Guardant Health offers the Guardant Health Portal app for healthcare professionals to track, access and download Guardant Health reports.
- Easily search, sort, and review reports
- On-call support for healthcare
professionals and patients
Comprehensive Genomic Profiling with a simple blood draw with an easy to interpret report.
Blood Sample
2x 10 ml tubes of blood
7 days
Comprehensive genomic
profiling results in
only 7 days
Take action
Clinically relevant
alterations
in 70+ cancer related genes.
For patients with advanced solid tumour cancers.
-
Before 1st Line Treatment
Get ahead of the challenges of tissue testing in
advanced cancer by utilizing Guardant360® to guide
1st line treatment decisions. -
At Progression
Get genomic information on over 70+ genes, including MSI
across multiple solid tumors to help inform cancer therapies and
clinical trials.
Published data
Prospective study of 323 NSCLC patients found
Guardant360® improved alteration detection
were unable to get complete
genomic results from tissue biopsy
genomic results from tissue biopsy
had targetable alterations detected
by Guardant360® and tissue testing
(n=82) versus tissue testing
alone (n=47)
by Guardant360® and tissue testing
(n=82) versus tissue testing
alone (n=47)
treated based on Guardant360® had a response or stable disease
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Consistently High
Concordance with Tissue
for targetable alterations before 1st NSCLC
therapy
Consistently High
Concordance with Tissue
- Best-in-class detection
- Extensively peer reviewed and published
- Published analytical and clinical validation (refs)
- Over 150 peer reviewed publications, more than 50 of which include associated clinical outcomes
Tissue has limitations beyond your control!
- Treatment delays
Results can be unpredictable, may take a month or longer, and can be incomplete - Insufficient availability of tissue
Exhausted by diagnostic needs and PD-L1 testing - Patient burden
Repeated tissue biopsies expose patients to potential adverse events - Practice/staff burden
Significant coordination involving multiple care team members
Relying solely on tissue can lead to undergenotyping
~ 1 in 2 NSCLC patients are unable to get
guideline-recommended genes for NSCLC2-6
EGFR
ALK
ROSI
BRAF
MET
RET
ERBB2 (HER2)
NTRK
