FDA approves new therapy for patients with previously treated multiple myeloma

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Today, the U.S. Food and Drug Administration (FDA) approved isatuximab-irfc, in combination with pomalidomide and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least two prior therapies including lenalidomide and a proteasome inhibitor.

This approval was based on the results from the ICARIA-MM clinical trial.

Isatuximab-irfc, administered through intravenous (IV) infusion, is a CD38-directed cytolytic antibody that works by helping certain cells in the immune system attack multiple myeloma cancer cells.

“Targeting cells has led to the development of important oncology treatments. While there is no cure for multiple myeloma, isatuximab-irfc is now another CD38-directed treatment option added to the list of FDA-approved treatments of patients with multiple myeloma who have progressive disease after previous therapies,” said Richard Pazdur, M.D., director of the FDA’s Oncology Center of Excellence and acting director of the Office of Oncologic Diseases in the FDA’s Center for Drug Evaluation and Research. “In the clinical trial, there was a 40% reduction in the risk of disease progression or death with this therapy.”

Multiple myeloma is a form of blood cancer that occurs in infection-fighting plasma cells (a type of white blood cell) found in the bone marrow.

These cancerous cells multiply, produce an abnormal protein and push out other healthy blood cells from the bone marrow.

The disease may result in a weakened immune system and cause other bone or kidney problems.

The National Cancer Institute estimates there would be 32,270 new cases of multiple myeloma and 12,830 related deaths in the United States in 2020.

The FDA approved isatuximab-irfc based on the results of a clinical trial involving 307 patients with relapsed and refractory multiple myeloma who had received at least two prior therapies, including lenalidomide and a proteasome inhibitor.

Half of the patients received isatuximab-irfc in combination with pomalidomide and low-dose dexamethasone and the other half received only pomalidomide and low-dose dexamethasone.

The efficacy of isatuximab-irfc was based on progression-free survival (PFS) – the amount of time a patient stays alive without the cancer growing.

Patients who received isatuximab-irfc in combination with pomalidomide and low-dose dexamethasone showed improvement in PFS with a 40% reduction in the risk of disease progression or death compared to patients who received pomalidomide and dexamethasone.

These patients also had an overall response rate of 60.4%.

In comparison, the patients who only received pomalidomide and low-dose dexamethasone had an overall response rate of 35.3%.

Common side effects for patients taking isatuximab-irfc were neutropenia (abnormally low levels of white blood cells), infusion-related reactions, pneumonia (infection of the air sacs in one or both of the lungs), upper respiratory tract infection, diarrhoea, anaemia, lymphopenia (decrease in the level of white blood cells) and thrombocytopenia (abnormally low levels of platelets). Isatuximab-irfc can cause serious side effects, which include the following.

Isatuximab-irfc can cause IV infusion-related reactions.

In a grade three or higher (severe) reaction, the isatuximab-irfc infusion should be permanently discontinued and health care professionals should institute appropriate medical management.

Isatuximab-irfc can also cause neutropenia and health care professionals should monitor a patient’s complete blood cell count periodically during treatment, as well as monitor patients with neutropenia for signs of infection.

Higher incidences of second primary malignancies (a second primary cancer that may occur in the same tissue or organ as the first cancer or in another region of the body) were observed in a controlled clinical trial of patients with multiple myeloma receiving isatuximab-irfc.

Therefore, health care professionals should monitor patients for the development of a second primary malignancy when taking isatuximab-irfc.

Laboratory test interference may be experienced with isatuximab-irfc.

Blood banks should be informed that patients are receiving isatuximab-irfc because the drug may interfere with certain tests that are done by blood banks (such as antibody screening) for patients who need a blood transfusion.

Health care professionals should type and screen patients prior to starting treatment with isatuximab-irfc.

Isatuximab-irfc may interfere with the assays (tests) used to monitor M-protein, which may impact the determination of complete response.

Health care professionals should advise pregnant women that isatuximab-irfc may cause harm to a developing foetus.

Women who are pregnant should not use isatuximab-irfc.

Women planning to become pregnant should use effective contraceptives during and for at least five months after treatment.


Source: The Food and Drug Administration (FDA)

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The ONA Editor curates oncology news, views and reviews from Australia and around the world for our readers. In aggregated content, original sources will be acknowledged in the article footer.

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