Evidence map›Paper›PMID 20546189›Full record

ReviewRespirology (Carlton, Vic.)2010

Current development and future prospects in chemotherapy of tuberculosis.

Eric L Nuermberger, Melvin K Spigelman, Wing Wai Yew

Registry-linked trialAbstract readReview
In one paragraph

Review in Respirology (Carlton, Vic.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03561753 (Pilot Clinical Trial of PRS TB Regimen I - Phase II), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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.

NCT03561753 phase4completednot on this mapstarted 2017, after this paper: background citation

Pilot Clinical Trial of PRS TB Regimen I - Phase II

TypeinterventionalSponsorShanghai Pulmonary Hospital, Shanghai, ChinaRan2017 to 2020Enrolled97ConditionsPulmonary Tuberculosis TB in Sputum: (+) MicroscopyArmsGroup A (the standard 2HRZE/4HR regimen), Group B (New short course PRS regimen, 4EZ(high dose)PtoCfz)
3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Ultra-short-course chemotherapy for spinal tuberculosis: five years of observation.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2013
    Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Rifamycins, Alone and in Combination.Cold Spring Harbor perspectives in medicine · 2016
    Review
  9. Article
  10. The role of delamanid in the treatment of drug-resistant tuberculosis.Therapeutics and clinical risk management · 2015
    Review
  11. Article
  12. Article
  13. Recent advances in tuberculosis: New drugs and treatment regimens.Current respiratory medicine reviews · 2013
    Article
  14. Article
  15. Article
  16. Article
  17. Antituberculosis therapy for 2012 and beyond.Expert opinion on pharmacotherapy · 2012
    Review
  18. Article
  19. Article
  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

3 authors.

Eric L NuermbergerCenter for Tuberculosis Research, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231-1002, USA. enuermb@jhmi.edu
Melvin K Spigelman
Wing Wai Yew

Funding

Advancing New Drug Regimens for MDR/XDR TBR01AI090820 · NIAID · JOHNS HOPKINS UNIVERSITY · PI NUERMBERGER, ERIC L · 2010 to 2012
$1.2M
NIAID NIH HHS R01 AI090820
6 · The paper itself

Abstract

Although treatment of drug-susceptible tuberculosis (TB) under ideal conditions may be successful in >or=95% of cases, cure rates in the field are often significantly lower due to the logistical challenges of administering and properly supervising the intake of combination chemotherapy for 6-9 months. Success rates are far worse for multidrug-resistant and extensively drug-resistant TB cases. There is general agreement that new anti-TB drugs are needed to shorten or otherwise simplify treatment for drug-susceptible and multidrug-resistant/extensively drug-resistant-TB, including TB associated with HIV infection. For the first time in over 40 years, a nascent pipeline of new anti-TB drug candidates has been assembled. Eleven candidates from seven classes are currently being evaluated in clinical trials. They include novel chemical entities belonging to entirely new classes of antibacterials, agents approved for use against infections other than TB, and an agent already approved for limited use against TB. In this article, we review the current state of TB treatment and its limitations and provide updates on the status of new drugs in clinical trials. In the conclusion, we briefly highlight ongoing efforts to discover new compounds and recent advances in alternative drug delivery systems.

Indexed as

AdamantaneAnimalsAntitubercular AgentsCarbapenemsClinical Trials as TopicDiarylquinolinesDrug Delivery SystemsEthylenediaminesFluoroquinolonesHumansIsonicotinic AcidsMiceMycobacterium tuberculosisNitroimidazolesOxazolidinonesPatient ComplianceAdamantaneAntitubercular AgentsbedaquilineCarbapenemsDiarylquinolinesEthylenediaminesFluoroquinolonesIsonicotinic AcidsN-geranyl-N'-(2-adamantyl)ethane-1,2-diamineNitroimidazolesOxazolidinonesPyrrolesQuinolinesRifamycinssudoterb

Identifiers

PMID20546189
PMCPMC4461445

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.