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02/01/2023-10/31/2026
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Correlation
Time Frame: 02/01/2023-10/31/2026
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Analyze the correlation among NRS-2002 score, PG-SGA score and the GLIM criteria.
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02/01/2023-10/31/2026
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Collaborators and Investigators
Investigators
- Study Chair: Yongshi Jia, M.D., Zhejiang Provincial People's Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Neoplasms
- Urogenital Neoplasms
- Neoplasms by Site
- Uterine Neoplasms
- Genital Neoplasms, Female
- Uterine Cervical Diseases
- Uterine Diseases
- Nutrition Disorders
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Genital Diseases
- Genital Diseases, Female
- Uterine Cervical Neoplasms
- Malnutrition
Other Study ID Numbers
- ZJPPH-RT-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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