Evidence map›Paper›PMID 25240917›Full record

ArticleOral oncology2014

Targeting of chemoprevention to high-risk potentially malignant oral lesions: challenges and opportunities.

Victor D Martinez, Calum E MacAulay, Martial Guillaud, Wan L Lam, Lewei Zhang, Kitty K Corbett, Miriam P Rosin

Abstract read
In one paragraph

Article in Oral oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

7 authors.

Victor D MartinezBC Cancer Research Centre, Department of Integrative Oncology, Vancouver, Canada.
Calum E MacAulayBC Cancer Research Centre, Department of Integrative Oncology, Vancouver, Canada.
Martial GuillaudBC Cancer Research Centre, Department of Integrative Oncology, Vancouver, Canada.
Wan L LamBC Cancer Research Centre, Department of Integrative Oncology, Vancouver, Canada.
Lewei ZhangFaculty of Dentistry, Departments of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Kitty K CorbettSchool of Public Health and Health Systems, University of Waterloo, Ontario, Canada.
Miriam P RosinBC Cancer Research Centre, Department of Cancer Control Research, Vancouver, Canada; Department of Biomedical Physiology and Kinesiology, Simon Fraser University, Burnaby, British Columbia, Canada. Electronic address: mrosin@bccrc.ca.

Funding

CLONAL CHANGES IN ORAL LESIONS OF HIGH-RISK PATIENTSR01DE013124 · NIDCR · BRITISH COLUMBIA CANCER AGENCY · PI ROSIN, MIRIAM P. · 1999 to 2007
$2.1M
Optical Techniques and Oral Precancer ManagementR01DE017013 · NIDCR · BRITISH COLUMBIA CANCER AGENCY · PI ROSIN, MIRIAM P. · 2005 to 2009
$1.9M
Whole genome array CGH of progressing oral dysplasiaR01DE015965 · NIDCR · BRITISH COLUMBIA CANCER AGENCY · PI LAM, WAN L · 2004 to 2007
$1.1M
NIDCR NIH HHS R01 DE013124NIDCR NIH HHS R01 DE015965NIDCR NIH HHS R01 DE017013NIDCR NIH HHS R01DE13124NIDCR NIH HHS R01DE17013
6 · The paper itself

Abstract

Worldwide, oral cancer is responsible for 170,000 deaths per year. Intervention to prevent this disease is a long sought after goal. Chemoprevention studies have focused on clinicopathological features of potentially malignant lesions (PML) in an effort to prevent their progression to cancer. However, prediction of future behavior for such lesions is difficult and remains a major challenge to such intervention. Different approaches to this problem have been tested in the past 20years. Early genetic progression models identified critical regions of allelic imbalance at 3p and 9p, and provided the basis for molecular markers to identify progressing PMLs. Subsequently, technological advances, such as genome-wide high-throughput array platforms, computer imaging, visualization technology and next generation sequencing, have broadened the scope for marker development and have the potential of further improving our ability to identify high-risk lesions in the near future either alone or in combination. In this article, we examine the milestones in the development of markers for PML progression. We emphasize the critical importance of networks among scientists, health professionals and community to facilitate the validation and application of putative markers into clinical practice. With a growing number of new agents to validate, it is necessary to coordinate the design and implementation of strategies for patient recruitment, integration of marker assessment, and the final translation of such approaches into clinical use.

Indexed as

Disease ProgressionBiomarkers, TumorHumansMouth NeoplasmsPrecancerous ConditionsRisk AssessmentRisk FactorsBiomarkers, TumorKnowledge translationLoss-of-heterozygosityOral potentially malignant lesionsOral premalignant lesionsProgression markers

Identifiers

PMID25240917
PMCPMC4539364

What OpenQuestion holds

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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.