Evidence map›Paper›PMID 21690376›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

The evolution of drug resistance and the curious orthodoxy of aggressive chemotherapy.

Andrew F Read, Troy Day, Silvie Huijben

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 149 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
149citing papers in PubMed, 1 pooled it
–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

149 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Interventions for the prevention of recurrent erysipelas and cellulitis.The Cochrane database of systematic reviews · 2017
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Competitive suppression and release in artemisinin-resistantEvolution, medicine, and public health · 2026
    Article
  7. The speed of vaccination rollout and the risk of pathogen adaptation.Journal of the Royal Society, Interface · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Design and synthesis of novel rigid dibenzo[Journal of enzyme inhibition and medicinal chemistry · 2023
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

89 more citing papers are in PubMed but not listed here.

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

3 authors.

Andrew F ReadCenter for Infectious Disease Dynamics, Department of Biology, Pennsylvania State University, University Park, PA 16802, USA. a.read@psu.edu
Troy Day
Silvie Huijben

Funding

Using Next-Generation Genomics to Study Antimalarial Drug Resistance in IndiaU19AI089676 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI OMPAD, DANIELLE C · 2010 to 2023
$22.6M
Within Host Selection of P. falciparum Variants by Artemisinin Combination TherapR01AI089819 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JULIANO, JONATHAN J · 2010 to 2014
$1.9M
The evolutionary biology of chemotherapy against infectious agents: towards ratiR01GM089932 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI READ, ANDREW F. · 2010 to 2013
$1.1M
NIAID NIH HHS R01 AI089819NIAID NIH HHS R01AI089819NIAID NIH HHS U19 AI089676NIAID NIH HHS U19AI089676NIGMS NIH HHS R01 GM089932NIGMS NIH HHS R01GM089932
6 · The paper itself

Abstract

The evolution of drug-resistant pathogens is a major challenge for 21st century medicine. Drug use practices vigorously advocated as resistance management tools by professional bodies, public health agencies, and medical schools represent some of humankind's largest attempts to manage evolution. It is our contention that these practices have poor theoretical and empirical justification for a broad spectrum of diseases. For instance, rapid elimination of pathogens can reduce the probability that de novo resistance mutations occur. This idea often motivates the medical orthodoxy that patients should complete drug courses even when they no longer feel sick. Yet "radical pathogen cure" maximizes the evolutionary advantage of any resistant pathogens that are present. It could promote the very evolution it is intended to retard. The guiding principle should be to impose no more selection than is absolutely necessary. We illustrate these arguments in the context of malaria; they likely apply to a wide range of infections as well as cancer and public health insecticides. Intuition is unreliable even in simple evolutionary contexts; in a social milieu where in-host competition can radically alter the fitness costs and benefits of resistance, expert opinion will be insufficient. An evidence-based approach to resistance management is required.

Indexed as

Biological EvolutionDrug ResistanceHumansMalariaPlasmodiumPublic Health

Identifiers

PMID21690376
PMCPMC3131826

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.