4.6 Review

Tissue biomarkers for predicting the risk of oral cancer in patients diagnosed with oral leukoplakia: A systematic review

Journal

ORAL DISEASES
Volume 27, Issue 8, Pages 1977-1992

Publisher

WILEY
DOI: 10.1111/odi.13747

Keywords

malignant transformation; oral dysplasia; oral leukoplakia; systematic-review; tissue biomarkers

Funding

  1. FundacAo de Amparo a Pesquisa e InvovacAo do Estado de Santa Catarina (FAPESC) [88887.200724/2018-00]
  2. CoordenacAo de Aperfeicoamento de Pessoal de Nivel Superior-Brasil (CAPES)

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A systematic review evaluated biomarkers related to oral leukoplakia, identifying some biomarkers associated with future cancer risk in OL patients. Heterogeneity and lack of standardized reporting were identified as issues in the studies.
Objectives We performed a systematic review to evaluate the published biomarkers related to oral leukoplakia (OL), aiming to identify the biomarkers that indicate any future risk of cancer in patients with oral leukoplakia. Methods A search strategy was developed for three main electronic databases: PubMed, Cochrane Library, and EBSCO, and also for Google Scholar, until February 28, 2020. The study selection was performed in a two-phase process aiming at studies assessing tissue biomarkers for malignant transformation of OL. Risk of bias analysis of included studies was performed using the Quality in Prognosis Studies Tool. Results From 3,130 articles initially identified by searching databases, a total of 46 studies were included in this systematic review, with a combined sample of 3,783 patients, of whom 1,047 presented with malignant transformation of a previously diagnosed OL as reported by the authors. The cancer incidence in the whole group was 27.6% (range: 5.4% to 54.1%). The studies were derived from different geographic areas, including Asia (n = 21), Europe (n = 15), North America (n = 9), and Oceania (n = 1). There were 49 different molecular biomarkers evaluated in the 46 included studies: p53 and podoplanin proteins were the most frequently reported, followed by abnormalities at particular chromosomal loci (e.g., LOH). Risk of bias analysis revealed concerns associated with measurement of prognostic factor, study confounding and statistical analysis and reporting. Conclusions Substantial heterogeneity and lack of standardized reporting of data among the studies were identified. The most promising biomarkers reported to have a significant association with the malignant transformation in OL included podoplanin and chromosomal loci abnormalities. A critical examination of the follow-up studies on OL published so far indicated that tissue biomarkers that could predict the risk of oral cancer in patients with OL are still in a discovery phase.

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