TECENTRIQ
Connecting patients to an important advancement in the management of lung cancer
With 6 indications across small- and non-small-cell lung cancer, TECENTRIQ is committed to advancing the standard of care in an area of high unmet need.1
TECENTRIQ—alone or in combination with cytotoxic therapy—has improved patient outcomes in metastatic non-small-cell lung cancer (NSCLC). It was also the first treatment advance in small-cell lung cancer (SCLC) in over 20 years, showing a significant survival benefit in a hard-to-treat patient population.2-6
Now, with adjuvant TECENTRIQ, the goal is cure
TECENTRIQ is the first and only approved adjuvant immunotherapy in PD-L1-high (≥50%) resected stage II-III* NSCLC, excluding EGFR/ALK+ disease. Learn how you can further reduce the risk of recurrence with adjuvant TECENTRIQ.1,7
Evidence-based treatment based on an extensive clinical trial programme addressing the unmet needs in patients with NSCLC and SCLC
TECENTRIQ indications1,8
Early-stage NSCLC
TECENTRIQ as monotherapy is indicated as adjuvant treatment following complete resection and platinum-based chemotherapy for adult patients with NSCLC with a high risk of recurrence whose tumours have PD-L1 expression on ≥50% of tumour cells (TC) and who do not have EGFR mutant or ALK positive NSCLC.
The staging edition agnostic "high risk of recurrence" definition refers to patients with stage II-IIIA per the 7th edition of the TNM staging system (select stage II-IIIB based on the 8th edition).
Metastatic NSCLC
TECENTRIQ, in combination with bevacizumab, paclitaxel and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous NSCLC. In patients with EGFR mutant or ALK-positive NSCLC, TECENTRIQ, in combination with bevacizumab, paclitaxel and carboplatin, is indicated only after failure of appropriate targeted therapies.
TECENTRIQ, in combination with nab-paclitaxel and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous NSCLC who do not have EGFR mutant or ALK-positive NSCLC.
TECENTRIQ as monotherapy is indicated for the first-line treatment of adult patients with metastatic NSCLC whose tumours have a PD-L1 expression ≥50% TC or ≥10% tumour-infiltrating immune cells (IC) and who do not have EGFR mutant or ALK-positive NSCLC.
TECENTRIQ as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic NSCLC after prior chemotherapy. Patients with EGFR mutant or ALK+ NSCLC should also have received targeted therapy before receiving TECENTRIQ.
SCLC
TECENTRIQ, in combination with carboplatin and etoposide, is indicated for first-line treatment of adult patients with extensive-stage small-cell lung cancer (ES-SCLC).
What this means for patients with lung cancer
Dr. John Conibear speaks about what recent advancements in immunotherapy mean for patient care.
Listen to Tommy, a lung cancer survivor who now uses his voice to raise awareness of the disease.