Evidence map›Paper›PMID 39269310›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2024

Androgen Deprivation Therapy Drives a Distinct Immune Phenotype in Localized Prostate Cancer.

Matthew C Dallos, Aleksandar Z Obradovic, Patrick McCann, Nivedita Chowdhury, Aditya Pratapa, David H Aggen, Christopher Gaffney, Karen A Autio, Renu K Virk, Angelo M De Marzo and 4 more

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. [A multi-level study of androgen deprivation therapy on the immune microenvironment in prostate cancer].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2026
    Article
  6. Molecular Mechanisms and Immune Regulation in Prostate Cancer: A Review.International journal of molecular sciences · 2026
    Review
  7. CD47 and FOXP3Cancers · 2026
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Androgens are a Key Factor Affecting Immune Related Diseases.The world journal of men's health · 2026
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Matthew C DallosGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-5412-3490
Aleksandar Z ObradovicDepartment of Medicine, Columbia University Medical Center, New York, New York.ORCID 0000-0002-8009-0186
Patrick McCannGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-1836-4617
Nivedita ChowdhuryAtreca Incorporated, San Carlos, California.ORCID 0000-0001-7327-3067
Aditya PratapaAkoya Biosciences Incorporated, Marlborough, Massachusetts.ORCID 0000-0002-3323-6250
David H AggenGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-3963-5751
Christopher GaffneyAkoya Biosciences Incorporated, Marlborough, Massachusetts.ORCID 0000-0002-7785-6611
Karen A AutioGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-0720-0390
Renu K VirkDepartment of Pathology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-2984-4202
Angelo M De MarzoDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0003-4847-5307
Emmanuel S AntonarakisDepartment of Medicine, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0003-0031-9655
Howard I ScherGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-6791-9324
Charles G DrakeDepartment of Medicine, Columbia University Medical Center, New York, New York.ORCID 0000-0001-9610-3677
Dana E RathkopfGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-4503-7582

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI ALAN KEITH MEEKER · 1985 to 2026
$208.6M
SPORE In Prostate CancerP50CA092629 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI David B. Solit · 2001 to 2026
$63.0M
TRANSGENIC MODELS FOR PROSTATE CANCER AND AUTOIMMUNITYP50CA058236 · NCI · JOHNS HOPKINS UNIVERSITY · PI NELSON, WILLIAM GEORGE · 1992 to 2020
$43.9M
Weill Cornell Medicine (WCM) SPORE in Prostate CancerP50CA211024 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GUDAS, LORRAINE J · 2017 to 2021
$10.9M
National Cancer Institute (NCI) 1P50CA211024-01A1 (P50)National Cancer Institute (NCI) P30 CA0006973National Cancer Institute (NCI) P50-CA58236National Cancer Institute (NCI) P50-CA92629NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA058236NCI NIH HHS P50 CA092629NCI NIH HHS P50 CA211024Prostate Cancer Foundation (PCF) 19YOUN27U.S. Department of Defense (DOD) W81XWH-18-2-0015
6 · The paper itself

Abstract

purposeAndrogen deprivation therapy (ADT) remains the backbone of prostate cancer treatment. Beyond the suppression of testosterone and tumor cell growth, emerging evidence suggests that ADT also modulates the immune tumor microenvironment. However, a more precise understanding of the timing and intricacies of these immunologic shifts is needed. EXPERIMENTAL

designIn this study, we analyzed 49 primary prostate cancers, comparing those surgically removed either without treatment or following treatment with degarelix at 4, 7, and 14 days before surgery. Utilizing next-generation DNA and RNA sequencing and multiplexed immunofluorescence, we examined alterations in immune phenotypes in the presence or absence of ADT.

resultsOur findings reveal that ADT rapidly transforms the typically bland prostate tumor microenvironment into an inflamed environment within days. Notably, we observed an increase in activated CD8 T cells along with an increase in suppressive regulatory T cells (Treg). We also found an expansion of the myeloid compartment, particularly proinflammatory M1-like tumor-associated macrophages. Intriguingly, discernable changes which have not previously been described also occurred in tumor cells, including upregulation of antigen presentation by MHC classes I and II and, unexpectedly, a decrease in the "do not eat me" signal CD47.

conclusionsThese observations underscore the critical role of timing and disease context in order to optimize the therapeutic efficacy of immune modulators combined with androgen ablation, for which the presurgical neoadjuvant setting may be ideal. Our findings warrant future prospective validation, which is currently underway.

Indexed as

Androgen AntagonistsProstatic NeoplasmsTumor MicroenvironmentAgedCD8-Positive T-LymphocytesHumansLymphocytes, Tumor-InfiltratingMaleMiddle AgedPhenotypeT-Lymphocytes, RegulatoryTumor-Associated MacrophagesAndrogen Antagonists

Identifiers

PMID39269310
PMCPMC11905119

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Registered trials

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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.