Overall survival improvement in patients with metastatic clear-cell renal cell carcinoma between 2000 and 2020: a retrospective cohort study.

Renal cell carcinoma clear-cell immune checkpoint inhibitors overall survival vascular endothelial growth factor receptor tyrosine kinase inhibitors

Journal

Acta oncologica (Stockholm, Sweden)
ISSN: 1651-226X
Titre abrégé: Acta Oncol
Pays: England
ID NLM: 8709065

Informations de publication

Date de publication:
Jan 2022
Historique:
pubmed: 30 10 2021
medline: 22 1 2022
entrez: 29 10 2021
Statut: ppublish

Résumé

Only a few recent phase III trials with targeted therapies or immune checkpoint inhibitors (ICIs) in metastatic clear-cell renal cell carcinoma (m-ccRCC) demonstrated an overall survival (OS) benefit compared to standard of care. We aimed to study the evolution of OS since the start of systemic therapy from 2000 to 2020. Retrospective study on all consecutively treated m-ccRCC patients in three Belgian hospitals starting with systemic therapy. The study outcome was OS since the start of systemic therapy. We used a univariable Cox model for OS with year of the start of therapy as a predictor, and a multivariable analysis including known prognostic factors. Linear and non-linear trends of time were tested. Five hundred patients were included. In a linear model, the HR for OS depending on the year of the start of therapy was 0.95 (95%CI 0.93-0.97; OS of m-ccRCC patients has been improving significantly over the last 15 years since the introduction of VEGFR-TKIs and ICIs.

Sections du résumé

BACKGROUND BACKGROUND
Only a few recent phase III trials with targeted therapies or immune checkpoint inhibitors (ICIs) in metastatic clear-cell renal cell carcinoma (m-ccRCC) demonstrated an overall survival (OS) benefit compared to standard of care. We aimed to study the evolution of OS since the start of systemic therapy from 2000 to 2020.
PATIENTS AND METHODS METHODS
Retrospective study on all consecutively treated m-ccRCC patients in three Belgian hospitals starting with systemic therapy. The study outcome was OS since the start of systemic therapy. We used a univariable Cox model for OS with year of the start of therapy as a predictor, and a multivariable analysis including known prognostic factors. Linear and non-linear trends of time were tested.
RESULTS RESULTS
Five hundred patients were included. In a linear model, the HR for OS depending on the year of the start of therapy was 0.95 (95%CI 0.93-0.97;
CONCLUSION CONCLUSIONS
OS of m-ccRCC patients has been improving significantly over the last 15 years since the introduction of VEGFR-TKIs and ICIs.

Identifiants

pubmed: 34711121
doi: 10.1080/0284186X.2021.1989720
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Vascular Endothelial Growth Factor A 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

22-29

Auteurs

Sofie Demasure (S)

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

Isabel Spriet (I)

Pharmacy Department, University Hospitals Leuven, Leuven, Belgium.

Philip R Debruyne (PR)

Department of General Medical Oncology, AZ Groeninge, Kortrijk, School of Life Sciences, Anglia Ruskin University, Cambridge, UK.

Annouschka Laenen (A)

Biostatistics and Statistical Bioinformatics Center, Leuven, Belgium.

Wim Wynendaele (W)

Department of Medical Oncology, Imelda Ziekenhuis, Bonheiden, Belgium.

Marcella Baldewijns (M)

Department of Pathology, University Hospitals Leuven, Leuven, Belgium.

Herlinde Dumez (H)

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

Paul M Clement (PM)

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

Hans Wildiers (H)

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

Patrick Schöffski (P)

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

Eduard Roussel (E)

Department of Urology, University Hospitals Leuven, Leuven, Belgium.

Lisa Kinget (L)

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

Maarten Albersen (M)

Department of Urology, University Hospitals Leuven, Leuven, Belgium.

Benoit Beuselinck (B)

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

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Classifications MeSH