Targeting

FGFR inhibitor FGFR3 PROOF 302 adjuvant cisplatin-based chemotherapy adjuvant therapy cisplatin-therapy refusal fusions or rearrangements infigratinib muscle-invasive urothelial carcinoma mutations neoadjuvant cisplatin-based chemotherapy phase III upper tract urothelial carcinoma urothelial bladder carcinoma urothelial carcinoma

Journal

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

Informations de publication

Date de publication:
Jul 2022
Historique:
pubmed: 25 5 2022
medline: 18 6 2022
entrez: 24 5 2022
Statut: ppublish

Résumé

PROOF 302 is an ongoing randomized, double-blind, placebo-controlled, adjuvant phase III trial (NCT04197986) in approximately 218 patients from 120 centers worldwide. Eligibility criteria include post-surgical high-risk muscle-invasive upper tract urothelial cancer (85% of patients) or urothelial bladder cancer (15%), susceptible Cancers of the bladder and other parts in the urinary system, especially those that are invasive and grow into the muscle layer, may need extra treatment after surgical removal of the tumor, particularly if there is a high risk of the cancer coming back. Chemotherapy regimens that include cisplatin are often used postoperatively, although some patients are unable to tolerate this treatment or refuse it. FGFR3, a protein that is encoded by the

Autres résumés

Type: plain-language-summary (eng)
Cancers of the bladder and other parts in the urinary system, especially those that are invasive and grow into the muscle layer, may need extra treatment after surgical removal of the tumor, particularly if there is a high risk of the cancer coming back. Chemotherapy regimens that include cisplatin are often used postoperatively, although some patients are unable to tolerate this treatment or refuse it. FGFR3, a protein that is encoded by the

Identifiants

pubmed: 35608106
doi: 10.2217/fon-2021-1629
doi:

Substances chimiques

Phenylurea Compounds 0
Pyrimidines 0
infigratinib A4055ME1VK
FGFR3 protein, human EC 2.7.10.1
Receptor, Fibroblast Growth Factor, Type 3 EC 2.7.10.1

Banques de données

ClinicalTrials.gov
['NCT04197986']

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2599-2614

Subventions

Organisme : QED Therapeutics
Organisme : Helsinn Healthcare S.A.

Auteurs

Sumanta K Pal (SK)

City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA.

Diederik M Somford (DM)

Canisius Wilhelmina Hospital, 6532 SZ Nijmegen, The Netherlands.

Petros Grivas (P)

Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, University of Washington, Seattle, WA 98195, USA.

Srikala S Sridhar (SS)

Princess Margaret Hospital, Toronto, ON M5G 2C1, Canada.

Shilpa Gupta (S)

Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH 44106, USA.

Joaquim Bellmunt (J)

Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
PSMAR-IMIM Laboratory, Boston, MA 02215, USA.

Guru Sonpavde (G)

Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Mark T Fleming (MT)

Virginia Oncology Associates, Norfolk, VA 23502, USA.

Seth P Lerner (SP)

Baylor College of Medicine, Houston, TX 77030, USA.

Yohann Loriot (Y)

Gustave Roussy, Villejuif, 94805, France.

Jean Hoffman-Censits (J)

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD 21287, USA.

Begoña P Valderrama (BP)

Hospital Universitario Virgen del Rocio, 41013 Seville, Spain.

Corina Andresen (C)

QED Therapeutics Inc., San Francisco, CA 94107, USA.

Marco J Schnabel (MJ)

University of Regensburg, 93053 Regensburg, Germany.

Suzanne Cole (S)

UT Southwestern Simmons Comprehensive Cancer Center, University of Texas, Dallas, TX 75390, USA.

Siamak Daneshmand (S)

Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.

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Classifications MeSH