Evidence map›Paper›PMID 30838430›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2019

Dosimetry-based high-activity therapy with

Jose Genolla, Trinidad Rodriguez, Pablo Minguez, Ricardo Lopez-Almaraz, Veronica Llorens, Aizpea Echebarria

Abstract read
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In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Milestones in dosimetry for nuclear medicine therapy.The British journal of radiology · 2022
    Review
  5. Article
  6. A safety and feasibility trial ofPediatric blood & cancer · 2021
    Article
  7. Article
  8. Upfront consolidation treatment withPediatric investigation · 2020
    Article
  9. 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

6 authors.

Jose GenollaDepartment of Nuclear Medicine, Cruces University Hospital, Plaza de Cruces s/n, 48903, Baracaldo, Vizcaya, Spain. jose.genollasubirats@osakidetza.eus.
Trinidad RodriguezDepartment of Nuclear Medicine, Cruces University Hospital, Plaza de Cruces s/n, 48903, Baracaldo, Vizcaya, Spain.
Pablo MinguezDepartment of Medical Physics and Radiation Protection, Cruces University Hospital, Plaza de Cruces s/n, 48903, Baracaldo, Vizcaya, Spain.
Ricardo Lopez-AlmarazDepartment of Pediatric Oncology and Hematology, Cruces University Hospital, Plaza de Cruces s/n, 48903, Baracaldo, Vizcaya, Spain.
Veronica LlorensDepartment of Nuclear Medicine, Cruces University Hospital, Plaza de Cruces s/n, 48903, Baracaldo, Vizcaya, Spain.
Aizpea EchebarriaDepartment of Pediatric Oncology and Hematology, Cruces University Hospital, Plaza de Cruces s/n, 48903, Baracaldo, Vizcaya, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePatients with high-risk neuroblastoma have an increased risk of recurrence and relapse of disease and a very poor prognosis.

methodsTen patients, between 3 and 20 years of age, were included. Nine patients had been refractory to several lines of chemotherapy and radiotherapy. One patient with a very high-risk neuroblastoma had received only induction therapy. Response was graded according to the International Neuroblastoma Staging System.

resultsRegarding treatment response, two patients achieved complete remission, one with relapse at 16 months, five achieved a partial remission, four showed progression at between 1 and 18 months; two showed stable disease with progression at between 1 and 5 months, and one showed progressive disease. Eight of the ten patients died with overall survival between 4 and 63 months, and two patients were still alive without disease at the time of this report: 52 and 32 months (patient had received only induction therapy). Acute and subacute adverse effects were mainly haematological, and one patient developed a differentiated thyroid cancer.

conclusionIn patients with high-risk refractory neuroblastoma, administration of high activities of

Indexed as

3-IodobenzylguanidineAdolescentChemoradiotherapyChildChild, PreschoolDisease ProgressionDrug Resistance, NeoplasmFemaleHumansMaleNeoplasm Recurrence, LocalNeuroblastomaProgression-Free SurvivalRadiometryRecurrenceRemission Induction3-IodobenzylguanidineTopotecan131I-mIBG therapyDosimetryHigh-risk neuroblastomaTopotecan

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.