Cloyd Jordan M, Kopecky Kimberly E, Norton Jeffrey A, Kunz Pamela L, Fisher George A, Visser Brendan C, Dua Monica M, Park Walter G, Poultsides George A
Department of Surgery, Stanford University, CA.
Division of Oncology, Stanford University, CA.
Surgery. 2016 Sep;160(3):708-13. doi: 10.1016/j.surg.2016.04.005. Epub 2016 May 20.
Although most pancreatic neuroendocrine tumors are solid, approximately 10% are cystic. Some studies have suggested that cystic pancreatic neuroendocrine tumors are associated with a more favorable prognosis.
A retrospective review of all patients with pancreatic neuroendocrine tumors who underwent operative resection between 1999 and 2014 at a single academic medical center was performed. Based on cross-sectional imaging performed before operation, pancreatic neuroendocrine tumors were classified according to the size of the cystic component relative to the total tumor size: purely cystic (100%), mostly cystic (≥50%), mostly solid (<50%), and purely solid (0%). Clinicopathologic characteristics and recurrence-free survival were assessed between groups.
In the study, 214 patients met inclusion criteria: 8 with purely cystic tumors, 7 with mostly cystic tumors, 15 with mostly solid tumors, and 184 with purely solid tumors. The groups differed in terms of tumor size (1.5 ± 0.5, 3.0 ± 1.7, 3.7 ± 2.6, and 4.0 ± 3.5 cm), lymph node positivity (0%, 0%, 26.7%, and 34.2%), intermediate or high grade (0%, 16.7%, 20.0%, and 31.0%), synchronous liver metastases (0%, 14.3%, 20.0%, and 26.6%) and need for pancreaticoduodenectomy (0%, 0%, 6.7%, and 25.0%), respectively. No cases of purely cystic pancreatic neuroendocrine tumors were associated with synchronous liver or lymph node metastasis, intermediate/high grade, recurrence, or death due to disease. Among patients presenting without metastatic disease, 10-year recurrence-free survival was 100% in patients with purely and mostly cystic tumors versus 53.0% in patients with purely and mostly solid tumors; however, this difference did not reach statistical significance.
Pancreatic neuroendocrine tumors demonstrate a spectrum of biologic behavior with an increasing cystic component being associated with more favorable clinicopathologic features and prognosis. Purely cystic pancreatic neuroendocrine tumors may represent 1 subset that can be safely observed without immediate resection.
虽然大多数胰腺神经内分泌肿瘤是实性的,但约10%为囊性。一些研究表明,囊性胰腺神经内分泌肿瘤的预后更有利。
对1999年至2014年在一家学术医疗中心接受手术切除的所有胰腺神经内分泌肿瘤患者进行回顾性研究。根据术前横断面成像,将胰腺神经内分泌肿瘤根据囊性成分相对于肿瘤总体积的大小进行分类:纯囊性(100%)、大部分为囊性(≥50%)、大部分为实性(<50%)和纯实性(0%)。评估各组之间的临床病理特征和无复发生存率。
在该研究中,214例患者符合纳入标准:8例为纯囊性肿瘤,7例为大部分为囊性肿瘤,15例为大部分为实性肿瘤,184例为纯实性肿瘤。各组在肿瘤大小(1.5±0.5、3.0±1.7、3.7±2.6和4.0±3.5cm)、淋巴结阳性率(0%、0%、26.7%和34.2%)、中或高级别(0%、16.7%、20.0%和31.0%)、同时性肝转移(0%、14.3%、20.0%和26.6%)以及是否需要胰十二指肠切除术(0%、0%、6.7%和25.0%)方面存在差异。纯囊性胰腺神经内分泌肿瘤无1例与同时性肝或淋巴结转移、中/高级别、复发或疾病死亡相关。在无转移性疾病的患者中,纯囊性和大部分为囊性肿瘤患者的10年无复发生存率为100%,而纯实性和大部分为实性肿瘤患者为53.0%;然而,这种差异未达到统计学意义。
胰腺神经内分泌肿瘤表现出一系列生物学行为,囊性成分增加与更有利的临床病理特征和预后相关。纯囊性胰腺神经内分泌肿瘤可能代表1个无需立即切除即可安全观察的亚组。