The Activated Stroma Index Is a Novel and Independent Prognostic Marker in Pancreatic Ductal Adenocarcinoma

被引:348
作者
Erkan, Mert [1 ]
Michalski, Christoph W. [1 ,2 ]
Rieder, Simon [1 ]
Reiser-Erkan, Carolin [1 ]
Abiatari, Ivane [1 ]
Kolb, Armin [2 ]
Giese, Nathalia A. [2 ]
Esposito, Irene [3 ]
Friess, Helmut [1 ]
Kleeff, Joerg [1 ]
机构
[1] Tech Univ Munich, Dept Gen Surg, D-81675 Munich, Germany
[2] Heidelberg Univ, Dept Gen Surg, Heidelberg, Germany
[3] Tech Univ Munich, Inst Pathol, D-81675 Munich, Germany
关键词
D O I
10.1016/j.cgh.2008.05.006
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Pancreatic ductal adenocarcinoma (PDAC) is a highly desmoplastic tumor with an innate resistance to therapy. Pancreatic stellate cells (PSCs) produce this excessively desmoplastic microenvironment. The impact of PSC activity on PDAC behavior in vivo is analyzed. Methods: 233 patients who underwent surgery for PDAC were evaluated by immunohistochemistry using antibodies against a-smooth muscle actin as a marker of PSC activity. Aniline was used to stain collagen deposition. The ratio of a-smooth muscle actin-stained area to collagen-stained area was defined as the activated stroma index (ASI). Survival analysis was performed using the Kaplan-Meier method. Prognostic factors were determined in a multivariable analysis using a Cox proportional hazards model. Results: Four major patterns of collagen deposition were defined with regard to PSC activity. The combination of high stromal activity and low collagen deposition was associated with a worse prognosis, whereas the combination of high collagen deposition and low stromal activity indicated a better prognosis. Patients with the lowest ASI had the best median survival rate (25.7 mo). The highest ASI was found in patients with the worst median survival rate (16.1 mo; P =.007; lowest vs highest ASI: hazard ratio, 1.61; 95% confidence interval, 1.014-2.562). ASI was an independent prognostic marker in multivariable survival analysis comparable with the nodal status of cancer. Conclusions: The activated stroma index is a novel independent prognostic marker in PDAC in cases undergoing surgery. This finding highlights the impact of the microenvironment in cancer progression and on patient survival.
引用
收藏
页码:1155 / 1161
页数:7
相关论文
共 33 条
[1]   Pancreatic carcinoma cells induce fibrosis by stimulating proliferation and matrix synthesis of stellate cells [J].
Bachem, MG ;
Schünemann, M ;
Ramadani, M ;
Siech, M ;
Beger, H ;
Buck, A ;
Zhou, SX ;
Schmid-Kotsas, A ;
Adler, G .
GASTROENTEROLOGY, 2005, 128 (04) :907-921
[2]   Identification, culture, and characterization of pancreatic stellate cells in rats and humans [J].
Bachem, MG ;
Schneider, E ;
Gross, H ;
Weidenbach, H ;
Schmid, RM ;
Menke, A ;
Siech, M ;
Beger, H ;
Grünert, A ;
Adler, G .
GASTROENTEROLOGY, 1998, 115 (02) :421-432
[3]  
Barcellos-Hoff MH, 2000, CANCER RES, V60, P1254
[4]   Putting tumours in context [J].
Bissell, MJ ;
Radisky, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :46-54
[5]   Matrix metalloproteinases play an active role in Wnt1-induced mammary tumorigenesis [J].
Blavier, L ;
Lazaryev, A ;
Dorey, F ;
Shackleford, GM ;
DeClerck, YA .
CANCER RESEARCH, 2006, 66 (05) :2691-2699
[6]   FIBROBLAST-MEDIATED ACCELERATION OF HUMAN EPITHELIAL TUMOR-GROWTH INVIVO [J].
CAMPS, JL ;
CHANG, SM ;
HSU, TC ;
FREEMAN, MR ;
HONG, SJ ;
ZHAU, HE ;
VONESCHENBACH, AC ;
CHUNG, LWK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :75-79
[7]  
CUBILLA AL, 1976, CANCER RES, V36, P2690
[8]   Loss of BNIP3 expression is a late event in pancreatic cancer contributing to chemoresistance and worsened prognosis [J].
Erkan, M ;
Kleeff, J ;
Esposito, I ;
Giese, T ;
Ketterer, K ;
Büchler, MW ;
Giese, NA ;
Friess, H .
ONCOGENE, 2005, 24 (27) :4421-4432
[9]   Periostin creates a tumor-supportive microenvironment in the pancreas by sustaining fibrogenic stellate cell activity [J].
Erkan, Mert ;
Kleeff, Joerg ;
Gorbachevski, Andre ;
Reiser, Carolin ;
Mitkus, Tomas ;
Esposito, Irene ;
Giese, Thomas ;
Buechler, Markus W. ;
Giese, Nathalia A. ;
Friess, Helmut .
GASTROENTEROLOGY, 2007, 132 (04) :1447-1464
[10]   Most pancreatic cancer resections are R1 resections [J].
Esposito, Irene ;
Kleff, Joerg ;
Bergmann, Frank ;
Reiser, Caroline ;
Herpel, Esther ;
Friess, Helmut ;
Schirmacher, Peter ;
Buechler, Markus W. .
ANNALS OF SURGICAL ONCOLOGY, 2008, 15 (06) :1651-1660