Pazopanib as Second-line Antiangiogenic Treatment in Metastatic Renal Cell Carcinoma After Tyrosine Kinase Inhibitor (TKI) Failure: A Phase 2 Trial Exploring Immune-related Biomarkers for Testing in the Post-immunotherapy/TKI Era.


Journal

European urology oncology
ISSN: 2588-9311
Titre abrégé: Eur Urol Oncol
Pays: Netherlands
ID NLM: 101724904

Informations de publication

Date de publication:
06 2021
Historique:
received: 04 06 2019
accepted: 19 07 2019
pubmed: 4 9 2019
medline: 2 2 2022
entrez: 4 9 2019
Statut: ppublish

Résumé

Pazopanib is an oral angiogenesis tyrosine kinase inhibitor (TKI) recommended in metastatic renal cell carcinoma (mRCC) for treatment-naïve patients or those experiencing cytokine failure. We conducted a phase 2, open-label, single-arm study in ten Spanish centres among mRCC patients whose disease progressed on first-line TKI. Patients received pazopanib until disease progression, death, or unacceptable toxicity. Twenty-seven patients were included (median age 62yr, 51.9% male). The objective overall response rate was 14.8% (95% confidence interval [CI] 1.4-28.2%). Median progression-free survival was 6.7mo (95% CI 3.7-11.2) and median overall survival was 20.6mo (95% CI 12.6-27.4). Lower circulating levels of IL-10 (p=0.002) were observed in responding patients at 8 wk after treatment. The median pazopanib treatment duration was 6.0mo (range 1.0-47.0). Most patients (48.1%) had mild or moderate adverse events (AEs), while 44.4% had severe AEs. Pazopanib was clinically active and well tolerated as a second-line treatment in mRCC patients after TKI failure, and circulating IL-10 levels could predict response. PATIENT SUMMARY: Pazopanib could be used as a second-line therapy for the treatment of metastatic renal cell carcinoma after failure of tyrosine kinase inhibitor (TKI) therapy when drugs such as nivolumab and cabozantinib are not available. Now that immunotherapy plus antiangiogenic therapy is a first-line option, IL-10 levels deserve further exploration as a potential predictor of response to sequential TKI-TKI therapy.

Identifiants

pubmed: 31477526
pii: S2588-9311(19)30117-8
doi: 10.1016/j.euo.2019.07.014
pii:
doi:

Substances chimiques

Biomarkers 0
Indazoles 0
Protein Kinase Inhibitors 0
Pyrimidines 0
Sulfonamides 0
pazopanib 7RN5DR86CK

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

502-505

Informations de copyright

Copyright © 2019 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Joaquim Bellmunt (J)

University Hospital del Mar, Barcelona, Spain. Electronic address: jbellmunt@parcdesalutmar.cat.

Emilio Esteban (E)

Hospital Universitario Central de Asturias, Oviedo, Spain.

Xabier García Del Muro (XG)

Instituto Catalán de Oncología, IDIBELL, Barcelona, Spain.

Juan Manuel Sepúlveda (JM)

Hospital Universitario 12 de Octubre, Madrid, Spain.

Pablo Maroto (P)

Hospital de Sant Pau, Barcelona, Spain.

Enrique Gallardo (E)

Institut d'Investigació i Innovació Parc Taulí, Parc Taulí Hospital Universitari, Barcelona, Spain.

Aranzazu González Del Alba (AG)

Servicio de Oncologia Médica, Hospital Universitario Son Dureta, Palma de Mallorca, Spain.

Olatz Etxaniz (O)

Instituto Catalán de Oncología, Badalona, Spain.

Marta Guix (M)

University Hospital del Mar, Barcelona, Spain.

Jose Luis González Larriba (JLG)

Hospital Clínico San Carlos, Madrid, Spain.

Jose A Arranz (JA)

Hospital Gregorio Marañón, Madrid, Spain.

Miriam Redrado (M)

CIBERONC/IDISNA Program of Solid Tumours and Biomarkers, CIMA and Department of Histology and Pathology, School of Medicine, University of Navarra, Pamplona, Spain.

Alfonso Calvo (A)

CIBERONC/IDISNA Program of Solid Tumours and Biomarkers, CIMA and Department of Histology and Pathology, School of Medicine, University of Navarra, Pamplona, Spain.

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Classifications MeSH