Well-Differentiated Bronchopulmonary Neuroendocrine Tumors: More Than One Entity

被引:7
|
作者
van den Broek, Medard F. M. [1 ]
Levy, Sonja [2 ]
Buikhuisen, Wieneke A. [3 ]
Dijke, Kim [2 ]
Hartemink, Koen J. [4 ]
van Leeuwaarde, Rachel S. [1 ]
Vriens, Menno R. [5 ]
Tesselaar, Margot E. T. [2 ]
Valk, Gerlof D. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Endocrine Oncol, Huispostnummer Q05-4-300,Postbus 85500, NL-3508 GA Utrecht, Netherlands
[2] Netherlands Canc Inst, Dept Med Oncol, Amsterdam, Netherlands
[3] Netherlands Canc Inst, Dept Thorac Oncol, Amsterdam, Netherlands
[4] Netherlands Canc Inst, Dept Surg Oncol, Amsterdam, Netherlands
[5] Univ Med Ctr Utrecht, Dept Endocrine Surg Oncol, Utrecht, Netherlands
关键词
Bronchopulmonary neuroendocrine tumor (NET); Survival; Multiple endocrine neoplasia type 1 (MEN1); Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH); Sporadic; ENDOCRINE NEOPLASIA TYPE-1; BRONCHIAL CARCINOID-TUMORS; SOCIETY EXPERT CONSENSUS; CELL HYPERPLASIA; PROGNOSTIC-FACTORS; MANAGEMENT; MEN1; GUIDELINES; DIAGNOSIS; CANCER;
D O I
10.1016/j.jtho.2021.07.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Until now, well-differentiated bronchopulmonary neuroendocrine tumors (bpNET) occurring either sporadically (sp-bpNET) or in the context of multiple endocrine neoplasia type 1 (MEN1) and diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) are regarded as similar entities. However, in contrast to sp-bpNET: MEN1-related and DIPNECH-related bpNET rarely metastasize or lead to bpNET-related death. We aimed to describe and compare the course of the disease of sp-bpNET, DIPNECH-and MEN1-related bpNET. Methods: All patients with histologically confirmed MEN1-related bpNET from the DutchMEN Study Group database (1990-2017), patients with resected sp-bpNET and DIPNECH patients referred to a Dutch European Neuroendocrine Tumor Society center between 2000 and 2018 were included. Fisher's exact test was used for comparison between groups. The primary end point was disease-specific mortality (DSM). Kaplan-Meier and log rank test were used to compare survival. Cox regression was used to identify risk factors for DSM in the sp-bpNET subgroup. Results: We included 112 sp-bpNET, 29 MEN1, and 27 DIPNECH patients. Tumor classification was similar across subgroups. A total of 20 patients (18%) with sp-bpNET died because of bpNET, compared with none in the MEN1 group and DIPNECH group. Median disease-specific survival was 12.3 (confidence interval: 6.3-18.3) years for patients with sp-bpNET, and not estimable for the other subgroups (p < 0.001). Differences in baseline characteristics did not explain worse survival in sp-bpNET. Tumor classification and age at diagnosis were independent risk factors for DSM in sp-bpNET. Conclusions: Patients with sp-bpNET have a significantly higher DSM compared with MEN1 or DIPNECH-related bpNET, unexplained by differences in baseline characteristics. This implies that not all bpNET are similar entities. (C) 2021 International Association for the Study of Lung Cancer. Published by Elsevier Inc.
引用
收藏
页码:1810 / 1820
页数:11
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