| Literature DB >> 31487927 |
Marco Cicciù1, Gabriele Cervino1, Luca Fiorillo2,3, Cesare D'Amico1, Giacomo Oteri1, Giuseppe Troiano4, Khrystyna Zhurakivska4, Lorenzo Lo Muzio4, Alan Scott Herford5, Salvatore Crimi6, Alberto Bianchi6, Dario Di Stasio7, Rosario Rullo7, Gregorio Laino7, Luigi Laino7.
Abstract
The fluorescence method is an innovative technique used by pathologists for examining body mucosa, and for the abnormalities tissue screening, potentially leading to the earlier discovery of pre-cancer, cancer or other disease processes. The early detection is one of the best mechanisms for enabling treatment success, increasing survival rates and maintaining a high quality of life. The purpose of this review is to evaluate the clinical efficiency of this diagnostic tool applied to the oral cavity (VELscope®). A literature systematic review has been performed. The initial research provided 53 results after applying the inclusion and exclusion criteria, and after a manual screening of the abstracts by the authors, only 25 results were eligible for review. The results and data contained in all the researches, no older than 10 years, were manually evaluated, and provided useful information on this diagnostic method. The VELscope® mean value about sensitivity and specificity resulted of 70.19% and 65.95%, respectively, by results analysis, but despite this some studies disagree about its clinical effectiveness, and this diagnostic method is still much debated in scientific and clinical medical literature. Surely being able to have efficient and effective tools from this point of view could help the clinician in the diagnosis, and also make timelier the pharmacological or surgical therapy, improving the quality of life of the patient, and in some cases guaranteeing a longer survival term.Entities:
Keywords: diagnostic techniques and procedures; optical imaging; oral cancer; oral neoplasms; oral surgery; precancerous conditions; quality of life
Year: 2019 PMID: 31487927 PMCID: PMC6784481 DOI: 10.3390/dj7030093
Source DB: PubMed Journal: Dent J (Basel) ISSN: 2304-6767
Synthesis of results.
| Authors (Year) | VELscope Investigation | Oral Pathology | Results | Statistical Analysis | Sample Size |
|---|---|---|---|---|---|
| Farah et al. (2018) [ | Differences between white light and autofluorescence on oral potentially malignant disorders (OPMD) detected margins. | Oral epithelial dysplasia, oral lichen planus, oral lichenoid dysplasia | Autofluorescence determined margins are safer | 11 | |
| Canjau et al. (2018) [ | Conventional oral examination vs. visual fluorescence evaluation with VELscope® | Malignant lesions and premalignant lesions | Fluorescence examination cannot replace histopathology, but it may add sensitivity to the conventional examination | 18 | |
| Amirchagmaghi et al. (2018) [ | Fluorescence evaluation in patients with oral lesions | Dysplasia and oral carcinoma | This method is not capable to distinguish malignant from benign lesions. | 45 | |
| Yamamoto et al. (2017) [ | Detection accuracy of VELscope on epithelial dysplasia of the tongue | Leukoplakia with and without dysplasia | Autofluorescence visualization could be an auxiliary method for diagnosis | Luminance ration on malignant lesion: | 79 |
| Huang et al. (2017) [ | White light vs. VELscope® method | Oral cancer, precancerous lesions | Fluorescence examination could be used to differentiate oral cancer and precancerous lesions from normal mucosa. | 140 | |
| Ganga et al. (2017) [ | Conventional Oral examination vs. VELscope method | Fluorescence examination could not provide a definitive diagnosis | 76% of specificity and sensitivity | 200 | |
| Cicciù et al. (2017) [ | Tissue fluorescence imaging vs. conventional oral examination or biopsy | Oral squamous cell carcinoma | The main criticism of autofluorescence on performing a diagnosis of cancer was the impossibility of discriminating high-risk from low-risk lesions, but it could be a quick and noninvasive method. | 1 | |
| Burian et al. (2017) [ | Tissue fluorescence examination VELscope® | Oral soft tissue lesions or carcinoma in situ | VELscope® could help clinicians and help to define biopsy margins | Sensitivity of VELscope | 90 |
| Scheer et al. (2016) [ | Tissue fluorescence examination VELscope® | Oral squamous cell carcinomas | VELscope® reveals no additional information to analysis | Sensitivity and specificity were 33.3% and 88.6% | 41 |
| Ohnishi et al. (2016) [ | Tissue fluorescence examination VELscope® | Carcinoma in situ | Fluorescence examination could represent a simple, cost-effective screening. | Sensitivity 95% and specificity 100% | 17 |
| Nagi et al. (2016) [ | Chemoluminescence and tissue autofluorescence in detection of Oral Squamous Cell Carcinoma (OSCC) and OPMD | OSCC and OPMD | Chemoluminescence and autofluorescence are simple and not invasive tests. | Sensitivity range 22% to 100% and specificity 16% to 100% | Review |
| Kordbacheh et al. (2016) [ | Molecular pathways associated with fluorescence properties of OPMD | OSCC, Oral epithelial dysplasia (OED), Oral lichen planus (OLP), Oral epithelial hyperplasia (OEH) | Uncovering these molecular mechanisms could provide a reduction in false positive or negative findings with VELscope® | 42 | |
| Rashid et Warnakulasuriya (2015) [ | Chemoluminescence vs. tissue autofluorescence in detection of OPMD | OPMD | VELscope® may detect erythematous lesions or benign inflammations as a false positive | Review | |
| Jane-Salas et al. (2015) [ | Conventional oral examination vs. Autofluorescence technique VELscope® | Oral lesions | No clinical benefits were obtained using the VELscope® system | Not significant results | 60 |
| Elvers et al. (2015) [ | Photo examination vs. autofluorescence examination VELscope® | OPMD | This technique enables clinicians to measure the extent of lesions beyond visible margins | 20 | |
| Hanken et al. (2013) [ | Early detection with VELscope® | OPMD | VELscope® is a simple noninvasive way to find OPMD | Sensitivity 22% specificity 8.4% | 120 |
| Rana et al. (2012) [ | Autofluorescence examination vs. white light examination | OPMD | VELscope® is a useful new diagnostic device for the detection of oral cancer diseases. | Sensitivity 100% specificity 74% | 289 |
| McNamara et al. [ | COE vs. Fluorescence examination VELscope® | OPMD | Biopsy does not confirm VELscope diagnosis | Scalpel biopsy vs. VELscope®
| 42 |
| Farah et al. (2012) [ | Tissue autofluorescence VELscope® in oral mucosa lesions detection | OPMD | VELscope® cannot provide a definitive diagnosis alone | Sensitivity 30% Specificity 63% | 112 |
| Scheer et al. (2011) [ | Autofluorescence evaluation VELscope® | OPMD, OSCC, squamous intraepithelial neoplasia | VELscope® can assist the clinician during the identification of OPMD, but it does not help in discriminating benign or malignant conditions | Sensitivity 100%, specificity 80% | 64 |
| Matsumoto (2011) [ | Autofluorescence evaluation VELscope® | OSCC, moderate and severe epithelial dysplasia lesions, mild dysplasia lesions and lichen planus. | VELscope® could be a valuable tool in an early detection of potentially malignant and malignant lesions in oral mucosa. | 74 | |
| Lopez-Jornet et al. (2011) [ | Autofluorescence evaluation VELscope® | Oral cancer | This device needed a conventional oral examination too | Sensitivity 98% to 100% Specificity 94% to 100% | Review |
| Fricain (2011) [ | Autofluorescence evaluation VELscope® vs. spectroscopy | OPMD | Histological examination remains the gold standard of OPMD diagnosis, VELscope® could only support clinicians | Sensibility 78% to 100% Specificity 75% to 100% | Review |
| Awan et al. (2011) [ | Autofluorescence vs. COE and oral biopsy | Oral leukoplakia, oral erythoplakia, oral lichen planus, hyperplastic candidiasis, rest frictional keratosis, oral sub-mucous fibrosis | VELscope® is not able to discriminate high or low risk lesions, but it can diagnose mucosal disorders | Sensibility 84.1% Specificity 15.3% | 126 |
| Mehrotra et al. (2010) [ | Autofluorescence techniques VELscope® vs. chemoluminescence ViziLite | OPMD | VELscope could provide a false negative | Sensitivity 50% Specificity 38.9% | 102 |
Statistical data results.
| 1342 Patient’s Data | Sensitivity or Sensibility | Specificity |
|---|---|---|
| VELscope® range | 22% to 100% | 8.4% to 100% |
| VELscope® weighted average | 70.19% | 65.95% |
Field of use.
| VELscope® | Oral leukoplakia, oral erythoplakia, oral lichen planus, hyperplastic candidiasis, rest frictional keratosis, oral sub-mucous fibrosis, oral squamous cell carcinoma, moderate and severe epithelial dysplasia lesions, mild dysplasia lesion, squamous intraepithelial neoplasia, oral carcinoma in situ |
Figure 1VELscope® results before a tongue biopsy. COE vs. VELscope®. For gentle concession of Prof. L. Laino.
Figure 2VELscope® results before a tongue biopsy. COE vs. VELscope®. For gentle concession of Prof. L. Laino.
Figure 3PRISMA flow chart.
Risk of bias.
| Authors (Year) | Risk of Bias | |||
|---|---|---|---|---|
| Unclear | Low | Moderate | High | |
| Farah et al. (2018) [ | x | |||
| Canjau et al. (2018) [ | x | |||
| Amirchagmaghi et al. (2018) [ | x | |||
| Yamamoto et al. (2017) [ | x | |||
| Huang et al. (2017) [ | x | |||
| Ganga et al. (2017) [ | x | |||
| Cicciù et al. (2017) [ | x | |||
| Burian et al. (2017) [ | x | |||
| Scheer et al. (2016) [ | x | |||
| Ohnishi et al. (2016) [ | x | |||
| Nagi et al. (2016) [ | x | |||
| Kordbacheh et al. (2016) [ | x | |||
| Rashid et Warnakulasuriya (2015) [ | x | |||
| Jane-Salas et al. (2015) [ | x | |||
| Elvers et al. (2015) [ | x | |||
| Hanken et al. (2013) [ | x | |||
| Rana et al. (2012) [ | x | |||
| McNamara et al. [ | x | |||
| Farah et al. (2012) [ | x | |||
| Scheer et al. (2011) [ | x | |||
| Matsumoto (2011) [ | x | |||
| Lopez-Jornet et al. (2011) [ | x | |||
| Fricain (2011) [ | x | |||
| Awan et al. (2011) [ | x | |||
| Mehrotra et al. (2010) [ | x | |||