Hellman Per, Lundström Tobias, Ohrvall Ulf, Eriksson Barbro, Skogseid Britt, Oberg Kjell, Tiensuu Janson Eva, Akerström Göran
Department of Surgery, University Hospital, SE-751 85 Uppsala, Sweden.
World J Surg. 2002 Aug;26(8):991-7. doi: 10.1007/s00268-002-6630-z. Epub 2002 May 21.
We have evaluated survival and tumor-related symptoms in the presence of mesenteric lymph node and liver metastases in relation to surgical procedures in 314 patients (148 women, mean age at diagnosis 61 years; 249 with liver metastases) treated for midgut carcinoid tumors. Of the operated patients, 46% presented with severe abdominal pain and intestinal obstruction and were operated on before the diagnosis. Medical treatment (somatostatin analogs, interferon-a) was initiated in 67% and 86%, respectively. Surgical attempts included small intestine or ileocecal/right-sided colon resection with excision of mesenteric lymph node metastases. Most of the patients (n = 286) had mesenteric lymph node metastases; 33% of them had unresectable mesenteric lymph node metastases and underwent surgery without mesenteric dissection. Patients who underwent resection for the primary tumor had a longer survival than those with no resection (median survival 7.4 vs. 4.0 years; p <0.01). Patients who underwent successful excision of mesenteric metastases had a significantly longer survival than those with remaining lymph node metastases. Patients operated on for a primary tumor but with remaining lymph nodes but no liver metastases and who subsequently received interferon and somatostatin analog treatment had a median survival of 7.4 years. Resection of the primary tumor and the mesenteric lymph node metastases led to a significant reduction in tumor-related symptoms. Surgery to remove the primary intestinal tumor including mesenteric lymph node metastases is supported by the present results, even in the presence of liver metastases. Liver metastases and significant preoperative weight loss are identified as major negative prognostic factors for survival.
我们评估了314例接受中肠类癌肿瘤治疗的患者(148名女性,诊断时平均年龄61岁;249例有肝转移)在存在肠系膜淋巴结和肝转移情况下的生存率及肿瘤相关症状,这些症状与手术方式相关。在接受手术的患者中,46%出现严重腹痛和肠梗阻,且在诊断前就接受了手术。分别有67%和86%的患者开始接受药物治疗(生长抑素类似物、干扰素-α)。手术尝试包括小肠或回盲部/右侧结肠切除并切除肠系膜淋巴结转移灶。大多数患者(n = 286)有肠系膜淋巴结转移;其中33%有无法切除的肠系膜淋巴结转移,未进行肠系膜清扫就接受了手术。接受原发性肿瘤切除的患者比未切除的患者生存期更长(中位生存期7.4年对4.0年;p<0.01)。成功切除肠系膜转移灶的患者比仍有淋巴结转移的患者生存期显著更长。因原发性肿瘤接受手术但仍有淋巴结且无肝转移,随后接受干扰素和生长抑素类似物治疗的患者中位生存期为7.4年。原发性肿瘤和肠系膜淋巴结转移灶的切除导致肿瘤相关症状显著减轻。即使存在肝转移,目前的结果也支持手术切除包括肠系膜淋巴结转移灶的原发性肠道肿瘤。肝转移和术前显著体重减轻被确定为生存的主要负面预后因素。