PIVOT-10: Phase II study of bempegaldesleukin plus nivolumab in cisplatin-ineligible advanced urothelial cancer.


Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
Jan 2021
Historique:
pubmed: 18 9 2020
medline: 11 8 2021
entrez: 17 9 2020
Statut: ppublish

Résumé

The choice of first-line therapy for patients with metastatic urothelial cancer (mUC) is based on cisplatin-eligibility and programmed death-ligand 1 (PD-L1) status. For patients with mUC who are ineligible for cisplatin and with low PD-L1 expression, chemotherapy-based regimens are the only approved first-line option. In a Phase I/II trial of the chemotherapy-free regimen, bempegaldesleukin (BEMPEG; NKTR-214) plus nivolumab, patients with locally advanced or mUC experienced tumor responses regardless of baseline PD-L1 expression (objective response rates: 50 and 45% in patients with PD-L1-positive and -negative tumors, respectively). The Phase II PIVOT-10 study (NCT03785925), evaluates efficacy and safety of first-line BEMPEG plus nivolumab in cisplatin-ineligible patients with locally advanced or mUC. Most patients will have low PD-L1 expression. Primary end point: objective response rates (including complete response).

Identifiants

pubmed: 32938232
doi: 10.2217/fon-2020-0795
doi:

Substances chimiques

Biomarkers, Tumor 0
Interleukin-2 0
Nivolumab 31YO63LBSN
Polyethylene Glycols 3WJQ0SDW1A
bempegaldesleukin BNO1JG5MZC
Cisplatin Q20Q21Q62J

Types de publication

Clinical Trial, Phase II Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

137-149

Subventions

Organisme : Nektar Therapeutics

Auteurs

Robert A Huddart (RA)

The Royal Marsden NHS Foundation Trust, Sutton, Surrey SM2 5PT, UK.

Arlene O Siefker-Radtke (AO)

The University of Texas MD Anderson Cancer Center, Department of Genitourinary Medical Oncology, Houston, TX 77030, USA.

Arjun V Balar (AV)

New York University Langone Health, Perlmutter Cancer Center, New York, NY 10016, USA.

Mehmet A Bilen (MA)

Emory University School of Medicine, Winship Cancer Institute, Atlanta, GA 30322, USA.

Thomas Powles (T)

Barts Cancer Institute, Queen Mary University of London, London EC1M 6BE, UK.

Aristotelis Bamias (A)

National & Kapodistrian University of Athens, 2nd Propaedeutic Dept of Internal Medicine, ATTIKON University Hospital, Athens 12462, Greece.

Daniel Castellano (D)

Hospital Universitario 12 de Octubre, Madrid 28041, Spain.

Maged F Khalil (MF)

Lehigh Valley Hospital, The Lehigh Valley Health Network, Allentown, PA 18103, USA.

Michiel S Van Der Heijden (MS)

The Netherlands Cancer Institute, Amsterdam 1066 CX, The Netherlands.

Vadim S Koshkin (VS)

Division of Hematology/Oncology, Department of Medicine, University of California San Francisco, San Francisco, CA 94158, USA.

David W Pook (DW)

Department of Medical Oncology, Monash Health, Melbourne, VIC 3168, Australia.

Mustafa Özgüroğlu (M)

Istanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, 34320 Avcilar/Istanbul, Turkey.

Linda Santiago (L)

Nektar Therapeutics, San Francisco, CA 94158, USA.

Bob Zhong (B)

Nektar Therapeutics, San Francisco, CA 94158, USA.

David Chien (D)

Nektar Therapeutics, San Francisco, CA 94158, USA.

Wei Lin (W)

Nektar Therapeutics, San Francisco, CA 94158, USA.

Mary A Tagliaferri (MA)

Nektar Therapeutics, San Francisco, CA 94158, USA.

Yohann Loriot (Y)

Université Paris-Sud, Université Paris-Saclay, INSERM 981, Institute Gustave Roussy, 94 805 Villejuif Cedex, France.

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Classifications MeSH