TARCEVA (erlotinib)
TherapyGenentech
TARCEVA (erlotinib) from Genentech is an EGFR inhibitor used in biomarker-defined lung cancer.
Approvals
6
Indications
1
Biomarkers
1
Mapped tests
5
Where this therapy is approved with a companion diagnostic
Each row represents a defined combination of indication, biomarker criteria, and TARCEVA. Select a testing pathway to see the eligible companion diagnostic tests.
Indication-specific approvals
Approvals where TARCEVA is tied to a specific indication and biomarker definition.
| Indication | Biomarker criteria | Notes | |
|---|---|---|---|
Non-Small Cell Lung Cancer (NSCLC) Solid Tumor · Lung | EGFR (HER1)
| View testing pathway → |
Tumor-agnostic approvals
Approvals defined at the solid tumor level where biomarker criteria determine eligibility for TARCEVA.
No tumor-agnostic companion diagnostic approvals are currently mapped for this therapy.
Tests used in these approvals
These assays are identified in FDA labeling or sponsor materials as companion diagnostics or acceptable tests when considering TARCEVA for eligible patients.
Test
cobas EGFR Mutation Test v2
Roche Molecular Systems, Inc. (Roche Diagnostics)
Method
PCR
Specimen
Tissue (FFPE)
2 approvalsView test profile →
Test
FoundationOne CDx
Foundation Medicine, Inc.
Method
NGS
Specimen
Tissue (FFPE)
1 approvalView test profile →
Test
FoundationOne Liquid CDx
Foundation Medicine, Inc.
Method
NGS
Specimen
Whole blood
1 approvalView test profile →
Test
MI Cancer Seek (MCS)
Caris Life Sciences
Method
NGS
Specimen
Tissue (FFPE)
1 approvalView test profile →
Test
ONCO/Reveal Dx Lung & Colon Cancer Assay (O/RDx-LCCA)
Pillar Biosciences, Inc.
Method
NGS
Specimen
Tissue (FFPE)
1 approvalView test profile →