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    This website is intended for healthcare professionals (HCPs) only. If you are an HCP, register free to access the full content.

    • Unmet need

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    • TECENTRIQ®▼ (atezolizumab)
    • HCC
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    1. Roche Medicines
    2. Oncology
    3. TECENTRIQ®▼ (atezolizumab)
    4. eNSCLC
    5. Unmet need

    Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to Roche Products Ltd. Please contact Roche Drug Safety Centre by emailing welwyn.uk_dsc@roche.com or calling +44 (0)1707 367554.

    Prescribing Information

    TECENTRIQ®▼(atezolizumab) Great Britain

    Adverse event reporting and additional monitoring

    For over 15 years, there have been limited advances in adjuvant systemic therapies for early-stage NSCLC3

    • Lung cancer remains one of the most prevalent forms of cancer in the UK, with approximately 52,000 cases in 20204
    • Unfortunately, NSCLC is associated with poor overall survival, even for those diagnosed early5,6
    • In the early setting, preventing recurrence is key as most of the mortality in postresectional NSCLC is related to recurrence5
    • Surgery is the cornerstone of treatment3,7,8 and for those who are fit enough, adjuvant chemotherapy can further reduce patients’ risk of recurrence9
    • However, for many patients it is not enough5,6 – the International Adjuvant Lung Cancer Trial showed that at 5 years, approximately 60% of patients with stage I-III NSCLC saw their disease return6

    DFS in the International Adjuvant Lung Cancer Trial6

    Adapted from Arriagada6

    Now though, adjuvant TECENTRIQ may allow more eligible patients to live free of disease recurrence than the current standard of care2

    • TECENTRIQ is the first immunotherapy licensed for use in adult patients with stage II to IIIA (7th edition of the UICC/AJCC-staging system) NSCLC and PD-L1 expression on ≥50% of tumour cells1,2
    • After complete resection and 1–4 cycles of platinum-based chemotherapy, TECENTRIQ may improve DFS and reduce eligible patients’ risk of recurrence vs active monitoring2

     

    Click here to learn about what you could offer your eligible patients with TECENTRIQ

    AJCC, American Joint Committee on Cancer; DFS, disease-free survival; NSCLC, non-small cell lung cancer; PD-L1, programmed death ligand 1; TC, tumour cell; UICC, Union for International Cancer Control.

    References:

    1. TECENTRIQ GB Summary of Product Characteristics.
    2. Felip E et al. Lancet 2021; 398(10308): 1344–1357.
    3. Vansteenkiste J et al. Ann Oncol 2019; 30(8): 1244–1253.
    4. International Agency for Research on Cancer. United Kingdom. Globocan 2020. Available at: https://gco.iarc.fr/today/data/factsheets/populations/826-united-kingdom-fact-sheets.pdf accessed January 2022.
    5. Taylor MD et al. Ann Thorac Surg 2012; 93(6): 1813–1821.
    6. Arriagada R et al. J Clin Oncol 2010; 28(1): 35–42.
    7. Postmus PE et al. Ann Oncol 2017; 28(suppl 4): iv1–iv21.
    8. NICE Pathways. Non-small-cell lung cancer: treatments with curative intent. July 2021.
    9. Burdett S et al. Cochrane Database Syst Rev 2015; (3): CD011430.

    M-GB-00005179.

    Date of preparation: February 2022.

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    Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to Roche Products Ltd. Please contact Roche Drug Safety Centre by emailing welwyn.uk_dsc@roche.com or calling +44 (0)1707 367554. ▼Additional monitoring: Medicinal products associated with this symbol are subject to additional monitoring. Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. For biological medicines, healthcare professionals should report adverse reactions by brand name and batch number. This is a promotional website intended for HCPs, designed, built and funded by Roche Products Ltd. Commentary and other materials, including external links, posted on this site are not intended to amount to advice on which reliance should be placed. We therefore disclaim all liability and responsibility arising from any reliance placed on such materials by any visitor to our site, or by anyone who may be informed of any of its contents. M-GB-00006977 Date of Preparation April 2022.