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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 (...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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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. |
format | Online Article Text |
id | pubmed-5173054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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