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Integrative Analysis of Large-cell Lung Cancer

Integrative Analysis of Large-cell Lung Carcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02917369
Acronym
LCLC
Enrollment
1000
Registered
2016-09-28
Start date
2016-01-31
Completion date
2026-12-31
Last updated
2016-09-28

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

Conditions

Lung Cancer

Keywords

LCLC; Integrative Analysis; Metastasis

Brief summary

Integrative analysis of LCLC

Detailed description

The investigators will analyzed proteomes of paired normal lung tissues and LCLC with or without liver metastasis, sequenced transcriptomes, perform whole exome sequencing, and single nucleotide polymorphism (SNP) array profiling for triplets, each comprising normal lung tissue, primary LCLC carcinoma, and its synchronous matched metastasis, as well as analyzed genomics of lung cancer characterized previously by The Cancer Genome Atlas (TCGA) to conduct integrated proteogenomic analyses.

Interventions

OTHERNormal lung tissue

The investigators will extract total protein, DNA and RNA from LCLC patients.

Sponsors

Shanghai Pulmonary Hospital, Shanghai, China
CollaboratorOTHER
Shanghai 10th People's Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age ≤ 75 years with histologically proven LCLC * No severe major organ dysfunction * World Health Organization (WHO) performance status of 0 or 1 * No prior cancer chemotherapy

Exclusion criteria

* Age ≥ 76 * Severe major organ dysfunction * WHO performance status of \>1 * Prior cancer chemotherapy

Design outcomes

Primary

MeasureTime frame
5 years overall survival5 years

Secondary

MeasureTime frame
5 years disease-free survival5 years

Countries

China

Contacts

Primary ContactDa Fu, PhD
fu800da900@126.com00-86-21-66301604

Outcome results

None listed

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