Clinical Pharmacokinetics of Radiopharmaceuticals from SPECT/CT Image Acquisition by Contouring in Patients with Gastroenteropancreatic Neuroendocrine Tumors: Lu-177 DOTATATE (Lutathera


Journal

European journal of drug metabolism and pharmacokinetics
ISSN: 2107-0180
Titre abrégé: Eur J Drug Metab Pharmacokinet
Pays: France
ID NLM: 7608491

Informations de publication

Date de publication:
Jul 2023
Historique:
accepted: 19 04 2023
medline: 7 7 2023
pubmed: 15 5 2023
entrez: 15 5 2023
Statut: ppublish

Résumé

Lu-177 DOTATATE (Lutathera From a retrospective study, SPECT/CT images were acquired at 4 h, 24 h, 72 h, and 192 h postadministration. From these images, volumic activities were calculated in blood and bone marrow. An individual non-compartmental pharmacokinetic analysis was performed, and the mean pharmacokinetic parameters of each tissue were compared together and with reference data. Blood volumic activities were then used to perform a population pharmacokinetic analysis (NONMEM). The pharmacokinetic parameters (non-compartmental analysis) obtained from blood (clearance [CL] = 2.65 L/h, volume of distribution at steady state [Vss] = 309 L, elimination half-life [t This study is a proof of concept that obtaining pharmacokinetic parameters with image-based blood concentration is possible. Obtaining observed concentrations from SPECT/CT images, without the need for blood sampling, is a real advantage for the patient and the drug monitoring. Pharmacokinetic modeling could be combined with a deep learning model for automatic contouring and allow precise patient-specific dose adjustment in a non-invasive manner.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
Lu-177 DOTATATE (Lutathera
METHODS METHODS
From a retrospective study, SPECT/CT images were acquired at 4 h, 24 h, 72 h, and 192 h postadministration. From these images, volumic activities were calculated in blood and bone marrow. An individual non-compartmental pharmacokinetic analysis was performed, and the mean pharmacokinetic parameters of each tissue were compared together and with reference data. Blood volumic activities were then used to perform a population pharmacokinetic analysis (NONMEM).
RESULTS RESULTS
The pharmacokinetic parameters (non-compartmental analysis) obtained from blood (clearance [CL] = 2.65 L/h, volume of distribution at steady state [Vss] = 309 L, elimination half-life [t
CONCLUSION CONCLUSIONS
This study is a proof of concept that obtaining pharmacokinetic parameters with image-based blood concentration is possible. Obtaining observed concentrations from SPECT/CT images, without the need for blood sampling, is a real advantage for the patient and the drug monitoring. Pharmacokinetic modeling could be combined with a deep learning model for automatic contouring and allow precise patient-specific dose adjustment in a non-invasive manner.

Identifiants

pubmed: 37184824
doi: 10.1007/s13318-023-00829-5
pii: 10.1007/s13318-023-00829-5
doi:

Substances chimiques

lutetium Lu 177 dotatate AE221IM3BB
copper dotatate CU-64 0
Lutetium-177 BRH40Y9V1Q
Radioisotopes 0
Radiopharmaceuticals 0
Lutetium 5H0DOZ21UJ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

329-339

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Références

Hennrich U, Kopka K. Lutathera®: The First FDA- and EMA-Approved Radiopharmaceutical for Peptide Receptor Radionuclide Therapy. Pharmaceuticals. Multidisciplinary Digital Publishing Institute; 2019;12:114.
Pouget J-P, Santoro L, Piron B, Paillas S, Ladjohounlou R, Pichard A, et al. From the target cell theory to a more integrated view of radiobiology in targeted radionuclide therapy: The Montpellier group’s experience. Nucl Med Biol. 2021;104–105.
Gupta SK, Singla S, Thakral P, Bal CS. Dosimetric analyses of kidneys, liver, spleen, pituitary gland, and neuroendocrine tumors of patients treated with 177Lu-DOTATATE. Clin Nucl Med. 2013;38:188–94.
doi: 10.1097/RLU.0b013e3182814ac1 pubmed: 23412597
Bodei L, Cremonesi M, Grana CM, Fazio N, Iodice S, Baio SM, et al. Peptide receptor radionuclide therapy with 177Lu-DOTATATE: the IEO phase I-II study. Eur J Nucl Med Mol Imaging. 2011;38(12):2125–35.
doi: 10.1007/s00259-011-1902-1 pubmed: 21892623
Sabet A, Ezziddin K, Pape U-F, Ahmadzadehfar H, Mayer K, Pöppel T, et al. Long-term hematotoxicity after peptide receptor radionuclide therapy with 177Lu-octreotate. J Nucl Med. 2013;54:1857–61.
doi: 10.2967/jnumed.112.119347 pubmed: 24009272
Del Prete M, Buteau F-A, Arsenault F, Saighi N, Bouchard L-O, Beaulieu A, et al. Personalized 177Lu-octreotate peptide receptor radionuclide therapy of neuroendocrine tumours: initial results from the P-PRRT trial. Eur J Nucl Med Mol Imaging. 2019;46:728–42.
doi: 10.1007/s00259-018-4209-7 pubmed: 30506283
Sundlöv A, Gleisner KS, Tennvall J, Ljungberg M, Warfvinge CF, Holgersson K, et al. Phase II trial demonstrates the efficacy and safety of individualized, dosimetry-based 177Lu-DOTATATE treatment of NET patients. Eur J Nucl Med Mol Imaging. 2022;49:3830–40.
doi: 10.1007/s00259-022-05786-w pubmed: 35451612 pmcid: 9399027
Siebinga H, de Wit-van der Veen BJ, Stokkel MDM, Huitema ADR, Hendrikx JJMA. Current use and future potential of (physiologically based) pharmacokinetic modelling of radiopharmaceuticals: a review. Theranostics. Ivyspring International Publisher; 2022;12:7804–20.
Forrer F, Krenning EP, Kooij PP, Bernard BF, Konijnenberg M, Bakker WH, et al. Bone marrow dosimetry in peptide receptor radionuclide therapy with [177Lu-DOTA0, Tyr3]octreotate. Eur J Nucl Med Mol Imaging. 2009;36:1138–46.
doi: 10.1007/s00259-009-1072-6 pubmed: 19247653 pmcid: 2691529
Santoro L, Pitalot L, Trauchessec D, Mora-Ramirez E, Kotzki PO, Bardiès M, et al. Clinical implementation of PLANET® Dose for dosimetric assessment after [177Lu]Lu-DOTA-TATE: comparison with Dosimetry Toolkit® and OLINDA/EXM® V1.0. EJNMMI Res. 2021;11:1.
Shen S, Meredith RF, Duan J, Macey DJ, Khazaeli MB, Robert F, et al. Improved prediction of myelotoxicity using a patient-specific imaging dose estimate for non-marrow-targeting (90)Y-antibody therapy. J Nucl Med. 2002;43:1245–53.
pubmed: 12215566
PKanalix version 2021R2. Antony, France: Lixoft SAS, 2021. Available from: https://lixoft.com/products/pkanalix/ . Access date: 04/04/2022.
FDA, Highlights of prescribing information - LUTATHERA - 2018. https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/208700s000lbl.pdf . Access date: 04/02/2022.
Nolain P, Combet R, Marchionni D, Speth H, Martinez JM, Fabre D. PopkinR: a suite of Shiny applications focused on the pharmacometrics workflow. Poster presented to Population Approach Group Europe (PAGE) meeting. Switzerland, 2018. https://www.page-meeting.org/?abstract=8684 . Access date: 07/04/2023.
Lindbom L, Pihlgren P, Jonsson N. PsN-Toolkit—a collection of computer intensive statistical methods for non-linear mixed effect modeling using NONMEM. Comput Methods Programs Biomed. 2005;79:241–57.
doi: 10.1016/j.cmpb.2005.04.005 pubmed: 16023764
Lindbom L, Ribbing J, Jonsson EN. Perl-speaks-NONMEM (PsN): a Perl module for NONMEM related programming. Comput Methods Programs Biomed. 2004;75:85–94.
doi: 10.1016/j.cmpb.2003.11.003 pubmed: 15212851
Hagmarker L, Svensson J, Rydén T, van Essen M, Sundlöv A, Gleisner KS, et al. Bone marrow absorbed doses and correlations with hematologic response during 177Lu-DOTATATE treatments are influenced by image-based dosimetry method and presence of skeletal metastases. J Nucl Med. 2019;60:1406–13.
doi: 10.2967/jnumed.118.225235 pubmed: 30902877 pmcid: 6785794
Puszkiel A, Bauriaud-Mallet M, Bourgeois R, Dierickx L, Courbon F, Chatelut E. Evaluation of the interaction of amino acid infusion on 177Lu-dotatate pharmacokinetics in patients with gastroenteropancreatic neuroendocrine tumors. Clin Pharmacokinet. 2019;58:213–22.
doi: 10.1007/s40262-018-0674-1 pubmed: 29736841
Jiménez-Franco LD, Glatting G, Prasad V, Weber WA, Beer AJ, Kletting P. Effect of tumor perfusion and receptor density on tumor control probability in 177Lu-DOTATATE therapy: an in silico analysis for standard and optimized treatment. J Nucl Med. 2021;62:92–8.
doi: 10.2967/jnumed.120.245068 pubmed: 32646878
Chan Kwong AH-XP, O'Jeanson A and Khier S. Model-informed therapeutic drug monitoring of meropenem in critically ill patients: improvement of the predictive ability of literature models with the PRIOR approach. Eur J Drug Metab Pharmacokinet. 2021 ;46(3):415-426.
Chan Kwong AH-XP, Calvier EAM, Fabre D, Gattacceca F, Khier S. Prior information for population pharmacokinetic and pharmacokinetic/pharmacodynamic analysis: overview and guidance with a focus on the NONMEM PRIOR subroutine. J Pharmacokinet Pharmacodyn. 2020;47:431–46.
Lutathera European public assessment report. https://www.ema.europa.eu/en/documents/assessment-report/lutathera-epar-public-assessment-report_en.pdf . Accessed on 02 July 2022.
Lubberink M, Wilking H, Öst A, Ilan E, Sandström M, Andersson C, et al. In vivo instability of 177 Lu-DOTATATE during peptide receptor radionuclide therapy. J Nucl Med. 2020;61(9):1337–40.
doi: 10.2967/jnumed.119.237818 pubmed: 32005767 pmcid: 7456166
Ljungberg M, Celler A, Konijnenberg MW, Eckerman KF, Dewaraja YK, Sjögreen-Gleisner K. MIRD Pamphlet No. 26: Joint EANM/MIRD Guidelines for Quantitative 177Lu SPECT applied for dosimetry of radiopharmaceutical therapy. J Nucl Med. 2016;57(1):151-62.

Auteurs

Anissa Barakat (A)

Pharmacokinetics and Pharmacometrics Department, School of Pharmacy, UFR Pharmacie, Montpellier University, 15 Avenue Charles Flahault, 34000, Montpellier, France.
Probabilities and Statistics Department, Institut Montpelliérain Alexander Grothendieck (IMAG), CNRS, UMR 5149, Inria, Montpellier University, Montpellier, France.
Nuclear Medicine Department, Montpellier Cancer Institute, Montpellier University, Montpellier, France.

Lore Santoro (L)

Nuclear Medicine Department, Montpellier Cancer Institute, Montpellier University, Montpellier, France.
Institut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Montpellier University, Montpellier, France.

Myrtille Vivien (M)

Biostatistics, Informatics and pharmaceutical physic Laboratory, School of Pharmacy, UFR Pharmacie, Montpellier University, 15 Av. Ch. Flahault, 34000, Montpellier, France.
Institute of Functional Genomic (IGF)- UMR 5203, INSERM U1191, Montpellier, France.

Pierre-Olivier Kotzki (PO)

Nuclear Medicine Department, Montpellier Cancer Institute, Montpellier University, Montpellier, France.
Institut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Montpellier University, Montpellier, France.

Emmanuel Deshayes (E)

Nuclear Medicine Department, Montpellier Cancer Institute, Montpellier University, Montpellier, France.
Institut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Montpellier University, Montpellier, France.

Sonia Khier (S)

Pharmacokinetics and Pharmacometrics Department, School of Pharmacy, UFR Pharmacie, Montpellier University, 15 Avenue Charles Flahault, 34000, Montpellier, France. sonia.khier@umontpellier.fr.
Probabilities and Statistics Department, Institut Montpelliérain Alexander Grothendieck (IMAG), CNRS, UMR 5149, Inria, Montpellier University, Montpellier, France. sonia.khier@umontpellier.fr.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH