van Essen Martijn, Krenning Eric P, Bakker Willem H, de Herder Wouter W, van Aken Maarten O, Kwekkeboom Dik J
Department of Nuclear Medicine, Erasmus MC, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands.
Eur J Nucl Med Mol Imaging. 2007 Aug;34(8):1219-27. doi: 10.1007/s00259-006-0355-4. Epub 2007 Jan 27.
Foregut carcinoid tumours have a different embryological origin than other gastroenteropancreatic neuroendocrine tumours (GEP NETs). In the total group of GEP NETs (n = 131), treatment with (177)Lu-octreotate resulted in tumour remission in 47% of patients, with a median time to progression (TTP) of >36 months. As patients with foregut carcinoids may respond differently, we here present the effects of this treatment in a subgroup of patients with foregut carcinoids of bronchial, gastric or thymic origin.
Nine patients with bronchial, five with gastric and two with thymic carcinoids were treated. All patients had metastasised disease. The intended cumulative dose of (177)Lu-octreotate was 22.2-29.6 GBq. Southwest Oncology Group criteria were used for response evaluation.
Bronchial carcinoids: Five patients had partial remission, one had minor response (MR, tumour size reduction: > or =25%, <50%), two had stable disease (SD) and one had progressive disease (PD). Median TTP was 31 months. Gastric carcinoids: One patient had complete remission, one had MR and two had SD, including one with PD at baseline. One patient developed PD. Thymic carcinoids: One patient had SD. In the other patient, disease remained progressive. All patients: Overall remission rate was 50%, including MR.
(177)Lu-octreotate treatment can be effective in patients with bronchial and gastric carcinoids. Its role in thymic carcinoids cannot be determined yet because of the limited number of patients. The overall remission rate of 50% in patients with the studied foregut carcinoids is comparable to that in the total group of GEP NETs.
前肠类癌瘤与其他胃肠胰神经内分泌肿瘤(GEP NETs)有着不同的胚胎学起源。在GEP NETs的总体队列(n = 131)中,使用(177)镥奥曲肽治疗可使47%的患者出现肿瘤缓解,中位疾病进展时间(TTP)>36个月。由于前肠类癌患者的反应可能不同,我们在此展示该治疗方法对一组支气管、胃或胸腺来源的前肠类癌患者的疗效。
对9例支气管类癌、5例胃类癌和2例胸腺类癌患者进行了治疗。所有患者均有转移性疾病。(177)镥奥曲肽的预期累积剂量为22.2 - 29.6 GBq。采用西南肿瘤协作组标准进行疗效评估。
支气管类癌:5例患者部分缓解,1例轻度反应(MR,肿瘤大小缩小:≥25%,<50%),2例疾病稳定(SD),1例疾病进展(PD)。中位TTP为31个月。胃类癌:1例患者完全缓解,1例MR,2例SD,其中1例基线时为PD。1例患者发生PD。胸腺类癌:1例患者SD。另一例患者疾病持续进展。所有患者:总体缓解率为50%,包括MR。
(177)镥奥曲肽治疗对支气管和胃类癌患者可能有效。由于患者数量有限,其在胸腺类癌中的作用尚无法确定。所研究的前肠类癌患者总体缓解率为50%,与GEP NETs总体队列中的缓解率相当。