Nutrition-support-team Based Intervention in Patients With Advanced Gastrointestinal Cancer (NSTBIPAGC)

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Xi'an Jiaotong University

Status

Unknown

Conditions

Malnutrition
Gastrointestinal Cancer
Nutrition Aspect of Cancer

Treatments

Other: NST group

Study type

Interventional

Funder types

Other

Identifiers

NCT03631537
XJTU1AF-CRF-2017-027

Details and patient eligibility

About

The research studies patients with advanced gastrointestinal cancer who receive chemotherapy in the medical oncology department of the First Affiliated Hospital of Xian Jiaotong University. All patients receive the nutritional risk assessment by the nutritional support team first, and patients with nutritional risk or malnutrition are randomly assigned to the study group and the control group. The study group receive nutritional intervention from the nutritional support team during the period of chemotherapy, while the control group receive routine nutritional support from their clinicians. In the control group, nurses execute the doctors' advice on nutrition, and the nutrition support team does not actively communicate with doctors about the nutritional risk of patients or interfere with it. The baseline characteristics, chemotherapy efficacy, adverse events and prognosis are collected in both groups. At last, data are analyzed to clarify the nutritional status and related factors of patients with advanced gastrointestinal cancer in our hospital, and most important to explore the effect of nutrition-support-team intervention on nutritional status, chemotherapy tolerance and prognosis of patients with advanced gastrointestinal cancer.

Full description

Baseline data include age, gender, pain, sleep condition, family care, tumor type, tumor stage, combined disease, chemotherapy regimen and concomitant medication. Nutritional risk assessments are performed by the nutrition support team just after enrollment, every two cycles of chemotherapy and at the end of the study. The adverse events of chemotherapy are collected and recorded at the end of each cycle. CT or MRI is performed to evaluate efficacy of chemotherapy every two treatment cycles. Patient after one treatment cycle can receive CT or MRI in advance if the clinical condition is worsening.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

advanced (recurrent or metastatic) gastrointestinal malignancies confirmed by pathology, plan to be treated with chemotherapy the expected life period is more than 3 months did not receive chemotherapy, radiotherapy, molecular targeted therapy or surgery in the last 4 weeks has been recovered from the acute toxicity of previous treatment (if patient received surgery, the wound must have completely healed) at least one measurable lesion according to RECIST 1.1 edition (the measurable lesion has not received radiotherapy) normal function of main organs:Blood routine examination needs to be met: Hb≥90g/L (without blood transfusions within 14 days); ANC≥1.5×109/L; PLT≥80×109/LBiochemical examination should conform to the following standards: TBIL≤1.5×ULN (upper limit of normal value); ALT and AST≤2.5×ULN (ALT and AST≤5×ULN, in case of liver metastasis); Serum creatinine ≤1×ULN, creatinine clearance rate >50ml/min (Cockcroft-Gault formula) volunteer to participate in the study, sign the informed consent, and cooperate with good compliance

Exclusion criteria

pregnancy or lactation having a long-term unhealed wound, traumatic or pathological fracture urinary protein > 2+ or 24 hour urinary protein >1.0g suffering from mental illness with hypertension and fail to get good control through antihypertensive medication (systolic pressure >140mmHg and/or diastolic pressure >90mmHg) serious diabetes, heart disease (including but not limited to myocardial ischemia, myocardial infarction, cardiac insufficiency, congestive heart failure), thrombotic diseases (including but not limited to cerebral hemorrhage, deep venous thrombosis and pulmonary embolism) long-term use of steroid for other medical reasons with diseases that may increasing the underlying research risk judged by researchers having a bleeding tendency or a great worry of gastrointestinal bleeding with infection requiring antibiotic treatment history of immunodeficiency, including HIV positive, organ transplantation and other acquired/congenital immunodeficiency disorders patients with Hepatitis B(except inactive carrier) or Hepatitis C took part in other clinical studies or is involved in other research projects at present

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

NST group
Experimental group
Description:
Nutrition support team gives the dietary supplement or other nutritional support during the period of chemotherapy
Treatment:
Other: NST group
routine group
No Intervention group
Description:
clinicians decide whether to give and how to give the dietary supplement and other nutritional support

Trial contacts and locations

1

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Central trial contact

Lingxiao Zhang, doctor

Data sourced from clinicaltrials.gov

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