NSE/Alb as a Prognostic Biomarker for Lung Cancer
NARPBLC
A Prospective Cohort Study on NSE/Alb as a Prognostic Biomarker for Lung Cancer Patients in Multicenter
1 other identifier
observational
202
1 country
1
Brief Summary
The incidence and mortality rate of lung cancer is the highest in the world. Current studies have found that tumor markers, inflammatory or nutritional indicators have a good predictive value for the prognosis of patients with non-small cell lung cancer (NSCLC). Neuron specific enolase (NSE) and serum albumin (Alb) are important indicators for monitoring tumor progression and nutritional status in lung cancer patients, respectively. Previous studies suggested that the higher the NSE, the worse prognosis of NSCLC patients, while the lower the Alb, the worse the prognosis of patients with malignant tumors. Through a retrospective study, the investigators found that NAR (NSE Alb Ratio) was higher and prognosis was poorer in patients undergoing NSCLC surgery. This is better than the previous assessment indicators PLR (platelet to lymphocyte ratio), NLR (neutrophil to lymphocyte ratio), AGR (albumin to globulin ratio), NAR can better assess prognosis. Therefore, on the basis of the previous retrospective analysis, the optimal NAR cut-off value was calculated according to ROC curve, and the value was grouped into multi-center prospective cohort study, and the relationship between NAR and other clinical indicators was studied by chi-square test. Univariate and multivariate analysis of Cox proportional hazard regression model was used to determine the prognostic factors. Finally, NSCLC patients were stratified according to tumor stage and pathological classification, and the differences of survival time between high NAR group and low NAR group were compared again under different stages and types, and the different stages of NAR in NSCLC patients were further analyzed. The clinical significance of typing. By exploring and validating the relationship between NAR and the prognosis of NSCLC patients, the investigators try to establish a new prognostic index. Obviously, it has important value for clinical application.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2017
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2017
CompletedFirst Submitted
Initial submission to the registry
October 28, 2018
CompletedFirst Posted
Study publicly available on registry
October 30, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2019
CompletedMay 21, 2019
August 1, 2018
2.5 years
October 28, 2018
May 19, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Overall survival
The time from randomization to death due to any cause. The last follow-up time is usually calculated as the time of death for those who have been lost before death.
2 years.
Secondary Outcomes (1)
Disease-free survival
2 years.
Study Arms (2)
high NAR
Neuron-Specific Enolase to Albumin Ratio is higher than 3.2×10-7
low NAR
Neuron-Specific Enolase to Albumin Ratio is lower than 3.2×10-7
Interventions
Previous studies have shown that inflammation and nutrition-related factors such as CRP/Alb (C-reactive protein-albumin ratio), PLR (platelet-to-lymphocyte ratio), NLR (neutrophil-to-lymphocyte ratio) can help to assess the prognosis of malignant tumors. This study is the first time to combine NSCLC tumor marker NSE and patient nutrition-related indicators Alb to predict the prognosis of patients, trying to find high sensitivity and specificity for NSCLC prognostic indicators to guide clinical work.
Eligibility Criteria
Sample sources: Xi'an Jiaotong University First Affiliated Hospital, Second Affiliated Hospital, Shaanxi Provincial People's Hospital, Shaanxi Provincial Cancer Hospital and other hospitals. Subject recruitment process: 1. Subject screening: Subjects were screened according to inclusion and exclusion criteria. 2. Recruitment of the research subject: In the course of clinical diagnosis and treatment, the competent doctor recruits. 3. Subject informed consent: inform patients to collect their clinical data and follow up for clinical studies, signing informed consent.
You may qualify if:
- (1) pathological diagnosis of non-small cell lung cancer
- (2) 18-70 years of age and no gender restriction.
- (3) patients who were admitted for the first time and underwent routine blood tests, three lung cancer and liver function tests.
You may not qualify if:
- (1) pregnant or lactating women
- (2) patients with other malignancies at the same time
- (3) patients with acute and chronic inflammation, autoimmune diseases, and patients with obvious liver and renal insufficiency.
- (4) patients with incomplete clinical and pathological data.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- First Affiliated Hospital Xi'an Jiaotong Universitylead
- Second Affiliated Hospital of Xi'an Jiaotong Universitycollaborator
- Shaanxi Provincial Cancer Hospitalcollaborator
- Shaanxi Provincial People's Hospitalcollaborator
- Xi'an Central Hospitalcollaborator
Study Sites (1)
First hospital affiliated Xi'an jiaotong university
Xi'an, Shaanxi, 710061, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Sida Qin, MD PhD
First Affiliated Hospital Xi'an Jiaotong University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 28, 2018
First Posted
October 30, 2018
Study Start
January 1, 2017
Primary Completion
June 30, 2019
Study Completion
June 30, 2019
Last Updated
May 21, 2019
Record last verified: 2018-08