Evidence map›Paper›PMID 42226023›Full record

ReviewJNCI cancer spectrum2026

Emerging role of radiopharmaceutical therapy in oncology: advances, challenges, and future directions.

Laura Ordas, Sean Foster, Phuc Pham, Andy Ollendorff, Varun Gnanasekar, Mahmoud Toulany, Quaovi H Sodji

Abstract readReview
In one paragraph

Review in JNCI cancer spectrum, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Linking In Vivo Imaging to Therapeutic Outcome withInternational journal of molecular sciences · 2026
    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

7 authors.

Laura OrdasDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Sean FosterDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Phuc PhamDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Andy OllendorffDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Varun GnanasekarDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Mahmoud ToulanyDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Quaovi H SodjiDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.ORCID 0000-0002-9469-1388

Funding

Targeted Radionuclide Therapy to Enhance the Efficacy of CAR T Cells Against NeuroblastomaK08CA285941 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Quaovi H Sodji · 2024 to 2026
$479k
NIH HHS K08CA285941
6 · The paper itself

Abstract

Radiopharmaceutical therapy has transformed cancer management by enabling systemic delivery of ionizing radiation via molecularly targeted pharmaceutics, complementing external beam radiotherapy, which primarily treats localized, radiographically defined lesions. By coupling diagnostic imaging with therapy, in a "radiotheranostic" paradigm, radiopharmaceutical therapy supports patient-specific target selection, dosimetry, and on-treatment monitoring. Progress in target discovery, radioligand chemistry, and optimization of pharmacokinetics and biodistribution has improved efficacy and safety, culminating in US Food and Drug Administration approvals of [177Lu]Lu-PSMA-617 (Pluvicto) for metastatic castration-resistant prostate cancer and [177Lu]Lu-DOTA-TATE (Lutathera) for neuroendocrine tumors. These successes highlight radiopharmaceutical therapy's expanding role across oncology. This review summarizes the evolution of radiopharmaceutical therapy from early clinical milestones to modern regulatory approvals, then surveys emerging radioligands directed at new molecular pathways. We also discuss strategies to enhance therapeutic response including rational combinations with DNA damage response agents such as poly(adenosine diphosphate-ribose) polymerase inhibitors or immunotherapies. Finally, we outline key challenges such as optimal patient selection, dosimetry standardization, therapeutic resistance, and access and highlight a few ways to accelerate broader clinical integration and continued innovation.

Indexed as

Neuroendocrine TumorsProstatic Neoplasms, Castration-ResistantRadiopharmaceuticalsDipeptidesHumansLutetiumMaleMolecular Targeted TherapyOctreotideOrganometallic CompoundsProstate-Specific AntigenRadioisotopesDipeptidesLutetiumLutetium-177lutetium (177Lu) vipivotide tetraxetanlutetium Lu 177 dotatateOctreotideOrganometallic CompoundsProstate-Specific AntigenRadioisotopesRadiopharmaceuticals

Identifiers

PMID42226023
PMCPMC13310479

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.