| Literature DB >> 30977385 |
Javier Cortés1, Fabrice André2, Anthony Gonçalves3, Sherko Kümmel4, Miguel Martín5, Peter Schmid6, Florian Schuetz7, Sandra M Swain8, Valerie Easton9, Erika Pollex10, Regula Deurloo11, Rebecca Dent12.
Abstract
The PD-L1 inhibitor atezolizumab received US FDA accelerated approval as treatment for PD-L1-positive metastatic triple-negative breast cancer (TNBC). In IMpassion130, combining atezolizumab with first-line nab-paclitaxel for metastatic TNBC significantly improved progression-free survival and showed a clinically meaningful effect on overall survival in patients with PD-L1-positive tumors. The placebo-controlled randomized Phase III IMpassion132 (NCT03371017) trial is evaluating atezolizumab with first-line chemotherapy (capecitabine [mandatory in platinum-pretreated patients] or gemcitabine/carboplatin) for inoperable locally advanced/metastatic TNBC recurring ≤12 months after completing standard (neo)adjuvant anthracycline and taxane chemotherapy. Stratification factors are: visceral metastases, tumor immune cell PD-L1 status and selected chemotherapy. Patients are randomized to atezolizumab 1200 mg or placebo every 3 weeks with the chosen chemotherapy, continued until progression, unacceptable toxicity or withdrawal. The primary end point is overall survival.Entities:
Keywords: PD-L1; atezolizumab; capecitabine; carboplatin; gemcitabine; immunotherapy; overall survival; triple-negative breast cancer
Year: 2019 PMID: 30977385 DOI: 10.2217/fon-2019-0059
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404