ECLC: Early Cancer Detection Test - Lung Cancer China

Sponsor
Bai Chunxue (Other)
Overall Status
Unknown status
CT.gov ID
NCT04216511
Collaborator
Gene Tech (Shanghai) Company Limited (Other)
1,000
3
21.3
333.3
15.6

Study Details

Study Description

Brief Summary

Lung cancer is the most common cancer in China from both incidence and mortality rate point of view, with significantly lower 5-year survival rate than average. Early detection is the recognized solution. LDCT is more and more popular accepted as an effective screening methodology but leads to numerous indeterminate pulmonary nodules for physicians to distinguish too. The value of autoantibody test in risk assessing of IPNs as well as early detection of lung cancer in high risk population has been demonstrated in clinical practice and trial but mainly in Caucasian. Purpose of this study is to understand the sensitivity, specificity and accuracy of candidate autoantibodies, and consequently explore the autoantibody combination with best clinical performance in Chinese population.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Tumor autoantibody detection

Study Design

Study Type:
Observational
Anticipated Enrollment :
1000 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Clinic Validation of Autoantibody Panel for Lung Cancer Diagnosis in Chinese Population
Actual Study Start Date :
Aug 22, 2019
Anticipated Primary Completion Date :
Oct 1, 2020
Anticipated Study Completion Date :
Jun 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Case-Lung Cancer

Patients with definite lung cancer diagnosis

Diagnostic Test: Tumor autoantibody detection
Level of a set of autoantibodies potentially relative with lung cancer will be tested for each of the participants.

Control

Either patients with benign pulmonary nodule, or healthy individuals without pulmonary nodule but with risk factors to develop lung cancer matched to lung cancer group

Diagnostic Test: Tumor autoantibody detection
Level of a set of autoantibodies potentially relative with lung cancer will be tested for each of the participants.

Outcome Measures

Primary Outcome Measures

  1. Autoantibody panel with best clinical performance in Chinese population [Oct.30, 2020]

    The combination which can achieve best sensitivity at 90% specificity, and its sensitivity, accuracy and PPV.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Male or female aged 18 or above.

  • Individuals complying with either of the following

  1. diagnosed as lung cancer (histopathologically confirmed);

  2. diagnosed as benign pulmonary nodule (confirmed by pathology or by follow-up based on 2018 Chinese Consensus on Pulmonary Nodule Diagnosis and Treatment);

  3. without pulmonary nodule but with lung cancer risk factor, age & gender matched recruited lung cancer patients.

  • Participant is willing and able to provide necessary information required in CRF.

  • Participant is willing and able to give informed consent for participation in the study.

Exclusion Criteria:
  • History of any cancer;

  • Lung cancer patient who received or is receiving any treatment, including but not limited to surgery, radiotherapy, chemotherapy, targeted therapy and immunotherapy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Zhongshan Hospital of Fudan University Shanghai Shanghai China 200000
2 Shanghai Chest Hospital Shanghai China
3 Henan Province People's Hospital Zhengzhou China

Sponsors and Collaborators

  • Bai Chunxue
  • Gene Tech (Shanghai) Company Limited

Investigators

  • Principal Investigator: Chunxue Bai, MD, Fudan University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Bai Chunxue, Chairman, Chinese Alliance Against Lung Cancer
ClinicalTrials.gov Identifier:
NCT04216511
Other Study ID Numbers:
  • CAALC-007-EarlyCDT Lung China
First Posted:
Jan 2, 2020
Last Update Posted:
Jan 2, 2020
Last Verified:
Dec 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Bai Chunxue, Chairman, Chinese Alliance Against Lung Cancer
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 2, 2020