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Prospective Genomics Initiative on Multiple Synchronous Lung Cancer (PGI-MSLC)

Prospective Genomics Initiative on Multiple Synchronous Lung Cancer (PGI-MSLC)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03795155
Enrollment
100
Registered
2019-01-07
Start date
2018-12-01
Completion date
2023-11-30
Last updated
2020-06-11

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

Conditions

Multiple Synchronous Lung Cancers (MSLCs)

Brief summary

This prospective study is to characterize the genomic landscape and genetic heterogeneity of multiple synchronous lung cancer (MSLC) in correlation with comprehensive clinical, histopathological and medical imaging information, in order to improve disease diagnosis and tailored treatment for MSLC patients.

Detailed description

* To initiate a prospective registry of MSLC patients with high-quality clinical samples and detailed medical data. * To define the clonal relationship, genomic landscape and potential driver alterations of MSLC using whole-genome sequencing. * To determine the intrapatient and intratumor genetic heterogeneity of MSLC. * To correlate molecular features with clinical parameters and patient outcome. * To serve as a continuous infrastructure for a large variety of research purposes including: A. Diagnostic research B. Prognostic research C. Biological research D. Interventional trial design testing new therapies in MSLC.

Interventions

None listed

Sponsors

RenJi Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years or older * Confirmed diagnosis of multiple synchronous lung cancers (MSLCs) without metastatic disease * Signed informed consent

Exclusion criteria

* Medical or psychiatric condition that would preclude informed consent * History of known high-risk infections * With metastatic tumors except lung

Design outcomes

Primary

MeasureTime frameDescription
Genomic characters of synchronous lessions in each MSLC patientNovember 30, 2021Whole-genome sequencing reveals the mutation, copy number variation and structure variation of MSLCs. We will analysis the genomic characters of synchronous lesions in each MSLC patient.

Countries

China

Contacts

Primary ContactPengfei Ma, Ph.D.
pengfei0820@163.com+8613671806647

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026