Eriksson B, Oberg K
Medical Department, University Hospital, Uppsala, Sweden.
Acta Oncol. 1993;32(2):203-8. doi: 10.3109/02841869309083913.
In the present study, we have updated our results with chemotherapy, alpha-interferon, octreotide and combinations of treatment modalities in patients with malignant endocrine pancreatic tumor (EPT). In our patient material of 134 EPT, 92 subjects had malignant tumors as evidenced by the presence of metastases or growth into adjacent organs. Seventy-eight patients had liver metastases. Streptozotocin plus 5-fluorouracil produced objective responses in 17/31 (54%) patients with a median duration of response of 23 months. The use of 5-HT3-antagonists as antiemetics has dramatically improved the quality of life during treatment by reducing the frequency of nausea to only 12.5%. The objective response rate to alpha-interferon (alpha-IFN) treatment, given as first-line treatment in 29 patients and after chemotherapy in 28 patients, was 51% (29/57) with a median duration of response of 20 months. Octreotide, which is still used as third-line treatment in most patients, produced significant biochemical responses in 6/19 (31%) patients with a median duration of 16 months. Combinations of alpha-IFN plus chemotherapy and a alpha-IFN plus octreotide in a small number of patients might indicate additive or synergistic effects. The median survival from start of treatment in the 92 malignant cases was 56.5 months, and for those with liver metastases (n = 78) at start of treatment 50 months. In conclusion, there are at least three effective therapies for malignant EPT and by combining them simultaneously or consecutively, a median survival of more than four years can be obtained.
在本研究中,我们更新了恶性内分泌胰腺肿瘤(EPT)患者接受化疗、α干扰素、奥曲肽及联合治疗方式的结果。在我们134例EPT患者资料中,92例有转移或侵犯邻近器官证据的患者患有恶性肿瘤。78例患者有肝转移。链脲佐菌素加5-氟尿嘧啶使17/31(54%)的患者产生客观缓解,缓解持续时间中位数为23个月。使用5-HT3拮抗剂作为止吐药,通过将恶心频率降至仅12.5%,显著改善了治疗期间的生活质量。在29例患者中作为一线治疗以及在28例患者中化疗后使用α干扰素(α-IFN)治疗,客观缓解率为51%(29/57),缓解持续时间中位数为20个月。奥曲肽在大多数患者中仍用作三线治疗,使6/19(31%)的患者产生显著的生化缓解,持续时间中位数为16个月。少数患者中α-IFN加化疗以及α-IFN加奥曲肽的联合治疗可能显示出相加或协同作用。92例恶性病例从开始治疗起的中位生存期为56.5个月,治疗开始时伴有肝转移(n = 78)的患者中位生存期为50个月。总之,对于恶性EPT至少有三种有效疗法,通过同时或连续联合使用这些疗法,可获得超过四年的中位生存期。