Evidence map›Paper›PMID 26169786›Full record

ArticleScientific reports2015

Automated astatination of biomolecules--a stepping stone towards multicenter clinical trials.

Emma Aneheim, Per Albertsson, Tom Bäck, Holger Jensen, Stig Palm, Sture Lindegren

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Production and Supply of α-Particle-Emitting Radionuclides for Targeted α-Therapy.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Review
  6. Synthesis of [Scientific reports · 2021
    Article
  7. Evaluation of therapeutic efficacy ofTranslational oncology · 2021
    Article
  8. Labeling Monoclonal Antibody with α-emittingCancer biotherapy & radiopharmaceuticals · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Rapid Cu-Catalyzed [Organic letters · 2018
    Article
  14. Article
  15. Review
  16. Improved production ofNuclear medicine and biology
    Article
  17. 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

6 authors.

Emma AneheimTargeted Alpha Therapy, Department of Radiation Physics, Sahlgrenska Academy at Gothenburg University, Gothenburg 41345, Sweden.
Per AlbertssonTargeted Alpha Therapy, Department of Radiation Physics, Sahlgrenska Academy at Gothenburg University, Gothenburg 41345, Sweden.
Tom BäckTargeted Alpha Therapy, Department of Radiation Physics, Sahlgrenska Academy at Gothenburg University, Gothenburg 41345, Sweden.
Holger JensenPET and Cyclotron unit, KF3982, Copenhagen University Hospital, Copenhagen, Denmark.
Stig PalmTargeted Alpha Therapy, Department of Radiation Physics, Sahlgrenska Academy at Gothenburg University, Gothenburg 41345, Sweden.
Sture LindegrenTargeted Alpha Therapy, Department of Radiation Physics, Sahlgrenska Academy at Gothenburg University, Gothenburg 41345, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To facilitate multicentre clinical studies on targeted alpha therapy, it is necessary to develop an automated, on-site procedure for conjugating rare, short-lived, alpha-emitting radionuclides to biomolecules. Astatine-211 is one of the few alpha-emitting nuclides with appropriate chemical and physical properties for use in targeted therapies for cancer. Due to the very short range of the emitted α-particles, this therapy is particularly suited to treating occult, disseminated cancers. Astatine is not intrinsically tumour-specific; therefore, it requires an appropriate tumour-specific targeting vector, which can guide the radiation to the cancer cells. Consequently, an appropriate method is required for coupling the nuclide to the vector. To increase the availability of astatine-211 radiopharmaceuticals for targeted alpha therapy, their production should be automated. Here, we present a method that combines dry distillation of astatine-211 and a synthesis module for producing radiopharmaceuticals into a process platform. This platform will standardize production of astatinated radiopharmaceuticals, and hence, it will facilitate large clinical studies focused on this promising, but chemically challenging, alpha-emitting radionuclide. In this work, we describe the process platform, and we demonstrate the production of both astaine-211, for preclinical use, and astatine-211 labelled antibodies.

Indexed as

Clinical Trials as TopicMulticenter Studies as TopicAntibodies, MonoclonalAstatineAutomation, LaboratoryDistillationHumansIsotope LabelingNeoplasmsRadiopharmaceuticalsAntibodies, MonoclonalAstatineRadiopharmaceuticals

Identifiers

PMID26169786
PMCPMC4500947

What OpenQuestion holds

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Registered trials

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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.