Evidence map›Paper›PMID 29641256›Full record

ArticleCancer biotherapy & radiopharmaceuticals2018

CLR 125 Auger Electrons for the Targeted Radiotherapy of Triple-Negative Breast Cancer.

Joseph Grudzinski, Ian Marsh, Benjamin Titz, Justin Jeffery, Marc Longino, Kevin Kozak, Kristofer Lange, Jason Larrabee, Ashley Weichmann, Amy Moser and 1 more

Abstract read
In one paragraph

Article in Cancer biotherapy & radiopharmaceuticals, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 20% 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.

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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Radionuclide-based theranostics - a promising strategy for lung cancer.European journal of nuclear medicine and molecular imaging · 2023
    Review
  5. Review
  6. Article
  7. Preclinical Characterization ofJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2019
    Article
  8. Preclinical Pharmacokinetics and Dosimetry Studies ofJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2019
    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

11 authors at 2 institutions in 1 country.

Joseph Grudzinski1 Department of Medical Physics, University of Wisconsin-Madison , Madison, Wisconsin.
Ian Marsh1 Department of Medical Physics, University of Wisconsin-Madison , Madison, Wisconsin.
Benjamin Titz2 Cellectar Biosciences, Inc. , Madison, Wisconsin.
Justin Jeffery3 University of Wisconsin Carbone Cancer Center , Madison, Wisconsin.
Marc Longino2 Cellectar Biosciences, Inc. , Madison, Wisconsin.
Kevin Kozak2 Cellectar Biosciences, Inc. , Madison, Wisconsin.
Kristofer Lange2 Cellectar Biosciences, Inc. , Madison, Wisconsin.
Jason Larrabee2 Cellectar Biosciences, Inc. , Madison, Wisconsin.
Ashley Weichmann3 University of Wisconsin Carbone Cancer Center , Madison, Wisconsin.
Amy Moser3 University of Wisconsin Carbone Cancer Center , Madison, Wisconsin.
Bryan Bednarz1 Department of Medical Physics, University of Wisconsin-Madison , Madison, Wisconsin.
University of Wisconsin Carbone Cancer Center · USUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAuger electrons emitted by radioisotopes such as

methodsA Current Good Manufacturing Practice (cGMP) method to radiolabel

resultsDosimetry analysis estimated that CLR 125 would impart the largest absorbed dose to the tumor per injected activity (0.261 ± 0.023 Gy/MBq) while the bone marrow, which is generally the dose-limiting organ for CLR1404, appears to have the lowest (0.063 ± 0.005 Gy/MBq). At administered activities of up to 74 MBq (3.7 GBq/kg), mice did not experience signs of toxicity. In addition, a single dose of CLR 125 reduced the volume of orthotopic primary TNBC xenografts by ∼60% compared to control vehicle (p < 0.001) and significantly extended survival. In addition, CLR 125 was efficacious against preclinical metastatic TNBC models by inhibiting the progression of micrometastases (p < 0.01).

conclusionsTargeted radionuclide therapy with CLR 125 displayed significant antitumor efficacy in vivo, suggesting promise for treatment of TNBC micrometastases.

Indexed as

AnimalsApoptosisCell ProliferationElectronsFemaleHumansIodine RadioisotopesLung NeoplasmsMiceMice, NudeMonte Carlo MethodTriple Negative Breast NeoplasmsTumor Cells, CulturedXenograft Model Antitumor AssaysIodine-125Iodine RadioisotopesAuger electronsCLR1404targeted radionuclide therapytheranosticstriple-negative breast cancer

Identifiers

PMID29641256
PMCPMC5905872
OpenAlexW2798083297

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.