Heterogeneity of small duct- and large duct-type intrahepatic cholangiocarcinoma

被引:1
|
作者
Kinzler, Maximilian N. [1 ,6 ]
Schulze, Falko [2 ]
Jeroch, Jan [2 ]
Schmitt, Christina [2 ]
Ebner, Silvana [2 ]
Gretser, Steffen [2 ]
Bein, Julia [2 ]
Finkelmeier, Fabian [1 ,3 ]
Trojan, Joerg [1 ]
Zeuzem, Stefan [1 ]
Schnitzbauer, Andreas A. [4 ]
Demes, Melanie C. [2 ]
Reis, Henning [2 ]
Wild, Peter J. [2 ,3 ,5 ]
Walter, Dirk [1 ]
机构
[1] Goethe Univ Frankfurt, Univ Hosp, Med Clin 1, Frankfurt, Germany
[2] Goethe Univ Frankfurt, Univ Hosp, Dr Senckenberg Inst Pathol, Frankfurt, Germany
[3] Goethe Univ Frankfurt, Frankfurt Canc Inst FCI, Frankfurt, Germany
[4] Goethe Univ, Univ Hosp Frankfurt, Dept Gen Visceral Transplant & Thorac Surg, D-60590 Frankfurt, Germany
[5] Frankfurt Inst Adv Studies FIAS, Frankfurt, Germany
[6] Goethe Univ Frankfurt, Univ Hosp, Med Clin 1, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
关键词
cholangiocarcinoma; heterogeneity; intrahepatic; molecular; pathology; surgical oncology;
D O I
10.1111/his.15162
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
AimsThe histological subtype of intrahepatic cholangiocarcinoma (iCCA) is associated with different mutational characteristics that impact clinical management. So far, data are lacking on the presence of small duct iCCA (SD-iCCA) and large duct iCCA (LD-iCCA) in a single patient. The aim of the current study was to determine the presence and degree of intratumoural heterogeneity of SD- and LD-iCCA features in different tumour regions.Methods and resultsAll patients treated with surgically resected iCCA at Frankfurt University Hospital between December 2005 and March 2023 were retrospectively analysed. Histomorphological features of SD- and LD-iCCA were evaluated by an expert hepatobiliary pathologist. Tissue samples suspicious for subtype heterogeneity were further investigated. Immunohistochemistry for N-cadherin, S100P, MUC5AC, MUC6, TFF1 and AGR2 and mutational profiling with the Illumina TruSight Oncology 500 (TSO500) assay were performed separately for the SD- and LD-iCCA regions. Of 129 patients with surgically resected iCCA, features of either SD- or LD-iCCA were present in 67.4% (n = 87) and 24.8% of the patients (n = 32), respectively; 7.8% (n = 10) had histomorphological features of both SD- and LD-iCCA, seven patients (5.4%) of which had sufficient formalin-fixed, paraffin-embedded tissue for further analysis. Heterogeneity of both subtypes could be confirmed with immunohistochemistry. In five of seven (71.4%) patients, molecular profiling revealed intratumoural differences in genetic alterations between the SD- and LD-iCCA region. In one patient, a BRAF mutation (p.V600E) was found in the SD-iCCA but not in the LD-iCCA region of the tumour.ConclusionsA marked portion of patients with iCCA exhibits both SD- and LD-iCCA in different tumour regions. In case of the presence of histopathological heterogeneity, mutational profiling should be considered to avoid missing therapeutically relevant genetic alterations.
引用
收藏
页码:1061 / 1067
页数:7
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