TECENTRIQ, in combination with carboplatin and etoposide, is indicated for the first-line treatment of adult patients with extensive-stage small-cell lung cancer
(ES-SCLC).1
TECENTRIQ was the first treatment advance in SCLC in over 20 years, showing a significant survival benefit in a hard-to-treat patient population.2
A Phase 3 study in patients (n=403) with extensive-stage SCLC randomised to receive induction therapy with carboplatin and etoposide in combination with TECENTRIQ or placebo, and then TECENTRIQ or placebo maintenance therapy until disease progression or unacceptable toxicity. Primary endpoints included OS and PFS.2
Carbo/etop; carboplatin/etoposide.
*The 1- and 2-year overall survival (OS) rates were pre-specified secondary endpoints in IMpower133 (n=201 for the Tecentriq + CP/ET arm and n=202 for control arm), 2,4,5 the median follow-up was 35.7 months for the experimental arm and 26.4 months for the control arm (CCOD: 24 Sept 2022). †The 3-, 4-, and 5-year OS rates from the exploratory merged analysis of IMpower133 and IMbrella A extension (n=18 patients who rolled over from the Tecentriq + CP/ET arm of IMpower133) were not pre-specified and are considered exploratory; the median follow-up was 59.4 months (CCOD: 16 March 2023).6
CCOD=clinical cutoff date
Carbo/etop, carboplatin/etoposide.
Carbo/etop; carboplatin/etoposide.
Carbo/etop; carboplatin/etoposide.
†As of data cut-off date 24th January 2019, median follow-up: 22.9 months.