Evidence map›Paper›PMID 35159082›Full record

ArticleCancers2022

Modeled Early Longitudinal PSA Kinetics Prognostic Value in Rising PSA Prostate Cancer Patients after Local Therapy Treated with ADT +/- Docetaxel.

Aurore Carrot, Reza-Thierry Elaidi, Olivier Colomban, Denis Maillet, Michel Tod, Benoit You, Stéphane Oudard

Registry-linked trialAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00764166 (Non-Metastatic High-Risk Prostate Cancer Patients With Biochemical Relapse Only After Local Treatment. A Prospective Randomized Phase III Study Comparing Hormonal Therapy +/-Docetaxel), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

NCT00764166 phase3unknown statusnot on this map

Non-Metastatic High-Risk Prostate Cancer Patients With Biochemical Relapse Only After Local Treatment. A Prospective Randomized Phase III Study Comparing Hormonal Therapy +/-Docetaxel

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2003 to 2010Enrolled254ConditionsAdenocarcinoma of the ProstateArmsDocetaxel + hormonal treatment (LH-RH agonist), Hormonal treatment (LH-RH agonist)
3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
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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

7 authors.

Aurore CarrotEA3738 CICLY, UCBL-HCL, Faculté de Médecine Lyon-Sud, Université Claude Bernard Lyon 1, 69100 Villeurbanne, France.ORCID 0000-0002-8835-2865
Reza-Thierry ElaidiAssociation Pour la Recherche sur les Thérapeutiques en Cancérologie, 20 Rue Leblanc, CEDEX 15, 75908 Paris, France.ORCID 0000-0003-2049-7600
Olivier ColombanEA3738 CICLY, UCBL-HCL, Faculté de Médecine Lyon-Sud, Université Claude Bernard Lyon 1, 69100 Villeurbanne, France.
Denis MailletInstitut de Cancérologie des Hospices Civils de Lyon (IC-HCL), Oncologie médicale, CITOHL, 69002 Lyon, France.
Michel TodEA3738 CICLY, UCBL-HCL, Faculté de Médecine Lyon-Sud, Université Claude Bernard Lyon 1, 69100 Villeurbanne, France.
Benoit YouEA3738 CICLY, UCBL-HCL, Faculté de Médecine Lyon-Sud, Université Claude Bernard Lyon 1, 69100 Villeurbanne, France.ORCID 0000-0002-3177-8857
Stéphane OudardCentre Hospitalier Lyon-Sud, Department of Medical Oncology, Georges Pompidou Hospital, 20 Rue Leblanc, CEDEX 15, 75908 Paris, France.ORCID 0000-0003-0893-285X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn metastatic prostate cancer (PCa) patients, androgen-deprivation therapy (ADT) combined with chemotherapy or next-generation androgen receptor targeted agents is a new standard treatment. The objective of the present study is to assess longitudinal PSA kinetics during treatment using mathematical modeling, to identify the modeled PSA kinetic parameters able to exhibit early prognostic/predictive values.

methodsPhase III clinical trial dataset (NCT00764166) comparing ADT +/- docetaxel in 250 locally treated patients for PCa with rising PSA levels, who were at high risk of metastatic disease was assessed. A kinetic-pharmacodynamic (K-PD) model was used to fit PSA kinetics during the first 100 treatment days, to estimate the modeled PSA production rate K (KPROD) and elimination constant rate K (KELIM). The prognostic value of these parameters, considered as categorized (favorable vs. unfavorable) covariates regarding PSA progression-free survival (PSA-PFS) and overall survival (OS), was assessed using univariate/multivariate analyses.

resultsData from 177/250 patients was assessed. KELIM exhibited a significant prognostic value regarding PSA-PFS and KPROD regarding OS (univariate analysis). In the PSA-PFS final multivariate model, KELIM and the primary therapy type were significant. The OS multivariate model integrated both KPROD and baseline PSA doubling-time.

conclusionIn this first study assessing the modeled PSA kinetics prognostic value in PCa patients treated with systemic treatments, KELIM and KPROD exhibited respective prognostic values regarding PSA-PFS and OS.

Indexed as

kineticsmodelsprostate-specific antigenprostatic neoplasmssurvivaltheoretical

Identifiers

PMID35159082
PMCPMC8834031

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Registered trials

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.