Tejani Mohamedtaki Abdulaziz, Saif Muhammad Wasif
Division of Hematology and Oncology, University of Rochester. Rochester, NY, USA.
JOP. 2014 Mar 10;15(2):132-4. doi: 10.6092/1590-8577/2301.
Pancreatic neuroendocrine tumors (pNETs) are rare well-differentiated neoplasms which can be functional or non-functional. They tend to have a worse prognosis than their counterpart carcinoid tumors. Current systemic treatment options for advanced, unresectable disease include somatostatin analogs, everolimus and sunitinib. Low response rates and toxicity profiles have, thus far, limited the widespread use of cytotoxic chemotherapy in this setting. In this update, we review three abstracts from the 2014 ASCO Gastrointestinal Cancers Symposium that present outcomes of the use of combination capecitabine and temozolomide in patients with advanced pNET. We summarize their results and discuss the role of this regimen in treatment algorithms for metastatic pNET.
胰腺神经内分泌肿瘤(pNETs)是罕见的高分化肿瘤,可分为功能性或非功能性。它们的预后往往比类癌肿瘤更差。目前,针对晚期不可切除疾病的全身治疗选择包括生长抑素类似物、依维莫司和舒尼替尼。迄今为止,低反应率和毒性特征限制了细胞毒性化疗在这种情况下的广泛应用。在本次更新中,我们回顾了2014年美国临床肿瘤学会(ASCO)胃肠道癌症研讨会的三篇摘要,这些摘要展示了晚期pNET患者使用卡培他滨和替莫唑胺联合治疗的结果。我们总结了它们的结果,并讨论了该方案在转移性pNET治疗算法中的作用。