- How is breast cancer treated?
- Surgery for breast cancer
- Radiation therapy for breast cancer
- Chemotherapy for breast cancer
- Hormone therapy for breast cancer
- Targeted therapy for breast cancer
- Bone-directed therapy for breast cancer
- Clinical trials for breast cancer
- Complementary and alternative therapies for breast cancer
- Treatment of non-invasive (stage 0) breast cancer
- Treatment of invasive breast cancer, by stage
- Treatment of breast cancer during pregnancy
- More treatment information for breast cancer
Targeted therapy for breast cancer
As researchers have learned more about the gene changes in cells that cause cancer, they have been able to develop newer drugs that specifically target these changes. These targeted drugs work differently from standard chemotherapy (chemo) drugs. They often have different (and less severe) side effects.
If you’d like more information on a drug used in your treatment or a specific drug mentioned in this section, see our Guide to Cancer Drugs , or call us with the names of the medicines you’re taking.
Drugs that target the HER2/neu protein
In about 1 in 5 patients with breast cancer, the cancer cells have too much of a growth-promoting protein known as HER2/neu (or just HER2) on their surface. Breast cancers with too much of this protein tend to grow and spread more aggressively without special treatment. A number of drugs have been developed that target this protein.
None of these drugs are safe during pregnancy because they can cause harm or even death to the fetus. Women who had not gone through menopause before starting treatment need to use effective birth control while on any of these drugs.
Trastuzumab (Herceptin): Trastuzumab is a type of drug known as a monoclonal antibody—a man-made version of a very specific immune system protein. It attaches to HER2 and can help slow the growth of cancer cells with too much HER2. It may also stimulate the immune system to more effectively attack the cancer.
Trastuzumab is given as an injection into a vein (IV), usually once a week or as a larger dose every 3 weeks.
Trastuzumab is often used as adjuvant therapy for HER2-positive cancers to reduce the risk of the cancer coming back. It is given with chemo at first, and then on its own, usually for a total of a year of treatment. This may also be started before surgery as neoadjuvant therapy.
Trastuzumab is also used to treat HER2-positive advanced breast cancers that return after treatment or continue to grow during treatment. Treatment that combines trastuzumab with chemo generally works better than chemo alone. If a cancer gets worse while a patient is getting trastuzumab and chemo, often the trastuzumab is continued and the chemo is changed.
Compared with chemo drugs, the side effects of trastuzumab are relatively mild. These side effects are rare and may include fever and chills, weakness, nausea, vomiting, cough, diarrhea, and headache. These side effects are generally mild and occur less often after the first dose.
A more serious potential side effect is heart damage leading to a problem called congestive heart failure. For most (but not all) women, this effect is temporary and has improved when the drug is stopped. The risk of heart problems is higher when trastuzumab is given with certain chemo drugs such as doxorubicin (Adriamycin) and epirubicin (Ellence). For this reason heart function is checked regularly during treatment with trastuzumab. Major symptoms of congestive heart failure are shortness of breath, leg swelling, and severe fatigue. Women having these symptoms should call their doctor right away.
Ado-trastuzumab emtansine (TDM-1, Kadcyla™): Ado-trastuzumab emtansine is a type of drug known as an antibody-drug conjugate. It is made up of the same monoclonal antibody found in trastuzumab attached to a chemo drug known as DM-1. In this type of drug, the antibody acts as a homing device, taking the chemo drug directly to the cancer cells.
This drug is given by itself (without chemo) to treat advanced breast cancer. It is given as an injection into a vein (IV) every 3 weeks. Common side effects include fatigue, nausea, muscle and bone pain, low platelet counts, headache, and constipation. This drug can also cause more serious side effects, such as severe allergic reactions, liver damage, heart damage, and lung problems.
Pertuzumab (Perjeta®): Like trastuzumab, pertuzumab is a monoclonal antibody that attaches to the HER2 protein. It seems to target a different part of the protein than trastuzumab does. This drug can be used along with docetaxel (Taxotere) and trastuzumab to treat advanced breast cancer. This 3 drug combination can also be used to treat earlier-stage breast cancers before surgery (as neoadjuvant therapy).
This drug is given as an infusion into a vein every 3 weeks. When given with trastuzumab and docetaxel, common side effects included diarrhea, hair loss, nausea, fatigue, rash, and low white blood cell counts (sometimes with fever). Many side effects, such as hair loss, nausea, and fatigue occur at about the same rate as in those who get just docetaxel and trastuzumab.
Like trastuzumab, pertuzumab cannot be given to patients with poor heart function as it can weaken the heart. Your doctor will check tests of heart function before starting this drug and again every few months during treatment with pertuzumab.
Lapatinib (Tykerb): Lapatinib is another drug that targets the HER2 protein. This drug is given as a pill to women with advanced HER2-positive breast cancer that is no longer helped by chemo and trastuzumab. It has also been studied as an adjuvant therapy in patients with HER2-positive cancer. The chemo drug capecitabine (Xeloda) is often given in combination with lapatinib to treat metastatic breast cancer. It may also be given with letrozole (Femara) in patients with HER2-positive advanced breast cancer that is also ER-positive.
In one study, giving lapatinib along with trastuzumab helped patients with advanced breast cancer live longer than giving it alone.
The most common side effects of this drug include diarrhea, nausea, vomiting, rash, and hand-foot syndrome (this was discussed in the section about chemotherapy). Diarrhea is a common side effect and can be severe, so it is very important to let your health care team know about any changes in bowel habits as soon as they happen.
In rare cases lapatinib may cause liver problems or a decrease in heart function (that can lead to shortness of breath), although this seems to go away once treatment is finished.
Everolimus is a type of targeted therapy that blocks mTOR, a protein in cells that normally promotes their growth and division. By blocking this protein, everolimus can help stop cancer cells from growing. Everolimus may also stop tumors from developing new blood vessels, which can help limit their growth. In treating breast cancer, this drug seems to help hormone therapy drugs work better.
Everolimus is a pill taken once a day.
This drug is approved to treat advanced hormone receptor−positive, HER2−negative, breast cancer in women who have gone through menopause. It is meant to be used with exemestane (Aromasin) in these women if their cancers have grown while they were being treated with either letrozole or anastrozole (or the cancer started growing shortly after treatment with these drugs was stopped). This approval was based on a study that showed that giving everolimus with exemestane was better than exemestane alone in shrinking tumors and stopping their growth in post-menopausal women with hormone receptor−positive, HER2−negative breast cancer that had stopped responding to letrozole or anastrozole.
Common side effects of this drug include mouth sores, diarrhea, nausea, fatigue, feeling weak or tired, low blood counts, shortness of breath, and cough. Everolimus can also increase blood lipids (cholesterol and triglycerides) and blood sugars, so your doctor will check your blood work periodically while you are on this drug. It can also increase your risk of serious infections, so your doctor will watch you closely for infection while you are on treatment.
Everolimus is also being studied for use for earlier stage breast cancer, with other hormone therapy drugs, and combination with other treatments. This is discussed further in the section, “What’s new in breast cancer research and treatment?”
Tumors need to develop and maintain new blood vessels to grow. Drugs that target these blood vessels are helpful against a variety of cancers, and have been studied for use in breast cancer.
Bevacizumab is a monoclonal antibody that has been used in patients with metastatic breast cancer. This antibody is directed against vascular endothelial growth factor, a protein that helps tumors form new blood vessels.
Bevacizumab is given by intravenous (IV) infusion. It is most often used in combination with chemo.
Rare, but possibly serious side effects include bleeding, holes forming in the colon (requiring surgery to correct), and slow wound healing.
More common side effects include high blood pressure, tiredness, blood clots, low white blood cell counts, headaches, mouth sores, loss of appetite, and diarrhea. High blood pressure is very common, so it is very important that your doctor watches your blood pressure carefully during treatment.
Bevacizumab was first approved by the US Food and Drug Administration (FDA) as part of the treatment for metastatic breast cancer in 2008. The approval was based on a study in which the women who received bevacizumab with the chemo drug paclitaxel (Taxol) had a longer time without their cancers growing than the women who received paclitaxel alone.
New study results presented at a July 2010 FDA meeting did not show a real benefit for the women receiving bevacizumab as a part of their treatment. Although bevacizumab seemed to slow cancer growth for a short-time in some of the women, it didn't help them live longer. Those given bevacizumab also had much more severe side effects. The FDA concluded that the risks of this drug outweigh the benefits in the treatment of metastatic breast cancer. On November 18, 2011, the FDA withdrew the breast cancer "indication" for bevacizumab. This does not mean that the drug will become unavailable, since it is still FDA-approved to treat some other cancers. It does mean that the company making bevacizumab can’t market the drug for breast cancer—the company can’t tell doctors or patients that the drug is useful in treating breast cancer. At this time, women who are taking bevacizumab can continue to do so, but they should discuss this treatment with their doctors.
More information about monoclonal antibodies can be found in our document, Immunotherapy.
For more information about targeted therapy drugs, see our document Targeted Therapy.
Last Medical Review: 09/11/2013
Last Revised: 01/31/2014