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1.
Oral Oncol ; 110: 104875, 2020 11.
Article in English | MEDLINE | ID: mdl-32622292

ABSTRACT

PURPOSE: Increasing evidence is accumulating for an alarming rising incidence of oral tongue SCC in a younger cohort, particularly in developed countries. The aim of this study is to analyse the change in incidence of OSCC in patients under the age of 45 in developed nations in the Asia-Pacific region. PATIENTS AND METHODS: Population data was extracted from the Australian Cancer Incidence and Mortality 2017 database and National Registry of Diseases Office, Singapore to allow calculation of the incidence in the Australian and Singaporean populations. This was compared to multi-institutional data from four tertiary Australian institutions. The inclusion criteria were as follows: a) diagnosis of primary SCC of the mobile tongue; b) treatment with curative intent; c) complete histopathologic data; d) complete adjuvant treatment data; e) follow up data. RESULTS: Analysis of ACIM data demonstrated that there was a significant increase in the incidence of tongue SCC in those under the age of 45 in the Australian and Singaporean populations (p < 0.001). When analysed for gender, the incidence of tongue SCC increased at a significantly higher rate in females than males (p < 0.001). Similarly, in the multi-institutional analysis including 1814 patients, the number of females under the age of 45 with tongue SCC significantly increased over time (p < 0.001), with the proportion of smokers in this cohort decreasing over time. CONCLUSION: The incidence of tongue SCC is rising in young females in developed nations in the Asia Pacific region, in keeping with observed epidemiological trends worldwide.


Subject(s)
Carcinoma, Squamous Cell/epidemiology , Tongue Neoplasms/epidemiology , Adult , Female , Humans
2.
Histopathology ; 74(6): 817-828, 2019 May.
Article in English | MEDLINE | ID: mdl-30589949

ABSTRACT

AIMS: Indoleamine 2,3-dioxygenase (IDO), an immunomodulatory enzyme, facilitates immune escape by tumours and promotes tumour progression. IDO inhibitors with and without additional anti-PD-1 therapy have been evaluated in recent and ongoing melanoma clinical trials, but IDO expression in melanoma tumours, and therefore its potential role as a predictive biomarker remains unknown. This study sought to evaluate IDO expression in immunotherapy-naive metastatic melanoma patients in order to determine patterns of expression in corresponding primary melanomas, locoregional metastases and distant metastases. METHODS AND RESULTS: Here, we evaluated IDO expression using immunohistochemistry in 99 melanoma tumour samples from 43 immunotherapy-naive patients with metastatic melanoma to determine patterns of expression in primary melanomas (n = 29), locoregional metastases (n = 36) and distant metastases (n = 34). Thirty-seven per cent of patients demonstrated tumour IDO expression in at least one specimen. Twelve of 35 patients (34%) with longitudinal specimens (i.e. two or more separate specimens from different disease stages in the same patient) displayed heterogeneous IDO staining between samples. Tumour IDO expression positively correlated with tumour-infiltrating lymphocyte (TIL) score as well as the number of IDO-expressing mononuclear cells in the primary melanoma (P < 0.0001 and P = 0.0011, respectively) and nodal metastases (P = 0.049 and P = 0.037, respectively), but not in distant metastases. Furthermore, tumour IDO expression correlated positively with PD-L1 expression by melanoma cells among all specimens (P = 0.0073). CONCLUSIONS: Therefore, while assessment of tumour IDO expression warrants evaluation in melanoma patient cohorts treated with IDO inhibitors dosed at levels proven to inhibit the target by pharmacodynamic assessment, its utility as a biomarker may be limited by intertumoral heterogeneity.


Subject(s)
Indoleamine-Pyrrole 2,3,-Dioxygenase/biosynthesis , Melanoma/enzymology , Skin Neoplasms/enzymology , Tumor Microenvironment , Adult , Aged , Biomarkers, Tumor/analysis , Female , Humans , Indoleamine-Pyrrole 2,3,-Dioxygenase/analysis , Male , Middle Aged , Melanoma, Cutaneous Malignant
3.
Pathology ; 50(6): 648-653, 2018 Oct.
Article in English | MEDLINE | ID: mdl-30177220

ABSTRACT

Malignant gastrointestinal neuroectodermal tumour (GNET) is a recently characterised rare and aggressive tumour that typically arises in association with the small intestine of adults. We present a novel case of this entity and expand the spectrum of its reported morphological features. The patient was a 5-year-old female, the youngest reported patient affected by the condition, and presented with extra-abdominal disease. The histopathological features included the presence of a junctional component of the palatal tumour, which mimicked mucosal melanoma, a feature that has not been previously reported in GNET. Whole genome and RNA sequencing was performed that demonstrated the EWSR1-ATF1 translocation characteristic of GNET. Knowledge of this entity and its features, together with careful morphological assessment supplemented by judicious immunohistochemical and molecular studies should enable the correct diagnosis to be established.


Subject(s)
Neuroectodermal Tumors/pathology , Parotid Neoplasms/genetics , Parotid Neoplasms/pathology , Transcription Factors/genetics , Child, Preschool , Diagnosis, Differential , Female , Germ-Line Mutation , Humans , Melanoma/diagnosis , Melanoma/pathology , Neuroectodermal Tumors/diagnosis , Neuroectodermal Tumors/genetics , Parotid Neoplasms/diagnosis , Pedigree
4.
Head Neck Pathol ; 12(3): 407-418, 2018 Sep.
Article in English | MEDLINE | ID: mdl-30069837

ABSTRACT

Squamous cell carcinoma (SCC) is the most common primary malignancy to affect the temporal bone, including primary cutaneous SCC of the pinna, external auditory canal, middle and inner ear. This anatomically complex region generates complicated three-dimensional specimens that can be a challenge for macroscopic and microscopic pathologic assessment. A universally accepted staging classification for these malignancies is still to be established. A brief summary of the regional anatomy, etiology and epidemiology, presentation and diagnosis, radiologic assessment and treatment follows with a review of the pathologic assessment of the different types of specimens generated and an update on staging for SCC of the temporal bone.


Subject(s)
Ear Canal/pathology , Ear Neoplasms/pathology , Squamous Cell Carcinoma of Head and Neck/pathology , Temporal Bone/pathology , Humans
5.
Methods Mol Biol ; 1756: 77-83, 2018.
Article in English | MEDLINE | ID: mdl-29600361

ABSTRACT

Pathological assessment of tissue is the gold standard for diagnosis and staging of neoplasia and provides key prognostic information for clinical management. Proper macroscopic assessment and cut-up technique is essential to ensure that the overall assessment is correct and reproducible. Endoscopic mucosal resection is a technique used for removing early neoplastic glandular lesions of the esophagus at the level of submucosa. Here, we describe the macroscopic assessment and dissection techniques used for the routine handling of endoscopic mucosal resection specimens in the clinical laboratory.


Subject(s)
Endoscopic Mucosal Resection , Esophageal Mucosa/pathology , Esophageal Neoplasms/pathology , Esophagoscopy , Histocytological Preparation Techniques/methods , Biomarkers, Tumor/analysis , Biopsy , Esophageal Mucosa/surgery , Esophageal Neoplasms/surgery , Histocytological Preparation Techniques/instrumentation , Humans
6.
Methods Mol Biol ; 1756: 85-92, 2018.
Article in English | MEDLINE | ID: mdl-29600362

ABSTRACT

An esophagogastrectomy is a surgical procedure that is performed for treatment of confirmed localized esophageal and esophagogastric junction adenocarcinoma. Proper macroscopic assessment and cut-up technique is essential to ensure that the overall assessment is correct and reproducible. Here, we describe a standard for macroscopic assessment and dissection to be used for routine handling of esophagogastrectomy specimens in the clinical laboratory.


Subject(s)
Adenocarcinoma/pathology , Dissection/methods , Esophageal Neoplasms/pathology , Esophagogastric Junction/pathology , Histocytological Preparation Techniques/methods , Stomach Neoplasms/pathology , Adenocarcinoma/surgery , Dissection/instrumentation , Esophageal Neoplasms/surgery , Esophagectomy , Esophagogastric Junction/surgery , Gastrectomy , Histocytological Preparation Techniques/instrumentation , Humans , Stomach Neoplasms/surgery
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