Evidence map›Paper›PMID 30601585›Full record

ReviewBritish journal of clinical pharmacology2019

Clinical and translational pharmacology of drugs for the prevention and treatment of bone metastases and cancer-induced bone loss.

Maria Rita Dionísio, André Mansinho, Catarina Abreu, Joana Cavaco-Silva, Sandra Casimiro, Luís Costa

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of clinical pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 12% 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, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Drugs for the treatment of metabolic bone diseases.British journal of clinical pharmacology · 2019
    Article
  12. Pharmacology of bisphosphonates.British journal of clinical pharmacology · 2019
    Review
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

6 authors at 2 institutions in 1 country.

Maria Rita DionísioOncology Division, Hospital de Santa Maria - CHLN, Lisbon, Portugal.ORCID 0000-0002-8296-9768
André MansinhoOncology Division, Hospital de Santa Maria - CHLN, Lisbon, Portugal.ORCID 0000-0001-8771-0838
Catarina AbreuOncology Division, Hospital de Santa Maria - CHLN, Lisbon, Portugal.ORCID 0000-0003-3558-3966
Joana Cavaco-SilvaOncology Division, Hospital de Santa Maria - CHLN, Lisbon, Portugal.ORCID 0000-0002-8737-0439
Sandra CasimiroLuis Costa Lab, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal.ORCID 0000-0002-6917-4477
Luís CostaOncology Division, Hospital de Santa Maria - CHLN, Lisbon, Portugal.ORCID 0000-0002-4782-7318
Hospital de Santa Maria · PTUniversity of Lisbon · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone disease is a frequent event in cancer patients, both due to cancer spread to bone and to cancer therapies. Bone is the organ most frequently affected by metastatic disease when considering the two most frequent cancers in the Western world (breast and prostate cancers). Bone metastases can have a substantial detrimental effect on patients' quality of life, as well as significant morbidity due to complications collectively known as skeletal-related events (SREs), which include hypercalcaemia, pathological fractures, spinal cord compression, and need of radiotherapy or surgery to the bone. These have been successfully mitigated with the development of bone-targeted agents (BTAs; bisphosphonates and denosumab), focused on inhibiting osteoclast activity. The potential direct antitumour effect of bisphosphonates, as well as the impact of osteoclast inhibition with subsequent decrease in bone metabolism, have also propelled investigation on the role of BTAs in preventing cancer relapse in bone. In this review, the authors aimed to discuss the role of BTAs in the treatment and prevention of bone metastases, as well as their potential value in preventing cancer treatment-induced bone loss (CTIBL). The review will focus on breast and prostate cancers, with the aim of providing the most relevant clinical data emerging from bench to bedside translational research in the field of cancer-induced bone disease.

Indexed as

AnimalsAntineoplastic AgentsBone Density Conservation AgentsBone Diseases, MetabolicBone NeoplasmsBone RemodelingBreast NeoplasmsChemotherapy, AdjuvantFemaleHumansMalePalliative CareProstatic NeoplasmsRisk FactorsTreatment OutcomeAntineoplastic AgentsBone Density Conservation Agentsbisphosphonatesbone metastasesbone-targeted agentsdenosumabRa-223

Identifiers

PMID30601585
PMCPMC6533479
OpenAlexW2907591491

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.