TY - JOUR
T1 - Intraarterial Administration of Peptide Receptor Radionuclide Therapy in Patients with Advanced Meningioma
T2 - Initial Safety and Efficacy
AU - Amerein, Adriana
AU - Maurer, Christoph
AU - Kircher, Malte
AU - Gäble, Alexander
AU - Krebold, Anne
AU - Rinscheid, Andreas
AU - Viering, Oliver
AU - Pfob, Christian H.
AU - Bundschuh, Ralph A.
AU - Behrens, Lars
AU - Braat, Arthur J.A.T.
AU - Berlis, Ansgar
AU - Lapa, Constantin
N1 - Publisher Copyright:
© 2024 by the Society of Nuclear Medicine and Molecular Imaging.
PY - 2024/12/1
Y1 - 2024/12/1
N2 - Peptide receptor radionuclide therapy (PRRT) is a treatment option for patients with advanced meningioma. Recently, intraarterial application of the radiolabeled somatostatin receptor agonists has been introduced as an alternative to standard intravenous administration. In this study, we assessed the safety and efficacy of intraarterial PRRT in patients with advanced, progressive meningioma. Methods: Patients with advanced, progressive meningioma underwent intraarterial PRRT with [177Lu]Lu-HA-DOTATATE. The safety of PRRT was evaluated according to the Common Terminology Criteria for Adverse Events version 5.0. Treatment response was assessed according to the proposed Response Assessment in Neuro-Oncology criteria for meningiomas and somatostatin receptor–directed PET/CT. Results: Thirteen patients (8 women, 5 men; mean age, 65 6 13 y) with advanced meningioma underwent 1–4 cycles (median, 4 cycles) of intraarterial PRRT with [177Lu]Lu-HA-DOTATATE (mean activity per cycle, 7,428 6 237 MBq; range, 6,000–7,700 MBq). Treatment was well tolerated with mainly grade 1–2 hematologic toxicity. Ten of 13 patients showed radiologic disease control at follow-up after therapy (1/10 complete remission, 1/10 partial remission, 8/10 stable disease), and 9 of 13 patients showed good control of clinical symptoms. Conclusion: Intraarterial PRRT in patients with advanced meningioma is feasible and safe. It may result in improved radiologic and clinical disease control compared with intravenous PRRT. Further research to validate these initial findings and to investigate long-term outcomes is highly warranted.
AB - Peptide receptor radionuclide therapy (PRRT) is a treatment option for patients with advanced meningioma. Recently, intraarterial application of the radiolabeled somatostatin receptor agonists has been introduced as an alternative to standard intravenous administration. In this study, we assessed the safety and efficacy of intraarterial PRRT in patients with advanced, progressive meningioma. Methods: Patients with advanced, progressive meningioma underwent intraarterial PRRT with [177Lu]Lu-HA-DOTATATE. The safety of PRRT was evaluated according to the Common Terminology Criteria for Adverse Events version 5.0. Treatment response was assessed according to the proposed Response Assessment in Neuro-Oncology criteria for meningiomas and somatostatin receptor–directed PET/CT. Results: Thirteen patients (8 women, 5 men; mean age, 65 6 13 y) with advanced meningioma underwent 1–4 cycles (median, 4 cycles) of intraarterial PRRT with [177Lu]Lu-HA-DOTATATE (mean activity per cycle, 7,428 6 237 MBq; range, 6,000–7,700 MBq). Treatment was well tolerated with mainly grade 1–2 hematologic toxicity. Ten of 13 patients showed radiologic disease control at follow-up after therapy (1/10 complete remission, 1/10 partial remission, 8/10 stable disease), and 9 of 13 patients showed good control of clinical symptoms. Conclusion: Intraarterial PRRT in patients with advanced meningioma is feasible and safe. It may result in improved radiologic and clinical disease control compared with intravenous PRRT. Further research to validate these initial findings and to investigate long-term outcomes is highly warranted.
KW - meningioma
KW - peptide receptor radionuclide therapy
KW - PRRT
KW - somatostatin receptor
KW - theranostics
UR - http://www.scopus.com/inward/record.url?scp=85211360070&partnerID=8YFLogxK
U2 - 10.2967/jnumed.124.268217
DO - 10.2967/jnumed.124.268217
M3 - Article
C2 - 39448269
AN - SCOPUS:85211360070
SN - 0161-5505
VL - 65
SP - 1911
EP - 1916
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 12
ER -