Evidence map›Paper›PMID 31897602›Full record

ReviewWorld journal of urology2021

Navigating systemic therapy for metastatic castration-naïve prostate cancer.

E M Kwan, I A Thangasamy, J Teh, O Alghazo, N J Sathianathen, N Lawrentschuk, A A Azad

Abstract readReview
PubMed Publisher
In one paragraph

Review in World journal of urology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Whole bloodTranslational andrology and urology · 2021
    Article
  6. Advanced prostate cancer.World journal of urology · 2021
    Article
  7. Article
  8. 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

7 authors at 3 institutions in 1 country.

E M KwanDepartment of Medicine, School of Clinical Sciences, Monash University, Melbourne, Australia.
I A ThangasamyDivision of Cancer Surgery, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Australia.
J TehDivision of Cancer Surgery, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Australia.
O AlghazoDivision of Cancer Surgery, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Australia.
N J SathianathenDivision of Cancer Surgery, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Australia.
N LawrentschukDivision of Cancer Surgery, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Australia.
A A AzadDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia. arun.azad@petermac.org.
Peter MacCallum Cancer Centre · AUUniversity of Melbourne · AUMonash University · AU

Funding

National Health and Medical Research Council APP1133107
6 · The paper itself

Abstract

introductionThe last decade has seen a remarkable shift in the treatment landscape of advanced prostate cancer, none more so than in the management of metastatic castration-naïve disease.

methodsThis narrative review will examine existing and emerging evidence supporting systemic therapy use for metastatic castration-naïve prostate cancer (mCNPC) and provide guidance on the selection of these agents with respect to optimising patient outcomes.

resultsThe addition of either docetaxel (chemohormonal approach) or an AR pathway inhibitor (abiraterone, enzalutamide or apalutamide) is a reasonable standard of care option for men commencing long-term ADT for mCNPC. While the issue of disease volume as a predictive biomarker for docetaxel benefit has previously been debated, recent data support consideration of upfront docetaxel in all patients, regardless of metastatic burden. Decisions regarding systemic treatment for men with mCNPC should be based on comprehensive consideration of disease, patient and logistical factors. Multiple novel therapeutics for mCNPC are currently under active investigation.

conclusionThe introduction of potent systemic therapy earlier in the mCNPC disease course has resulted in dramatic improvements in clinical outcomes for patients. As the management of mCNPC continues to evolve, the future remains promising, with the expectation of ongoing improvements to patient outcomes and quality of life.

Indexed as

Androgen AntagonistsAndrogen Receptor AntagonistsAntineoplastic AgentsHumansMaleNeoplasm MetastasisProstatic NeoplasmsAndrogen AntagonistsAndrogen Receptor AntagonistsAntineoplastic AgentsAbirateroneAndrogen receptor pathway inhibitorsApalutamideCastration-naïveDocetaxelEnzalutamideHormone-sensitiveMetastatic prostate cancer

Identifiers

PMID31897602
OpenAlexW2997412766

What OpenQuestion holds

Textmetadata
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.