ObjectivesTo estimate the effectiveness of endoscopic screening programme in reducing incidence and mortality of upper gastrointestinal cancer in high risks areas of China.DesignThis multicentre population-based cohort study was conducted in six areas in China from 2005 to 2015. All permanent residents aged 40 to 69 years were identified as target subjects. We refer to those who were invited for screening collectively as the invited group. Of these, we classify those who were invited and undertook endoscopic screening as the screened group and those who were invited but did not accept screening as the non-screened group. Target subjects who were not invited to the screening were assigned to the control group. The effectiveness of the endoscopic screening and screening programme were evaluated by comparing reductions in incidence and mortality from upper gastrointestinal cancer in the screened and invited group with control group.ResultsOur cohort analysis included 637 500 people: 299 483 in the control group and 338 017 in the invited to screening group, 113 340 (33.53%) of whom were screened eventually. Compared with subjects in the control group, upper gastrointestinal cancer incidence and mortality decreased by 23% (relative risk (RR)=0.77, 95% CI 0.74 to 0.81) and 57% (RR=0.43, 95% CI 0.40 to 0.47) in the screened group, respectively, and by 14% (RR=0.86, 95% CI 0.84 to 0.89) and 31% (RR=0.69, 95% CI 0.66 to 0.72) in the invited group, respectively.ConclusionAmong individuals aged 40 to 69 years in high risk areas of upper gastrointestinal cancer, one-time endoscopic screening programme was associated with a significant decrease in upper gastrointestinal cancer incidence and mortality.
SEPT9 gene methylation was validated as a biomarker for colorectal cancer (CRC) for >10 years and available as the Epi proColon test as an aid in CRC detection for >6 years. It was proven to be an accurate, reliable, fast, and convenient molecular test. In this opportunistic screening study, we validated a further simplified SEPT9 gene methylation assay in 1031 subjects in Chinese hospitals. The sensitivity for CRC detection was 76.6% at a specificity of 95.9%, and the results showed a satisfactory detection rate for each CRC stage, including early stages. The new SEPT9 assay, with enhanced technical simplicity, convenience, and lower cost, did not differ in performance compared with Epi proColon 2.0, the commercialized SEPT9 assay. The CRC detection sensitivity was further enhanced when the assay was combined with carcinoembryonic antigen (sensitivity, 86.4%) or fecal immunochemical test (sensitivity, 94.4%), suggesting that the combined tests may be an effective option for future opportunistic screening. In brief, our study has validated a new SEPT9 assay and combined testing as an aid in cancer detection, providing a new approach for opportunistic CRC screening.
BackgroundLung cancer is the leading cause of cancer-related death in China. Results from a randomized controlled trial using annual low-dose computed tomography (LDCT) in specific high-risk groups demonstrated a 20% reduction in lung cancer mortality.MethodsA China national lung cancer screening guideline was developed by lung cancer early detection and treatment expert group appointed by the National Health and Family Planning Commission, based on results of the National Lung Screening Trial, systematic review of evidence related to LDCT screening, and protocol of lung cancer screening program conducted in rural China.ResultsAnnual lung cancer screening with LDCT is recommended for high risk individuals aged 50–74 years who have at least a 20 pack-year smoking history and who currently smoke or have quit within the past five years. Individualized decision making should be conducted before LDCT screening. LDCT screening also represents an opportunity to educate patients as to the health risks of smoking; thus, education should be integrated into the screening process in order to assist smoking cessation.ConclusionsA lung cancer screening guideline is provided for the high-risk population in China.
Background and Aims
In recent years, high-resolution microendoscopy (HRME) has shown potential to improve screening for esophageal squamous cell neoplasia (ESCN). Furthering its utility in a clinical setting, especially in lower-resource settings, could be accomplished by reducing the size and cost of the system as well as incorporating the ability of real-time, objective feedback. This article describes a tablet-interfaced HRME with fully automated, real-time image analysis.
Methods
The performance of the tablet-interfaced HRME was assessed by acquiring images from the oral mucosa in a normal volunteer. An automated, real-time analysis algorithm was developed and evaluated using training, test, and validation images from a previous in vivo study of 177 patients referred for screening or surveillance endoscopy in China. The algorithm was then implemented in a tablet HRME that was used to obtain and analyze images from esophageal tissue in 3 patients. Images were displayed alongside the probability that the imaged region was neoplastic.
Results
The tablet-interfaced HRME demonstrated comparable imaging performance at lower cost compared with first-generation laptop-interfaced HRME systems. In a post-hoc quantitative analysis, the algorithm identified neoplasia with a sensitivity and specificity of 95% and 91% in the validation set, compared with 84% and 95% achieved in the original study.
Conclusion
The tablet-based HRME is a low-cost tool that provides quantitative diagnostic information to the endoscopist in real-time. This could especially be beneficial in lower-resource settings for operators with less experience interpreting HRME images.
Background & Aims
High-resolution microendoscopy is an optical imaging technique with the
potential to improve the accuracy of endoscopic screening for esophageal squamous
neoplasia. Although these microscopic images can readily be interpreted by trained
personnel, quantitative image analysis software could facilitate the use of this
technology in low-resource settings. In this study we developed and evaluated
quantitative image analysis criteria for the evaluation of neoplastic and non-neoplastic
squamous esophageal mucosa.
Methods
We performed image analysis of 177 patients undergoing standard upper endoscopy
for screening or surveillance of esophageal squamous neoplasia, using high-resolution
microendoscopy, at 2 hospitals in China and 1 in the United States from May 2010 to
October 2012. Biopsies were collected from imaged sites (n=375); a consensus diagnosis
was provided by 2 expert gastrointestinal pathologists and used as the standard.
Results
Quantitative information from the high-resolution images was used to develop an
algorithm to identify high-grade squamous dysplasia or invasive squamous cell cancer,
based on histopathology findings. Optimal performance was obtained using mean nuclear
area as the basis for classification, resulting in sensitivities and specificities of
93% and 92% in the training set, 87% and 97% in the test
set, and 84% and 95% in an independent validation set, respectively.
Conclusions
High-resolution microendoscopy with quantitative image analysis can aid in the
identification of esophageal squamous neoplasia. Use of software-based image guides may
overcome issues of training and expertise in low-resource settings, allowing for
widespread use of these optical biopsy technologies.
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