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Risk factors for oral epithelial dysplasias to become malignant: clinical implications

Authors :
E. Chimenos-Küstner
C. Arranz
S. Gómez-Armayones
B. Quirós
S. Tous
M. Mena
R.M. Penín
Laia Alemany
Miren Taberna
S. Marquez
Octavio Servitje
Source :
International Journal of Oral and Maxillofacial Surgery. 51:473-480
Publication Year :
2022
Publisher :
Elsevier BV, 2022.

Abstract

There is a lack of effective clinical management of oral epithelial dysplasias to reduce their risk of malignant transformation and considerable gaps in knowledge regarding the most effective means of treating such lesions. A retrospective cohort of biopsy-confirmed oral epithelial dysplasias consecutively diagnosed in the period 1995–2014 and followed-up until 2017 was identified from pathology department files. Demographic, clinical and follow-up information was collected. Multivariate Cox proportional-hazards models were performed to evaluate sociodemographic, clinical and pathological factors associated with progression to oral squamous cell carcinoma. The study included 144 oral epithelial dysplasias, of which 42% progressed to oral cancer at the end of follow-up (21 years). Clinical aspect of the lesion was described for 77 (53.5%) of the patients. Treatment, age, grade of the lesion and diagnostic period were independent prognostic factors for progression. When considering only patients with described clinical aspect, only treatment and grade of the lesion were independently associated with cancer. The results from this non-selected retrospective cohort of oral epithelial dysplasias underscore the existing limitations of the current standard-of-care of the patients and provide novel insights on the management of these lesions with and without described clinical aspect. Well-designed, robust prospective studies, a homogenized staging system and multidisciplinary treatment guidelines are warranted.

Details

ISSN :
09015027
Volume :
51
Database :
OpenAIRE
Journal :
International Journal of Oral and Maxillofacial Surgery
Accession number :
edsair.doi.dedup.....c12bd9ced2e89ba372b2e321b652fd97