Clinical Effectiveness Assessment of VeriStrat® Testing and Validation of Immunotherapy Tests in NSCLC Subjects (INSIGHT)
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| ClinicalTrials.gov Identifier: NCT03289780 |
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Recruitment Status :
Recruiting
First Posted : September 21, 2017
Last Update Posted : December 7, 2022
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| Condition or disease |
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| Non-Small Cell Lung Cancer |
The primary purpose of this observational study is to assess the physician's clinical practice patterns while using VeriStrat testing in subjects with NSCLC whose tumors are epidermal growth factor receptor (EGFR) wild-type (negative) or have unknown EGFR mutational status. This study will also attempt to further validate that VeriStrat test results stratify subjects by clinical outcomes in the real world, uncontrolled clinical setting while exploring whether certain therapeutic approaches may yield opportunities for further study.
Predictive tests that aid physician therapeutic decision making are critical for optimizing subject outcomes while minimizing toxicity and associated treatment costs. This study will provide data for the validation of immunotherapy tests currently being developed. Immunotherapy mechanisms are dependent upon the interactions between the tumor, tumor microenvironment, and the patient immune system. As such, a successful predictive test will reflect the complex interplay between tumor and host. The multivariate tests from Biodesix have the advantage of being able to assess this complex biology.
The information gained from this research will not only guide the adoption of the VeriStrat test and inform medical decision making, including treatment choice, but will allow the validation of additional mass-spectrometry-based proteomic tests.
| Study Type : | Observational |
| Estimated Enrollment : | 5000 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | An Observational Study Assessing the Clinical Effectiveness of VeriStrat and Validating Immunotherapy Tests in Subjects With Non-Small Cell Lung Cancer |
| Actual Study Start Date : | April 4, 2016 |
| Estimated Primary Completion Date : | December 2025 |
| Estimated Study Completion Date : | December 2025 |
- Physician Treatment Patterns Description [ Time Frame: 3 years ]Physician Treatment patterns Description: To describe physician treatment patterns pre and post-veriStrat testing. Describe the impact of the VeriStrat test results on treatment decisions, including but not limited to: percentage change in treatment decision, differences in chosen treatments between patients classified as VeriStrat good and those classified as VeriStrat Poor. Change in percentage of patients receiving systemic therapy or supportive therapies only.
- Immunotherapy Stratification by Overall Survival [ Time Frame: 3 years ]To determine whether immunotherapy test(s) stratify immunotherapy-treated subjects by overall survival.
- Immunotherapy Stratification by Progression-Free Survival [ Time Frame: 3 years ]To determine whether immunotherapy test(s) stratify immunotherapy-treated subjects by progression-free survival.
- VeriStrat Poor vs. Good Outcomes [ Time Frame: 3 years ]To compare progression free survival (PFS) and overall survival (OS) outcomes between those classified as VeriStrat-Poor and VeriStrat-Good.
- Platinum-based therapy outcomes in VeriStrat Poor vs. Good subjects. [ Time Frame: 3 years ]To compare outcomes in subjects classified as VeriStrat-Poor and VeriStrat-Good and treated with platinum-based therapy.
- Immunotherapy outcomes in VeriStrat Poor vs. Good subjects. [ Time Frame: 3 years ]To compare outcomes in subjects classified as VeriStrat-Poor and VeriStrat-Good and treated with immunotherapy.
- Single agent chemotherapy outcomes in VeriStrat Poor vs. Good Subjects [ Time Frame: 3 years ]To compare outcomes in subjects classified as VeriStrat-Poor and VeriStrat-Good and treated with single agent chemotherapy.
- VeriStrat label changes over time. [ Time Frame: 3 years ]To compare the longitudinal changes in VeriStrat classification over the course of the study
- Determination of Immunotherapy tests ability to stratify subjects based on treatment. [ Time Frame: 3 years ]To determine whether immunotherapy test(s) stratify subjects treated with chemotherapy or targeted therapies by outcome.
- Correlation between the VeriStrat test and Immunotherapy tests. [ Time Frame: 3 years ]To observe the correlation between VeriStrat classification and immunotherapy test(s) classification at baseline and longitudinally.
- Longitudinal changes in Immunotherapy tests. [ Time Frame: 3 years ]To describe the longitudinal changes in immunotherapy test classification over the course of the study.
- Stratification of Immunotherapy Test(s) [ Time Frame: 3 years ]To determine whether immunotherapy test(s) stratify immunotherapy-treated subjects by other clinically meaningful factors or endpoints.
- Changes in GeneStrat [ Time Frame: 3 years ]To observe changes in GeneStrat status across lines of therapy.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Subject must be 18 years of age or older at time of signing informed consent form (ICF).
- A diagnosis of NSCLC.
- Subject is willing to provide serum samples for VeriStrat testing.
- EGFR mutation status wild-type (negative) or a tested unknown.
- For subjects with untested/unknown EGFR status only: The subject must be willing to provide blood samples for GeneStrat testing.
- Subject is willing to provide serum samples for research, understanding that no test results will be made available either to the subject or the treating physician.
- Subject is able to read and understand the ICF and agrees to comply with study procedures and requirements.
Exclusion Criteria:
1. Subject's ability to understand the requirements of the protocol or to provide informed consent is impaired or subject is unwilling to comply with the protocol requirements.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03289780
| Contact: Niki Givens, B.S. | 720-495-1583 | niki.givens@biodesix.com |
Show 42 study locations
| Principal Investigator: | Linda Traylor, Ph.D | Biodesix, Inc. |
Documents provided by Biodesix, Inc.:
Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Biodesix, Inc. |
| ClinicalTrials.gov Identifier: | NCT03289780 |
| Other Study ID Numbers: |
BDX-00146 |
| First Posted: | September 21, 2017 Key Record Dates |
| Last Update Posted: | December 7, 2022 |
| Last Verified: | December 2022 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Lung Neoplasms Carcinoma, Non-Small-Cell Lung Respiratory Tract Neoplasms Thoracic Neoplasms Neoplasms by Site |
Neoplasms Lung Diseases Respiratory Tract Diseases Carcinoma, Bronchogenic Bronchial Neoplasms |