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NCT Number: NCT06349148

The Effects of Immunonutrition Therapy on Locally Advanced Cervical Cancer Patients

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?

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years;
  • Pathological histological diagnosis confirmed as cervical squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma;
  • Confirmed as Locally Advanced Cervical Cancer (LACC) based on gynecological examination and imaging assessment;
  • Undergoing CCRT/RT treatment;
  • Patients are conscious, able to communicate without barriers, and able to answer questions.
  • diagnosed with malnutrition according to the GLIM criteria;

Exclusion criteria

  • Patients who received neoadjuvant chemotherapy or immunotherapy before treatment;
  • Patients with concomitant other malignant tumors or a history of malignant tumors;
  • Patients with special pathological types of tumors such as cervical small cell carcinoma or neuroendocrine tumors;
  • Patients staged as Ⅳb according to the International Federation of Gynecology and Obstetrics(FIGO) 2018 staging system;
  • Patients with other severe chronic debilitating diseases, such as severe heart failure (New York Heart Association Class II-IV), severe liver damage (alanine aminotransferase ≥ 3 times the upper limit of normal), severe renal insufficiency (GFR < 30 ml/min*1.73 m²), etc.;
  • Eastern Cooperative Oncology Group(ECOG) performance status ≥ 2;
  • Presence of other contraindications to CCRT/RT.

Treatment and study plan

enteral immunonutrition

Dietary Supplement

Patients in this group receives 2 bottles of immunonutrients per day (Impact, Nestlé, approximately 700 kcal).

standard oral enteral nutrition

Dietary Supplement

Patients in the control group receives isoenergetic standard oral enteral nutrition ( emulsion or Nutrison).

Primary outcomes

  1. Dose-limiting toxicity

    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).

  2. DLT-free survival

    Time frame: 5-6 weeks

    Time from start of treatment to onset of DLT

Secondary outcomes

  1. compliance

    Time frame: 5-6 weeks

    the proportion of people who complete the prescribed treatment plan

  2. Prevalence of malnutrition

    Time frame: 5-6 weeks, 3 months post-treatment

    assessed by GLIM criteria

  3. Prevalence of sarcopenia

    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

  4. QoL (Quality of life)

    Time frame: 5-6 weeks, 3 months post-treatment

    Quality of life measured by standardized EORTC quality of life questionnaire(QLQ)-C30

  5. Objective response rate (ORR)

    Time frame: 3 months post-treatment

    evaluated by RECIST

  6. laboratory tests

    Time frame: 5-6 weeks, 3 months post-treatment

    inflammation and immune-related indicators

  7. 2-year overall survival

    Time frame: 2 years

    the time from the start of treatment until the date of death from any cause

  8. 2-year progression-free survival

    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

Study contacts

Contact information is provided by the study sponsor or research team.

SHUANGZHENG JIA, PhD

CONTACT

[email protected]

00-86-010-87788276

Sponsors and collaborators

Lead sponsor

SHUANG ZHENG JIA, PhD

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Apr 5, 2024
Registry last updated
Dec 5, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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