Capivasertib Plus Paclitaxel Versus Placebo Plus Paclitaxel As First-Line Therapy for Metastatic Triple-Negative Breast Cancer: The PAKT Trial.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
10 02 2020
Historique:
pubmed: 17 12 2019
medline: 9 9 2020
entrez: 17 12 2019
Statut: ppublish

Résumé

The phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway is frequently activated in triple-negative breast cancer (TNBC). The AKT inhibitor capivasertib has shown preclinical activity in TNBC models, and drug sensitivity has been associated with activation of PI3K or AKT and/or deletions of PTEN. The PAKT trial was designed to evaluate the safety and efficacy of adding capivasertib to paclitaxel as first-line therapy for TNBC. This double-blind, placebo-controlled, randomized phase II trial recruited women with untreated metastatic TNBC. A total of 140 patients were randomly assigned (1:1) to paclitaxel 90 mg/m Median PFS was 5.9 months with capivasertib plus paclitaxel and 4.2 months with placebo plus paclitaxel (hazard ratio [HR], 0.74; 95% CI, 0.50 to 1.08; 1-sided Addition of the AKT inhibitor capivasertib to first-line paclitaxel therapy for TNBC resulted in significantly longer PFS and OS. Benefits were more pronounced in patients with

Identifiants

pubmed: 31841354
doi: 10.1200/JCO.19.00368
doi:

Substances chimiques

Placebos 0
Pyrimidines 0
Pyrroles 0
Class I Phosphatidylinositol 3-Kinases EC 2.7.1.137
PIK3CA protein, human EC 2.7.1.137
AKT1 protein, human EC 2.7.11.1
Proto-Oncogene Proteins c-akt EC 2.7.11.1
PTEN Phosphohydrolase EC 3.1.3.67
PTEN protein, human EC 3.1.3.67
Paclitaxel P88XT4IS4D
capivasertib WFR23M21IE

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

423-433

Subventions

Organisme : Department of Health
Pays : United Kingdom
Organisme : Cancer Research UK
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Auteurs

Peter Schmid (P)

Barts ECMC, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Barts Hospital NHS Trust, London, United Kingdom.

Jacinta Abraham (J)

Velindre National Health Service (NHS) Trust, Cardiff, United Kingdom.

Stephen Chan (S)

Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.

Duncan Wheatley (D)

Royal Cornwall Hospitals NHS Trust, Truro, United Kingdom.

Adrian Murray Brunt (AM)

University Hospitals of North Midlands NHS Trust, Stoke-on-Trent, United Kingdom.

Gia Nemsadze (G)

Institute of Clinical Oncology, Tbilisi, Georgia.

Richard D Baird (RD)

Cancer Research UK Cambridge Centre, Cambridge, United Kingdom.

Yeon Hee Park (YH)

Samsung Medical Centre, Seoul, Republic of Korea.

Peter S Hall (PS)

Edinburgh Cancer Research Centre, University of Edinburgh, Edinburgh, United Kingdom.

Timothy Perren (T)

Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.

Robert C Stein (RC)

National Institute for Health Research Biomedical Research Centre, University College London Hospitals NHS Foundation Trust, University College London, London, United Kingdom.

László Mangel (L)

Institute of Oncology, Medical University of Pécs, Pecs, Hungary.

Jean-Marc Ferrero (JM)

Centre Antoine Lacassagne, Nice, France.

Melissa Phillips (M)

Barts Hospital NHS Trust, London, United Kingdom.

John Conibear (J)

Barts Hospital NHS Trust, London, United Kingdom.

Javier Cortes (J)

Ramon y Cajal University Hospital, Madrid, Spain.

Andrew Foxley (A)

AstraZeneca, Cambridge, United Kingdom.

Elza C de Bruin (EC)

AstraZeneca, Cambridge, United Kingdom.

Robert McEwen (R)

AstraZeneca, Cambridge, United Kingdom.

Daniel Stetson (D)

AstraZeneca, Waltham, MA.

Brian Dougherty (B)

AstraZeneca, Waltham, MA.

Shah-Jalal Sarker (SJ)

Barts ECMC, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.

Aaron Prendergast (A)

Barts ECMC, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.

Max McLaughlin-Callan (M)

Barts ECMC, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.

Matthew Burgess (M)

Barts ECMC, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.

Cheryl Lawrence (C)

Barts ECMC, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.

Hayley Cartwright (H)

Barts ECMC, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.

Kelly Mousa (K)

Barts ECMC, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.

Nicholas C Turner (NC)

Institute of Cancer Research, London, United Kingdom.
Royal Marsden Hospital, London, United Kingdom.

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Classifications MeSH