Literature DB >> 25846099

Accepting risk in the acceleration of drug development for rare cancers.

David Ashley1, David Thomas2, Lia Gore3, Rob Carter4, John R Zalcberg5, Renée Otmar6, Julian Savulescu7.   

Abstract

Rare cancers collectively contribute a disproportionate fraction of the total burden of cancer. The oncology community is increasingly facing small numbers of patients with each cancer subtype, requiring cooperation and collaboration to complete multicentre trials that advance knowledge and patient care. At the same time, new insights into the biology of rare cancers have led to an explosion in knowledge and development of targeted agents. These insights and techniques are set to revolutionise the care of patients with cancer. However, drug development strategies and the availability of new agents for rare cancers are at risk of stalling owing to the ever-increasing complexity and costs of clinical trials. Finding solutions to these problems is imperative to the future of cancer care. We propose that a greater degree of risk sharing is needed than is currently accepted to enable the use of new methods with confidence, and to keep pace with scientific advancement.
Copyright © 2015 Elsevier Ltd. All rights reserved.

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Year:  2015        PMID: 25846099     DOI: 10.1016/S1470-2045(14)71153-2

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  6 in total

Review 1.  Managing Expectations in the Transition to Proof of Concept Studies.

Authors:  Thomas Kieber-Emmons; Issam Makhoul; Angela Pennisi; Eric R Siegel; Peter D Emanuel; Bejotaloh Monzavi-Karbassi; Zenon Steplewski; J Thaddeus Beck; Laura F Hutchins
Journal:  Rev Recent Clin Trials       Date:  2017

2.  Development of a Framework Based on Reflective MCDA to Support Patient-Clinician Shared Decision-Making: The Case of the Management of Gastroenteropancreatic Neuroendocrine Tumors (GEP-NET) in the United States.

Authors:  Monika Wagner; Dima Samaha; Hanane Khoury; William M O'Neil; Louis Lavoie; Liga Bennetts; Danielle Badgley; Sylvie Gabriel; Anthony Berthon; James Dolan; Matthew H Kulke; Mireille Goetghebeur
Journal:  Adv Ther       Date:  2017-12-21       Impact factor: 3.845

3.  Are products with an orphan designation for oncology indications different from products for other rare indications? A retrospective analysis of European orphan designations granted between 2002-2012.

Authors:  Kim Pauwels; Isabelle Huys; Minne Casteels; Kristina Larsson; Caroline Voltz; Karri Penttila; Thomas Morel; Steven Simoens
Journal:  Orphanet J Rare Dis       Date:  2017-02-16       Impact factor: 4.123

4.  Working to improve the management of sarcoma patients across Europe: a policy checklist.

Authors:  Bernd Kasper; Estelle Lecointe-Artzner; Suzanne Wait; Shannon Boldon; Roger Wilson; Alessandro Gronchi; Claudia Valverde; Mikael Eriksson; Sarah Dumont; Nora Drove; Athanasia Kanli; Markus Wartenberg
Journal:  BMC Cancer       Date:  2018-04-16       Impact factor: 4.430

5.  Applying Reflective Multicriteria Decision Analysis (MCDA) to Patient-Clinician Shared Decision-Making on the Management of Gastroenteropancreatic Neuroendocrine Tumors (GEP-NET) in the Spanish Context.

Authors:  Monika Wagner; Dima Samaha; Jesus Cuervo; Harshila Patel; Marta Martinez; William M O'Neil; Paula Jimenez-Fonseca
Journal:  Adv Ther       Date:  2018-07-09       Impact factor: 3.845

6.  Adapting to a Pandemic - Conducting Oncology Trials during the SARS-CoV-2 Pandemic.

Authors:  Aaron C Tan; David M Ashley; Mustafa Khasraw
Journal:  Clin Cancer Res       Date:  2020-04-20       Impact factor: 12.531

  6 in total

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