Use of DNA image cytometry in conducting oral cancer screening in rural India

被引:4
|
作者
Datta, Madhurima [1 ,2 ]
Guillaud, Martial [3 ,4 ]
Chaitanya, Nallan [5 ]
Ndvn, Shyam [6 ]
Palat, Gayatri [7 ]
Kumari, Priya [8 ]
Rapelli, Vineela [7 ]
Jn, Jagannath [7 ]
Kumari, Sanjeeva [7 ]
Broughton, Sandra [9 ]
Sutcliffe, Simon [9 ]
Laronde, Denise M. [1 ,2 ]
机构
[1] Univ British Columbia, Fac Dent, 2199 Wesbrook Mall, Vancouver, BC V6T 1Z3, Canada
[2] BC Canc, Canc Control Res, Vancouver, BC, Canada
[3] BC Canc, Imaging Unit, Integrat Oncol, Vancouver, BC, Canada
[4] Univ British Columbia, Dept Stat, Vancouver, BC, Canada
[5] RAK Coll Dent Sci, Ras Al Khaymah, U Arab Emirates
[6] Osmania Univ, Govt Dent Coll, Hyderabad, India
[7] MNJ Inst Oncol & Reg Canc Ctr, Hyderabad, India
[8] Nizams Coll, Dept Zool, Hyderabad, India
[9] Two Worlds Canc Collaborat Fdn, Kelowna, BC, Canada
关键词
cytology; DNA aneuploidy; DNA image cytometry; fluorescence visualisation; oral cancer; oral epithelial dysplasia; oral potentially malignant lesions; CHROMOSOMAL INSTABILITY; DECISION-MAKING; DYSPLASIA; LESIONS; CYTOLOGY; PLOIDY; RISK;
D O I
10.1111/cyt.13159
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objectives Oral cancer screening can assist in the early detection of oral potentially malignant lesions (OPMLs) and prevention of oral cancers. It can be challenging for clinicians to differentiate OPMLs from benign conditions. Adjunct screening tools such as fluorescence visualisation (FV) and DNA image cytometry (DNA-ICM) have shown success in identifying OPMLs in high-risk clinics. For the first time we aimed to assess these technologies in Indian rural settings and evaluate if these tools helped clinicians identify high-risk lesions during screening. Methods Dental students and residents screened participants in five screening camps held in villages outside of Hyderabad, India, using extraoral, intraoral, and FV examinations. Lesion and normal tissue brushings were collected for DNA-ICM analysis and cytology. Results Of the 1116 participants screened, 184 lesions were observed in 152 participants. Based on white light examination (WLE), 45 lesions were recommended for biopsy. Thirty-five were completed on site; 25 (71%) were diagnosed with low-grade dysplasias (17 mild, 8 moderate) and the remaining 10 showed no signs of dysplasia. FV loss was noted in all but one dysplastic lesion and showed a sensitivity of 96% and specificity of 17%. Cytology combined with DNA-ICM had a sensitivity of 64% and specificity of 86% in detecting dysplasia. Conclusion DNA-ICM combined with cytology identified the majority of dysplastic lesions and identified additional lesions, which were not considered high-risk during WLE and biopsy on site. Efforts to follow-up with these participants are ongoing. FV identified most high-risk lesions but added limited value over WLE.
引用
收藏
页码:600 / 610
页数:11
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