Clinical trial · Observational
Registry of Guardant360® Use and Outcomes In People With Advanced Cancer
NCT03477474CI-TRIAL-00041089GEODEterminatedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Alternative data published
Summary
Brief summary (as posted)
The purpose of this registry is to collect data that describes the characteristics of people with advanced cancer for whom the Guardant360 assay is ordered and to observe their clinical outcomes after receiving their results.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-small Cell Lung Cancer Metastatic | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Estimate Progression Free Survival (PFS)
- timeFrame
- 24 Months
Secondary outcomes (10)
- measure
- Duration of treatment response
- timeFrame
- 24 Months
- measure
- Time of tumor progression
- timeFrame
- 24 Months
- measure
- time to treatment failure
- timeFrame
- 24 Months
- measure
- Overall survival
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
General Inclusion Criteria: 1. 18 Years of age or older 2. Ability to provide written informed consent 3. Blood collected for the most recent Guardant360 test within 8 weeks prior to enrollment General Exclusion Criteria 1. Pregnancy at the time of the qualifying Guardant360 blood collection 2. History of the allogeneic organ or tissue transplant Module 1 (Non-Small Cell Lung Cancer) Inclusion Criteria 1. NSCLC, confirmed by histology or cytology 2. Advanced disease, defined as: stage IIIB or IV NSCLC at the time of the qualifying Guardant360 blood collection; or for subjects with an initial diagnosis of Stage I-IIIA disease, NSCLC that is recurrent or metastatic at the time of the qualifying Guardant360 blood collection 3. One of the following conditions at the time of the qualifying Guardant360 blood collection: * No prior systemic therapy for advanced disease OR * All three of the following conditions: 1\. A history of prior systemic therapy for advanced disease, 2. Disease progression within the previous four weeks, \& 3. No new systemic therapy for advanced disease Exclusion Criteria Subjects with a diagnosis or history of any cancer involving the lung that is not classified as NSCLC, including but not limited to small cell carcinoma, neuroendocrine or carcinoid tumor, lymphoma, mesothelioma, metastatic non-lung carcinoma, or cancer of unknown primary.
References
Publications (0)
Data not yet available
No reference posted for this study.