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Molecular Analysis and Treatment Options of SCLC

Molecular Landscape Analysis and Clinical Implications for SCLC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05945745
Enrollment
500
Registered
2023-07-14
Start date
2016-01-01
Completion date
2028-12-31
Last updated
2024-11-29

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

Conditions

Small-cell Lung Cancer, Small Cell Lung Cancer, Combined Type, Small Cell Lung Cancer Extensive Stage, Small Cell Lung Cancer Limited Stage, Small Cell Lung Carcinoma

Brief summary

Small cell lung cancer (SCLC) is an aggressive disease that is characterized by rapid growth and the early development of metastases. Patients typically respond to initial chemotherapy but quickly experience relapse, resulting in a poor long-term outcome. Therapeutic innovations that substantially improve survival have historically been limited, and reliable, predictive biomarkers are lacking. Ongoing research has advanced the understanding of molecular categories and the immunologic microenvironment of SCLC, which in turn has helped improve disease classification and staging. Considering the role of molecular alterations has not yet fully to be defined in the treatment of SCLC, there is an urgent recognition that molecular alterations in the SCLC are important to predict response and survival for novel therapies and ongoing clinical trials. Advances in research have revealed critical information regarding biologic characteristics of the disease, which may lead to the identification of vulnerabilities and the development of new therapies. Further research focused on identifying biomarkers and evaluating innovative therapies will be paramount to improving treatment outcomes for patients with SCLC. In summary, identification of (genetic) biomarkers in SCLC is increasingly essential to perform molecular diagnostics and individualized treatments. This project aims to create a registry of patients with SCCL to further the characterization of molecular alterations and develop (novel) treatments based on the detection.

Interventions

DRUGChemotherapy

different treatments based on the molecular analysis

Sponsors

Shanghai Chest Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Histologically proven diagnosis of SCLC * 18 years of age or older * Ability to understand and the willingness to sign a written informed consent document

Exclusion criteria

* Histologically proven diagnosis of non-SCLC

Design outcomes

Primary

MeasureTime frameDescription
Objective response rate (ORR)20 yearsCollect detailed clinical information on patients with SCLC via the electronic medical records
Disease control rate (DCR)20 yearsCollect detailed clinical information on patients with SCLC via the electronic medical records
Progression-free survival (PFS)20 yearsCollect detailed clinical information on patients with SCLC via the electronic medical records

Secondary

MeasureTime frameDescription
Overall survival (OS)20 yearsCollect detailed clinical information on patients with SCLC via the electronic medical records

Countries

China

Contacts

Primary ContactXiaomin Niu
ar_tey@hotmail.com, artey@sjtu.edu.cn021-22200000

Outcome results

None listed

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