IMpassion132 Phase III trial: atezolizumab and chemotherapy in early relapsing metastatic triple-negative breast cancer.
Adult
Antibodies, Monoclonal, Humanized
/ pharmacology
Antineoplastic Combined Chemotherapy Protocols
/ pharmacology
B7-H1 Antigen
/ antagonists & inhibitors
Capecitabine
/ therapeutic use
Carboplatin
/ therapeutic use
Chemotherapy, Adjuvant
/ methods
Clinical Trials, Phase III as Topic
Deoxycytidine
/ analogs & derivatives
Female
Humans
Mastectomy
Multicenter Studies as Topic
Neoplasm Recurrence, Local
/ drug therapy
Placebos
/ administration & dosage
Randomized Controlled Trials as Topic
Treatment Outcome
Triple Negative Breast Neoplasms
/ mortality
Gemcitabine
PD-L1
atezolizumab
capecitabine
carboplatin
gemcitabine
immunotherapy
overall survival
triple-negative breast cancer
Journal
Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629
Informations de publication
Date de publication:
Jun 2019
Jun 2019
Historique:
pubmed:
13
4
2019
medline:
7
1
2020
entrez:
13
4
2019
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 30977385
doi: 10.2217/fon-2019-0059
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
B7-H1 Antigen
0
CD274 protein, human
0
Placebos
0
Deoxycytidine
0W860991D6
atezolizumab
52CMI0WC3Y
Capecitabine
6804DJ8Z9U
Carboplatin
BG3F62OND5
Gemcitabine
0
Types de publication
Clinical Trial Protocol
Journal Article
Langues
eng
Sous-ensembles de citation
IM