Trastuzumab (Kanjinti)

How is this drug name pronounced?

Trastuzumab: tras-TOO-zoo-mab

Kanjinti: kan-JIN-tee

Kanjinti (trastuzumab-anns) is “biosimilar” to Herceptin (trastuzumab). Kanjinti has been shown to be similar to Herceptin in the way in which it works, how well it works, and how safe it is. Other approved drugs that are biosimilar to Herceptin are Ogivri (trastuzumab-dkst), Ontruzant (trastuzumab-dttb), Herzuma (trastuzumab-pkrb), and Trazimera (trastuzumab-gyyp).


What cancer(s) does this drug treat?

Kanjinti is approved for:

Early breast cancer
Advanced breast cancer
Advanced stomach cancer

Early breast cancer

Kanjinti is approved for:

  • Patients with breast cancer that

    • tests positive for high amounts of the HER2 molecule and has spread into the lymph nodes (but not beyond the lymph nodes), OR
    • tests positive for high amounts of the HER2 molecule and has not spread into the lymph nodes, but the patient is at high risk.

In such cases, Kanjinti is used after surgical removal of all known disease. It may be used:

  • together with doxorubicin, cyclophosphamide, and either paclitaxel or docetaxel chemotherapy, OR
  • together with docetaxel and carboplatin chemotherapy, OR
  • by itself in patients who have previously received combination chemotherapy containing anthracyclines such as doxorubicin.

Advanced breast cancer

Kanjinti is approved for:

  • Patients with advanced breast cancer that tests positive for high amounts of the HER2 molecule and has spread to other parts of the body beyond the breast and lymph nodes, and who have not received treatment for their advanced disease. In such cases, Kanjinti is used in combination with the chemotherapy paclitaxel.
  • Patients with advanced breast cancer that tests positive for high amounts of the HER2 molecule and has spread to other parts of the body, and who have received one or more chemotherapy treatments for their advanced disease. In such cases, Kanjinti is used alone.

Advanced stomach cancer

Kanjinti is approved for:

  • Patients with gastric adenocarcinoma (stomach cancer) or gastroesophageal junction adenocarcinoma (cancer of the area where the stomach meets the esophagus) that tests positive for high amounts of the HER2 molecule and has spread to other parts of the body, and who have not received treatment for their advanced disease. In such cases, Kanjinti is used in combination with cisplatin and capecitabine or 5-fluorouracil chemotherapy.

Limitations of Use:

Age: The safety and efficacy of Kanjinti in patients under 18 years of age have not been established.
Pregnancy/Breastfeeding: Treatment with Kanjinti can cause serious side effects and death to a fetus. Patients should use effective contraception to prevent pregnancy during treatment with Kanjinti and for at least seven months after the last dose of Kanjinti. Kanjinti may cause adverse reactions to a breastfed child. Women are advised not to breastfeed during treatment with Kanjinti and for at least seven months after the last dose of Kanjinti.
Drug interactions: Treatment with anthracycline-based chemotherapy (e.g., doxorubicin) should be avoided for up to 7 months after stopping Kanjinti. Patients who receive anthracycline-based chemotherapy less than 7 months after stopping Kanjinti may be at increased risk to develop heart problems.


What type of immunotherapy is this?


How does this drug work?

  • Target: Human epidermal growth factor receptor 2 (HER2)

Kanjinti is an antibody that was made in the laboratory and was designed to attach to a protein molecule called HER2. HER2 is present on the surface of some normal cells in the body, but is present in much higher quantities on the surface of breast and stomach cancer cells. Higher-than-normal amounts of HER2 on cancer cells make these cells the main target of Kanjinti. 

Kanjinti and other antibody molecules have an overall “Y” shape. The two tips of the upper arms of the “Y” shape are the parts of the antibody that can very precisely bind to their target. For Kanjinti, tips of the upper arms bind to HER2. The stem of Kanjinti’s “Y” shape can attract immune cells or other parts of the immune system.

Kanjinti works to kill cancer cells in at least two ways.

Cancer cell growth inhibition
When HER2 on the surface of cells binds to itself or to other HER2-related proteins, it sends signals into the cell. These signals cause the cell to multiply, or in other ways promote the cell’s survival (such as causing cancer cells to produce molecules that enhance the growth of blood vessels, which help feed the tumor and support its growth). Higher-than-normal amounts of HER2 allow cancer cells to grow and multiply out of control. Binding of Kanjinti to HER2 blocks HER2 from pairing up and sending these signals into the cancer cells, preventing the cells from persisting and multiplying.

Antibody-dependent cell-mediated cytotoxicity (ADCC)
When bound to HER2 on the surface of cancer cells, the stem of Kanjinti can also attract and bind immune cells (like NK cells). This allows Kanjinti to act as a bridge between the target cell and the immune cell. The immune cell then releases molecules that can kill the cell Kanjinti is bound to.

Illustration showing how Kanjinti works


How is this drug given to patients?

Before starting treatment with Kanjinti, a small tumor sample is collected from a patient and is tested to determine if the tumor is positive for high amounts of the HER2 molecule.

The first dose of Kanjinti is administered via a tube into a vein (intravenous infusion, or i.v.) over the course of 90 minutes. Subsequent doses of Kanjinti are also given by intravenous infusion, but are typically lower in amount and are delivered over the course of 30-90 minutes. Kanjinti is usually administered weekly or every 3 weeks, and treatment continues out to one year, or until the cancer starts to grow again. Administration of Kanjinti does not require a hospital stay. The dose and schedule for treatment with Kanjinti differs slightly for the different diseases it is approved for, and may change if other drugs are part of the therapy.

Prior to the starting treatment with Kanjinti, patients undergo a thorough assessment of the condition of their heart. Patients also have their hearts monitored every 3 months during treatment with Kanjinti and upon completion of Kanjinti treatment.


What are the observed clinical results?

For: 

Early breast cancer (previously untreated after surgical removal of all known disease)
Early breast cancer (previously treated after surgical removal of all known disease)
Advanced breast cancer (previously untreated)
Advanced breast cancer (previously treated)
Advanced stomach cancer

It is important to keep in mind that each patient’s outcome is individual and may be different from the results observed in the clinical studies. In addition, with immunotherapy, it sometimes takes several months for responses to be observed.

Early breast cancer (previously untreated after surgical removal of all known disease)

In two large clinical trials, 4063 patients with breast cancer were either treated with doxorubicin and cyclophosphamide chemotherapy followed by paclitaxel plus trastuzumab (trastuzumab is the active ingredient in Kanjinti) OR with doxorubicin and cyclophosphamide chemotherapy followed by paclitaxel alone to prevent the return of disease after surgical removal of all known disease.

In an analysis of 3752 patients, at a median follow-up of 2 years:

Results of Doxorubicin + Cyclophosphamide followed by Paclitaxel + Trastuzumab vs. Doxorubicin + Cyclophosphamide followed by Paclitaxel alone (diagram)

In an analysis of 4063 patients at a median follow-up of 8.3 years:

Prognosis Doxorubicin + Cyclophosphamide followed by Paclitaxel + Trastuzumab vs. Doxorubicin + Cyclophoshamide followed by Paclitaxel alone (diagram)

In another clinical trial, 3222 patients with breast cancer were treated with either 

  • Docetaxel and carboplatin plus trastuzumab (trastuzumab is the active ingredient in Kanjinti), OR 
  • Doxorubicin and cyclophosphamide followed by docetaxel plus trastuzumab, OR
  • Doxorubicin and cyclophosphamide followed by docetaxel

to prevent the return of disease after surgical removal of all known disease.

At the time of data analysis:

Results of Docetaxel + Carboplatin + Trastuzumab vs. Doxorubicin + Cyclophosphamide followed by Docetaxel + Trastuzumab vs. Doxorubicin + Cyclophosphamide followed by Docetaxel alone (diagram)

Early breast cancer (previously treated after surgical removal of all known disease)

In a clinical trial, 3386 patients with breast cancer who had already been treated with chemotherapy to prevent the return of disease after surgical removal of all known disease, were either treated with trastuzumab (trastuzumab is the active ingredient in Kanjinti) for one or two years or were observed with no additional treatment.

At a median follow-up at 1 year:

Results after chemotherapy followed by Trastuzumab vs. chemotherapy alone (diagram)

At a median follow-up of 8 years, no added benefit in treating with trastuzumab for 2 years versus 1 year was found when looking at the percentage of patients who were disease-free or the percentage of patients who were alive.

Advanced breast cancer (previously untreated)

In a clinical trial, 469 patients with advanced breast cancer that tested positive for high amounts of the HER2 molecule and had spread to other parts of the body, and who had not been treated for their advanced disease, were treated with chemotherapy (anthracycline [doxorubicin or epirubicin] together with cyclophosphamide or paclitaxel) plus trastuzumab (trastuzumab is the active ingredient in Kanjinti) or chemotherapy alone.

Results after chemotherapy + Trastuzumab vs. chemotherapy alone (diagram)

(For the definition of “median”, click HERE.)

Advanced breast cancer (previously treated)

In a clinical trial, 222 patients with advanced breast cancer that tested positive for high amounts of the HER2 molecule and had spread to other parts of the body, and who had been previously treated with chemotherapy, but the disease had returned, were treated with trastuzumab (trastuzumab is the active ingredient in Kanjinti) alone. 12% of patients saw their tumors shrink and 2% of patients saw their tumors completely disappear. Complete disappearance of the tumors was only seen in patients with disease limited to skin and lymph nodes.

Advanced stomach cancer

In a clinical trial, 594 patients gastric adenocarcinoma (stomach cancer) or gastroesophageal junction adenocarcinoma (cancer of the area where the stomach meets the esophagus) that tested positive for the HER2 molecule and had spread to other parts of the body, and who had not received treatment for their advanced disease, were treated with either trastuzumab (trastuzumab is the active ingredient in Kanjinti) plus cisplatin and capecitabine or 5-fluorouracil chemotherapy or with chemotherapy alone. Half the patients treated with trastuzumab and chemotherapy lived for 14 months, compared with 11 months for patients treated with chemotherapy alone.


What are the side effects?

The most common side effects associated with treating breast cancer with Kanjinti are: fever, nausea, vomiting, reactions to the infusion, diarrhea, infections, cough, headache, fatigue, shortness of breath, rash, low white and red blood cell count, and muscle soreness.

The most common adverse reactions associated with treating stomach cancer with Kanjinti are: low white blood cell count, low platelet count, diarrhea, fatigue, irritation to mucous membranes (swelling of the lining of the mouth, nose, or throat), weight loss, upper respiratory tract infections, fever, and loss of taste.

Treatment with Kanjinti in combination with chemotherapy can cause a decrease in neutrophils, a type of immune cell that helps fight infections, making patients more likely to get an infection.

Heart problems
Kanjinti can cause potentially serious side effects, the most important of which is damage to the heart. Treatment with Kanjinti can cause a type of heart disease in which the heart is abnormally enlarged and the heart muscle becomes thickened and/or stiffened. As a result, the heart’s ability to pump blood is less efficient. The frequency of this side effect and its severity is highest in patients receiving Kanjinti together with chemotherapy containing anthracyclines, such as doxorubicin. Kanjinti can also cause other heart-related problems including high blood pressure and changes to the heart’s rhythm. Prior to starting treatment with Kanjinti, patients undergo a thorough assessment of the condition of their heart. Patients also have their hearts monitored every 3 months during treatment with Kanjinti and upon completion of Kanjinti treatment. Treatment with Kanjinti will be discontinued if severe heart issues occur.

Lung problems 
Treatment with Kanjinti can also cause serious lung side effects, including difficulty breathing, formation of scar tissue in the lungs, accumulation of some types of blood cells in the lung, accumulation of fluid around the lung, low blood oxygen levels, and more.

Infusion reactions
Treatment with Kanjinti can cause a set of reactions caused by the injection. The reactions may include flu-like symptoms such as fever and chills, and occasionally nausea, vomiting, pain, headache, dizziness, shortness of breath, low blood pressure, rash, and weakness. In very few patients, infusion reactions are serious and can be life-threatening; in these cases, the infusion should be immediately stopped and appropriate interventions and monitoring should be initiated. Symptoms usually occur during the infusion or within 24 hours of the infusion.

Patients should report any symptoms to their healthcare provider, who can then initiate actions to limit or reverse the side effects. For a more complete list of possible side effects, see the full prescribing information.


Additional information

Manufacturer 

Amgen

Approval

FDA and EMA 

Last updated on April 6, 2021


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