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Cochrane Database of Systematic Reviews

Targeted therapy for metastatic renal cell carcinoma

Esta versión no es la más reciente

Información

DOI:
https://doi.org/10.1002/14651858.CD012796Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 15 septiembre 2017see what's new
Tipo:
  1. Intervention
Etapa:
  1. Protocol
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Urología

Copyright:
  1. Copyright © 2017 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

Cifras del artículo

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Contraer

Autores

  • Fabian Hofmann

    Correspondencia a: Department of Urology, Sunderby Sjukhus, Umeå University, Luleå, Sweden

    [email protected]

  • Lorenzo SO Marconi

    Department of Urology and Renal Transplantation, Centro Hospitalar e Universitario de Coimbra, Coimbra, Portugal

  • Fiona Stewart

    c/o Cochrane Incontinence Group, Institute of Health & Society, Newcastle University, Newcastle Upon Tyne, UK

  • Thomas BL Lam

    Academic Urology Unit, University of Aberdeen, Aberdeen, UK

  • Axel Bex

    Division of Surgical Oncology, Department of Urology, The Netherlands Cancer Institute, Amsterdam, Netherlands

  • Steven E Canfield

    Division of Urology, Department of Surgery, The University of Texas Medical School at Houston, Houston, USA

  • Börje Ljungberg

    Department of Surgical and Perioperative Sciences, Umeå University, Umeå, Sweden

Contributions of authors

Contributions to the protocol

This protocol version concept and design: Fabian Hofmann, Thomas BL Lam, Axel Bex

Submitted and revised protocol: final approval by all authors.

Contributions to the review

To be decided after discussion and consensus

Sources of support

Internal sources

  • BC Cancer Agency, Canada.

External sources

  • No sources of support supplied

Declarations of interest

F Hofmann: declares the following relevant activities outside the submitted work: employed as a urologist, serves as guideline associate of European Association of Urology Renal Cell Carcinoma Guideline Panel and reports receiving no compensation for panel membership.

LSO Marconi: none known

F Steward: none known.

C Coppin: declares the following activities related to the submitted work: received support from BC Cancer Agency for travel to a meeting for the study or other purposes. Declares the following relevant activities outside the submitted work: received payment for contracted employment from BC Cancer Agency, a Canadian provincial government cancer agency with treatment policies that include agents described in the submitted work.

TBL Lam: declares the following relevant activity outside the submitted work: serves as member of European Association of Urology Renal Cell Carcinoma Guideline Panel and reports receiving no compensation for panel membership.

A Bex: declares the following relevant activities outside the submitted work: received consultancy support paid to his institution by Pfizer and Novartis for taking part in advisory boards; received payment from Pfizer and GlaxoSmithKline for presenting at Pfizer and GlaxoSmithKline sponsored symposia and conferences. These companies produce interventions (mTOR inhibitors and VEGF‐targeting therapy) that are researched in the review. Dr. Bex also reports that he is principal investigator of the European Organisation for Research and Treatment of Cancer (EORTC) SURTIME trial, a randomised phase III trial comparing immediate versus deferred nephrectomy in patients with synchronous metastatic renal cell carcinoma, which is in part supported by a grant from Pfizer to the sponsor (EORTC).

SE Canfield: none known.

B Ljungberg: declares the following relevant activities outside the submitted work: received support from Pfizer, GlaxoSmithKline and Novartis for advisory board attendance, most recently in early 2013, on the topic of renal cell carcinoma. Most interventions assessed in the review are produced by these companies.

Acknowledgements

We thank Cochrane Urology Review Group representatives Alea Miller and Philipp Dahm, for facilitating this collaboration and for editorial suggestions, and Molly M Neuberger, for administrative assistance. We wish to acknowledge additional authors contributing to previous versions of this review, Chris Coppin (Canada), Christian Kollmannsberger (Canada), Lyly Le (Canada), Franz Porzsolt (Germany), and Timothy J Wilt (USA). We also thank all members of the EAU Renal Cell Cancer Guideline Panel for support and individual contributions.

Version history

Published

Title

Stage

Authors

Version

2020 Oct 14

Targeted therapy for metastatic renal cell carcinoma

Review

Fabian Hofmann, Eu Chang Hwang, Thomas BL Lam, Axel Bex, Yuhong Yuan, Lorenzo SO Marconi, Börje Ljungberg

https://doi.org/10.1002/14651858.CD012796.pub2

2017 Sep 15

Targeted therapy for metastatic renal cell carcinoma

Protocol

Fabian Hofmann, Lorenzo SO Marconi, Fiona Stewart, Thomas BL Lam, Axel Bex, Steven E Canfield, Börje Ljungberg

https://doi.org/10.1002/14651858.CD012796

Notes

This is a protocol for a Cochrane Review that will serve to update and replace the existing Cochrane Review entitled, "Targeted therapy for advanced renal cell carcinoma" (Coppin 2008).

We have based parts of the Methods section of this Cochrane protocol on a standard template established by the CMED Group.

Keywords

MeSH

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.

Table 1. Individual targeted agents to be searched

Axitinib

Bevacizumab

Dovitinib

Erlotinib

Everolimus

Lapatinib

Pazopanib

Sorafenib

Sunitinib

Temsirolimus

Thalidomide

Tivozanib

Other agents identified during search

Figuras y tablas -
Table 1. Individual targeted agents to be searched