Evidence map›Paper›PMID 24935010›Full record

ReviewNature reviews. Clinical oncology2014

European perspective for effective cancer drug development.

Denis Lacombe, Sabine Tejpar, Roberto Salgado, Fatima Cardoso, Vassilis Golfinopoulos, Daniela Aust, Gunnar Folprecht, Arnaud Roth, Roger Stupp

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Clinical oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Trial
  2. Article
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  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Societal challenges of precision medicine: Bringing order to chaos.European journal of cancer (Oxford, England : 1990) · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Clinical cancer research: the past, present and the future.Nature reviews. Clinical oncology · 2014
    Review
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Denis LacombeEORTC Headquarters, Avenue Mounier 83/11, 1200 Brussels, Belgium.
Sabine TejparU.Z. Leuven Campus Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium.
Roberto SalgadoInstitut Jules Bordet, Rue Heger-Bordet 1, 1000 Brussels, Belgium.
Fatima CardosoChampalimaud Cancer Centre, Avenue De Brasília, Doca de Pedrouços, 1400-048 Lisboa, Portugal.
Vassilis GolfinopoulosEORTC Headquarters, Avenue Mounier 83/11, 1200 Brussels, Belgium.
Daniela AustUniversitaetsklinikum Carl Gustav Carus, Fetscherstrasse 74, 01307 Dresden, Germany.
Gunnar FolprechtUniversitaetsklinikum Carl Gustav Carus, Fetscherstrasse 74, 01307 Dresden, Germany.
Arnaud RothHôpitaux Universitaires de Genève, rue Gabrielle-Perret-Gentil 4, 1211 Geneve 14, Switzerland.
Roger StuppUniversitaetsSpital Zurich, Division of Oncology, Raemistrasse 100, 8091 Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Health systems and the clinical research landscape evolve continuously owing to increased risk aversion, scrutiny by funding bodies, and costs of clinical trials. In this context, however, current drug development procedures are far from optimal, as exemplified by the late-stage failure of several drugs. The identification of new drugs urgently requires approaches based on a solid understanding of cancer biology, and that will support the design of robust confirmatory trials. The complexity and the costs of drug development are now beyond the knowledge and operational capacity of single organisations, therefore, a drastic deviation from the traditional path of drug discovery and new forms of multidisciplinary partnerships are needed to succeed in this sector. The European Organisation for Research and Treatment of Cancer (EORTC) proposes the use of collaborative molecular screening platforms (CMSPs) as a new approach to tackle this issue. These CMSPs have the advantage of optimizing the expertise of several partners and combining efforts alongside with cost-sharing models for efficient patient selection. This article describes some of the challenges to advancing drug development and improving medical treatments and how these hurdles can be overcome.

Indexed as

Antineoplastic AgentsDrug DiscoveryEuropeHumansNeoplasmsAntineoplastic Agents

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.