Cancer Hospital, Chinese Academy of Medical Sciences
Beijing, 100021, China
Location status: Recruiting
Location contact
SHUANGZHENG JIA, PhD
CONTACT
NCT Number: NCT06349148
The goal of this open-label randomized control trial is to study the effect of immunonutrition in locally advanced cervical cancer (LACC) with standard concurrent chemoradiotherapy. LACC patients undergoing radical synchronous chemoradiotherapy will be randomized into the experimental group receiving enteral immunonutrition therapy and the control group receiving standard enteral nutrition support.The main purpose it aims to answer are:1)Can immunonutrition therapy improve patients' dose-limiting toxicity(DLT) and DLT-free survival? 2)Can immunonutrition therapy improve patients' nutritional status and quality of life?
Interested in participating?
Request Info18 year and older
Female
Interventional
Not applicable
Beijing, 100021, China
Location status: Recruiting
SHUANGZHENG JIA, PhD
CONTACT
Malnutrition is one of the most common complications in patients with Locally Advanced Cervical Cancer (LACC) undergoing radical concurrent chemoradiotherapy (CCRT). Tumor patients often experience significant immune imbalance, metabolic abnormalities, and inflammatory responses. Immunonutrition therapy involves the use of specific immunonutrients such as polyunsaturated fatty acids, arginine, nucleotides, etc., to prevent and correct malnutrition in cancer patients, regulate immune function, alleviate harmful or excessive inflammatory responses, and thereby improve patients' clinical outcomes.
This study is an open-label randomized controlled trial, including patients with LACC who all receive radical radiotherapy. Using the Nutritional Risk Screening 2002 (NRS2002) at screening, patients identified as having nutritional risk are further assessed by nutritionists and physicians using the Patient-Generated Subjective Global Assessment (PG-SGA) score and modified Global leadership initiative on malnutrition (GLIM) criteria. Patients with moderate or severe malnutrition are randomly allocated into the enteral immunonutrition therapy group (experimental group) and the standard enteral nutrition support group (control group). The experimental group receives immunonutrients per day, while the control group receives isoenergetic standard oral enteral nutrition. Upon admission, all patients receive nutritional education from specialized nurses and consult with nutritionists, and nutritional support is provided during the concurrent chemoradiotherapy for a total of 5 weeks (W0-W5).GLIM score, quality of life score and peripheral blood inflammation and immune indicators were collected within 48 hours after admission (before treatment), W5, W8, and W20; CTCAE v 5.0 score was used for treatment side effects.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients in this group receives 2 bottles of immunonutrients per day (Impact, Nestlé, approximately 700 kcal).
Patients in the control group receives isoenergetic standard oral enteral nutrition ( emulsion or Nutrison).
Time frame: 5-6 weeks
Patients need to receive cisplatin treatment at 40 mg/m2 weekly for 5-6 weeks. During this period, any serious adverse reactions that lead to treatment interruption, delay, or chemotherapy dose reduction are defined as dose-limiting toxicities(DLT).
Time frame: 5-6 weeks
Time from start of treatment to onset of DLT
Time frame: 5-6 weeks
the proportion of people who complete the prescribed treatment plan
Time frame: 5-6 weeks, 3 months post-treatment
assessed by GLIM criteria
Time frame: 5-6 weeks, 3 months post-treatment
assessed by Skeletal muscle index(SMI) at the third lumbar vertebra(L3-SMI )calculated based on CT
Time frame: 5-6 weeks, 3 months post-treatment
Quality of life measured by standardized EORTC quality of life questionnaire(QLQ)-C30
Time frame: 3 months post-treatment
evaluated by RECIST
Time frame: 5-6 weeks, 3 months post-treatment
inflammation and immune-related indicators
Time frame: 2 years
the time from the start of treatment until the date of death from any cause
Time frame: 2 years
the date of the treatment to the date of disease progression or death from any cause in the absence of progression
Contact information is provided by the study sponsor or research team.
SHUANG ZHENG JIA, PhD
Other
The Effects of Immunonutrition Therapy on the Nutritional Status, Immune Function, and Quality of Life of Locally Advanced Cervical Cancer Patients With Malnutrition: an Open-label Randomized Controlled Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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