Phosphorylated Akt Expression as a Favorable Prognostic Factor for Patients Undergoing Curative Resection and Adjuvant Chemoradiotherapy for Proximal Extrahepatic Bile Duct Cancer

Objectives: To evaluate the prognostic significance of phosphorylated Akt (p-Akt), phosphorylated mammalian target of rapamycin (p-mTOR), and total phosphatase and tensin homolog deleted on chromosome 10 (PTEN) expressions in patients undergoing adjuvant chemoradiotherapy (CRT) for proximal extrahepatic bile duct (EHBD) cancer. Methods: Sixty-three patients with proximal EHBD cancer who underwent curative resection followed by adjuvant CRT were enrolled into this study. Postoperative radiotherapy was delivered to tumor bed and regional lymph nodes up to a median of 40 Gy (range, 40 to 54 Gy). Fifty-nine patients also received fluoropyrimidine chemotherapy as a radiosensitizer. p-Akt, p-mTOR, and PTEN expression were assessed with immunohistochemical staining on the tissue microarray. Results: p-Akt, p-mTOR, and PTEN were expressed in 23 (36.5%), 17 (27.0%), and 24 patients (38.1%), respectively. p-Akt expression was associated with distant metastasis and overall survival (OS), but not with locoregional recurrence. The 5-year distant metastasis-free and OS rates were 25.8% versus 58.2% (P=0.007), and 27.5% versus 50.2% (P=0.0167) in patients with negative and positive expression, respectively. On multivariate analysis, nodal involvement was the only significant prognosticator predicting inferior distant metastasis-free survival (P=0.0105), whereas p-Akt expression had a borderline significance (P=0.0541). As for OS, p-Akt expression was a marginally significant prognosticator (P=0.0635), whereas other risk factors lost the statistical significance. Conclusion: p-Akt expression tended to be associated with a favorable prognosis in patients undergoing curative resection followed by adjuvant CRT for proximal EHBD cancer.

[1]  J. Bussink,et al.  Low phosphorylated AKT expression in laryngeal cancer: indications for a higher metastatic risk. , 2013, International journal of radiation oncology, biology, physics.

[2]  H. Min,et al.  Molecular biomarkers in extrahepatic bile duct cancer patients undergoing chemoradiotherapy for gross residual disease after surgery , 2012, Radiation oncology journal.

[3]  D. Ganeshan,et al.  Extrahepatic biliary cancer: New staging classification. , 2012, World journal of radiology.

[4]  Jin‐Young Jang,et al.  Adjuvant Chemoradiotherapy After Curative Resection for Extrahepatic Bile Duct Cancer: A Long-term Single Center Experience , 2012, American journal of clinical oncology.

[5]  A. Allal,et al.  Is adjuvant radiotherapy needed after curative resection of extrahepatic biliary tract cancers? A systematic review with a meta-analysis of observational studies. , 2012, Cancer treatment reviews.

[6]  W. Lau,et al.  Current therapy of hilar cholangiocarcinoma. , 2012, Hepatobiliary & pancreatic diseases international : HBPD INT.

[7]  Sarat Chandarlapaty,et al.  AKT inhibition relieves feedback suppression of receptor tyrosine kinase expression and activity. , 2011, Cancer cell.

[8]  W. Kim,et al.  Extrahepatic bile duct cancers: surgery alone versus surgery plus postoperative radiation therapy. , 2010, International journal of radiation oncology, biology, physics.

[9]  Hong-shan Liu,et al.  [Expression of Survivin protein in extrahepatic cholangiocarcinoma and its relationship with the prognosis]. , 2009, Zhonghua wai ke za zhi [Chinese journal of surgery].

[10]  Seung‐Mo Hong,et al.  The Expression of Phospho-AKT, Phospho-mTOR, and PTEN in Extrahepatic Cholangiocarcinoma , 2009, Clinical Cancer Research.

[11]  S. Curley,et al.  Extrahepatic Bile Duct Adenocarcinoma: Patients at High-Risk for Local Recurrence Treated with Surgery and Adjuvant Chemoradiation Have an Equivalent Overall Survival to Patients with Standard-Risk Treated with Surgery Alone , 2008, Annals of Surgical Oncology.

[12]  M. Nagino,et al.  Expression of matrix metalloproteinase 7 is an unfavorable postoperative prognostic factor in cholangiocarcinoma of the perihilar, hilar, and extrahepatic bile ducts. , 2008, Human pathology.

[13]  Y. Ku,et al.  Frequent activation of mitogen-activated protein kinase relative to Akt in extrahepatic biliary tract cancer , 2007, Journal of Gastroenterology.

[14]  T. Khoury,et al.  Akt expression may predict favorable prognosis in cholangiocarcinoma , 2006, Journal of gastroenterology and hepatology.

[15]  A. Toker,et al.  Akt signaling and cancer: surviving but not moving on. , 2006, Cancer research.

[16]  W. Travis,et al.  Evaluation of two phosphorylation sites improves the prognostic significance of Akt activation in non-small-cell lung cancer tumors. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[17]  D. Gouma,et al.  Recurrent disease after microscopically radical (r0) resection of periampullary adenocarcinoma in patients without adjuvant therapy , 2004, Journal of Gastrointestinal Surgery.

[18]  D. Troyer,et al.  Phosphorylation of Akt (Ser473) is an Excellent Predictor of Poor Clinical Outcome in Prostate Cancer , 2004, Cancer Research.

[19]  T. Okumura,et al.  Serine/Threonine Kinase AKT Is Frequently Activated in Human Bile Duct Cancer and Is Associated with Increased Radioresistance , 2004, Cancer Research.

[20]  W. Jarnagin,et al.  Surgical management of cholangiocarcinoma. , 2004, Seminars in liver disease.

[21]  M. D'Angelica,et al.  Patterns of initial disease recurrence after resection of gallbladder carcinoma and hilar cholangiocarcinoma , 2003, Cancer.

[22]  D. Heo,et al.  Role of postoperative radiotherapy in the management of extrahepatic bile duct cancer. , 2002, International journal of radiation oncology, biology, physics.

[23]  C. Sawyers,et al.  The phosphatidylinositol 3-Kinase–AKT pathway in human cancer , 2002, Nature Reviews Cancer.

[24]  Kyusam Choi,et al.  The expression of phospho-AKT1 and phospho-MTOR is associated with a favorable prognosis independent of PTEN expression in intrahepatic cholangiocarcinomas , 2012, Modern Pathology.