Evidence map›Paper›PMID 34675084›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2022

Novel Redirected T-Cell Immunotherapies for Advanced Prostate Cancer.

Tanya B Dorff, Vivek Narayan, Stephen J Forman, Peter D Zang, Joseph A Fraietta, Carl H June, Naomi B Haas, Saul J Priceman

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 53 citations in OpenAlex.

  1. Phase II Trial of Pembrolizumab and Anti-CD3 x Anti-HER2 Bispecific Antibody-Armed Activated T Cells in Metastatic Castration-Resistant Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Trial
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  10. Immunotherapy in metastatic prostate cancer.Therapeutic advances in medical oncology · 2025
    Review
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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

8 authors at 3 institutions in 1 country.

Tanya B Dorff *Department of Medical Oncology and Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, California.
Vivek Narayan *Division of Hematology/Medical Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-8205-738X
Stephen J FormanDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope Comprehensive Cancer Center, Duarte, California.
Peter D ZangUniversity of Southern California, Los Angeles, California.ORCID 0000-0002-5644-380X
Joseph A FraiettaCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, Pennsylvania.
Carl H JuneCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0003-0241-3557
Naomi B HaasDivision of Hematology/Medical Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
Saul J PricemanDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope Comprehensive Cancer Center, Duarte, California.
University of Pennsylvania · USCity of Hope · USUniversity of Southern California · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI John Charles Williams · 1985 to 2026
$86.3M
UCLA SPORE IN PROSTATE CANCERP50CA092131 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REITER, ROBERT E · 2002 to 2023
$42.6M
Directing the metabolic fate of CAR T cellsR01CA226983 · NCI · UNIVERSITY OF PENNSYLVANIA · PI JUNE, CARL H. · 2018 to 2022
$2.1M
Department of Defense W81XWH-17-1-0208NCI NIH HHS P30 CA033572NCI NIH HHS P50 CA092131NCI NIH HHS R01 CA226983Prostate Cancer Foundation PCFYOUNG18
6 · The paper itself

Abstract

Immunotherapy has failed to achieve durable remissions in advanced prostate cancer patients. More potent T-cell-redirecting strategies may be needed to overcome the immunologically exclusive and suppressive tumor microenvironment. Clinical trials are underway, seeking to define the optimal target for T-cell redirection, such as PSMA, PSCA, or STEAP-1, as well as the optimal strategy, with CAR or bispecific antibodies. As results continue to emerge from these trials, understanding differential toxicity and efficacy of these therapies based on their targets and functional modifications will be key to advancing these promising therapies toward clinical practice. This review provides a unique depth and breadth of perspective regarding the diverse immunotherapy strategies currently under clinical investigation for men with advanced prostate cancer.

Indexed as

Antibodies, BispecificProstatic NeoplasmsHumansImmunotherapyMaleT-LymphocytesTumor MicroenvironmentAntibodies, Bispecific

Identifiers

PMID34675084
PMCPMC8866199
OpenAlexW3206052651

What Socratic holds

Textmetadata
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 Socratic graph.