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Targeted therapy medicines attack certain proteins or cell functions that help cancer cells grow. Like chemotherapy, these medicines go all through the body, but they work in different ways. This means they can sometimes help even if chemotherapy isn’t working. These medicines mainly target cancer cells. So the side effects are often different and sometimes less severe than chemotherapy side effects.
Not everyone with colorectal cancer will need targeted therapy. Deciding if targeted therapy is a choice for you will depend mainly on these factors:
The stage of your cancer
Details about your cancer cells, such as specific proteins found on the surface of the cancer cells or certain gene changes in the cells. Cancer cells are tested for these proteins and gene changes in a lab.
Your age and overall health
Your concerns about side effects
What treatments you may have had before
Targeted medicines are used to treat some colorectal cancers that have spread to other parts of the body. Some of these medicines are also being studied to see if they might help if given after surgery for less advanced cancers.
These medicines are most often given along with chemotherapy. But some may also be used alone if chemotherapy is no longer working.
Several types of targeted medicines are now used for colorectal cancer.
Tumors need new blood vessels to grow beyond a certain size. Some targeted medicines work by blocking new blood vessels from forming. These include:
Bevacizumab
Ramucirumab
Ziv-aflibercept
Epidermal growth factor receptor or EGFR is a protein that's often found in high levels on cancer cells and helps them grow. Some targeted medicines work by attacking the EGFR protein. These include:
Cetuximab
Panitumumab
These medicines don’t work in people whose cancer cells have certain gene mutations. Your healthcare provider will test a sample of your tumor for these mutations before you get one of these medicines.
Regorafenib is a type of targeted medicine known as a multikinase inhibitor. It blocks several different proteins (kinases) in cancer cells that normally help them grow.
Encorafenib is another targeted therapy medicine that can shrink tumors or slow cancer growth. It works by attacking a protein that helps cancer cells grow.
Larotrectinib targets a specific gene change found in some colorectal cancer cells. It might be used if other treatments aren't working any more.
Before treatment starts, you'll meet with a medical oncologist. This is a healthcare provider who specializes in treating cancer with medicines. They will discuss your treatment choices with you and explain what you might expect.
How you get targeted therapy depends on which medicines are used. Some are pills that you take at home. Others go right into your blood through an IV (intravenous) line in a vein. This may take several minutes or hours.
In most cases, you will have targeted therapy as an outpatient. This means that you get it at a hospital clinic, infusion center, or your healthcare provider's office, and you go home the same day. Rarely, you may need to stay in the hospital during treatment.
You'll be watched for reactions during your treatments.
Some targeted medicines are given along with chemotherapy. Others are given alone.
Side effects of targeted therapy are different for everyone. They also depend on which medicine you get. Ask your healthcare provider about possible side effects you should watch for. Tell your provider about any changes or side effects you notice. There may be ways to help you feel better and keep side effects from getting worse. In most cases, side effects will get better over time after treatment ends.
These are some of the possible side effects of targeted therapy:
Allergic reactions, often during the infusion. If you have a reaction, it will likely be short-term and treatable. If this happens, your healthcare provider will talk with you about whether you can keep taking this type of medicine.
Acne-like skin changes on your face and chest. Treatment can’t prevent these skin changes. But there are ways to make them less of a problem and keep them from getting infected.
High blood pressure
Headaches
Fever
Higher risk for infection because of a low white blood cell count
Feeling very tired during and for a while after treatment
Loss of appetite
Belly (abdominal) pain
Sores in the mouth and throat
Weight loss
Diarrhea
Joint pain
Rare, but more severe side effects are:
Blood clots and an increased risk for heart attack and stroke. Your healthcare provider will watch you for this side effect. Let them know right away if you have chest pain, shortness of breath, or numbness or weakness, or if you feel dizzy or faint.
A GI perforation. This is an opening in the stomach or intestine. Tell your healthcare team right away if you have any new pain, constipation, or vomiting.
Bleeding inside the body (internal bleeding). Symptoms include coughing up blood, having blood in your stools or urine, or bleeding from your nose or gums.
Protein in the urine. This is a sign of kidney damage. Your healthcare provider will check a urine sample before and during your treatment to see if there is too much protein in it.
Hand-foot syndrome. Symptoms include redness, irritation, or pain in your hands and feet.
Liver damage. Symptoms include yellowing of your skin or the whites of your eyes.
Slow wound healing. Let your healthcare provider know if you have any wounds that aren’t healing well.
It's important to know which medicines you're taking. Write down the names of your medicines. Ask your healthcare team how they work, how to take them, and what side effects they might have.
Talk with your healthcare providers about what signs to look for and when to call them. Know what number to call with problems or questions. Is there a different number for evenings, holidays, and weekends?
It may be helpful to keep a diary of your side effects. A written list will make it easier for you to remember your questions when you go to your appointments. It will also make it easier for you to work with your healthcare team to make a plan to manage your side effects.