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1.
World J Gastroenterol ; 24(45): 5167-5178, 2018 Dec 07.
Article in English | MEDLINE | ID: mdl-30568393

ABSTRACT

AIM: To integrate clinically significant variables related to prognosis after curative resection for gallbladder carcinoma (GBC) into a predictive nomogram. METHODS: One hundred and forty-two GBC patients who underwent curative intent surgical resection at Peking Union Medical College Hospital (PUMCH) were included. This retrospective case study was conducted at PUMCH of the Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS & PUMC) in China from January 1, 2003 to January 1, 2018. The continuous variable carbohydrate antigen 19-9 (CA19-9) was converted into a categorical variable (cCA19-9) based on the normal reference range. Stages 0 to IIIA were merged into one category, while the remaining stages were grouped into another category. Pathological grade X (GX) was treated as a missing value. A multivariate Cox proportional hazards model was used to select variables to construct a nomogram. Discrimination and calibration of the nomogram were performed via the concordance index (C-index) and calibration plots. The performance of the nomogram was estimated using the calibration curve. Receiver operating characteristic (ROC) curve analysis and decision curve analysis (DCA) were performed to evaluate the predictive accuracy and net benefit of the nomogram, respectively. RESULTS: Of these 142 GBC patients, 55 (38.7%) were male, and the median and mean age were 64 and 63.9 years, respectively. Forty-eight (33.8%) patients in this cohort were censored in the survival analysis. The median survival time was 20 months. A series of methods, including the likelihood ratio test and Akaike information criterion (AIC) as well as stepwise, forward, and backward analyses, were used to select the model, and all yielded identical results. Jaundice [hazard ratio (HR) = 2.9; 95% confidence interval (CI): 1.60-5.27], cCA19-9 (HR = 3.2; 95%CI: 1.91-5.39), stage (HR = 1.89; 95%CI: 1.16-3.09), and resection (R) (HR = 2.82; 95%CI: 1.54-5.16) were selected as significant predictors and combined into a survival time predictive nomogram (C-index = 0.803; 95%CI: 0.766-0.839). High prediction accuracy (adjusted C-index = 0.797) was further verified via bootstrap validation. The calibration plot demonstrated good performance of the nomogram. ROC curve analysis revealed a high sensitivity and specificity. A high net benefit was proven by DCA. CONCLUSION: A nomogram has been constructed to predict the overall survival of GBC patients who underwent radical surgery from a clinical database of GBC at PUMCH.


Subject(s)
Cholecystectomy , Gallbladder Neoplasms/mortality , Jaundice, Obstructive/epidemiology , Nomograms , Adult , Aged , Aged, 80 and over , China/epidemiology , Female , Gallbladder/pathology , Gallbladder/surgery , Gallbladder Neoplasms/complications , Gallbladder Neoplasms/pathology , Gallbladder Neoplasms/surgery , Humans , Jaundice, Obstructive/etiology , Kaplan-Meier Estimate , Male , Middle Aged , Neoplasm Staging , ROC Curve , Retrospective Studies
2.
World J Gastroenterol ; 22(46): 10254-10259, 2016 Dec 14.
Article in English | MEDLINE | ID: mdl-28028375

ABSTRACT

Gallbladder cancer (GBC), although considered as a relatively rare malignancy, is the most common neoplasm of the biliary tract system. The late diagnosis and abysmal prognosis present challenges to treatment. The overall 5-year survival rate for metastatic GBC patients is extremely low. BRCA1 and BRCA2 are the breast cancer susceptibility genes and their mutation carriers are at a high risk for cancer development, both in men and women. Olaparib, an oral poly ADP-ribose polymerase inhibitor, has been approved by the Food and Drug Administration and the European Commission for the treatment of ovarian cancer with any BRCA1/2 mutations. The first case of a BRCA1-mutated GBC patient who responded to olaparib treatment is reported here.


Subject(s)
Antineoplastic Agents/therapeutic use , Gallbladder Neoplasms/drug therapy , Genes, BRCA1 , Liver Neoplasms/drug therapy , Phthalazines/therapeutic use , Piperazines/therapeutic use , Aged , Gallbladder Neoplasms/diagnostic imaging , Gallbladder Neoplasms/genetics , Gallbladder Neoplasms/pathology , Humans , Liver Neoplasms/diagnostic imaging , Liver Neoplasms/genetics , Liver Neoplasms/secondary , Male , Mutation , Tomography, X-Ray Computed , Treatment Outcome
3.
World J Gastroenterol ; 22(18): 4459-65, 2016 May 14.
Article in English | MEDLINE | ID: mdl-27182157

ABSTRACT

Combined hepatocellular cholangiocarcinoma (CHC) accounts for 0.4%-14.2% of primary liver cancer cases and possesses pathological features of both hepatocellular carcinoma and cholangiocarcinoma. Since this disease was first described and classified in 1949, the classification of CHC has continuously evolved. The latest definition and classification of CHC by the World Health Organization is based on the speculation that CHC arises from hepatic progenitor cells. However, there is no evidence demonstrating the common origin of different components of CHC. Furthermore, the definition of CHC subtypes is still ambiguous and the identification of CHC subtype when a single tumor contains many components has remained unresolved. In addition, there is no summary on the newly recognized histopathology features or the contribution of CHC components to prognosis and outcome of this disease. Here we provide a review of the current literature to address these questions.


Subject(s)
Bile Duct Neoplasms/pathology , Bile Ducts, Intrahepatic/pathology , Carcinoma, Hepatocellular/pathology , Cholangiocarcinoma/pathology , Liver Neoplasms/pathology , Neoplasms, Complex and Mixed , Bile Duct Neoplasms/classification , Bile Duct Neoplasms/genetics , Carcinoma, Hepatocellular/classification , Carcinoma, Hepatocellular/genetics , Cell Differentiation , Cell Lineage , Cholangiocarcinoma/classification , Cholangiocarcinoma/genetics , Genetic Predisposition to Disease , Humans , Liver Neoplasms/classification , Liver Neoplasms/genetics , Phenotype , Prognosis
4.
World J Gastroenterol ; 21(42): 12190-6, 2015 Nov 14.
Article in English | MEDLINE | ID: mdl-26576103

ABSTRACT

Liver cancer is a common malignancy and surgery is the main treatment strategy. However, the prognosis is still poor because of high frequencies of postoperative recurrence and metastasis. In recent years, cancer stem cell (CSC) theory has evolved with the concept of stem cells, and has been applied to oncological research. According to cancer stem cell theory, liver cancer can be radically cured only by eradication of liver cancer stem cells (LCSCs). This notion has lead to the isolation and identification of LCSCs, which has become a highly researched area. Analysis of LCSC markers is considered to be the primary method for identification of LCSCs. Here, we provide an overview of the current research progress and prospects of surface markers for LCSCs.


Subject(s)
Biomarkers, Tumor/metabolism , Liver Neoplasms/metabolism , Neoplastic Stem Cells/metabolism , Side-Population Cells/metabolism , Animals , Humans , Liver Neoplasms/genetics , Liver Neoplasms/pathology , Neoplastic Stem Cells/pathology , Phenotype , Predictive Value of Tests , Prognosis , Side-Population Cells/pathology
5.
World J Gastroenterol ; 19(46): 8595-604, 2013 Dec 14.
Article in English | MEDLINE | ID: mdl-24379576

ABSTRACT

Intraductal papillary neoplasm of the bile duct (IPNB) is a variant of bile duct carcinoma that is characterized by intraductal growth and better outcomes compared with common cholangiocarcinoma. IPNBs are mainly found in patients from Far Eastern areas, where hepatolithiasis and clonorchiasis are endemic. According to the immunohistochemical profiles of the mucin core proteins, IPNBs are classified into four types: pancreaticobiliary, intestinal, gastric, and oncocytic. Approximately 40%-80% of IPNBs contain a component of invasive carcinoma or tubular or mucinous adenocarcinoma, suggesting that IPNB is a disease with high potential for malignancy. It is difficult to make an accurate preoperative diagnosis because of IPNB's low incidence and the lack of specificity in its clinical manifestation. The most common abnormal preoperative imaging findings of IPNB are intraductal masses and the involvement of bile duct dilation. Simultaneous proximal and distal bile duct dilation can be detected in some cases, which has diagnostic significance. Cholangiography and cholangioscopy are needed to confirm the pathology and demonstrate the extent of the lesions. However, pathologic diagnosis by biopsy cannot reflect the actual stage in many cases because different foci may be of different stages and because mixed pathologic findings may exist in the same lesion. Surgical resection is the major treatment. Systematic cholangioscopy with staged biopsies and frozen sections is recommended during resection to ensure that no minor tumors are left and that curative resection is achieved. Staging, histologic subtype, curative resection and lymph node metastasis are factors affecting long-term survival.


Subject(s)
Adenocarcinoma, Mucinous/pathology , Bile Duct Neoplasms/pathology , Bile Ducts/pathology , Carcinoma, Papillary/pathology , Papilloma/pathology , Adenocarcinoma, Mucinous/chemistry , Adenocarcinoma, Mucinous/mortality , Adenocarcinoma, Mucinous/surgery , Bile Duct Neoplasms/chemistry , Bile Duct Neoplasms/mortality , Bile Duct Neoplasms/surgery , Bile Ducts/chemistry , Bile Ducts/surgery , Biliary Tract Surgical Procedures , Biomarkers, Tumor/analysis , Biopsy , Carcinoma, Papillary/chemistry , Carcinoma, Papillary/mortality , Carcinoma, Papillary/surgery , Diagnosis, Differential , Diagnostic Imaging/methods , Dilatation, Pathologic , Endoscopy, Digestive System , Humans , Neoplasm Invasiveness , Neoplasm Staging , Papilloma/chemistry , Papilloma/mortality , Papilloma/surgery , Predictive Value of Tests , Risk Factors , Treatment Outcome
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