Drug |
Cancer Type |
Stage |
Use |
Biomarker |
Type of Agent |
Avastin (bevacizumab) |
Colorectal cancer |
Metastatic (stage 4) |
Combined with intravenous 5-fluorouracil-based chemotherapy for first- or second-line treatment |
No biomarker required |
Monoclonal antibody |
Avastin (bevacizumab) |
Colorectal cancer |
Metastatic (stage 4) |
In combination with chemotherapy for second-line treatment in patients who have progressed on a first-line Avastin-containing regimen |
No biomarker required |
Monoclonal antibody |
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 |
Monoclonal antibody |
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 required |
Monoclonal antibody |
Avastin (bevacizumab) |
Ovarian, fallopian tube, or primary peritoneal cancer |
Recurrent platinum-resistant disease |
Combined with chemotherapy for platinum-resistant recurrent disease who received no more than 2 prior chemotherapy regimens |
No biomarker required |
Monoclonal antibody |
Avastin (bevacizumab) |
Ovarian, fallopian tube, or primary peritoneal cancer |
Recurrent platinum-sensitive disease |
Combined with chemotherapy, followed by Avastin as a single agent, for platinum-sensitive recurrent diesase |
No biomarker required |
Monoclonal antibody |
Cyramza (ramucirumab) |
Colorectal cancer |
Metastatic (stage 4) |
Combined with FOLFIRI chemotherapy, for treatment after disease progression on, or after prior therapy with bevacizumab, oxaliplatin, and a fluoropyrimidine |
No biomarker required |
Monoclonal antibody |
Datroway (datopotamab deruxtecan-dlnk) |
Breast cancer |
Metastatic (stage 4) or unresectable |
Treatment for cancers that have progressed after hormone therapy and chemotherapy |
Hormone receptor position (HR-positive), HER2-negative |
Antibody-drug conjugate |
Elahere (mirvetuximab soravtansine-gynx) |
Ovarian, fallopian tube, or primary peritoneal cancer |
Stage 3 or 4 |
As second-line or later treatment of platinum-resistant or platinum-sensitive recurrent ovarian cancer |
Positive for FRα (folate receptor alpha) |
Antibody-drug conjugate |
Enhertu (fam-trastuzumab-deruxtecan-nxki) |
Breast cancer |
Metastatic (stage 4) |
Treatment for people who have: - received a prior anti-HER2 therapy for metastatic breast cancer, or
- had their breast cancer come back during or within 6 months of completing treatment for their early-stage breast cancer
|
HER2 overexpression (HER2-positive) |
Antibody-drug conjugate |
Enhertu (fam-trastuzumab-deruxtecan-nxki) |
Breast cancer |
Metastatic (stage 4) |
Treatment for people with tumors that are HER2-low who: - received chemotherapy in the metastatic setting and whose cancer no longer responds to hormonal therapy
- received chemotherapy in the adjuvant setting and whose cancer came back within 6 months of completing chemotherapy
|
HER2-low |
Antibody-drug conjugate |
Enhertu (fam-trastuzumab-deruxtecan-nxki) |
Solid tumors |
Metastatic (stage 4) or unresectable |
For adult patients with advanced solid tumors who have received prior treatment and have no alternative treatment options |
HER2 overexpression (HER2-positive) |
Antibody-drug conjugate |
Kadcyla (trastuzumab emtansine) |
Breast cancer |
Metastatic (stage 4) |
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-drug conjugate |
Kadcyla (trastuzumab emtansine) |
Breast cancer |
Early stage (stage 2-3) |
As adjuvant therapy for people who have residual invasive disease after neoadjuvant taxane and Herceptin |
HER2 overexpression (HER2-positive) |
Antibody-drug conjugate |
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) |
Monoclonal antibody |
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) |
Monoclonal antibody |
Trodelvy (sacituzumab govitecan-hziy) |
Breast cancer |
Metastatic (stage 4) |
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 |
Trodelvy (sacituzumab govitecan-hziy) |
Breast cancer |
Metastatic (stage 4) |
For metastatic breast cancer breast after endocrine-based therapy and at least 2 additional systemic therapies in the metastatic setting |
Hormone receptor-positive (HR-positive), HER2-negative |
Antibody-drug conjugate |
Trodelvy (sacituzumab govitecan-hziy) |
Breast cancer |
Metastatic (stage 4) |
For metastatic breast cancer breast after endocrine-based therapy and at least 2 additional systemic therapies in the metastatic setting |
Hormone receptor-positive (HR-positive), HER2-negative |
Antibody-drug conjugate |
Vectibix (panitumumab) |
Colorectal cancer |
Metastatic (stage 4) |
Combined with FOLFOX for first-line treatment |
Negative for KRAS and NRAS mutations |
Monoclonal antibody |
Vectibix (panitumumab) |
Colorectal cancer |
Metastatic (stage 4) |
As a single therapy following disease progression after prior treatment with fluoropyrimidine, oxaliplatin, and irinotecan-containing chemotherapy |
Negative for KRAS and NRAS mutations |
Monoclonal antibody |