ALK expression is absent in pancreatic ductal adenocarcinoma

被引:4
|
作者
Ormanns, Steffen [1 ]
Assmann, Gerald [1 ]
Reu, Simone [1 ]
Gallmeier, Eike [2 ]
Bader, Dominik C. [2 ]
Kleespies, Axel [3 ]
Haas, Michael [4 ,5 ]
Kruger, Stephan [4 ,5 ]
Heinemann, Volker [4 ,5 ]
Kirchner, Thomas [1 ]
Boeck, Stefan [4 ,5 ]
机构
[1] Univ Munich, Inst Pathol, D-80337 Munich, Germany
[2] Univ Munich, Klinikum Grosshadern, Dept Internal Med 2, D-80337 Munich, Germany
[3] Univ Munich, Klinikum Grosshadern, Dept Gen Visceral Transplantat Vasc & Thorac Surg, D-80337 Munich, Germany
[4] Univ Munich, Klinikum Grosshadern, Dept Internal Med 3, D-80337 Munich, Germany
[5] Univ Munich, Klinikum Grosshadern, Ctr Comprehens Canc, D-80337 Munich, Germany
关键词
ALK; Biomarker; Pancreatic cancer; NATIONAL-CANCER-INSTITUTE; REARRANGEMENT; GEMCITABINE; CRIZOTINIB; PHASE-3; TRIAL;
D O I
10.1007/s00432-014-1774-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It has not yet been clearly defined whether anaplastic lymphoma kinase (ALK) expression can be detected in pancreatic ductal adenocarcinoma (PDAC). Within a retrospective study, archival PDAC surgical specimens were screened for ALK expression in tumor and normal tissue by immunohistochemistry (IHC) with the use of a specific ALK detection kit on a tissue microarray (TMA). PDAC tumor tissue was available from 99 resected cases: fifty-eight out of 99 patients (59 %) had nodal-positive disease, and 80 patients (81 %) had pT3 tumors. Forty-nine patients underwent R0 resection, and in 48 cases, resection status was classified R1. Regarding ALK expression, five cases showed faint immunoreactivity on TMA, which was negative on whole mount sections. All other 94 cases showed no ALK expression. In 99 PDAC cases, no ALK expression was detected by IHC; ALK thus may not serve as a relevant drug target in PDAC.
引用
收藏
页码:1625 / 1628
页数:4
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