Abstract 374P
Background
Oral lichen planus (OLP) is an autoimmune disorder that causes a persistent inflammatory condition that affects the oral mucosa. The precise cause of OLP is unknown, however it is thought to be a combination of genetic predisposition, environmental factors, and immunological dysregulation. Oral lichen planus is classified as a potentially oral malignant lesion (POML) because it has the potential to develop into oral squamous cell cancer (OSCC).
Methods
34 individuals with OLP were followed for three years in this prospective clinic-histologic investigation. Tissue samples from these patients were immunohistochemically and histomorphometrically examined for CD34 and CD105 (Endoglin). The patients received routine oral preventive therapy at three-month intervals and were followed for up to three years. The possibility for a malignant transformation was evaluated clinically, and in the event of clinical suspicion, a repeat biopsy was undertaken to rule out malignancy.
Results
The clinical and histological parameters were analyzed using the paired 't' test with the assumption of normal distribution and with an appropriate sample size of 34. During the three-year follow-up period, 73% (n=25/34) of the total patients never developed oral cancer. OSCC was the most typically found, with the Gingivo-Buccal Sulcus area being the most prevalent site. The mean Vascular Caliber (VC) utilizing CD 34 and CD 105 (μm2) in PMOL was 8.5 ± 2.0 μm2 and 5.4 ± 1.2 μm2, respectively. The mean VC - CD 34 and CD105 did differ statistically (p-value<0.05). It has been reported that patients with 'erosive' OLP had a higher malignant transformation potential (n=09/34) and higher levels of CD34 and CD105 than patients without malignant transformation (p-value<0.01).
Conclusions
CD 34 and CD105 markers were found to be beneficial in predicting the malignant transformation potential of Erosive OLP when utilized in evaluating micro vessel density and vessel morphometry. This suggests that CD34 and CD105 may be useful immunohistological indicators for assessing the early stage of malignant transformation potential in POMLs, particularly OLP, well before 3.0 years. As a result, CD34 and Endoglin are being recommended as IHC Panel Markers for determining OLP prognosis.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
397P - Comparison between Y-site co-infusion versus standard dexamethasone for preventing hypersensitivity reactions from oxaliplatin administration: A randomized controlled trial
Presenter: jarearnjit Phavirunsiri
Session: Poster Display
Resources:
Abstract
398P - Evaluation of the effectiveness of denosumab therapy giant cell tumor of the pelvis
Presenter: Abbos Nurjabov
Session: Poster Display
Resources:
Abstract
399P - Long-term outcomes of patients with gastric cancer who received the best supportive care without any anticancer treatment
Presenter: Yohei Arihara
Session: Poster Display
Resources:
Abstract
401TiP - Oral opioid vs intravenous patient-controlled analgesia (PCA) with hydromorphone bolus-only or continuous infusion to maintain analgesia for severe cancer pain: A randomized phase III trial
Presenter: Cheng Huang
Session: Poster Display
Resources:
Abstract
407P - K-TrackTM: A streamlined personalized assay to detect molecular residual disease in solid tumors
Presenter: Nam Vo
Session: Poster Display
Resources:
Abstract
408P - Increased EGFR and MET expression and corresponding tumor microenvironment (TME) change in hepatocellular carcinoma (HCC) tissues after sorafenib (Sora) treatment
Presenter: Chia Jui Yen
Session: Poster Display
Resources:
Abstract
410P - Systematic evaluation of cell-free DNA fragmentation patterns for cancer diagnosis and enhanced cancer detection through integration of multiple fragmentations
Presenter: Xiangy-Yu Meng
Session: Poster Display
Resources:
Abstract
412P - Multiplex digital spatial profiling (DSP) of protein reveals distinct immune and molecular phenotypes in hepatocellular carcinoma
Presenter: Chia Jui Yen
Session: Poster Display
Resources:
Abstract
413P - Clinical utility of advanced features provided by circulating tumor DNA-based comprehensive genomic profiling
Presenter: Young-gon Kim
Session: Poster Display
Resources:
Abstract
414P - Landscape of ERBB2 mutations in advanced cancers (AC) using circulating tumor DNA (ctDNA) next-generation sequencing (NGS) in Asia and Middle East (AME)
Presenter: Byoung Chul Cho
Session: Poster Display
Resources:
Abstract