The joint IAEA, EANM, and SNMMI practical guidance on peptide receptor radionuclide therapy (PRRNT) in neuroendocrine tumours

被引:605
作者
Zaknun, John J. [2 ,3 ]
Bodei, L. [1 ]
Mueller-Brand, J. [4 ]
Pavel, M. E. [5 ]
Baum, R. P. [6 ]
Hoersch, D. [6 ]
O'Dorisio, M. S. [7 ]
O'Dorisiol, T. M. [8 ]
Howe, J. R. [9 ]
Cremonesi, M. [10 ]
Kwekkeboom, D. J. [11 ]
机构
[1] European Inst Oncol, Div Nucl Med, Milan, Italy
[2] IAEA, Div Human Hlth, Nucl Med Sect, A-1400 Vienna, Austria
[3] ENETS Ctr Excellence, Ctr Mol Radiotherapy & Mol Imaging, Zent Klin Bad Berka, Bad Berka, Germany
[4] Univ Basel, Klin & Inst Nukl Med, Basel, Switzerland
[5] Charite, Campus Virchow Klinikum, Klin Gastroenterol Hepatol Endokrinol Diabet & St, D-13353 Berlin, Germany
[6] ENETS Ctr Excellence, Dept Internal Med Gastroenterol & Endocrinol, Zent Klin Bad Berka, Bad Berka, Germany
[7] Univ Iowa, Dept Pediat, RJ & LA Carver Coll Med, Iowa City, IA 52242 USA
[8] Univ Iowa, Dept Internal Med, RJ & LA Carver Coll Med, Iowa City, IA 52242 USA
[9] Univ Iowa, Dept Surg Oncol, RJ & LA Carver Coll Med, Iowa City, IA USA
[10] European Inst Oncol, Serv Hlth Phys, Milan, Italy
[11] Erasmus MC, Dept Nucl Med, Rotterdam, Netherlands
关键词
Peptide receptor radionuclide therapy; PRRNT; neuroendocrine tumours; guideline/s; renal protection; RADIOLABELED SOMATOSTATIN ANALOG; ENETS CONSENSUS GUIDELINES; PHASE-II; SURVIVAL BENEFIT; LIVER METASTASES; NUCLEAR-MEDICINE; CARCINOID-TUMORS; THYROID-CANCER; FOLLOW-UP; DOSIMETRY;
D O I
10.1007/s00259-012-2330-6
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
100231 [临床病理学]; 100902 [航空航天医学];
摘要
Peptide receptor radionuclide therapy (PRRNT) is a molecularly targeted radiation therapy involving the systemic administration of a radiolabelled peptide designed to target with high affinity and specificity receptors overexpressed on tumours. PRRNT employing the radiotagged somatostatin receptor agonists Y-90-DOTATOC ([Y-90-DOTA(0),Tyr(3)]-octreotide) or Lu-177-DOTATATE ([Lu-177-DOTA(0),Tyr(3),Thr(8)]-octreotide or [Lu-177-DOTA(0),Tyr(3)]-octreotate) have been successfully used for the past 15 years to target metastatic or inoperable neuroendocrine tumours expressing the somatostatin receptor subtype 2. Accumulated evidence from clinical experience indicates that these tumours can be subjected to a high absorbed dose which leads to partial or complete objective responses in up to 30 % of treated patients. Survival analyses indicate that patients presenting with high tumour receptor expression at study entry and receiving Lu-177-DOTATATE or Y-90-DOTATOC treatment show significantly higher objective responses, leading to longer survival and improved quality of life. Side effects of PRRNT are typically seen in the kidneys and bone marrow. These, however, are usually mild provided adequate protective measures are undertaken. Despite the large body of evidence regarding efficacy and clinical safety, PRRNT is still considered an investigational treatment and its implementation must comply with national legislation, and ethical guidelines concerning human therapeutic investigations. This guidance was formulated based on recent literature and leading experts' opinions. It covers the rationale, indications and contraindications for PRRNT, assessment of treatment response and patient follow-up. This document is aimed at guiding nuclear medicine specialists in selecting likely candidates to receive PRRNT and to deliver the treatment in a safe and effective manner. This document is largely based on the book published through a joint international effort under the auspices of the Nuclear Medicine Section of the International Atomic Energy Agency.
引用
收藏
页码:800 / 816
页数:17
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