Molecular Imaging and Therapeutic Nuclear Medicine, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Molecular Imaging and Therapeutic Nuclear Medicine, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia;
J Nucl Med. 2022 Feb;63(2):218-225. doi: 10.2967/jnumed.120.260760. Epub 2021 May 28.
The purpose of this study was to assess the efficacy and safety of Lu-DOTATATE in patients with somatostatin receptor (SSR)-positive lung neuroendocrine tumors (NETs). This is a retrospective review of the outcome of patients with typical carcinoid (TC) and atypical carcinoid (AC), treated with Lu-DOTATATE at 2 ENETS Centers of Excellence. Morphologic imaging (RECIST 1.1) and Ga-DOTATATE PET/CT responses were assessed at 3 mo after completion of Lu-DOTATATE. Concordance between 2 response assessment methods was evaluated by κ statistics. Progression-free survival (PFS) and overall survival (OS) were estimated by Kaplan-Meier analysis and compared by Log-rank test. Treatment-related adverse events (AEs) were graded based on Common Terminology Criteria for Adverse Events, version 5. Of 48 patients (median age, 63 y; 13 women), 43 (90%) had AC and 5 (10%) TC. Almost all patients (47, 98%) were treated due to progression. Most patients (40, 83%) received somatostatin analogs, and 10 patients (20%) had prior everolimus, chemotherapy, or both. All patients had high SSR expression (≥ modified Krenning score 3) on pretreatment Ga-DOTATATE PET/CT. Patients received a median 4 (range, 1-4) cycles of Lu-DOTATATE (33% with concurrent radiosensitizing chemotherapy) to a median cumulative activity of 27 GBq (range, 6-43GBq). At a median follow-up of 42 mo, the median PFS and OS were 23 mo (95% CI, 18-28 mo) and 59 mo (95% CI, 50-not reached [NR]), respectively. Of 40 patients with RECIST-measurable disease and 39 patients with available Ga-DOTATATE PET/CT, response categories were partial response, 20% (95% CI, 10%-35%) and 44% (95% CI, 30%-59%); stable disease, 68% (95% CI, 52%-80%) and 44% (95% CI, 30%-59%); and progressive disease, 12% (95% CI, 5%-27%) by both, respectively. There was a moderate concordance between response categories by RECIST and Ga-DOTATATE PET/CT, weighted κ of 0.51 (95% CI, 0.21-0.68). Of patients with stable disease by RECIST, those with partial response on Ga-DOTATATE PET/CT had a longer OS than those with no response, NR versus 52 mo (95% CI, 28-64), hazard ratio 0.2 (95% CI, 0.1-0.6), < 0.001. Most grade 3/4 AEs were reversible and the most common was lymphopenia (14%) with no incidence of myelodysplasia or leukemia. In patients with advanced progressive lung NET and satisfactory SSR expression, Lu-DOTATATE is effective and safe with a high disease control rate and encouraging PFS and OS.
本研究旨在评估 Lu-DOTATATE 在生长抑素受体(SSR)阳性肺神经内分泌肿瘤(NETs)患者中的疗效和安全性。这是对在 2 个欧洲神经内分泌肿瘤学会卓越中心接受 Lu-DOTATATE 治疗的典型类癌(TC)和非典型类癌(AC)患者的结局进行的回顾性分析。在完成 Lu-DOTATATE 治疗后 3 个月,通过 RECIST 1.1 进行形态学影像学评估和 Ga-DOTATATE PET/CT 反应评估。采用κ统计评估两种反应评估方法之间的一致性。采用 Kaplan-Meier 分析估计无进展生存期(PFS)和总生存期(OS),并采用 Log-rank 检验进行比较。根据常见不良事件术语标准,第五版(CTCAE v5)对治疗相关不良事件(AE)进行分级。48 例患者(中位年龄 63 岁;13 名女性)中,43 例(90%)为 AC,5 例(10%)为 TC。几乎所有患者(47 例,98%)均因疾病进展而接受治疗。大多数患者(40 例,83%)接受了生长抑素类似物治疗,10 例患者(20%)接受过依维莫司、化疗或两者联合治疗。所有患者在 Ga-DOTATATE PET/CT 预处理时均具有高 SSR 表达(≥改良 Krenning 评分 3)。患者接受了中位数为 4(范围 1-4)个周期的 Lu-DOTATATE(33%的患者同时接受放射增敏化疗),累积活度中位数为 27GBq(范围 6-43GBq)。中位随访 42 个月时,中位 PFS 和 OS 分别为 23 个月(95%CI,18-28 个月)和 59 个月(95%CI,50-NR)。在 40 例可测量疾病的患者和 39 例可进行 Ga-DOTATATE PET/CT 的患者中,RECIST 可测量疾病的反应类别为部分缓解(95%CI,10%-35%)和 44%(95%CI,30%-59%);稳定疾病(95%CI,52%-80%)和 44%(95%CI,30%-59%);疾病进展(95%CI,5%-27%),两者的加权 κ 值为 0.51(95%CI,0.21-0.68)。在 RECIST 评估为稳定疾病的患者中,Ga-DOTATATE PET/CT 评估为部分缓解的患者 OS 长于无反应的患者,NR 与 52 个月(95%CI,28-64)相比,危险比为 0.2(95%CI,0.1-0.6),P<0.001。大多数 3/4 级 AE 是可逆的,最常见的是淋巴细胞减少(14%),没有骨髓增生异常或白血病的发生。在晚期进展性肺 NET 且 SSR 表达满意的患者中,Lu-DOTATATE 治疗具有较高的疾病控制率,PFS 和 OS 令人鼓舞,且安全有效。