Nuklearmedizin 2019; 58(02): 129
DOI: 10.1055/s-0039-1683541
Vorträge
Theranostik: NET und Radioembolisation
Georg Thieme Verlag KG Stuttgart · New York

Long-term Nephrotoxicity After PRRT: Mythos or Reality?

J Zhang
1   Zentralklinik Bad Berka, Theranostics Center for Molecular Radiotherapy & Molecular Imaging, Bad Berka
,
HR Kulkarni
1   Zentralklinik Bad Berka, Theranostics Center for Molecular Radiotherapy & Molecular Imaging, Bad Berka
,
A Singh
1   Zentralklinik Bad Berka, Theranostics Center for Molecular Radiotherapy & Molecular Imaging, Bad Berka
,
K Niepsch
1   Zentralklinik Bad Berka, Theranostics Center for Molecular Radiotherapy & Molecular Imaging, Bad Berka
,
C Schuchardt
1   Zentralklinik Bad Berka, Theranostics Center for Molecular Radiotherapy & Molecular Imaging, Bad Berka
,
T Langbein
1   Zentralklinik Bad Berka, Theranostics Center for Molecular Radiotherapy & Molecular Imaging, Bad Berka
,
RP Baum
1   Zentralklinik Bad Berka, Theranostics Center for Molecular Radiotherapy & Molecular Imaging, Bad Berka
› Author Affiliations
Further Information

Publication History

Publication Date:
27 March 2019 (online)

 
 

    Ziel/Aim:

    The aim of this study was to assess nephrotoxicity of peptide receptor radionuclide therapy (PRRT) in a large cohort of patients with neuroendocrine neoplasms (NEN) treated over the last 20 years in our institution.

    Methodik/Methods:

    A total of 1361 patients with NEN (male 767; mean age 60.0 ± 11.8y), treated with Lu-177-DOTATATE/-TOC, Y-90-DOTATATE/-TOC, DUO-PRRT, or TANDEM-PRRT were included with all parameters prospectively documented in a structured database (comprising over 250 items per patient). Kidney function (serum creatinine, blood urea nitrogen, cGFR, electrolytes) was evaluated prior to each PRRT cycle and in follow up. Renal function was further quantified by measuring the TER ans GFR. Treatment-related adverse events were graded according to CTCAE v.5.0.

    Ergebnisse/Results:

    5448 cycles of PRRT were administered, in addition, 4052 records were available for restaging. The median overall survival was 70.1 months with a median follow-up time of 91.8 months. Baseline creatinine was normal in 82.0% of subjects, grade 1 (G1) renal insufficiency (RI) was present prior to PRRT in 16.2%, G2 in 1.7%, and G3 in 0.1%. After treatment, renal function was normal in 78.2%, 18.9% had G1, and 1.9% had G2 RI. G3 events were recorded in only four patients (0.3%), of which two had a history of recurrent urinary tract infections and two had already GTC-3 at baseline. No CTC-4 or 5 nephrotoxicity was observed. TER changed from 207.7 ± 56.6 to 186.3 ± 53.8 ml/min; 45.5% had a clinically non-significant fall in renal function, whereas 32% showed an improvement after treatment. GFR changed from 83.9 ± 24.3 to 76.4 ± 25.7 ml/min/1.73 m2, including a clinically not relevant decline in 46.2%, whereas 33.0% showed an improvement. For subgroup who received 8 – 10 cycles of PRRT, the annual loss of the mean value of TER between 2003 and 2017 were 10%.

    Schlussfolgerungen/Conclusions:

    This retrospective analysis with prospective documentation in a large cohort of 1361 NEN patients, receiving 5448 cycles of PRRT with optimal nephroprotection, treated at a single institution over 20 years (with a median follow-up time of 91.8 months) did not reveal any evidence of significant long-term nephrotoxicity after PRRT.


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