Molecular Profile |
Indication/Tumor Type |
Response Type |
Relevant Treatment Approaches |
Therapy Name |
Approval Status |
Evidence Type |
Efficacy Evidence |
References |
FBXW7 R465H
|
lung adenocarcinoma
|
sensitive |
|
Temsirolimus
|
Clinical Study |
Actionable |
In a clinical case report, a patient with lung adenocarcinoma harboring FBXW7 R465H demonstrated tumor shrinkage when treated with Torisel (temsirolimus) (PMID: 24360397).
|
24360397
|
FBXW7 R465H
|
T-cell adult acute lymphocytic leukemia
|
resistant |
|
MRK-003
|
Preclinical |
Actionable |
In a preclinical study, FBXW7 R465H conferred resistance to gamma secretase inhibitor, MRK-003, by activation of the NOTCH pathway and stablization of MYC as demonstrated in T cell acute lymphoblastic leukemia (T-ALL) cell lines (PMID: 17646409).
|
17646409
|
FBXW7 R505C
|
T-cell adult acute lymphocytic leukemia
|
resistant |
|
MRK-003
|
Preclinical |
Actionable |
In a preclinical study, FBXW7 R505C conferred resistance to gamma secretase inhibitor, MRK-300, by activation of the NOTCH pathway and stablization of MYC as demonstrated in T cell acute lymphoblastic leukemia (T-ALL) cell lines (PMID: 17646409).
|
17646409
|
FBXW7 R505C
|
head and neck squamous cell carcinoma
|
sensitive |
|
Vorinostat
|
Preclinical |
Actionable |
In a preclinical study, Zolinza (vorinostat) inhibited growth of a head and neck squamous cell carcinoma cell line harboring FBXW7 R505C in culture (PMID: 23274910).
|
23274910
|
FBXW7 R505C
|
colorectal cancer
|
resistant |
|
Regorafenib
|
Preclinical - Cell culture |
Actionable |
In a preclinical study, colorectal cell lines with FBXW7 R505C demonstrated acquired resistance in regorafenib (PMID: 27399335).
|
27399335
|
FBXW7 R465C
|
T-cell adult acute lymphocytic leukemia
|
resistant |
|
MRK-003
|
Preclinical |
Actionable |
In a preclinical study, FBXW7 R465C conferred resistance to gamma secretase inhibitor, MRK-003, by activation of the NOTCH pathway and stablization of MYC as demonstrated in T cell acute lymphoblastic leukemia (T-ALL) cell lines (PMID: 17646409).
|
17646409
|
FBXW7 del
|
T-cell adult acute lymphocytic leukemia
|
resistant |
|
MRK-003
|
Preclinical |
Actionable |
In a preclinical study, homozygous deletion of FBXW7 is conferred resistance to gamma secretase inhibitor, MRK-003, by activation of the NOTCH pathway and stablization of MYC as demonstrated in T cell acute lymphoblastic leukemia (T-ALL) cell lines (PMID: 17646409).
|
17646409
|
FBXW7 loss
|
colon cancer
|
sensitive |
|
Sirolimus
|
Preclinical |
Actionable |
In a preclinical study, Rapamune (sirolimus) inhibited epithelial-mesenchymal transition, motility, and invasiveness in colon cancer cells lacking FBXW7 in culture (PMID: 23558291)
|
23558291
|
FBXW7 R505L
|
T-cell adult acute lymphocytic leukemia
|
resistant |
|
MRK-003
|
Preclinical |
Actionable |
In a preclinical study, FBXW7 R505L may conferred resistance to gamma secretase inhibitor, MRK-003, by activation of the NOTCH pathway and stablization of MYC as demonstrated in T cell acute lymphoblastic leukemia (T-ALL) cell lines (PMID: 17646409).
|
17646409
|
FBXW7 R479Q
|
T-cell adult acute lymphocytic leukemia
|
resistant |
|
MRK-003
|
Preclinical |
Actionable |
In a preclinical study, FBXW7 R479Q conferred resistance to gamma secretase inhibitor, MRK-003, by activation of the NOTCH pathway and stablization of MYC as demonstrated in T cell acute lymphoblastic leukemia (T-ALL) cell lines (PMID: 17646409).
|
17646409
|
FBXW7 E192A
|
fibrolamellar carcinoma
|
predicted - sensitive |
|
Sirolimus
|
Phase I |
Actionable |
In a Phase I study, Rapamune (sirolimus) resulted in prolonged stable disease in a patient with hepatocellular fibrolamellar carcinoma harboring FBXW7 E192A (PMID: 24586741).
|
24586741
|
FBXW7 inact mut
|
Advanced Solid Tumor
|
sensitive |
|
Belinostat
|
Preclinical |
Actionable |
In a preclinical study, Beleodaq (belinostat) inhibited human cancer cell lines harboring FBXW7 inactivating mutations in culture (PMID: 23274910).
|
23274910
|
FBXW7 inact mut
|
Advanced Solid Tumor
|
sensitive |
|
Entinostat
|
Preclinical |
Actionable |
In a preclinical study, entinostat (MS-275) inhibited cancer cells from advanced solid tumors and hematological cells harboring FBXW7 inactivating mutations in culture (PMID: 23274910).
|
23274910
|
FBXW7 inact mut
|
breast cancer
|
sensitive |
|
Sirolimus
|
Preclinical - Cell line xenograft |
Actionable |
In a preclinical study, breast cancer cells harboring a FBXW7 mutation demonstrated sensitivity to Rapamune (sirolimus) in culture and in cell line xenograft models (PMID: 18787170).
|
18787170
|
FBXW7 inact mut
|
hematologic cancer
|
sensitive |
|
Entinostat
|
Preclinical |
Actionable |
In a preclinical study, entinostat (MS-275) inhibited cancer cells from advanced solid tumors and hematological cells harboring FBXW7 inactivating mutations in culture (PMID: 23274910).
|
23274910
|
FBXW7 inact mut
|
hematologic cancer
|
sensitive |
|
AR-42
|
Preclinical |
Actionable |
In a preclinical study, AR-42 inhibited human hematologic cancer cell lines harboring FBXW7 inactivating mutations in culture (PMID: 23274910).
|
23274910
|
FBXW7 inact mut
|
hematologic cancer
|
sensitive |
|
Belinostat
|
Preclinical |
Actionable |
In a preclinical study, Beleodaq (belinostat) inhibited human hematologic cancer cell lines harboring FBXW7 inactivating mutations in culture (PMID: 23274910).
|
23274910
|
FBXW7 inact mut
|
Advanced Solid Tumor
|
sensitive |
|
AR-42
|
Preclinical |
Actionable |
In a preclinical study, AR-42 inhibited human cancer cell lines harboring FBXW7 inactivating mutations in culture (PMID: 23274910).
|
23274910
|
FBXW7 inact mut
|
Advanced Solid Tumor
|
resistant |
|
Docetaxel
|
Preclinical |
Actionable |
In a preclinical study, human cancer cell lines harboring FBXW7 inactivating mutations were resistant to docetaxel in culture (PMID: 23274910).
|
23274910
|
FBXW7 mutant
|
Her2-receptor negative breast cancer
|
predicted - sensitive |
|
LY3039478
|
Phase I |
Actionable |
In a Phase I trial, LY3039478 treatment resulted in partial response lasted 9.5 months in a patient with hormone receptor-positive, Erbb2 (Her2)-negative breast cancer harboring FBXW7 mutation (PMID: 30060061; NCT01695005).
|
30060061
|