Table1.
Molecular aberrations defining administration of approved targeted agents in different solid tumor diagnoses
| Cancer type (alphabetically) | Molecular target | Assessment technique | Molecular aberration | Approved targeted agent (chronologically) |
| AI: aromatase inhibitor, ALK: anaplastic lymphoma kinase, EGFR: epidermal growth factor receptor, ER: estrogen receptor, FISH: fluorescent in situ hybridization, GIST: gastrointestinal stromal tumor, HER2: human epidermal growth factor receptor 2, IHC: immunohistochemistry, PgR: progesterone receptor, T-DM1: trastuzumab DM1. | ||||
| Breast cancer | ER and/or PgR | IHC | Overexpression | Tamoxifen, AIs fulvestrant |
| HER2 | IHC FISH | Overexpression and/or amplification | Trastuzumab, lapatinib pertuzumab T-DM1 | |
| Colorectal cancer | KRAS | DNA | Mutation | Cetuximab, panitumumab |
| Gastric cancer | HER2 | IHC FISH | Overexpression and/or amplification | Trastuzumab |
| GIST | KIT | IHC | Mutation | Imatinib |
| Lung cancer | EGFR | DNA | Mutation | Gefitinib, erlotinib |
| ALK and/or ROS | FISH | Rearrangement | Crizotinib | |
| RET | FISH | Rearrangement | Vandetanib | |
| Melanoma | BRAF | DNA | Mutation | Vemurafenib, dabrafenib |