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131I-间碘苄胍在转移性中肠类癌肿瘤治疗中的应用

131I-meta-iodobenzylguanidine in the management of metastatic midgut carcinoid tumors.

作者信息

Sywak Mark S, Pasieka Janice L, McEwan Alexander, Kline Greg, Rorstad Otto

机构信息

Royal North Shore Hospital, St Leonards, New South Wales, Australia.

出版信息

World J Surg. 2004 Nov;28(11):1157-62. doi: 10.1007/s00268-004-7603-1.

Abstract

The management of metastatic neuroendocrine tumors incorporates multimodal therapy with surgery, biotherapy, and chemotherapy. Tumor-targeted therapies using radiolabeled octreotide and metaiodobenzylguanidine (mIBG) represent a novel treatment approach. The aim of this study was to evaluate the effectiveness of 131I-mIBG in the treatment of metastatic midgut carcinoid tumors. survival outcomes were assessed for patients treated at two regional cancer centers and then compared. One center used 131I-mIBG routinely in the management of metastatic carcinoid tumors (center A), and the other did not use this modality (center B). Only patients with histologically proven metastatic carcinoid tumor shown, or thought most likely, to be of midgut origin were included in the study. During the period 1980 to 2002, a series of 58 patients from center A with metastatic carcinoid tumor arising from the midgut underwent multimodality therapy with the addition of 131I-mIBG. Their median age was 64 years. The median dose of 131I-mIBG administered was 6751 MBq, and there was an average of 2.8 treatments per patient. During the same period, 58 patients with metastatic carcinoid were treated at center B with similar multimodality therapy without the use of 131I-mIBG therapy. Their median age was 65 years. Survivals at 3 and 5 years were 77% and 63%, respectively (95% CI 47-75), for group A. The 3- and 5-year survivals for group B were 56% and 47% (95% CI 34-59), respectively. The mean follow-up was 6.6 years for group A and 5.0 years for group B. Although retrospective in nature, this study suggests that the addition of 131I-mIBG therapy to the treatment protocol of patients with metastatic midgut carcinoid tumors prolongs survival.

摘要

转移性神经内分泌肿瘤的治疗采用手术、生物治疗和化疗的多模式疗法。使用放射性标记的奥曲肽和间碘苄胍(mIBG)的肿瘤靶向治疗是一种新的治疗方法。本研究的目的是评估131I-mIBG治疗转移性中肠类癌肿瘤的有效性。对在两个地区癌症中心接受治疗的患者的生存结果进行评估,然后进行比较。一个中心在转移性类癌肿瘤的管理中常规使用131I-mIBG(A中心),另一个中心不使用这种方法(B中心)。只有组织学证实为转移性类癌肿瘤且显示或被认为最可能起源于中肠的患者才被纳入研究。在1980年至2002年期间,A中心的一系列58例源于中肠的转移性类癌肿瘤患者接受了多模式治疗,并加用了131I-mIBG。他们的中位年龄为64岁。给予的131I-mIBG的中位剂量为6751 MBq,每位患者平均接受2.8次治疗。在同一时期,B中心的58例转移性类癌患者接受了类似的多模式治疗,但未使用131I-mIBG治疗。他们的中位年龄为65岁。A组3年和5年生存率分别为77%和63%(95%CI 47-75)。B组3年和5年生存率分别为56%和47%(95%CI 34-59)。A组的平均随访时间为6.6年,B组为5.0年。尽管本研究本质上是回顾性的,但它表明在转移性中肠类癌肿瘤患者的治疗方案中添加I-mIBG治疗可延长生存期。

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