Antiproliferative Systemic Therapies for Metastatic Small Bowel Neuroendocrine Tumours
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Oncology
Link
https://link.springer.com/content/pdf/10.1007/s11864-021-00863-y.pdf
Reference52 articles.
1. Dasari A, et al. Trends in the incidence, prevalence, and survival outcomes in patients with neuroendocrine tumors in the United States. JAMA Oncol. 2017;3(10):1335–42. https://doi.org/10.1001/jamaoncol.2017.0589.
2. Rindi G, Bordi C. Aetiology, molecular pathogenesis and genetics. Best Pract Res Clin Gastroenterol. 2005;19(4 SPEC. ISS) Bailliere Tindall Ltd:519–34. https://doi.org/10.1016/j.bpg.2005.03.005.
3. Hofland J, Kaltsas G, De Herder WW. Advances in the diagnosis and management of well-differentiated neuroendocrine neoplasms. Endocr Rev. 2020;41(2) Endocrine Society. https://doi.org/10.1210/endrev/bnz004. Provided very important information about epidemiology of the small bowel NETs, as well as biological characteristics and the appropriate investigation of small bowel NETs.
4. Clift AK, et al. Neuroendocrine neoplasms of the small bowel and pancreas. Neuroendocrinology. 2020;110(6) S. Karger AG:444–76. https://doi.org/10.1159/000503721.
5. Williams ED, Sandler M. The classification of carcinoid tumours. Lancet. 1963. https://doi.org/10.1016/S0140-6736(63)90951-6.
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