Drug |
Cancer Type |
Stage |
Use |
Biomarker |
Type of Agent |
Afinitor (everolimus) |
Breast cancer |
Metastatic or advanced |
Combined with exemestane for postmenopausal women with advanced breast cancer which progressed with letrozole or anastrozole. |
HR-positive, HER2-negative |
MTOR inhibitor |
Afinitor (everolimus) |
Pancreatic neuro-endocrine tumors (PNET) |
Progressive PNETs |
Used to treat PNETs that have progressed on other treatments. |
No biomarker needed |
MTOR inhibitor |
Avastin (bevacizumab) |
Ovarian, fallopian tube or primary peritoneal cancer |
Stage 2-4 |
Combined with Lynparza (olaparib) for first-line maintenance therapy for platinum-sensitive cancer. |
Homologous Recombination Deficiency (HRD) testing |
VEGF inhibitor |
Avastin (bevacizumab) |
Ovarian, fallopian tube or primary peritoneal cancer |
Stage 3-4 |
Combined with chemotherapy, followed by Avastin as a single agent following initial surgical resection. |
No biomarker needed |
VEGF inhibitor |
Avastin (bevacizumab) |
Ovarian, fallopian tube or primary peritoneal cancer |
Recurrent |
Combined with chemotherapy for treating platinum-resistant, recurrent disease in people who received no more than 2 prior chemotherapy regimens. |
No biomarker needed |
VEGF inhibitor |
Avastin (bevacizumab) |
Ovarian, fallopian tube or primary peritoneal cancer |
Recurrent |
Combined with chemotherapy, followed by Avastin as a single agent, for platinum-sensitive recurrent disease. |
No biomarker needed |
VEGF inhibitor |
Avastin (bevacizumab) |
Colorectal cancer |
Metastatic |
Combined with intravenous 5-fluorouracil-based chemotherapy for first-, or second-line treatment. |
No biomarker needed |
VEGF inhibitor |
Avastin (bevacizumab) |
Colorectal cancer |
Metastatic |
Combined with chemotherapy for second-line treatment in patients who have progressed on a first-line Avastin-containing regimen. |
No biomarker needed |
VEGF inhibitor |
Braftovi (encorafenib) |
Colorectal cancer |
Metastatic |
Combined with cetuximab, for the treatment of adult patients with metastatic colorectal cancer. |
BRAF V600E tumor mutation |
BRAF inhibitor |
Braftovi (encorafenib) |
Melanoma |
Metastatic |
Combined with Mektovi (binimetinib), for the treatment of patients with unresectable or metastatic melanoma. |
BRAF V600E or V600K tumor mutation |
BRAF inhibitor |
Cotellic (cobimetinib) |
Melanoma |
Metastatic |
Combined with Zelboraf (vemurafenib) for the treatment of patients with unresectable or metastatic melanoma. |
BRAF V600E or V600K tumor mutation |
BRAF inhibitor |
Cyramza (ramucirumab) |
Colorectal cancer |
Metastatic |
Combined with FOLFIRI chemotherapy, for treatment after disease progression on, or after prior therapy with bevacizumab, oxaliplatin, and a fluoropyrimidine. |
No biomarker required |
VEGF inhibitor |
Datroway (datopotamab deruxtecan-dlnk) |
Breast cancer |
Metastatic |
Treatment for cancers that have progressed after hormone therapy and chemotherapy. |
Hormone receptor position (HR-positive), HER2-negative |
Antibody-drug conjugate (chemotherapy attached to antibody targeting TROP-2) |
ELAHERE (mirvetuximab soravtansine-gynx) |
Ovarian cancer |
Stage 3-4 |
Used as second-line or later treatment of platinum-resistant or platinum-sensitive recurrent ovarian cancer. |
Positive for FRα (folate receptor alpha) |
Antibody-drug conjugate (chemotherapy attached to antibody targeting FR-α receptor) |
Enhertu (fam-trastuzumab-deruxtecan-nxki) |
Breast cancer |
Metastatic |
Treatment for people who have received a prior anti-HER2-based regimen either: - in the metastatic setting.
- in the neoadjuvant or adjuvant setting and developed a recurrence during or within six months of completing treatment.
|
HER2 overexpression (HER2-positive) |
Antibody-drug conjugate |
Enhertu (fam-trastuzumab-deruxtecan-nxki) |
Breast cancer |
Metastatic |
As treatment for people who have tumors that are HER2-low, received chemotherapy in the metastatic setting and whose cancer no longer responds to hormonal therapy. |
HR-positive and HER2-low |
Antibody-drug conjugate |
Enhertu (fam-trastuzumab-deruxtecan-nxki) |
Breast cancer |
Metastatic |
As treatment for people with HR-positive, HER2-low or HER2 ultralow that came back or got worse after one or more hormone therapies in the metastatic setting. |
HR-positive and HER2-low or HER2-ultra low |
Antibody-drug conjugate |
Enhertu (fam-trastuzumab-deruxtecan-nxki) |
Solid tumors (pan tumor) |
Metastatic or unresectable |
For adult patients with unresectable or metastatic, HER2-positive solid tumors (including colorectal cancer) who have received prior systemic treatment and have no alternative treatment options. |
HER2 overexpression (HER2-positive) |
Antibody-drug conjugate |
Erbitux (cetuximab) |
Colorectal cancer |
Metastatic |
Combined with FOLFIRI for first-line treatment, or combined with irinotecan for cancers that no longer respond to irinotecan-based chemotherapy or as a single agent in patients who have progressed after oxaliplatin- and irinotecan-based chemotherapy. |
EGFR positive and KRAS mutation negative |
EGFR inhibitor |
Fruzaqla (fruquintinib) |
Colorectal cancer |
Metastatic |
Used as a single agent when cancer has progressed after treatment with chemotherapy and targeted therapy. |
No biomarker required |
VEGF inhibitor |
Herceptin (trastuzumab) |
Breast cancer |
Early stage |
The treatment of Her2-positive breast cancer. |
HER2 overexpression (HER2-positive) |
Antibody targeting HER2 receptors |
Herceptin (trastuzumab) and Tukysa (tucatinib) combination |
Colorectal cancer |
Metastatic or unresectable |
For people who progressed after chemotherapy. |
HER2 overexpression (HER2-positive) |
Antibody targeting HER2 receptors and a kinase inhibitor that targets HER2 receptors |
Ibrance (palbociclib) |
Breast cancer |
Metastatic |
Combined with an aromatase inhibitor as treatment of advanced cancer as initial hormone therapy in postmenopausal women or in men. |
HR-positive and HER2-negative |
Targeted therapy known as a kinase inhibitor that blocks the CDK4/6 pathway |
Ibrance (palbociclib) |
Breast cancer |
Metastatic |
Combined with Faslodex (fulvestrant) as treatment in postmenopausal women or in men whose disease progressed following endocrine therapy. |
HR-positive and HER2-negative |
Targeted therapy known as a kinase inhibitor that blocks the CDK4/6 pathway |
Kadcyla (trastuzumab emtansine) |
Breast cancer |
Early stage |
Adjuvant therapy for people with early breast cancer who still have disease after neoadjuvant taxane and treatment with Herceptin |
HER2 overexpression (HER2-positive) |
Antibody targeting HER2 receptors |
Kadcyla (trastuzumab emtansine) |
Breast cancer |
Metastatic |
For treatment in people whose cancer got worse after receiving Herceptin and chemotherapy in the following settings: - for metastatic disease, or
- as adjuvant therapy, and experienced disease recurrence during or within 6 months of completing adjuvant therapy.
|
HER2 overexpression (HER2-positive) |
Antibody targeting HER2 receptors |
Kisqali (ribociclib) |
Breast cancer |
Metastatic |
Combined with an aromatase inhibitor for the treatment of pre/perimenopausal or postmenopausal women as initial hormone based therapy. |
HR-positive and HER2-negative |
Targeted therapy known as a kinase inhibitor that blocks the CDK4/6 pathway |
Kisqali (ribociclib) |
Breast cancer |
Metastatic |
Combined with Faslodex (fulvestrant) for the treatment of postmenopausal women, as initial hormone based therapy. |
HR-positive and HER2-negative |
Targeted therapy known as a kinase inhibitor that blocks the CDK4/6 pathway |
Krazati (adagrasib) |
Colorectal cancer |
Metastatic |
In combination with cetuximab for locally advanced or metastatic colorectal cancer (CRC) that has progressed after treatment with chemotherapy. |
KRASG12C mutation |
Targeted therapy against the KRASG12C protein |
Lenvima (lenvatinib) |
Endometrial cancer |
Advanced disease |
Combined with pembrolizumab, for the treatment of patients whose cancer has progressed after treatment and who are not candidates for surgery or radiation. |
Tumors that are not MSI-H or dMMR (or MMR-D) - they may be referred to as MSI-Low, MSS, pMMR or MMR-P) |
Targeted therapy known as a tyrosine kinase inhibitor |
Mekinist (trametinib) |
Melanoma |
Unresectable or metastatic |
As a single agent and in combination with dabrafenib for the treatment of unresectable or metastatic melanoma. |
BRAF V600E or V600K tumor mutation |
Targeted therapy known as a MEK inhibitor |
Mekinist (trametinib) |
Melanoma |
Lymph node positive |
Combined with Taflinar (dabrafenib) as adjuvant treatment of people with melanoma and involvement of lymph node(s), following complete resection. |
BRAF V600E or V600K tumor mutation |
Targeted therapy known as a MEK inhibitor |
Mektovi (binimetinib) |
Melanoma |
Unresectable or metastatic |
Combined with Braftovi (encorafenib), for the treatment of people with unresectable or metastatic melanoma. |
BRAF V600E or V600K tumor mutation |
Targeted therapy known as a MEK inhibitor |
Orserdu (elacestrant) |
Breast cancer |
Metastatic |
Used alone to treat men or postmenopausal women with HR-positive, HER2-negative breast cancer, which progressed after at least one line of hormone therapy therapy. |
HR-positive, HER2-negative with an ESR1 mutation |
Type of targeted hormonal therapy known as SERD (selective estrogen receptor degrader or downregulator) |
Perjeta (pertuzumab) |
Breast cancer |
Locally advanced, inflammatory or early stage |
Combined with Herceptin (trastuzumab) and docetaxel as treatment before surgery (neoadjuvant). |
HER2 overexpression (HER2-positive) |
Antibody targeting HER2 receptors |
Phesgo (pertuzumab, trastuzumab combined injection) |
Breast cancer |
Early stage |
- Before surgery (neoadjuvant) treatment for tumors larger than 2 cm or node-positive, or
- After surgery (adjuvant) treatment for early breast cancer that has a high likelihood of coming back.
|
HER2 overexpression (HER2-positive) |
Antibody targeting HER2 receptors |
Piqray (alpelisib) |
Breast cancer |
Metastatic |
Combined with Faslodex (fulvestrant) as treatment in men or post-menopausal women who progressed on or after treatment with hormone therapy. |
HR-positive, HER2-negative and positive for a PIK3CA tumor mutation |
Targeted therapy known as a kinase inhibitor that blocks the PIK3 pathway |
Pluvicto (lutetium Lu 177 vipivotide tetraxetan) |
Prostate cancer |
Metastatic castration-resistant prostate cancer (mCRPC) |
For treatment of mCRPC which has stopped responding or got worse after treatment with hormonal therapy using an androgen receptor inhibitor and taxane-based chemotherapy. |
Imaging with a PET scan that looks for prostate cancers with the marker PSMA |
Targeted radiation therapy (radioligand therapy) |
Retevmo (selpercatinib) |
Solid tumors (pan tumor) |
Metastatic or unresectable |
Second-line or later treatment for metastatic solid tumors for which there are no other treatment options. |
RET fusion |
Kinase inhibitor |
Stivarga (regorafenib) |
Colorectal cancer |
Metastatic |
For treatment of colorectal cancer that has progressed after treatment and for which there are no other treatment options. |
No biomarker required |
Targeted therapy known as a multi-kinase inhibitor |
Tafinlar (dabrafenib) |
Melanoma |
Unresectable or metastatic |
Combined with Mekinist (trametinib) for the treatment of people with unresectable or metastatic melanoma. |
BRAF V600E or V600K tumor mutation |
Targeted therapy known as a BRAF inhibitor |
Tafinlar (dabrafenib) |
Melanoma |
Lymph node positive |
Combined with Mekinist (trametinib) as adjuvant treatment of people with melanoma and involvement of lymph node(s), following complete resection. |
BRAF V600E or V600K tumor mutation |
Targeted therapy known as a BRAF inhibitor |
Trodelvy (sacituzumab govitecan-hziy) |
Breast cancer |
Metastatic |
For metastatic breast cancer that progressed, recurred or did not respond to at least two previous lines of treatment. |
Triple-negative (ER/PR-negative, HER2-negative) |
Antibody-drug conjugate (chemotherapy attached to antibody found in TNBC) |
Truqap (capivasertib) |
Breast cancer |
Metastatic |
Combined with fulvestrant as treatment for HR-positive, advanced or metastatic breast cancer which recurred or got worse after standard hormone therapy. |
PTEN, PIK3 or AKT1 mutation in the tumor |
Targeted therapy known as a kinase inhibitor that blocks the AKT pathway |
Tukysa (tucatinib) |
Breast cancer |
Metastatic or unresectable |
In combination with Herceptin (trastuzumab) to treat cancer which has progressed after at least one prior treatment with an anti-HER2 treatment in the metastatic setting. |
HER2 overexpression (HER2-positive) |
Targeted therapy known as a kinase inhibitor that targets HER2 receptors |
Vectibix (panitumumab) |
Colorectal cancer |
Metastatic |
Combined with FOLFOX for first-line treatment. |
Negative for KRAS and NRAS mutations |
Targeted therapy that targets a receptor known as EGFR |
Vectibix (panitumumab) |
Colorectal cancer |
Metastatic |
As a single therapy following disease progression after prior treatment with fluoropyrimidine, oxaliplatin, and irinotecan-containing chemotherapy. |
Negative for KRAS and NRAS mutations |
Targeted therapy that targets a receptor known as EGFR |
Verzenio (abemaciclib) |
Breast cancer |
Metastatic |
Used alone to treat breast cancer that has progressed after treatment with hormone therapy and chemotherapy in the metastatic setting. |
HR-positive and HER2-negative |
Targeted therapy known as a kinase inhibitor that blocks the CDK4/6 pathway |
Verzenio (abemaciclib) |
Breast cancer |
Metastatic |
Combined with Faslodex (fulvestrant) as treatment in women whose disease progressed following endocrine therapy. |
HR-positive and HER2-negative |
Targeted therapy known as a kinase inhibitor that blocks the CDK4/6 pathway |
Vitrakvi (larotrectinib) |
Solid tumors (pan tumor) |
Metastatic or unresectable |
For treatment in metastatic solid tumors for which there are no other treatment options. |
NTRK fusion |
Kinase inhibitor |
Xofigo (Radium 223 dichloride) |
Prostate cancer |
Metastatic castration-resistant prostate cancer (mCRPC) |
For treatment of mCRPC that has spread to the bones but has not to other organs. |
No biomarker needed |
Targeted radiation therapy (radioligand therapy) |
Zelboraf (vemurafenib) |
Melanoma |
Unresectable or metastatic |
Combined with Tecentriq (atezolizumab) and Cotellic (cobimetinib) in people with melanoma that has the BRAF gene mutation, when the cancer can’t be removed by surgery or has spread to other parts of the body. |
BRAF V600E or V600K tumor mutation |
Targeted therapy known as a BRAF inhibitor |