Blenrep (belantamab or belantamab mafodotin-blmf) is an antibody-drug conjugate (ADC) used to treat a certain type of blood cancer called multiple myeloma. Blenrep (belantamab) is given as an intravenous (IV) infusion at a doctor’s office or infusion center. Some side effects of Blenrep (belantamab) can be mild, such as nausea and diarrhea. But this medication can also cause serious eye problems that require special monitoring.
Please note: Blenrep (belantamab) is no longer FDA-approved in the United States and can only be accessed from the manufacturer through a special request process.
Advanced multiple myeloma that have previously been treated with at least 4 prior therapies
Blenrep (belantamab) is an antibody-drug conjugate (ADC). It's made up of two main parts that work together to kill cancer cells:
A monoclonal antibody part that finds and binds to cancer cells. In the case of multiple myeloma, the monoclonal antibody binds to proteins called BMCA and goes inside the cancer cells.
Once Blenrep (belantamab) is inside the tumor cells, the chemotherapy part of this medication kills the tumor cells.
Source: DailyMed
Side effects that you should report to your care team as soon as possible:
Side effects that usually do not require medical attention (report to your care team if they continue or are bothersome):
Because it’s an antibody drug conjugate, it uses a more targeted, specific approach to get chemotherapy to cancer cells
Each infusion only takes 30 minutes and is given every 3 weeks, so more convenient
Doesn’t typically cause hair loss, a common side effect of many anticancer medications
Commonly causes eye problems, which can be serious
Only available through a special request program (not currently approved in the United States)
Might cause infusion-related reactions, such as chills, fever, and nausea
Some people taking Blenrep (belantamab) experienced an infusion related reaction during treatment. If you have any symptoms such as itching, feeling hot, trouble breathing, or chest pain tell your nurse right away. They might need to pause your treatment or slow down the infusion. You might also need certain medications, such as diphenhydramine (Benadryl) or acetaminophen (Tylenol), before your next dose.
Some Blenrep (belantamab) side effects, such as liver enzyme and electrolyte changes in your blood, are monitored with lab tests. It’s important you keep all appointments to get labs drawn as your provider recommends, so they can monitor for these side effects.
Not all clinics or infusion centers are able to administer Blenrep (belantamab). Part of the REMS program requires the clinic to enroll in the program before they can give the medication. Your provider might need to refer you to a specific treatment center that’s registered to give Blenrep (belantamab).
Females who are taking Blenrep (belantamab) shouldn’t breastfeed. We don’t know if Blenrep (belantamab) passes into human milk. But because of the risk of harm to the nursing infant, it’s best to avoid nursing if you’re taking Blenrep (belantamab) and for 3 months after the last dose.
Blenrep (belantamab) can cause some serious health issues. This risk may be even higher for certain groups. If this worries you, talk to your doctor or pharmacist about other options.
People taking Blenrep (belantamab) commonly develop eye problems, typically within the first 2 treatment cycles. The most common eye problem is called keratopathy, which results in changes to the thin clear layer at the front of your eye (the cornea). Sometimes this condition doesn’t cause symptoms, but sometimes it can cause serious vision changes where you can’t see as well and blurred vision. Blenrep (belantamab) might also cause dry eyes and a sensation that something is in your eye. You’ll need to see an ophthalmologist before each dose so they can check for vision changes even if you don’t have symptoms. Your provider will recommend that you use preservatives-free eye drops 4 times a day throughout treatment. Avoid wearing contact lenses, unless your ophthalmologist says it's safe to do so. Depending on how this medication affects your eyesight, you might not be able to drive. If you do experience eye problems, you might need to pause Blenrep (belantamab), take it at a lower dose, or stop taking it altogether.
Because Blenrep (belantamab) can cause serious eye problems, it used to only be available through a special program called a Risk Evaluation and Mitigation Strategy (REMS). But since this medication has been withdrawn from the US market, this program is no longer available. If you’re receiving Blenrep (belantamab), your provider will give you more information about current safety programs.
Some people who receive Blenrep (belantamab) can develop low platelet counts in their body, typically within the first month of treatment. Platelets are the cells in your blood that form blood clots and prevent bleeding. So, when they’re low, your body can’t stop bleeding as well. Your provider will monitor your blood cell counts while you’re taking Blenrep (belantamab). If you have signs of low platelets such as bruising, nose bleeds, or blood in stool or urine, contact your provider right away. Your provider might need to stop, pause, or lower your dose of Blenrep (belantamab).
Some people receiving Blenrep (belantamab) developed an infusion reaction during their treatment. Symptoms of an infusion reaction might include itching, chills, chest pain or tightness, trouble breathing, and changes in blood pressure. Your nurse will monitor you during your infusion. If you have a reaction, your infusion might need to be paused, slowed down, or completely stopped depending on how severe your symptoms are. In addition, your provider will give you premedications for all future infusions to lower your risk of these reactions.
Blenrep (belantamab) hasn’t been studied in human pregnancy, but based on the way the medication works it can cause harm to an unborn baby or pregnancy loss (miscarriage). Your provider might require a negative pregnancy test before you start taking Blenrep (belantamab). Females who can get pregnant should use effective birth control while taking Blenrep (belantamab) and for 4 months after the last dose. Males who are sexually active with a female who can get pregnancy should use condoms while taking Blenrep (belantamab) and for 6 months after the last dose.
Your provider will determine your dose of Blenrep (belantamab) based on your body weight. The typical dose is 2.5 mg/kg given through the vein (intravenously) once every 3 weeks.
Advanced multiple myeloma that have previously been treated with at least 4 prior therapies
Advanced multiple myeloma in adults who've already tried at least four other therapies
Advanced multiple myeloma in adults (after at least two or more prior therapies)
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