Evidence map›Paper›PMID 35451612›Full record

Trial reportEuropean journal of nuclear medicine and molecular imaging2022

Phase II trial demonstrates the efficacy and safety of individualized, dosimetry-based

Anna Sundlöv, Katarina Sjögreen Gleisner, Jan Tennvall, Michael Ljungberg, Carl Fredrik Warfvinge, Kajsa Holgersson, Andreas Hallqvist, Peter Bernhardt, Johanna Svensson

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in European journal of nuclear medicine and molecular imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01456078 (A Multicenter Phase II-Study Evaluating Efficacy and Safety of 177Lu-DOTA-TATE Based on Kidney-Dosimetry in Patients With Disseminated Neuroendocrine Tumors), which is not on this map. Cited by 50 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 4 pooled it
10.8field-weighted citation impact, top 1% of its field
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.

NCT01456078 phase2completednot on this map

A Multicenter Phase II-Study Evaluating Efficacy and Safety of 177Lu-DOTA-TATE Based on Kidney-Dosimetry in Patients With Disseminated Neuroendocrine Tumors

TypeinterventionalSponsorLund University HospitalRan2011 to 2018Enrolled60ConditionsNeuroendocrine Tumors, Liver MetastasesArms177Lu-DOTA-TATE
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 4 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Is there a role for early SSTR-targeting PRRT in GEP-NET?European journal of nuclear medicine and molecular imaging · 2026
    Pooled it
  2. Pooled it
  3. Dosimetry of [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2024
    Pooled it
  4. EANM practice guideline for quantitative SPECT-CT.European journal of nuclear medicine and molecular imaging · 2023
    Guideline
  5. Trial
  6. Trial
  7. Patient Survival and Its Relation to Tumor Absorbed Dose in [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Article
  8. Dosimetry-Driven Personalization of Radiopharmaceutical Therapies: Evidence and Opportunities.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Review
  9. Response to the FDA Dosage Optimization Draft Guidance for Radiopharmaceutical Therapies.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Article
  10. Krenning score enhances integrated biomarker models for survival prediction in PRRT-treated GEP-NET: a retrospective cohort study.Cancer imaging : the official publication of the International Cancer Imaging Society · 2026
    Article
  11. Review
  12. Inter-center variability of dosimetry methodology and the impact on reported absorbed dose for [European journal of nuclear medicine and molecular imaging · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. [EJNMMI physics · 2026
    Article
  19. Review
  20. Article
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

9 authors at 2 institutions in 1 country.

Anna SundlövDepartment of Clinical Sciences, Oncology and Pathology, Skåne University Hospital, Lund University, Lund, Sweden.
Katarina Sjögreen GleisnerDepartment of Medical Radiation Physics, Clinical Sciences Lund, Lund University, Lund, Sweden.
Jan TennvallDepartment of Clinical Sciences, Oncology and Pathology, Skåne University Hospital, Lund University, Lund, Sweden.
Michael LjungbergDepartment of Medical Radiation Physics, Clinical Sciences Lund, Lund University, Lund, Sweden.
Carl Fredrik WarfvingeDepartment of Clinical Sciences, Oncology and Pathology, Skåne University Hospital, Lund University, Lund, Sweden.
Kajsa HolgerssonDepartment of Oncology, Sahlgrenska University Hospital, Blå Stråket 2, 413 45, Gothenburg, Sweden.
Andreas HallqvistDepartment of Oncology, Sahlgrenska University Hospital, Blå Stråket 2, 413 45, Gothenburg, Sweden.
Peter BernhardtDepartment of Radiation Physics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Johanna SvenssonDepartment of Oncology, Sahlgrenska University Hospital, Blå Stråket 2, 413 45, Gothenburg, Sweden. johanna.b.svensson@vgregion.se.ORCID 0000-0003-3292-7719
Lund University · SESahlgrenska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRadionuclide therapy with

methodsPatients were eligible if they had a progressive, somatostatin receptor-positive neuroendocrine tumor with a Ki 67 labeling index < 20%. They received cycles of 7.4 GBq of

resultsNinety-six patients who had received a median of 5 cycles (range 1-9) were evaluable for efficacy. The objective tumor response was 16% partial response, 66% stable disease, and 19% progressive disease. The median PFS and OS were 29 months and 47 months, respectively, and were significantly associated with kidney dose, performance status, and Ki 67 levels but not with tumor origin. The overall toxicity was mild, and the most common events were grade 1-2 anemia, thrombocytopenia, fatigue, nausea, and diarrhea. Grade 3-4 toxicity occurred in < 10% of patients and was mostly hematological, with no grade 3-4 renal toxicity.

conclusionIndividualized treatment with

trial registrationEudraCT 2011-000,240-16. NCT01456078. https://clinicaltrials.gov/ct2/show/NCT01456078.

Indexed as

Neuroendocrine TumorsOrganometallic CompoundsHumansKi-67 AntigenOctreotidePositron-Emission TomographyRadionuclide ImagingRadiopharmaceuticalsReceptors, Somatostatincopper dotatate CU-64Ki-67 AntigenOctreotideOrganometallic CompoundsRadiopharmaceuticalsReceptors, Somatostatin177Lu-DOTATATEDosimetryNeuroendocrine tumorsRadionuclide therapy

Identifiers

PMID35451612
PMCPMC9399027
OpenAlexW4224248946

What OpenQuestion holds

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Registered trials

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.