Gibril F, Venzon D J, Ojeaburu J V, Bashir S, Jensen R T
Digestive Diseases Branch, National Institute of Diabetes and Digestive, and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-1804, USA.
J Clin Endocrinol Metab. 2001 Nov;86(11):5282-93. doi: 10.1210/jcem.86.11.8011.
The natural history of pancreatic endocrine tumors (PETs) in patients with MEN1 is largely unknown. Recent studies in patients with sporadic PETs show that in a subset, tumor growth is aggressive. To determine whether PETs in patients with MEN1 show similar growth behavior, we report results from a long-term prospective study of 57 patients with MEN1 and Zollinger-Ellison syndrome. All patients had tumor imaging studies yearly, and the mean follow-up was 8 yr. Only patients with PETs 2.5 cm or larger underwent abdominal surgical exploration. Hepatic metastases occurred in 23%, and in 14% tumors demonstrated aggressive growth. Three tumor-related deaths occurred, each due to liver metastases, and in each, aggressive tumor growth was present. Overall, 4% of the study group, 23% with liver metastases and 38% with aggressive disease, died. Aggressive growth was associated with higher gastrins and larger tumors. Patients with liver metastases with aggressive growth differed from those with liver metastases without aggressive growth in age at MEN1 onset or diagnosis and primary tumor size. Survival was decreased (P = 0.0012) in patients with aggressive tumor growth compared with those with liver metastases without aggressive growth or with no liver metastases without aggressive growth. Based on these results a number of factors were identified that may be clinically useful in determining in which patients aggressive tumor growth may occur. These results demonstrate in a significant subset of patients with MEN1 and Zollinger-Ellison syndrome, aggressive tumor growth occurs and can lead to decreased survival. The identification of prognostic factors that identify this group will be important clinically in allowing more aggressive treatment options to be instituted earlier.
MEN1患者胰腺内分泌肿瘤(PETs)的自然病史在很大程度上尚不清楚。最近对散发性PETs患者的研究表明,在一部分患者中,肿瘤生长具有侵袭性。为了确定MEN1患者的PETs是否表现出类似的生长行为,我们报告了一项对57例MEN1和卓-艾综合征患者进行的长期前瞻性研究结果。所有患者每年都进行肿瘤影像学检查,平均随访时间为8年。只有PETs直径达到或超过2.5 cm的患者接受腹部手术探查。23%的患者发生肝转移,14%的肿瘤表现出侵袭性生长。发生了3例与肿瘤相关的死亡,均死于肝转移,且每例均存在侵袭性肿瘤生长。总体而言,研究组中有4%的患者死亡,肝转移患者中有23%死亡,侵袭性疾病患者中有38%死亡。侵袭性生长与胃泌素水平较高和肿瘤较大有关。发生侵袭性生长的肝转移患者与未发生侵袭性生长的肝转移患者在MEN1发病或诊断时的年龄以及原发肿瘤大小方面存在差异。与未发生侵袭性生长的肝转移患者或未发生肝转移且无侵袭性生长的患者相比,侵袭性肿瘤生长患者的生存率降低(P = 0.0012)。基于这些结果,确定了一些在临床上可能有助于判断哪些患者可能发生侵袭性肿瘤生长的因素。这些结果表明,在相当一部分MEN1和卓-艾综合征患者中,会出现侵袭性肿瘤生长并可导致生存率降低。识别出能确定这一群体的预后因素在临床上非常重要,这样可以更早地采取更积极的治疗方案。