Variant · Snv
ERBB2 T790M
CI-VAR-00004342Explore in graph →CIViC 4907
Curated evidence
Evidence by cancer (1 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
civicProvenance
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 38591867
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Neoplasm1 | ||||||||
| ERBB2 Activating Mutation OR ERBB2 T790M | Osimertinib | Predictive | B | Does Not Support Sensitivity Response | 3 | submitted | EID12026In this phase 2 clinical trial, 19 patients with tumours harbouring EGFR mutations (T790M or activation mutations) were treated with osimertinib, an EGFR TKI. Of the 19 patients, 13 were evaluable for… (full text at CIViC) PMID 38591867 · Chen et al., 2024 · Open in CIViC | civic |
ClinVar
Clinical significance (0)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
Data not yet available
No ClinVar interpretation attached to this variant.