| Cancer Type |
Test |
Therapeutic Impact |
‘Omic Category |
| Breast Cancer |
HER2 by FISH |
Response to trastuzumab [9,10] |
Genomics |
| HER2 by IHC |
Response to trastuzumab [9,10] |
Pathology/Proteomics |
| ER/PR by RT-PCR |
Response to hormonal therapies [88-90] |
Transcriptomics |
| DPD by PCR |
Fluorouracil toxicity [91] |
Genomics |
| PIK3CA Mutation Analysis |
Resistance to trastuzumab in HER2 positive tumors [92] |
Genomics |
| Colorectal Cancer |
KRAS mutation analysis |
Response to panitumamab, cetuximab [13] |
Genomics |
| BRAF mutation analysis |
Response to panitumamab, cetuximab [15] |
Genomics |
| EGFR amplication by FISH |
Response to cetuximab [93] |
Genomics |
| Thymidylate synthase by IHC |
Resistance to fluorouracil or related agents [94] |
Pathology/Proteomics |
| UGT1A1 Molecular Assay |
Increased risk of severe irinotecan toxcity [95] |
Genomics |
| DPD by PCR |
Fluorouracil toxicity [91,96] |
Genomics |
| PIK3CA Mutation analysis |
Resistance to cetuximab salvage therapy [97] |
Genomics |
| Non-Small Cell Lung Cancer |
EGFR Mutation analysis |
Response to gefitinib, erlotinib [98] |
Genomics |
| KRAS Mutation |
Resistance to gefitinib, erlotinib [14] |
Genomics |
| ALK by FISH |
Sensitivity to crizotinib [99] |
Genomics |
| ERCC1 by IHC |
Resistance to platinum-based chemotherapeutics [100] |
Pathology/Proteomics |
| EGFR Amplication by FISH |
Resistance to gefitinib, erlotinib, cetuximab plus paclitaxel, and carboplatin [101] |
Genomics |
| EGFR by IHC |
Response to cetuximab plus chemotherapy [102] |
Pathology/Proteomics |
| TS by RT-PCR |
Resistance to pemetrexed [103] |
Transcriptomics |
| UGT1A1 Molecular Assay |
Irinotecan toxicity [104] |
Genomics |
| ALK by FISH |
Response to crizotinib in metastatic disease [105] |
Genomics |
| Gastric Cancer |
HER2 by FISH |
Response to trastuzumab [11] |
Genomics |
| HER2 by IHC |
Response to trastuzumab [106,107] |
Pathology/Proteomics |
| ERCC1 by IHC |
Resistance to platinum-based chemotherapies [108] |
Pathology/Proteomics |
| Melanoma |
BRAF Mutation Analysis |
Response to vemurafenib [16] |
Genomics |
| Brain Cancer |
MGMT methylation |
Response to temozolomide [109] |
Epigenomics |
| Head and Neck Cancers |
DPD status |
Fluorouracil toxicity and efficacy [110] |
Metabolomics |
| CLL |
17p by FISH |
Resistance to fludarabine based regimens |
Genomics |
| |
P53 Mutation analysis |
Resistance to fludarabine based regimens [111] |
Genomics |
| CML |
BCR-ABL |
Recommended imatinib [112] |
Genomics |
| BCR-ABL KD Mutation V299L, T315A, F17L/V/I/C |
Response to nilotinib rather than dasatinib [41] |
Genomics |
| BCR-ABL KD Mutation Y253H, E255K/V, F359V/C/I |
Response to dasatinib rather than nilotinib [41] |
Genomics |
| BCR-ABL transcript mass by RQ-PCR |
Response tyrosine kinase inhibitors after therapy ihas been intiated [113] |
Transcriptomics |
| Myelodysplastic Syndrome |
Deletion 5q |
Response to lenalidomide [114] |
Genomics |
| Platelet derived growth factor receptor beta |
Indication for imatinib [115,116] |
Genomics |
| Non-Hodgkin’s Lymphoma |
MYC translocations |
Resistance to retuximab plus cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) in diffuse B-cell lymphoma [117] |
Genomics |
HER2: Human epidermal growth receptor 2