Evidence map›Paper›PMID 24668274›Full record

Trial reportEuropean journal of nuclear medicine and molecular imaging2014

Individualized dosimetry-based activity reduction of ⁹⁰Y-DOTATOC prevents severe and rapid kidney function deterioration from peptide receptor radionuclide therapy.

Sofie Van Binnebeek, Kristof Baete, Bert Vanbilloen, Christelle Terwinghe, Michel Koole, Felix M Mottaghy, Paul M Clement, Luc Mortelmans, Karin Haustermans, Eric Van Cutsem and 4 more

Abstract readClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in European journal of nuclear medicine and molecular imaging, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Trial
  2. IndividualisedEuropean journal of nuclear medicine and molecular imaging · 2017
    Trial
  3. Trial
  4. Review
  5. Pharmaceutics · 2023
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. DosingEuropean journal of nuclear medicine and molecular imaging · 2021
    Article
  11. First-in-human dosimetry of gastrin-releasing peptide receptor antagonist [European journal of nuclear medicine and molecular imaging · 2020
    Article
  12. Article
  13. Correlation of dose with toxicity and tumour response toEuropean journal of nuclear medicine and molecular imaging · 2018
    Review
  14. Review
  15. Article
  16. Review
  17. Nephrotoxicity after PRRT with (177)Lu-DOTA-octreotate.European journal of nuclear medicine and molecular imaging · 2016
    Article
  18. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Sofie Van BinnebeekNuclear Medicine, University Hospitals Leuven, Leuven, Belgium, sofie.vanbinnebeek@uzleuven.be.
Kristof Baete
Bert Vanbilloen
Christelle Terwinghe
Michel Koole
Felix M Mottaghy
Paul M Clement
Luc Mortelmans
Karin Haustermans
Eric Van Cutsem
Alfons Verbruggen
Kris Bogaerts
Chris Verslype
Christophe M Deroose

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAssessment of kidney function evolution after (90)Y-DOTATOC peptide receptor radionuclide therapy (PRRT) with capped activity administration based on a 37-Gy threshold of biological effective dose (BED) to the kidney.

methodsIn a prospective phase II study, patients with metastasized neuroendocrine tumours were evaluated for therapy using 185 MBq (111)In-pentetreotide with amino acid coinfusion. Planar whole-body images were acquired at four time-points after injection and kidney volumes were measured using CT/MRI. BED to the kidneys was estimated using an extended BED formula and biexponential renal clearance. Based on published BED dose-toxicity relationships, we allowed a maximal kidney BED of 37 Gy; if the calculated BED exceeded 37 Gy, treatment activity was reduced accordingly. Kidney function was assessed at baseline and at 18 months, predominantly using (51)Cr-EDTA. The rate of renal function decline was expressed as annual glomerular filtration rate loss (aGFRL).

resultsOnly 22 of 50 patients reached the 18-months time-point, with most missing patients having died due to disease progression. In the 22 patients who reached 18 months, no rapid kidney function deterioration was observed over the 18 months, aGFRL >33% was not seen, and only three patients showed an increase of one toxicity grade and one patient an increase of two grades. No significant correlations between kidney volume (p = 0.35), baseline GFR (p = 0.18), risk factors for renal function loss (p = 0.74) and aGFRL were observed. Among the 28 patients who did not reach 18 months, one developed grade 4 kidney toxicity at 15 months after PRRT.

conclusionProspective dosimetry using a 37 Gy BED as the threshold for kidney toxicity is a good guide for (90)Y-DOTATOC PRRT and is associated with a low risk of rapid renal function deterioration and evolution to severe nephrotoxicity.

Indexed as

Radiation DosageAdultAgedDigestive System NeoplasmsFemaleHumansKidneyKidney Function TestsLung NeoplasmsMaleMiddle AgedNeuroendocrine TumorsOctreotidePrecision MedicineRadiometryRadionuclide ImagingEdotreotideOctreotideRadiopharmaceuticalsYttrium Radioisotopes

Identifiers

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.