Evolution of the Mesenteric Mass in Small Intestinal Neuroendocrine Tumours

被引:18
作者
Blazevic, Anela [1 ,2 ]
Brabander, Tessa [2 ,3 ]
Zandee, Wouter T. [1 ,2 ,4 ,5 ]
Hofland, Johannes [1 ,2 ]
Franssen, Gaston J. H. [2 ,6 ]
van Velthuysen, Marie-Louise F. [2 ,7 ]
Feelders, Richard A. [1 ,2 ]
De Herder, Wouter W. [1 ,2 ]
机构
[1] Erasmus MC, ENETS Ctr Excellence, Dept Internal Med, Sect Endocrinol, NL-3015 GD Rotterdam, Netherlands
[2] Erasmus MC Canc Inst, NL-3015 GD Rotterdam, Netherlands
[3] Erasmus MC, ENETS Ctr Excellence, Dept Radiol & Nucl Med, NL-3015 GD Rotterdam, Netherlands
[4] Univ Med Ctr Groningen, Dept Endocrinol, NL-9700 RB Groningen, Netherlands
[5] Univ Groningen, NL-9700 RB Groningen, Netherlands
[6] Erasmus MC, ENETS Ctr Excellence, Dept Surg, NL-3015 GD Rotterdam, Netherlands
[7] Erasmus MC, ENETS Ctr Excellence, Dept Pathol, NL-3015 GD Rotterdam, Netherlands
关键词
neuroendocrine tumour; mesenteric metastases; progression; radiology; CT scan; PRRT; RECIST; 1;
D O I
10.3390/cancers13030443
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Around two-thirds of patients with small intestinal neuroendocrine tumours are present with a metastatic mesenteric mass. This mass is known to cause intestinal complications, however, little is known on its development over time in the era of targeted therapy. Therefore, we conducted a retrospective study to assess the growth and response to therapy. We found that the growth of the mesenteric mass was detectable in 13.5% over a median time of 3.4 years and peptide receptor radionuclide therapy resulted in size reduction in only 3.8%. This site-specific static growth behavior is important to note when assessing disease progression and therapeutic options. Background: A metastatic mesenteric mass is a hallmark of small intestinal neuroendocrine tumours (SI-NETs). However, little is known on its development over time. Therefore, we conducted a study to assess the evolution of a SI-NET-associated mesenteric mass over time. Methods: Retrospectively, 530 patients with proven SI-NET were included. The presence and growth of a mesenteric mass was assessed using RECIST 1.1 criteria on every consecutive CT-scan until the end of follow-up or resection. Results: At baseline, a mesenteric mass was present in 64% of the patients, of whom 13.5% showed growth of the mesenteric mass with a median time to growth of 40 months. Male gender was the only independent predictor of growth (OR 2.67). Of the patients without a mesenteric mass at the first evaluation, 2.6% developed a pathological mesenteric mass. Treatment with peptide receptor radionuclide therapy (PRRT; N = 132) resulted in an objective size reduction of the mesenteric mass in 3.8%. Conclusion: The metastatic mesenteric mass in SI-NETs has a static behavior over time. Therefore, site-specific growth behavior should be taken into account when selecting target lesions and assessing disease progression and therapeutic response. PRRT appears not to be effective for size reduction of the mesenteric mass.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 19 条
[1]   Immunohistochemical Expression and Prognostic Value of ER, PR and HER2/neu in Pancreatic and Small Intestinal Neuroendocrine Tumors [J].
Arnason, Thomas ;
Sapp, Heidi L. ;
Barnes, Penelope J. ;
Drewniak, Magdalena ;
Abdolell, Mohamed ;
Rayson, Daniel .
NEUROENDOCRINOLOGY, 2011, 93 (04) :249-258
[2]   Mesenteric fibrosis and palliative surgery in small intestinal neuroendocrine tumours [J].
Blazevic, Anela ;
Zandee, Wouter T. ;
Franssen, Gaston J. H. ;
Hofland, Johannes ;
van Velthuysen, Marie-Louise F. ;
Hofland, Leo J. ;
Feelders, Richard A. ;
de Herder, Wouter W. .
ENDOCRINE-RELATED CANCER, 2018, 25 (03) :245-254
[3]   Small intestinal neuroendocrine tumours and fibrosis: an entangled conundrum [J].
Blazevic, Anela ;
Hofland, Johannes ;
Hofland, Leo J. ;
Feelders, Richard A. ;
de Herder, Wouter W. .
ENDOCRINE-RELATED CANCER, 2018, 25 (03) :R115-R130
[4]   Association of a Prophylactic Surgical Approach to Stage IV Small Intestinal Neuroendocrine Tumors With Survival [J].
Daskalakis, Kosmas ;
Karakatsanis, Andreas ;
Hessman, Ola ;
Stuart, Heather C. ;
Welin, Staffan ;
Janson, Eva Tiensuu ;
Oberg, Kjell ;
Hellman, Per ;
Norlen, Olov ;
Stalberg, Peter .
JAMA ONCOLOGY, 2018, 4 (02) :183-189
[5]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[6]   Consensus guidelines for the management of patients with digestive neuroendocrine tumors -: Well-differentiated jejunal-ileal tumor/carcinoma [J].
Eriksson, Barbro ;
Kloeppel, Guenter ;
Krenning, Eric ;
Ahlman, Hakan ;
Ploeckinger, Ursula ;
Wiedenmann, Bertram ;
Arnold, Rudolf ;
Auernhammer, Christoph ;
Koerner, Meike ;
Rindi, Guido ;
Wildi, Stefan .
NEUROENDOCRINOLOGY, 2008, 87 (01) :8-19
[7]   Progesterone Receptor and PTEN Expression Predict Survival in Patients With Low- and Intermediate-Grade Pancreatic Neuroendocrine Tumors [J].
Estrella, Jeannelyn S. ;
Broaddus, Russell R. ;
Mathews, Amber ;
Milton, Denai R. ;
Yao, James C. ;
Wang, Huamin ;
Rashid, Asif .
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2014, 138 (08) :1027-1036
[8]   The Surgical Management of Small Bowel Neuroendocrine Tumors Consensus Guidelines of the North American Neuroendocrine Tumor Society [J].
Howe, James R. ;
Cardona, Kenneth ;
Fraker, Douglas L. ;
Kebebew, Electron ;
Untch, Brian R. ;
Wang, Yi-Zarn ;
Law, Calvin H. ;
Liu, Eric H. ;
Kim, Michelle K. ;
Menda, Yusuf ;
Morse, Brian G. ;
Bergsland, Emily K. ;
Strosberg, Jonathan R. ;
Nakakura, Eric K. ;
Pommier, Rodney F. .
PANCREAS, 2017, 46 (06) :715-731
[9]  
Laskaratos F, 2019, NEUROENDOCRINOLOGY, V108, P217
[10]   Progression of metastases and symptom improvement from laparotomy in midgut carcinoid tumors [J].
Makridis, C ;
Rastad, J ;
Oberg, K ;
Akerstrom, G .
WORLD JOURNAL OF SURGERY, 1996, 20 (07) :900-907