Molecular Analysis and Treatment Options of SCLC

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorShanghai Chest Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Histologically proven diagnosis of SCLC

18 years of age or older

Ability to understand and the willingness to sign a written informed consent document

Disqualifiers

Histologically proven diagnosis of non-SCLC

Trial population

Participants with SCLC are with the standard treatment and/or are enrolled in the clinical trials.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Chemotherapy

    Drug

    different treatments based on the molecular analysis

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Objective response rate (ORR)

Collect detailed clinical information on patients with SCLC via the electronic medical records

Time frame
20 years
2

Disease control rate (DCR)

Collect detailed clinical information on patients with SCLC via the electronic medical records

Time frame
20 years
3

Progression-free survival (PFS)

Collect detailed clinical information on patients with SCLC via the electronic medical records

Time frame
20 years

Secondary outcomes

1

Overall survival (OS)

Collect detailed clinical information on patients with SCLC via the electronic medical records

Time frame
20 years

Other outcomes

Sponsors and contacts

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