Treatment of Multiple Endocrine Neoplasia 1/2 Tumors: Case Report and Review of the Literature

Treatment of Multiple Endocrine Neoplasia 1/2 Tumors: Case Report and Review of the Literature
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多发性内分泌肿瘤1/2肿瘤的治疗:病例报告及文献复习

DOI:
--
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发表时间:
2012
期刊:
影响因子:
3.5
通讯作者:
R. Fine
R. Fine
中科院分区:
医学3区
文献类型:
--
作者:
A. Gulati;Benjamin A. Krantz;R. Moss;Wendy N Moyal;D. Tsushima;Kelley B. Mowatt;S. Schreibman;R. Fine

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Background: Neuroendocrine tumors are uncommon tumors that are histopathologically and biologically heterogeneous and include the multiple endocrine neoplasia (MEN) 1 and 2 syndromes. The morbidity of MEN-1 and MEN-2 is often due to the symptomatology of the endocrine hormones produced, and the mortality mainly occurs from hepatic dysfunction incurred by liver metastases. At present, there is essentially no effective cure once the tumor has metastasized to the liver. Patient: We present a patient with progressive, metastatic MEN-1 with the classic ‘3 P’s’ triad of neuroendocrine tumor of the pancreas, parathyroid adenoma and a pituitary adenoma. Results: After progression on high-dose Sandostatin LAR (60 mg/month) and multiple surgeries, the patient had a partial response (40% decrease) to a novel regimen of capecitabine and temozolomide (CAPTEM) and progression-free survival of 18 months. He had minor grade 1 toxicities and no grade 2, 3 or 4 toxicities. Discussion: The history and treatment options for MEN-1/2 cancers are reviewed, as well as the data behind our novel regimen, CAPTEM. Conclusion: The CAPTEM regimen is a tolerable, safe, easy to administer oral regimen with possible efficacy for MEN-1 tumors.
DOI: 10.1056/nejm199202203260804
发表时间: 1992-02-20
影响因子: 158.5
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发表时间: 2012-08-20
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