Evidence map›Paper›PMID 31018850›Full record

ArticleRadiation oncology (London, England)2019

Retrospective study on the benefit of adjuvant radiotherapy in men with intraductal carcinoma of prostate.

Vincent Q Trinh, Nazim Benzerdjeb, Ségolène Chagnon-Monarque, Nicolas Dionne, Guila Delouya, André Kougioumoutzakis, Jennifer Sirois, Roula Albadine, Mathieu Latour, Anne-Marie Mes-Masson and 7 more

Open access · goldAbstract read
In one paragraph

Article in Radiation oncology (London, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 23 citations in OpenAlex.

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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

17 authors at 4 institutions in 1 country.

Vincent Q TrinhDepartment of Pathology, Centre hospitalier de l'Université de Montréal, 1051 Sanguinet, Montréal, Québec, H2X 0C1, Canada.
Nazim BenzerdjebCentre de recherche du Centre hospitalier de l'Université de Montréal and Institut du cancer de Montréal, 900 Saint-Denis, Montréal, Québec, H2X 0A9, Canada.
Ségolène Chagnon-MonarqueCentre de recherche du Centre hospitalier de l'Université de Montréal and Institut du cancer de Montréal, 900 Saint-Denis, Montréal, Québec, H2X 0A9, Canada.
Nicolas DionneCentre de recherche du Centre hospitalier de l'Université de Montréal and Institut du cancer de Montréal, 900 Saint-Denis, Montréal, Québec, H2X 0A9, Canada.
Guila DelouyaDepartment of Radiation Oncology, Centre Hospitalier de l'Université de Montréal, 1051 Sanguinet, Montréal, Québec, H2X 0C1, Canada.
André KougioumoutzakisCentre de recherche du Centre hospitalier de l'Université de Montréal and Institut du cancer de Montréal, 900 Saint-Denis, Montréal, Québec, H2X 0A9, Canada.
Jennifer SiroisDepartment of Pathology, Centre hospitalier de l'Université de Montréal, 1051 Sanguinet, Montréal, Québec, H2X 0C1, Canada.
Roula AlbadineDepartment of Pathology, Centre hospitalier de l'Université de Montréal, 1051 Sanguinet, Montréal, Québec, H2X 0C1, Canada.
Mathieu LatourDepartment of Pathology, Centre hospitalier de l'Université de Montréal, 1051 Sanguinet, Montréal, Québec, H2X 0C1, Canada.
Anne-Marie Mes-MassonCentre de recherche du Centre hospitalier de l'Université de Montréal and Institut du cancer de Montréal, 900 Saint-Denis, Montréal, Québec, H2X 0A9, Canada.
Hélène HovingtonLaboratoire d'Uro-Oncologie Expérimentale, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université-Laval, Hôpital L'Hôtel-Dieu de Québec, 10 McMahon, Québec, G1R 3S1, Canada.
Alain BergeronLaboratoire d'Uro-Oncologie Expérimentale, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université-Laval, Hôpital L'Hôtel-Dieu de Québec, 10 McMahon, Québec, G1R 3S1, Canada.
Kevin C ZornCentre de recherche du Centre hospitalier de l'Université de Montréal and Institut du cancer de Montréal, 900 Saint-Denis, Montréal, Québec, H2X 0A9, Canada.
Yves FradetDepartment of Urology, Centre Hospitalier Universitaire de Québec-Université-Laval, Hôpital L'Hôtel-Dieu de Québec, 11 Côte du Palais, Québec, G1R 2J6, Canada.
Fred SaadCentre de recherche du Centre hospitalier de l'Université de Montréal and Institut du cancer de Montréal, 900 Saint-Denis, Montréal, Québec, H2X 0A9, Canada.
Daniel TausskyDepartment of Radiation Oncology, Centre Hospitalier de l'Université de Montréal, 1051 Sanguinet, Montréal, Québec, H2X 0C1, Canada.
Dominique TrudelDepartment of Pathology, Centre hospitalier de l'Université de Montréal, 1051 Sanguinet, Montréal, Québec, H2X 0C1, Canada. dominique.trudel.chum@ssss.gouv.qc.ca.
Centre Hospitalier de l’Université de Montréal · CAUniversité Laval · CAHôtel-Dieu de Québec · CAUniversité de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntraductal carcinoma of the prostate (IDC-P) is an independent biomarker of recurrence and survival with particular treatment response, yet no study has tested its response to radiotherapy. The aim of our project was to test the impact of adjuvant radiotherapy (ART) in patients with localized to locally advanced prostate cancer (PC) and IDC-P. MATERIALS AND

methodsWe performed a retrospective study of men with pT2-T3 PC treated by radical prostatectomy (RP) with or without ART, from two centres (1993-2015). Exclusion criteria were the use of another type of treatment prior to biochemical recurrence (BCR), and detectable prostate- specific antigen (PSA) following RP or ART. Primary outcome was BCR (2 consecutive PSA ≥ 0.2 ng/ml). Patients were grouped by treatment (RP

resultsWe reviewed 293 RP specimens (median follow-up 99 months, 69 BCR). Forty-eight patients (16.4%) were treated by RP + ART. Multivariate Cox regression for BCR indicated that IDC-P had the strongest impact (hazard ratio [HR] = 2.39, 95% confidence interval [CI]:1.44-3.97), while ART reduced the risk of BCR (HR = 0.38, 95%CI: 0.17-0.85). Other HRF were all significant except for pT3b stage. IDC-P[+] patients who did not receive ART had the worst BCR-free survival (log-rank P = 0.023). Furthermore, IDC-P had the same impact on BCR-free survival as ≥1 HRF (log-rank P = 0.955).

conclusionMen with IDC-P who did not receive ART had the highest BCR rates, and IDC-P had the same impact as ≥1 HRF, which are often used as ART indications. Once validated, ART should be considered in patients with IDC-P.

Indexed as

Carcinoma, Intraductal, NoninfiltratingHumansMaleMiddle AgedNeoplasm Recurrence, LocalPrognosisProstatic NeoplasmsRadiotherapy, AdjuvantRetrospective StudiesSurvival RateAdjuvant radiotherapyBiochemical recurrenceProstate cancerRadical prostatectomy

Identifiers

PMID31018850
PMCPMC6482557
OpenAlexW2946700400

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.