Evidence map›Paper›PMID 40138150›Full record

ReviewCurrent treatment options in oncology2025

Advances in PSMA-Targeted Radionuclide Therapeutics.

Samuel Ruder, Andres Ricaurte-Fajardo, Michael Sun, Sandra Huicochea Castellanos, Joseph R Osborne, Scott T Tagawa

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Lesion Absorbed Dose-Response Relationship in Patients with Metastatic Castration-Resistant Prostate Cancer Undergoing [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2025
    Article
  4. 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.

Samuel RuderDepartment of Medicine, Division of Hematology and Oncology, New York Presbyterian Weill Cornell Medical Center, 520 East 70th Street, Starr Pavilion, NY, NY, 10065, USA. spj9003@nyp.org.ORCID http://orcid.org/0000-0003-3676-2798
Andres Ricaurte-FajardoDepartment of Radiology, Division of Molecular Imaging and Therapeutics, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0002-7374-4460
Michael SunDepartment of Medicine, Division of Hematology and Oncology, New York Presbyterian Weill Cornell Medical Center, 520 East 70th Street, Starr Pavilion, NY, NY, 10065, USA.
Sandra Huicochea CastellanosDepartment of Radiology, Division of Molecular Imaging and Therapeutics, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0003-2907-8744
Joseph R OsborneDepartment of Radiology, Division of Molecular Imaging and Therapeutics, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0003-0232-5960
Scott T TagawaDepartment of Medicine, Division of Hematology and Oncology, New York Presbyterian Weill Cornell Medical Center, 520 East 70th Street, Starr Pavilion, NY, NY, 10065, USA. stt2007@med.cornell.edu.ORCID http://orcid.org/0000-0003-2777-8587

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementProstate-specific membrane antigen targeted radionuclide therapies (PSMA-TRT) such as 177Lu-PSMA-617 hold great promise in improving clinical outcomes at various stages of prostate cancer. The FDA approval of 177Lu-PSMA-617 represents a significant advancement in the treatment of metastatic castration-resistant prostate cancer (mCRPC). The VISION trial demonstrated improved radiographic progression-free survival (rPFS) and overall survival (OS) with 177Lu-PSMA-617 in patients with mCRPC who had already receive androgen receptor pathway inhibitor (ARPI) and taxane chemotherapy. Exploration of 177Lu-PSMA-617 in earlier stages of prostate cancer, such as in the PSMAfore trial for patients who have not received chemotherapy, holds great promise for improving long-term outcomes and delaying exposure to chemotherapy. Combining 177Lu-PSMA-617 with other therapies, including chemotherapy, PARP inhibitors, and immunotherapy, is an area of active investigation. This review will also discuss alternative radionuclides (such as actininum-225 and terbium-161) and delivery vehicles (such as PSMA-I&T), which we find promising. Predictive biomarkers and dosimetry will be crucial for identifying patients most likely to benefit from PSMA-TRT. Continued research and refinement of these therapies will lead to PSMA-targeted treatments becoming an integral part of prostate cancer management.

Indexed as

Antigens, SurfaceGlutamate Carboxypeptidase IIProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantRadioisotopesRadiopharmaceuticalsHumansLutetiumMaleMolecular Targeted TherapyTreatment OutcomeAntigens, SurfaceFOLH1 protein, humanGlutamate Carboxypeptidase IILutetiumRadioisotopesRadiopharmaceuticals177Lu-PSMA-617Metastatic castration-resistant prostate cancer (mCRPC)Prostate cancerPSMA-targeted therapyRadioligand therapyRadionuclide therapy

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.