Evidence map›Paper›PMID 30733316›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2019

Melanocortin 1 Receptor-Targeted α-Particle Therapy for Metastatic Uveal Melanoma.

Narges K Tafreshi, Christopher J Tichacek, Darpan N Pandya, Michael L Doligalski, Mikalai M Budzevich, HyunJoo Kil, Nikunj B Bhatt, Nancy D Kock, Jane L Messina, Epifanio E Ruiz and 11 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05496686 (First in Human Phase I Study of 225Actinium-MTI-201), which is not on this map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.8field-weighted citation impact, top 3% 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.

NCT05496686 phase1active not recruitingnot on this mapstarted 2022, after this paper: background citation

First in Human Phase I Study of 225Actinium-MTI-201 (225Ac-MTI-201) in Metastatic Uveal Melanoma

TypeinterventionalSponsorModulation Therapeutics, Inc.Ran2022 to 2029Enrolled16ConditionsUveal Melanoma, MetastaticArms4.7 microCi 225Ac-MTI-201, 9.5 microCi of 225Ac-MTI-201, 19 microCi of 225Ac-MTI-201, 38 microCi of 225Ac-MTI-201, 76 microCi of 225Ac-MTI-201
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  8. Article
  9. [MC1R is highly expressed in esophageal squamous cell carcinoma].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  10. Review
  11. HarnessingJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2022
    Review
  12. Review
  13. Targeted α-therapy in non-prostate malignancies.European journal of nuclear medicine and molecular imaging · 2021
    Review
  14. Current issues in molecular biology · 2021
    Article
  15. Preclinical evaluation of [European journal of nuclear medicine and molecular imaging · 2021
    Article
  16. Review
  17. Review
  18. Article
  19. Synthesis of DOTA-pyridine chelates forEJNMMI radiopharmacy and chemistry · 2021
    Article
  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

21 authors at 5 institutions in 1 country.

Narges K TafreshiDepartment of Cancer Physiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Christopher J TichacekDepartment of Cancer Physiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Darpan N PandyaDepartment of Cancer Biology, Wake Forest University Health Sciences, Winston-Salem, North Carolina.
Michael L DoligalskiDepartment of Cancer Physiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Mikalai M BudzevichSmall Animal Imaging Laboratory, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
HyunJoo KilDepartment of Pharmaceutical Sciences, Health Sciences Center, West Virginia University, and Modulation Therapeutics Inc., Morgantown, West Virginia.
Nikunj B BhattDepartment of Cancer Biology, Wake Forest University Health Sciences, Winston-Salem, North Carolina.
Nancy D KockSection on Comparative Medicine, Department of Pathology, Wake Forest University Health Sciences, Winston-Salem, North Carolina.
Jane L MessinaDepartments of Anatomic Pathology and Cutaneous Pathology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Epifanio E RuizSmall Animal Imaging Laboratory, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Nella C DelvaDepartment of Cancer Physiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Adam WeaverDivision of Research Integrity and Compliance, University of South Florida, Tampa, Florida.
William R GibbonsDivision of Research Integrity and Compliance, University of South Florida, Tampa, Florida.
David C BoulwareBiostatistics Core Facility, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Nikhil I KhushalaniDepartment of Cutaneous Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Ghassan El-HaddadDepartments of Diagnostic Imaging and Interventional Radiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida; and.
Pierre L TriozziDepartment of Hematology and Oncology, Wake Forest University Health Sciences, Winston-Salem, North Carolina.
Eduardo G MorosDepartment of Cancer Physiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Mark L McLaughlinDepartment of Pharmaceutical Sciences, Health Sciences Center, West Virginia University, and Modulation Therapeutics Inc., Morgantown, West Virginia.
Thaddeus J WadasDepartment of Cancer Biology, Wake Forest University Health Sciences, Winston-Salem, North Carolina.
David L MorseDepartment of Cancer Physiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida david.morse@moffitt.org.
Moffitt Cancer Center · USWake Forest University · USUniversity of South Florida · USModulation Therapeutics (United States) · USWest Virginia University · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sally Lynn Hodder · 2012 to 2026
$81.0M
NCI NIH HHS P30 CA076292NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

New effective therapies are greatly needed for metastatic uveal melanoma, which has a very poor prognosis with a median survival of less than 1 y. The melanocortin 1 receptor (MC1R) is expressed in 94% of uveal melanoma metastases, and a MC1R-specific ligand (MC1RL) with high affinity and selectivity for MC1R was previously developed.

Indexed as

Molecular Targeted TherapyAlpha ParticlesAnimalsAntineoplastic AgentsCell Line, TumorChelating AgentsFemaleHumansLanthanoid Series ElementsMaleMaximum Tolerated DoseMelanomaMiceMice, Inbred BALB CMice, SCIDNeoplasm MetastasisAntineoplastic AgentsChelating AgentsLanthanoid Series ElementsMC1R protein, humanRadiopharmaceuticalsReceptor, Melanocortin, Type 1225Ac alpha therapymelanocortin 1 receptormouse modeluveal melanoma

Identifiers

PMID30733316
PMCPMC6681690
OpenAlexW2913066485

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.