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The impact of (177)Lu-octreotide therapy on (99m)Tc-MAG3 clearance is not predictive for late nephropathy

Peptide Receptor Radionuclide Therapy (PRRT) for the treatment of neuroendocrine tumors may lead to kidney deterioration. This study aimed to evaluate the suitability of (99m)Tc-mercaptoacetyltriglycine ((99m)Tc­-MAG3) clearance for the early detection of PRRT-induced changes on tubular extraction (...

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Autores principales: Werner, Rudolf A., Beykan, Seval, Higuchi, Takahiro, Lückerath, Katharina, Weich, Alexander, Scheurlen, Michael, Bluemel, Christina, Herrmann, Ken, Buck, Andreas K., Lassmann, Michael, Lapa, Constantin, Hänscheid, Heribert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173054/
https://www.ncbi.nlm.nih.gov/pubmed/27259246
http://dx.doi.org/10.18632/oncotarget.9775
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author Werner, Rudolf A.
Beykan, Seval
Higuchi, Takahiro
Lückerath, Katharina
Weich, Alexander
Scheurlen, Michael
Bluemel, Christina
Herrmann, Ken
Buck, Andreas K.
Lassmann, Michael
Lapa, Constantin
Hänscheid, Heribert
author_facet Werner, Rudolf A.
Beykan, Seval
Higuchi, Takahiro
Lückerath, Katharina
Weich, Alexander
Scheurlen, Michael
Bluemel, Christina
Herrmann, Ken
Buck, Andreas K.
Lassmann, Michael
Lapa, Constantin
Hänscheid, Heribert
author_sort Werner, Rudolf A.
collection PubMed
description Peptide Receptor Radionuclide Therapy (PRRT) for the treatment of neuroendocrine tumors may lead to kidney deterioration. This study aimed to evaluate the suitability of (99m)Tc-mercaptoacetyltriglycine ((99m)Tc­-MAG3) clearance for the early detection of PRRT-induced changes on tubular extraction (TE). TE rate (TER) was measured prior to 128 PRRT cycles (7.6±0.4 GBq (177)Lu-octreotate/octreotide each) in 32 patients. TER reduction during PRRT was corrected for age-related decrease and analyzed for the potential to predict loss of glomerular filtration (GF). The GF rate (GFR) as measure for renal function was derived from serum creatinine. The mean TER was 234 ± 53 ml/min/1.73 m(2) before PRRT (baseline) and 221 ± 45 ml/min/1.73 m(2) after a median follow-up of 370 days. The age-corrected decrease (mean: −3%, range: −27% to +19%) did not reach significance (p=0.09) but significantly correlated with the baseline TER (Spearman p=−0.62, p<0.001). Patients with low baseline TER showed an improved TER after PRRT, high decreases were only observed in individuals with high baseline TER. Pre-therapeutic TER data were inferior to plasma creatinine-derived GFR estimates in predicting late nephropathy. TER assessed by (99m)Tc-MAG3­clearance prior to and during PRRT is not suitable as early predictor of renal injury and an increased risk for late nephropathy.
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spelling pubmed-51730542016-12-23 The impact of (177)Lu-octreotide therapy on (99m)Tc-MAG3 clearance is not predictive for late nephropathy Werner, Rudolf A. Beykan, Seval Higuchi, Takahiro Lückerath, Katharina Weich, Alexander Scheurlen, Michael Bluemel, Christina Herrmann, Ken Buck, Andreas K. Lassmann, Michael Lapa, Constantin Hänscheid, Heribert Oncotarget Research Paper Peptide Receptor Radionuclide Therapy (PRRT) for the treatment of neuroendocrine tumors may lead to kidney deterioration. This study aimed to evaluate the suitability of (99m)Tc-mercaptoacetyltriglycine ((99m)Tc­-MAG3) clearance for the early detection of PRRT-induced changes on tubular extraction (TE). TE rate (TER) was measured prior to 128 PRRT cycles (7.6±0.4 GBq (177)Lu-octreotate/octreotide each) in 32 patients. TER reduction during PRRT was corrected for age-related decrease and analyzed for the potential to predict loss of glomerular filtration (GF). The GF rate (GFR) as measure for renal function was derived from serum creatinine. The mean TER was 234 ± 53 ml/min/1.73 m(2) before PRRT (baseline) and 221 ± 45 ml/min/1.73 m(2) after a median follow-up of 370 days. The age-corrected decrease (mean: −3%, range: −27% to +19%) did not reach significance (p=0.09) but significantly correlated with the baseline TER (Spearman p=−0.62, p<0.001). Patients with low baseline TER showed an improved TER after PRRT, high decreases were only observed in individuals with high baseline TER. Pre-therapeutic TER data were inferior to plasma creatinine-derived GFR estimates in predicting late nephropathy. TER assessed by (99m)Tc-MAG3­clearance prior to and during PRRT is not suitable as early predictor of renal injury and an increased risk for late nephropathy. Impact Journals LLC 2016-06-01 /pmc/articles/PMC5173054/ /pubmed/27259246 http://dx.doi.org/10.18632/oncotarget.9775 Text en Copyright: © 2016 Werner et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Werner, Rudolf A.
Beykan, Seval
Higuchi, Takahiro
Lückerath, Katharina
Weich, Alexander
Scheurlen, Michael
Bluemel, Christina
Herrmann, Ken
Buck, Andreas K.
Lassmann, Michael
Lapa, Constantin
Hänscheid, Heribert
The impact of (177)Lu-octreotide therapy on (99m)Tc-MAG3 clearance is not predictive for late nephropathy
title The impact of (177)Lu-octreotide therapy on (99m)Tc-MAG3 clearance is not predictive for late nephropathy
title_full The impact of (177)Lu-octreotide therapy on (99m)Tc-MAG3 clearance is not predictive for late nephropathy
title_fullStr The impact of (177)Lu-octreotide therapy on (99m)Tc-MAG3 clearance is not predictive for late nephropathy
title_full_unstemmed The impact of (177)Lu-octreotide therapy on (99m)Tc-MAG3 clearance is not predictive for late nephropathy
title_short The impact of (177)Lu-octreotide therapy on (99m)Tc-MAG3 clearance is not predictive for late nephropathy
title_sort impact of (177)lu-octreotide therapy on (99m)tc-mag3 clearance is not predictive for late nephropathy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173054/
https://www.ncbi.nlm.nih.gov/pubmed/27259246
http://dx.doi.org/10.18632/oncotarget.9775
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