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Effect of enteral nutrition on the prognosis of patients with lung cancer or breast cancer treated with internal medicine: a single-center prospective cohort study

Effect of enteral nutrition on the prognosis of patients with lung cancer or breast cancer treated with internal medicine: a single-center prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070144
Enrollment
Unknown
Registered
2023-04-03
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung cancer, breast cancer

Interventions

EN group:N/A
PN group:N/A
Nutrition advisory group:N/A

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ?adult patients with unresectable locally advanced or metastatic lung or breast cancer diagnosed by histopathology and/or cytology; ?AJCC stage III or IV; ?having at least one measurable lesion confirmed by CT or MRI according to RECIST 1.1 criteria for assessing the objective efficacy of oncologic therapy. Target lesions located within the irradiated field of previous radiotherapy or within the area after local treatment were considered measurable if progression was confirmed; ? the presence of nutritional risk as assessed by NRS2002 or malnutrition as assessed by PG-SGA; ? expected survival = 3 months; ? planned to continue chemotherapy at our hospital for = 3 subsequent cycles (both surgical and non-surgical patients); ? patients and their families were informed of this study and signed Informed consent form

Exclusion criteria

Exclusion criteria: (1) Patients with double primary or multiple primary malignancies; (2) Patients without pathological confirmation; (3) Patients with severe cardiac, hepatic, or renal dysfunction or other life-threatening comorbidities; (4) Patients who did not cooperate with this study, withdrew from the manager midway, or were unable/unwilling to complete the follow-up program; (5) Patients with communication disorders or psychiatric disorders; (6) Patients who had received parenteral or enteral nutrition therapy prior to admission.

Design outcomes

Primary

MeasureTime frame
objective response rate;disease control rate;the QLQ-C30 score;

Secondary

MeasureTime frame
body mass;body mass index;total protein;arm circumference;Triceps skin fold thickness;albumin;hemoglobin;IgG;IgA;CD4+/CD8+;hypersensitive C-reactive protein;tumor necrosis factor a;prealbumin;NRS2002 score;PG-SGA score;CD4+ T-lymphocytes;CD8+ T-lymphocytes;IL-2;IL-4;IL-6;IL-10;adverse reaction rate;

Countries

China

Contacts

Public ContactChen Shi

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, China.

29136909@qq.com15807138405

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026