NCT03257735

Brief Summary

Primary lung cancer is one of the most common malignancies in China, with 57 percent of patients being diagnosed at advanced stage. At present, advanced lung cancer has entered the era of precise treatment. So it is very important to determine the gene mutation status of the tumor and prescribe drugs at the targets. Liquid biopsy is a suitable alternative when tumor tissues are difficult to obtain. Liquid biopsy technique refers to the use of human body fluid as a sample source to detect the information of related diseases, including blood, urine, saliva and cerebrospinal fluid. It is non-invasive, fast and simple, and can avoid the problem of insufficient sample size and support for repeated sampling to continuously monitor disease. With the increasing incidence of lung cancer and the development of diagnosis and treatment technology, the survival period of patients has been extended, and the incidence and diagnosis rate of the brain metastasis of lung cancer have increased year by year. The brain metastasis of lung cancer is the most common type of brain metastatic tumor. The incidence rate is about 40-50%, and the prognosis is poor--the natural median survival period is about 1-2 months. Because of the impractical intracranial tumor biopsy and very low level of DNA in peripheral blood, cerebrospinal fluid, which makes close contact with brain tumors, becomes potential available samples. Several studies have shown that genetic testing of cerebrospinal fluid is feasible. Therefore, this study aims to test the cerebrospinal fluid, blood and tissue by the latest second-generation sequencing technology at different time points, to dynamically monitor the gene mutation status of cerebrospinal fluid, blood and tissue, to explore the role of cerebrospinal fluid biopsy in the diagnosis and treatment of non-small cell lung cancer with brain metastases.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2017

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2017

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

August 5, 2017

Completed
17 days until next milestone

First Posted

Study publicly available on registry

August 22, 2017

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2018

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2019

Completed
Last Updated

August 22, 2017

Status Verified

August 1, 2017

Enrollment Period

1.7 years

First QC Date

August 5, 2017

Last Update Submit

August 21, 2017

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change from baseline gene mutation status at 2 months

    compare the gene mutation status of cerebrospinal fluid,blood and tumor tissue at baseline and after the first session

    2 months

  • Change from second line gene mutation status at 6 months

    compare the gene mutation status of cerebrospinal fluid,blood and tumor tissue after the first session and at the time of tumor progression

    6 months

Secondary Outcomes (2)

  • PFS

    From date of randomization until the date of first documented progression or date of death from any cause,whichever came first,assessed up to 60 months.

  • OS

    From date of randomization until the date of death from any cause,assessed up to 60 months

Interventions

1. Patients' cerebrospinal fluid, blood and tumor tissue were collected within 3 days before treatment at diagnosis. 2. Patients' cerebrospinal fluid and blood were extracted at the time of first evaluation of efficacy after treatment (TKI began after 1 month or chemotherapy after 2 cycles). 3. Patients' cerebrospinal fluid and blood were extracted at first time of tumor progression,and re-biopsy of tumor tissue was done as much as possible. All the samples were tested by next-generation sequencing.

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients were histologically confirmed with NSCLC and identified with new brain metastases by MRI.

You may qualify if:

  • Male or female, aged over 18 and less than 75 years old
  • The estimated survival period is greater than 12 weeks
  • ECOG score is less than 2
  • Histological diagnosis is non-small cell lung cancer, and there are enough tissue specimens for lung cancer related gene detection
  • The brain metastasis is confirmed by brain MRI, and the first line treatment of brain metastasis was considered as chemotherapy or target therapy
  • There must be at least one evaluable lesion based on the criteria of RECIST 1.1 (maximum diameter at least 10mm on spiral CT and MRI)
  • Patients are tolerable for lumbar puncture with no contraindication
  • Patients are able to comply with the research requirements and follow-up procedures
  • Patients must sign the informed consent prior to the beginning of any substantive test procedure (informed consent is subject to approval of the independent ethics committee)

You may not qualify if:

  • Brain metastases were treated
  • Intracranial symptoms were obvious, and radiotherapy/surgery was considered in the first line treatment
  • Histological specimens are not enough to detect lung cancer related genes
  • Patients were suffering from other types of malignancy
  • Patients have any contraindications of lumbar puncture
  • Patients have any uncontrolled systemic disease, including active infection, uncontrolled high blood pressure, diabetes, unstable angina and congestive heart failure, myocardial infarction (1 year) before the start of treatment, severe arrhythmia that needs drugs therapy, coagulant function abnormality, liver or kidney or metabolic disease
  • Pregnant and lactating pregnant women
  • Patients were not willing to be followed up

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, 510000, China

RECRUITING

Related Publications (1)

  • Li M, Chen J, Zhang B, Yu J, Wang N, Li D, Shao Y, Zhu D, Liang C, Ma Y, Ou Q, Hou X, Chen L. Dynamic monitoring of cerebrospinal fluid circulating tumor DNA to identify unique genetic profiles of brain metastatic tumors and better predict intracranial tumor responses in non-small cell lung cancer patients with brain metastases: a prospective cohort study (GASTO 1028). BMC Med. 2022 Nov 14;20(1):398. doi: 10.1186/s12916-022-02595-8.

Biospecimen

Retention: SAMPLES WITH DNA

We plan to detect the patients' cerebrospinal fluid,blood and tumor tissue with the method of next-generation sequencing.

MeSH Terms

Conditions

Lung NeoplasmsBrain Neoplasms

Condition Hierarchy (Ancestors)

Respiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract DiseasesCentral Nervous System NeoplasmsNervous System NeoplasmsBrain DiseasesCentral Nervous System DiseasesNervous System Diseases

Study Officials

  • Likun Chen, PhD

    Sun Yat-sen University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Delan Li, master

CONTACT

Likun Chen, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief Physician

Study Record Dates

First Submitted

August 5, 2017

First Posted

August 22, 2017

Study Start

May 1, 2017

Primary Completion

December 31, 2018

Study Completion

May 31, 2019

Last Updated

August 22, 2017

Record last verified: 2017-08

Data Sharing

IPD Sharing
Will not share

Individual participant data are not available to others.

Locations