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Efficacy and Safety of 177 Lu-DOTATATE in Lung Neuroendocrine Tumors: A Bicenter study.
- Source :
-
Journal of nuclear medicine : official publication, Society of Nuclear Medicine [J Nucl Med] 2022 Feb; Vol. 63 (2), pp. 218-225. Date of Electronic Publication: 2021 May 28. - Publication Year :
- 2022
-
Abstract
- The purpose of this study was to assess the efficacy and safety of <superscript>177</superscript> Lu-DOTATATE in patients with somatostatin receptor (SSR)-positive lung neuroendocrine tumors (NETs). Methods: This is a retrospective review of the outcome of patients with typical carcinoid (TC) and atypical carcinoid (AC), treated with <superscript>177</superscript> Lu-DOTATATE at 2 ENETS Centers of Excellence. Morphologic imaging (RECIST 1.1) and <superscript>68</superscript> Ga-DOTATATE PET/CT responses were assessed at 3 mo after completion of <superscript>177</superscript> 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. Results: 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 <superscript>68</superscript> Ga-DOTATATE PET/CT. Patients received a median 4 (range, 1-4) cycles of <superscript>177</superscript> 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 <superscript>68</superscript> 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 <superscript>68</superscript> 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 <superscript>68</superscript> 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), P < 0.001. Most grade 3/4 AEs were reversible and the most common was lymphopenia (14%) with no incidence of myelodysplasia or leukemia. Conclusion: In patients with advanced progressive lung NET and satisfactory SSR expression, <superscript>177</superscript> Lu-DOTATATE is effective and safe with a high disease control rate and encouraging PFS and OS.<br /> (© 2022 by the Society of Nuclear Medicine and Molecular Imaging.)
- Subjects :
- Adult
Aged
Aged, 80 and over
Female
Humans
Lung Neoplasms diagnostic imaging
Lung Neoplasms mortality
Male
Middle Aged
Neuroendocrine Tumors diagnostic imaging
Neuroendocrine Tumors mortality
Octreotide adverse effects
Octreotide therapeutic use
Organometallic Compounds adverse effects
Positron Emission Tomography Computed Tomography
Retrospective Studies
Lung Neoplasms radiotherapy
Neuroendocrine Tumors radiotherapy
Octreotide analogs & derivatives
Organometallic Compounds therapeutic use
Radiopharmaceuticals therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1535-5667
- Volume :
- 63
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of nuclear medicine : official publication, Society of Nuclear Medicine
- Publication Type :
- Academic Journal
- Accession number :
- 34049983
- Full Text :
- https://doi.org/10.2967/jnumed.120.260760