Evidence map›Paper›PMID 36057895›Full record

Observational studyWorld journal of urology2022

Development of castration resistance in prostate cancer patients treated with luteinizing hormone-releasing hormone analogues (LHRHa): results of the ANARESISTANCE study.

J C Angulo, J P Ciria Santos, A Gómez-Caamaño, R Poza de Celis, J L González Sala, J M García Garzón, J A Galán-Llopis, M Pérez Sampietro, V Perrot, J Planas Morin and 1 more

Open access · hybridAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in World journal of urology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

11 authors at 9 institutions in 2 countries.

J C AnguloClinical Department, Universidad Europea de Madrid; Hospital Universitario de Getafe, Madrid, Spain. javier.angulo@universidadeuropea.es.ORCID http://orcid.org/0000-0002-1735-8792
J P Ciria SantosRadiation Oncology Service, Hospital Universitario Donostia, Donostia, Spain.
A Gómez-CaamañoDepartment of Radiation Oncology, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain.
R Poza de CelisDepartment of Radiation Oncology, Hospital Universitario Araba, Gasteiz, Spain.
J L González SalaUrology Service, Corporació Sanitària Parc Taulí, Sabadell, Spain.
J M García GarzónUrology Service, Hospital General de Llerena, Llerena, Spain.
J A Galán-LlopisUrology Service, Hospital General Universitario de Alicante, Alicante, Spain.ORCID http://orcid.org/0000-0002-2168-2456
M Pérez SampietroIpsen Pharma, S.A.U, Barcelona, Spain.
V PerrotIpsen Pharma, S.A.U, Barcelona, Spain.
J Planas MorinUrology Service, Hospital Universitario Vall d'Hebrón, Barcelona, Spain.
ANARESISTANCE study group
Ipsen (Spain) · ESVall d'Hebron Hospital Universitari · ESComplejo Hospitalario Universitario de Santiago · ESCorporació Sanitària Parc Taulí · ESDonostiako Unibertsitate Ospitalea · ESHospital Arnau de Vilanova · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital Universitario Araba · ESUniversidad Europea · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEvaluate the percentage of patients with prostate cancer treated with luteinizing hormone-releasing hormone analogues (LHRHa) that develop castration resistance after a follow-up period of 3 years. The secondary objective is to evaluate the variables potentially related to the progression to castration resistant prostate cancer (CRPC).

methodsA post-authorization, nation-wide, multicenter, prospective, observational, and longitudinal study that included 416 patients treated with LHRHa between 2012 and 2017 is presented. Patients were followed for 3 years or until development of CRPC, thus completing a per-protocol population of 350 patients. A Cox regression analysis was carried out to evaluate factors involved in progression to CRPC.

resultsAfter 3 years of treatment with LHRHa 18.2% of patients developed CRPC. In contrast, in the subgroup analysis, 39.6% of the metastatic patients developed CRPC, compared with 8.8% of the non-metastatic patients. The patients with the highest risk of developing CRPC were those with a nadir prostate-specific antigen (PSA) > 2 ng/ml (HR 21.6; 95% CI 11.7-39.8; p < 0.001) and those receiving concomitant medication, most commonly bicalutamide (HR 1.8; 95% CI 1-3.1, p = 0.0431).

conclusionsThe proportion of metastatic patients developing CRPC after 3 years of treatment with LHRHa is consistent with what has been previously described in the literature. In addition, this study provides new findings on CRPC in non-metastatic patients. Concomitant medication and nadir PSA are statistically significant predictive factors for the time to diagnosis of CRPC, the nadir PSA being the strongest predictor.

Indexed as

Prostatic NeoplasmsProstatic Neoplasms, Castration-ResistantAndrogen AntagonistsCastrationGonadotropin-Releasing HormoneHumansLongitudinal StudiesMaleProspective StudiesProstate-Specific AntigenAndrogen AntagonistsGonadotropin-Releasing HormoneProstate-Specific AntigenCastration-resistant prostatic neoplasmsGonadotropin-releasing hormoneObservational studyProspective study

Identifiers

PMID36057895
PMCPMC9512882
OpenAlexW4294571682

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.