Evidence map›Paper›PMID 32068491›Full record

ArticleThe Journal of urology2020

Analysis of AR-FL and AR-V1 in Whole Blood of Patients with Castration Resistant Prostate Cancer as a Tool for Predicting Response to Abiraterone Acetate.

Kristina Stuopelyte, Rasa Sabaliauskaite, Arnas Bakavicius, Benedikta S Haflidadóttir, Tapio Visakorpi, Riina-Minna Väänänen, Chintan Patel, Daniel C Danila, Hans Lilja, Juozas R Lazutka and 3 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of urology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 5 countries.

Kristina StuopelyteInstitute of Biomedical Sciences, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
Rasa SabaliauskaiteNational Cancer Institute, Vilnius, Lithuania.
Arnas BakaviciusUrology Centre, Vilnius University, Vilnius, Lithuania.
Benedikta S HaflidadóttirProstate Cancer Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Tapio VisakorpiProstate Cancer Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Riina-Minna VäänänenDepartment of Biotechnology, University of Turku, Turku, Finland.
Chintan PatelDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Daniel C DanilaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Hans LiljaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Juozas R LazutkaInstitute of Biomedical Sciences, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
Albertas UlysNational Cancer Institute, Vilnius, Lithuania.
Feliksas JankeviciusNational Cancer Institute, Vilnius, Lithuania.
Sonata JarmalaiteInstitute of Biomedical Sciences, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
National Cancer Institute · LTMemorial Sloan Kettering Cancer Center · USVilnius University · LTLund University · SETampere University · FITampere University Hospital · FIUniversity of Turku · FI

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeReliable molecular diagnostic tools are still unavailable for making informed treatment decisions and monitoring the response in patients with castration resistant prostate cancer. We evaluated the significance of whole blood circulating androgen receptor transcripts of full length (AR-FL) and splice variants (AR-V1, AR-V3 and AR-V7) as biomarkers of abiraterone acetate treatment resistance in patients with castration resistant prostate cancer. MATERIALS AND

methodsAfter retrospective analysis in 112 prostate specimens AR-FL, AR-V1, AR-V3 and AR-V7 were evaluated in 185 serial blood samples, prospectively collected from 102 patients with castration resistant prostate cancer before and during abiraterone acetate therapy via reverse transcription quantitative polymerase chain reaction.

resultsAR-FL was present in all samples while AR-V1, AR-V3, AR-V7 and at least 1 of them was detected in 17%, 55%, 65% and 81% of castration resistant prostate cancer blood samples, respectively. The highest amount of AR-V1 was found in blood of patients whose response time was short and medium in comparison to extended. Patients with a higher level of AR-FL and/or AR-V1 had the shortest progression-free survival and overall survival (p <0.0001).

conclusionsBlood circulating AR-FL or AR-V1 can serve as blood based biomarkers for identification of the primary resistance to abiraterone acetate and the tool to monitor de novo resistance development during abiraterone acetate treatment.

Indexed as

Abiraterone AcetateAntineoplastic AgentsBiomarkers, TumorCase-Control StudiesDrug Resistance, NeoplasmFollow-Up StudiesHumansMaleMiddle AgedMultivariate AnalysisProgression-Free SurvivalProspective StudiesProstatic Neoplasms, Castration-ResistantProtein IsoformsReceptors, AndrogenRNAAbiraterone AcetateAntineoplastic AgentsAR protein, humanBiomarkers, TumorProtein IsoformsReceptors, AndrogenRNAabiraterone acetateandrogencastration-resistantdrug resistanceliquid biopsyneoplasmprostatic neoplasmsreceptors

Identifiers

PMID32068491
PMCPMC7301408
OpenAlexW2979388571

What OpenQuestion holds

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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.