Small Cell Lung Cancer Clinical Trial
Official title:
Tempus Small Cell Lung Cancer Observational Study (Sculptor): A Tissue and Longitudinal Circulating Tumor DNA (ctDNA) Biomarker Profiling Study of Patients With Small Cell Lung Cancer (SCLC) Using Comprehensive Next-Generation Sequencing (NGS) Assays
NCT number | NCT05257551 |
Other study ID # | TP-CA-003 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | July 13, 2022 |
Est. completion date | March 2026 |
Verified date | May 2024 |
Source | Tempus AI |
Contact | Sculptor Study |
Phone | 833-514-4187 |
sculptor-study[@]tempus.com | |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The study is a non-interventional evaluation of participants with SCLC who will receive diagnostic and (where possible) post-progression tumor tissue profiling, alongside plasma ctDNA biomarker profiling in addition to their standard of care therapy and disease surveillance.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | March 2026 |
Est. primary completion date | March 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Histologically confirmed small cell lung cancer diagnosis - Diagnosis made with excisional or core needle biopsy specimen (fine needle aspirate may be permitted with approval from the PI) - Subjects must submit fresh or archived FFPE tumor sample to the central laboratory - ECOG performance status of 0 or 1 at time of enrollment - Planned extensive stage first-line therapy of etoposide plus carboplatin plus PD-L1 inhibitor (atezolizumab or durvalumab) - Extensive stage disease at time of diagnosis - Willing and able to provide informed consent Exclusion Criteria: - History of prior systemic treatment of SCLC - History of radiotherapy or planned radiotherapy to all measurable disease foci - Prior diagnosis of non-small cell lung cancer - Mixed small cell and non-small cell histology - Suspected metastatic cancer from other sites (i.e., those without a known or suspected lung primary diagnosis) - Not willing to have additional blood samples collected |
Country | Name | City | State |
---|---|---|---|
United States | University of Colorado | Aurora | Colorado |
United States | Johns Hopkins University | Baltimore | Maryland |
United States | University of North Carolina | Chapel Hill | North Carolina |
United States | TriHealth Cancer Institute | Cincinnati | Ohio |
United States | OhioHealth Research Institute | Columbus | Ohio |
United States | Englewood Health Medical Center | Englewood | New Jersey |
United States | Cancer and Blood Specialty Clinic | Los Alamitos | California |
United States | Illinois Cancer Care | Peoria | Illinois |
United States | Oklahoma Cancer Specialists and Research Institutes | Tulsa | Oklahoma |
United States | Cancer Care Association of York | York | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Tempus AI | AstraZeneca |
United States,
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* Note: There are 22 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | To measure biomarkers of SCLC using the TEMPUS xT assay | To measure specific biomarkers of SCLC subtypes and outcomes using the TEMPUS xT assay | Up to 4 years | |
Other | To identify biomarkers and mechanisms of progression | To identify biomarkers and mechanisms of progression from EP + PDL1-i therapy | Up to 4 years | |
Other | To study progression free survival (PFS) and overall survival (OS) | To study real-world PFS and OS as measured by the treating clinician | Up to 4 years | |
Primary | To determine if tumor tissue transcriptional subtypes can be detected | To determine prospectively if SCLC tumor tissue transcriptional subtypes can be detected by Tempus|xT RNAseq | Up to 4 years | |
Primary | To characterize relationship between tissue transcriptional subtype and clinical outcomes | To characterize the relationship between tissue transcriptional subtype and clinical outcomes for EP+PDL1-i therapy based on collection of longitudinal information from medical records | Up to 4 years | |
Secondary | To assess the potential for liquid biopsy in SCLC | To use blood based assays to assess the complementarity of circulating biomarkers to tissue based methods | Up to 4 years | |
Secondary | To test which tissue and sample variables confound gene expression subtypes | To measure how variable transcriptional measurements are across tissue characteristics such as site of biopsy and type of biopsy | Up to 4 years |
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