Lim Lisi Elizabeth, Chan David L, Thomas David, Du Yang, Tincknell Gary, Kuchel Anna, Davis Alexander, Bailey Dale L, Pavlakis Nick, Cehic Gabrielle, Macdonald William, Wyld David, Segelov Eva
Department of Medical Oncology, Monash Health, Melbourne, Australia.
Department of Medical Oncology, Royal North Shore Hospital, Sydney, Australia.
Oncotarget. 2020 Jul 7;11(27):2636-2646. doi: 10.18632/oncotarget.27659.
Peptide receptor radionuclide therapy (PRRT) is an approved treatment modality for gastroenteropancreatic neuroendocrine tumours (GEP NETs), Although Phase III randomised clinical trial data is not available for NETs of other site of origin, in practice, PRRT is used more widely in clinical practice, based on its mechanism of targeting the somatostatin receptor. Use of PRRT for lung (bronchial) NET, specifically typical and atypical carcinoid (TC, AC), has been reported only in small retrospective case series. This multicentre study adds to the evidence regarding utility of PRRT for lung NETs.
A retrospective chart review of patients with TC and AC who received Lu-dotatate PRRT between January 2002 and June 2019 in six hospitals across Australia was undertaken. Data regarding demographics, efficacy and toxicity was evaluated at each site by the treating clinician.
Forty-eight patients (32 AC, 15 TC, 1 unclassified) received a median of four Lu-dotatate treatments. There was a median of one prior line of systemic treatment (range: 0-3). The response rate to Lu-dotatate was 33%, with a median overall survival of 49 months (range of 3-91), at a median follow up of 33 months. This compares favourably with GEP NET. Overall toxicity was recorded as modest.
Lu-dotatate PRRT in patients with lung NETs is used in real world practice, where it appears well-tolerated with some efficacy. Further evidence could be obtained through a global prospective clinical or registry trial.
肽受体放射性核素治疗(PRRT)是一种已获批准用于胃肠胰腺神经内分泌肿瘤(GEP NETs)的治疗方式。尽管目前尚无针对其他原发部位神经内分泌肿瘤的III期随机临床试验数据,但在实际应用中,基于其靶向生长抑素受体的机制,PRRT在临床实践中的应用更为广泛。关于PRRT用于肺(支气管)神经内分泌肿瘤,特别是典型和非典型类癌(TC,AC)的报道仅见于小型回顾性病例系列。这项多中心研究补充了有关PRRT用于肺神经内分泌肿瘤效用的证据。
对2002年1月至2019年6月期间在澳大利亚六家医院接受镥[177Lu]奥曲肽PRRT治疗的TC和AC患者进行回顾性病历审查。各治疗中心的临床医生对患者的人口统计学、疗效和毒性数据进行评估。
48例患者(32例AC,15例TC,1例未分类)接受了中位数为4次的镥[177Lu]奥曲肽治疗。既往全身治疗的中位数为1线(范围:0 - 3线)。镥[177Lu]奥曲肽的缓解率为33%,中位总生存期为49个月(范围3 - 91个月),中位随访时间为33个月。这与GEP NET相比具有优势。总体毒性记录为轻度。
镥[177Lu]奥曲肽PRRT在肺神经内分泌肿瘤患者的实际临床应用中显示出较好的耐受性和一定疗效。可通过全球前瞻性临床或注册试验获得更多证据。