Abstract:BACKGROUND
Patients with an history of carcinoma of the upper aerodigestive tract are at high risk for recurrence or the development of new tumors in this region. In the majority of follow‐up protocols, these patients undergo radiologic and endoscopic evaluation as a means of surveillance for the early detection of recurrence. The brush biopsy‐capsule technique represents a noninvasive and inexpensive screening device for this patient population. In the current study, the authors retrospectively assessed the s… Show more
“…Durch die SBC lässt sich der Anteil "inadäquater Proben" deutlich reduzieren. Die SBC läßt sich auf alle Tumoren des Kopf-Hals-Bereiches anwenden; Ösophagus und Hypopharynx, die einem gezielten Abstrich schwer zugänglich sind, kön-nen kursorisch mit einem schluckbaren Schwämmchen erfasst werden [222].…”
“…Durch die SBC lässt sich der Anteil "inadäquater Proben" deutlich reduzieren. Die SBC läßt sich auf alle Tumoren des Kopf-Hals-Bereiches anwenden; Ösophagus und Hypopharynx, die einem gezielten Abstrich schwer zugänglich sind, kön-nen kursorisch mit einem schluckbaren Schwämmchen erfasst werden [222].…”
“…All patients underwent OPB sampling before panendoscopy with oesophagoscopy, which excluded a second oesophageal tumour. Oesopharyngeal brush sampling was performed, as previously described (Leoni-Parvex et al, 2000). An abrasive sponge wrapped in a capsule (Oesotest s , Biodessa, France) was first swallowed and then withdrawn with a string.…”
Section: Patients and Sample Collectionmentioning
confidence: 99%
“…This definition of positivity was based on oeosophageal cytological criteria proposed by Shu (1983) and used by others (Leoni-Parvex et al, 2000). The cytological evaluation was considered negative only when there was no significant cytonuclear atypia in squamous cells and if the majority of cells were of the intermediate type.…”
Section: Cytological Criteriamentioning
confidence: 99%
“…Cytological screening (Ogden, 1997) has been developed by collecting saliva with or without an oral mucosal brush. Recently, an encapsulated oesopharyngeal brush (OPB) technique for cytological analysis was developed to detect recurrent and metachronous oesophageal carcinomas (Leoni-Parvex et al, 2000). Oesopharyngeal brush has also been shown to be capable of collecting exfoliated cells from oral or pharyngeal carcinoma.…”
Oesopharyngeal brush (OPB) sampling with cytological analysis can yield exfoliated cells from asymptomatic tumours of the upper aero-digestive tract and the oesophagus. In this study, we compared cytological evaluation and molecular analysis for the detection of exfoliated cancer cells sampled with an OPB. A total of 56 patients with a known unique head and neck squamous cell carcinoma (HNSCC) and five healthy controls were enrolled prospectively. Exfoliated cells from these 61 patients were collected with an OPB before initial endoscopy. p53 mutations and UT 5085 microsatellite instability (MI) were analysed in the HNSCC tumour, lymphocytes and the corresponding OPB DNA samples. p53 mutations and UT5085 MI were detected in 31 out of 56 and 14 out of 56 HNSCC, respectively, but not in any of the five controls. Direct sequencing of p53 was able to detect mutations in OPB DNA in only two out of 29 patients harbouring a p53-mutated primary tumour. Microsatellite instability was detected in OPB DNA of 11 out of 13 informative (bandshift detected in tumour) patients, whereas cytological analysis detected abnormal cells in only six of the same 13 patients (P ¼ 0.03). In informative patients, all positive OPB samples at cytological analysis were also positive at molecular analysis of UT5085, and both analyses confirmed the two negative samples. Molecular analysis of OPB from eight uninformative patients and from five healthy controls were all negative. OPB sampling with MI-based molecular analysis could be efficient for early detection of recurrent HNSCC. This result prompts us to use other microsatellite markers in order to maximise the percentage of informative patients.
“…Examination of exfoliated cells has never achieved the same success in the diagnosis of HNSCC as it has in the diagnosis of cancer of the uterine cervix (5). However, an encapsulated pharyngoesophageal brush (PEB) technique (Oesotest) for cytologic analysis was recently developed to detect esophageal carcinomas (6). This technique has been reported to have a sensitivity of 88.7% and a specificity of 90.7% in the detection of recurrent and metachronous neoplasms of the upper aerodigestive tract and seems to be safe and minimally invasive (6).…”
We sought to determine whether early-stage laryngopharyngeal squamous cell carcinomas (SCC) can be detected through molecular analysis of exfoliated cells collected with the use of a pharyngoesophageal brush (PEB). Experimental Design:Thirty-three patients with a single, untreated, early-stage (T1orT2) SCC of the supraglottic larynx or pharynx underwent collection of cells with a PEB, followed by endoscopic biopsy of the tumor. PEB specimens were also collected from five healthy subjects. PEB samples and tumor tissue were examined for hypermethylation of p16 INK4a (CDKN2) gene promoter CpG islands (assayed by methylation-specific PCR) and UT5085 tetranucleotide microsatellite instability (assayed by GeneScan analysis). PEB samples were also subjected to cytologic analysis. Results: Eight of 33 (24%) tumors exhibited a bandshift at UT5085, and14 of 33 (42%) exhibited hypermethylation at the p16 promoter. Overall,17 of 33 (52%) patients had at least one of the two markers in their tumor. Cytologic analysis of PEB samples revealed tumor in 4 of 33 (12%) patients; cytologic findings were normal in all five control subjects. Molecular analysis of PEB samples revealed tumor DNA in 13 of 17 (76%) patients with at least one of the two molecular markers in their tumor. Eight of14 (57%) patients with p16 hypermethylation in their tumor and 8 of 8 (100%) patients with UT5085 microsatellite instability in their tumor had similar findings in the PEB samples. None of the PEB samples from the control subjects or patients withneither molecular markerin their tumor displayed abnormality. Conclusion: Molecular analysis of PEB samples holds promise for the early detection of earlystage laryngopharyngeal SCCs. New molecular markers need to be identified to increase the sensitivity of molecular screening.
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