1771.1 – Axicabtagene ciloleucel therapy for patients with relapsed or refractory follicular lymphoma

Find out about the service or technology in this application and the medical condition it addresses. You can also view the application documents, the deadlines for providing consultation input, and the outcome of the application when the MSAC process is complete.

  • Status Assessment
  • Type Re-application
  • Pre-PASC consultation Not applicable
  • Pre-MSAC consultation Open
  • Outcome Pending

Application details

Applicant

Gilead Sciences Pty Limited

Reason for application

Funding for a high cost, highly specialised therapy under the National Health Reform Agreement.

Service or technology in this application

Axicabtagene ciloleucel is a CAR T-cell therapy that is produced using a patient’s own T-cells (another form of immune cell), making the product unique to each patient. For CAR-T therapy, a patient’s T-cells are collected and genetically modified in a lab to express an anti-CD19 chimeric antigen receptor (CAR) that targets the lymphoma B-cells. The modified T-cells are multiplied and then infused back into the patient where they target and kill the cancerous lymphoma B-cells, thereby treating the lymphoma.

Axicabtagene ciloleucel is used when patients with follicular lymphoma do not respond to (refractory), or relapse (come back) after, other types of treatment, such as chemotherapy.

Type: Therapeutic technology

Medical condition this application addresses

Follicular Lymphoma (FL) is a type of blood cancer that changes certain blood cells in the body called B-cell lymphocytes (B-cells). It can affect lymph nodes (sometimes called glands) and the lymphatic system. Follicular lymphoma is considered an indolent lymphoma, which means it is usually slow growing.

Previous applications

Consultation survey and deadlines

The following consultation deadlines apply:

  • Pre-PASC consultation deadline: Expedited - bypassing PASC
  • Pre-MSAC consultation deadline: Friday 13 June 2025 11:59 pm AEST  

For other ways to provide input, see how to have your say.

We welcome input from everyone. We are especially keen to hear from those with lived experience of the health condition, service or technology the applications are addressing.

Find out more about consultation.

Meetings to consider this application

This application will be considered at the following meetings:

  • PASC meeting: Bypassing PASC
  • ESC meeting: 12-13 June 2025
  • MSAC meeting: 31 July - 1 August 2025

Find out more about our meetings.

Outcome details

The outcome of this application is pending.

More information