
VIDEOS
Changes to the BTC treatment landscape and international guidelines
What factors do you consider when choosing an immunotherapy for your patients living with BTC?
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(01:52)
TOPAZ Phase III trial design and results
Patient-centred experience
Which patients are suitable for IMFINZI? Are there any subgroups that are unsuitable?
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(02:45)
What do you tell your patients about IMFINZI and what to expect from their treatment?
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(01:40)
PBS Information: Authority required (STREAMLINED) for NSCLC. Refer to PBS Schedule for full authority information. PLEASE CLICK HERE TO REVIEW FULL PRODUCT INFORMATION BEFORE PRESCRIBING. ▼ This medicinal product is subject to additional monitoring in Australia. This will allow quick identification of new safety information. AE: adverse event; BICR: Blinded Independent Central Review; CI: confidence interval; CRT: chemoradiation therapy; HR: hazard ratio; irAE: immune-related adverse event; NSCLC: non-small cell lung cancer; OS: overall survival; PFS: progression-free survival; RECIST: Response Evaluation Criteria in Solid Tumors. References: 1. Girard N, et al. J Thorac Oncol 2023;18:181-193. 2. Spigel DR, et al. J Clin Oncol 2022;1301-1311. 3. Antonia SJ, et al. N Engl J Med 2017;377:1919-1929. IMFINZI® is a registered trademark of the AstraZeneca group of companies. Registered user AstraZeneca Pty. Ltd. ABN 54 009 682 311. 66 Talavera Road, Macquarie Park, NSW 2113. https://www.astrazeneca.com.au. For Medical Information enquiries or to report an adverse event or product quality complaint: Telephone 1800 805 342 or via https://contactazmedical.astrazeneca.com or email Medical Information enquiries to medinfo.australia@astrazeneca.com. AU-15640 ASTR0828/EMBC Date of preparation: January 2023. |