Evidence map›Paper›PMID 32949185›Full record

ArticleThe Prostate2020

Impact of baseline serum IL-8 on metastatic hormone-sensitive prostate cancer outcomes in the Phase 3 CHAARTED trial (E3805).

Lauren C Harshman, Victoria X Wang, Anis A Hamid, Gabriella Santone, Charles G Drake, Michael A Carducci, Robert S DiPaola, Raina N Fichorova, Christopher J Sweeney

Open access · greenAbstract read
In one paragraph

Article in The Prostate, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Liquid biopsy to personalize treatment for metastatic prostate cancer.American journal of translational research · 2024
    Review
  6. Review
  7. Review
  8. Cabozantinib plus Nivolumab Phase I Expansion Study in Patients with Metastatic Urothelial Carcinoma Refractory to Immune Checkpoint Inhibitor Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. 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

9 authors at 6 institutions in 1 country.

Lauren C HarshmanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Lank Center for Genitourinary Oncology, Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0002-7636-1588
Victoria X WangDepartment of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Anis A HamidDepartment of Medical Oncology, Dana-Farber Cancer Institute, Lank Center for Genitourinary Oncology, Harvard Medical School, Boston, Massachusetts, USA.
Gabriella SantoneDepartment of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Charles G DrakeDepartment of Medicine, Division of Oncology, Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, New York, USA.ORCID 0000-0001-9610-3677
Michael A CarducciDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, USA.
Robert S DiPaolaDepartment of Medicine, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
Raina N FichorovaDepartment of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Christopher J SweeneyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Lank Center for Genitourinary Oncology, Harvard Medical School, Boston, Massachusetts, USA.
Harvard University · USBrigham and Women's Hospital · USColumbia University Irving Medical Center · USDana-Farber Cancer Institute · USSidney Kimmel Comprehensive Cancer Center · USUniversity of Kentucky · US

Funding

Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer, MITCHELL D. SCHNALL · 2014 to 2026
$167.6M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO · 2014 to 2026
$111.2M
ECOG-ACRIN Biospecimen Bank to Support NCTNU24CA196172 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI STANLEY R. HAMILTON, Scott D Jewell · 2015 to 2026
$41.1M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareUG1CA233180 · NCI · DANA-FARBER CANCER INST · PI Harold John Burstein · 2019 to 2026
$8.6M
NCTN LAPS at Johns HopkinsUG1CA233196 · NCI · JOHNS HOPKINS UNIVERSITY · PI DEBORAH K ARMSTRONG, Julie Renee Brahmer · 2019 to 2026
$4.6M
Analysis of Blood Borne Markers in Hormone Sensitive Metastatic Prostate CancerR01CA208254 · NCI · DANA-FARBER CANCER INST · PI SWEENEY, CHRISTOPHER J · 2016 to 2018
$1.6M
NCI NIH HHS R01 CA208254NCI NIH HHS U10 CA180794NCI NIH HHS U10 CA180820NCI NIH HHS U24 CA196172NCI NIH HHS UG1 CA233180NCI NIH HHS UG1 CA233196NIH HHS R01CA208254-01NIH HHS U10CA180794NIH HHS U10CA180820NIH HHS UG1CA233180NIH HHS UG1CA233196
6 · The paper itself

Abstract

backgroundThe immunosuppressive cytokine interleukin- 8 (IL-8), produced by tumor cells and some myeloid cells, promotes inflammation, angiogenesis, and metastasis. In our discovery work, elevated serum IL-8 at androgen deprivation therapy (ADT) initiation portended worse overall survival (OS). Leveraging serum samples from the phase 3 CHAARTED trial of patients treated with ADT +/- docetaxel for metastatic hormone-sensitive prostate cancer (mHSPC), we validated these findings.

methodsTwo hundred and thirty-three patients had serum samples drawn within 28 days of ADT initiation. The samples were assayed using the same Mesoscale Multiplex ELISA platform employed in the discovery cohort. After adjusting for performance status, disease volume, and de novo/metachronous metastases, multivariable Cox proportional hazards models assessed associations between IL-8 as continuous and binary variables on OS and time to castration-resistant prostate cancer (CRPC). The median IL-8 level (9.3 pg/ml) was the a priori binary cutpoint. Fixed-effects meta-analyses of the discovery and validation sets were performed.

resultsHigher IL-8 levels were prognostic for shorter OS (continuous: hazard ratio [HR] 2.2, 95% confidence interval [CI]: 1.4-3.6, p = .001; binary >9.3: HR 1.7, 95% CI: 1.2-2.4, p = .007) and time to CRPC (continuous: HR 2.3, 95% CI: 1.6-3.3, p < .001; binary: HR 1.8, 95% CI: 1.3-2.5, p < .001) and independent of docetaxel use, disease burden, and time of metastases. Meta-analysis including the discovery cohort, also showed that binary IL-8 levels >9.3 pg/ml from patients treated with ADT alone was prognostic for poorer OS (HR 1.8, 95% CI: 1.2-2.7, p = .007) and shorter time to CRPC (HR 1.4, 95% CI: 0.99-1.9, p = .057).

conclusionsIn the phase 3 CHAARTED study of men with mHSPC at ADT initiation, elevated IL-8 portended worse survival and shorter time to castration-resistant prostate cancer independent of docetaxel administration, metastatic burden, and metachronous versus de novo metastatic presentation. These findings support targeting IL-8 as a strategy to improve mHSPC outcomes.

Indexed as

AdultAgedAged, 80 and overAndrogen AntagonistsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsDocetaxelHumansInterleukin-8MaleMiddle AgedPrognosisProstatic NeoplasmsSurvival RateTreatment OutcomeAndrogen AntagonistsAntineoplastic AgentsDocetaxelInterleukin-8ADTcytokineshormone sensitive prostate cancerIL-8MCPTNF-α

Identifiers

PMID32949185
PMCPMC7606809
OpenAlexW3087692268

What OpenQuestion holds

Textmetadata
LicenceTDM
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.