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Efficacy and Safety of <sup>177</sup>Lu-DOTATATE in Lung Neuroendocrine Tumors: A Bicenter study

Lamiaa Zidan, Amir Iravani, Kira Oleinikov, Simona Ben‐Haim, David J. Gross, Amichay Meirovitz, Ophra Maimon, Tim Akhurst, Michael Michael, Rodney J. Hicks, Simona Grozinsky‐Glasberg, Grace Kong

2021Journal of Nuclear Medicine50 citationsDOIOpen Access PDF

Abstract

To assess the efficacy and safety of <sup>177</sup>Lu-DOTATATE in patients with somatostatin receptor (SSR) positive lung neuroendocrine tumor (NET). <b>Methods:</b> This is a retrospective review of the outcome of patients with typical carcinoid (TC) and atypical carcinoid (AC), treated with <sup>177</sup>Lu-DOTATATE at two ENETS Centres of Excellence. Morphological imaging (RECIST 1.1) and <sup>68</sup>Ga-DOTATATE PET/CT responses were assessed at 3 months after completion of <sup>177</sup>Lu-DOTATATE. Concordance between two response assessment methods was evaluated by Kappa statistics. Progression-free survival (PFS) and overall survival (OS) was estimated by Kaplan-Meier analysis and compared by Log-rank test. Treatment-related adverse events (AEs) were graded based on CTCAE version 5. <b>Results:</b> Of 48 patients (median age, 63 years, 13 female), 43 (90%) had AC and 5 (10%) TC. Almost all patients (47, 98%) were treated due to progression. Majority (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 pre-treatment <sup>68</sup>Ga-DOTATATE PET/CT. Patients received a median 4 (range 1-4) cycles of <sup>177</sup>Lu-DOTATATE (33% with concurrent radiosensitizing chemotherapy) to a median cumulative activity of 27GBq (range 6-43GBq). At median follow-up of 42 months, the median PFS and OS were 23 months (95% CI 18-28 months) and 59 months (95% CI 50-not reached [NR]), respectively. Of 40 patients with RECIST-measurable disease and 39 patients with available <sup>68</sup>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 <sup>68</sup>Ga-DOTATATE PET/CT, weighted Kappa of 0.51 (95% CI 0.21-0.68). Of patients with stable disease by RECIST, those with partial response on <sup>68</sup>Ga-DOTATATE PET/CT had longer OS compared to those with no response, NR vs 52 months (95% CI 28-64), HR 0.2 (95% CI 0.1-0.6), p 0.001. Most grade 3/4 AEs were reversible and the most common was lymphopenia (14%) with no incidence of myelodysplasia/leukemia. <b>Conclusion:</b> In patients with advanced progressive lung NET and satisfactory SSR expression, <sup>177</sup>Lu-DOTATATE is effective and safe with a high disease control rate and encouraging PFS and OS.

Topics & Concepts

MedicineCommon Terminology Criteria for Adverse EventsNeuroendocrine tumorsResponse Evaluation Criteria in Solid TumorsInternal medicineAdverse effectSomatostatin receptorConcordanceRetrospective cohort studyNuclear medicineGastroenterologySomatostatinChemotherapyProgressive diseaseNeuroendocrine Tumor Research AdvancesLung Cancer Research StudiesNeuroblastoma Research and Treatments
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