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Glofitamab Approved by NHS as Potential Curative Treatment for Aggressive Blood Cancer

2 years ago2 min read
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Key Insights

  • The NHS has approved glofitamab (Columvi®) for diffuse large B-cell lymphoma (DLBCL) patients who have undergone two or more ineffective treatments.

  • Clinical trials have demonstrated glofitamab's potential to cure DLBCL, offering a new treatment option for approximately 5,500 people diagnosed annually in England.

  • Glofitamab, administered intravenously, activates the patient's own T-cells to target and eliminate lymphoma cells, reducing the need for chemotherapy and its associated side effects.

The National Health Service (NHS) in England is set to offer glofitamab (Columvi®) as a potentially curative treatment for patients with diffuse large B-cell lymphoma (DLBCL), an aggressive form of blood cancer. This approval by the Medicines and Healthcare products Regulatory Agency (MHRA) and the National Institute of Health and Care Excellence (NICE) provides a new option for patients who have relapsed or are refractory to previous treatments.

Clinical Efficacy and Mechanism of Action

Clinical trials have indicated that glofitamab has the potential to induce remission and even cure DLBCL in some patients. One such patient, John Sharp, had previously been reliant on a wheelchair, but after glofitamab treatment, he achieved complete remission and regained the ability to walk. Glofitamab is a bispecific antibody that redirects a patient's own T-cells to target and kill lymphoma cells. This mechanism reduces the need for traditional chemotherapy, thereby minimizing side effects and improving the patient's quality of life.
Dr. Wendy Osborne, a consultant haematologist at Freeman Hospital in Newcastle, explained, "Bispecific antibodies use the patient’s own white blood cells to attack and kill the lymphoma... By bringing these cells together, the patient’s own immune system is activated and kills the cancer cell and so chemotherapy is not required."

Availability and Access

Glofitamab will be made available through the Cancer Drugs Fund (CDF), ensuring fast-tracked access for eligible patients. This is particularly significant for those who have not responded to or are ineligible for CAR T-cell therapy. The intravenous administration of glofitamab can be offered at more cancer treatment sites across the country, increasing accessibility for patients.

Impact and Future Implications

Approximately 5,500 people are diagnosed with DLBCL in England each year, predominantly men aged 65 and over. The introduction of glofitamab represents a significant advancement in the treatment landscape, offering a chemotherapy-free option with the potential for long-term remission and cure.
Amanda Pritchard, NHS Chief Executive, stated, "The approval of Glofitamab is incredible news for those who have this advanced and aggressive form of blood cancer... it is so wonderful to hear the impact that it has already had on patients like John who can now walk again and spend time with his family, thanks to this lifechanging treatment."
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