Evidence map›Paper›PMID 25173680›Full record

ArticleClinical & experimental metastasis2014

Improving treatment strategies for patients with metastatic castrate resistant prostate cancer through personalized computational modeling.

Jill Gallaher, Leah M Cook, Shilpa Gupta, Arturo Araujo, Jasreman Dhillon, Jong Y Park, Jacob G Scott, Julio Pow-Sang, David Basanta, Conor C Lynch

Abstract read
In one paragraph

Article in Clinical & experimental metastasis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Hybrid modeling frameworks of tumor development and treatment.Wiley interdisciplinary reviews. Systems biology and medicine · 2020
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Homeostasis Back and Forth: An Ecoevolutionary Perspective of Cancer.Cold Spring Harbor perspectives in medicine · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Current and emerging therapies for bone metastatic castration-resistant prostate cancer.Cancer control : journal of the Moffitt Cancer Center · 2015
    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

10 authors.

Jill GallaherDepartment of Integrated Mathematical Oncology, SRB, H. Lee Moffitt Cancer Center and Research Institute, 12902 Magnolia Dr., Tampa, FL, 33612, USA.
Leah M Cook
Shilpa Gupta
Arturo Araujo
Jasreman Dhillon
Jong Y Park
Jacob G Scott
Julio Pow-Sang
David Basanta
Conor C Lynch

Funding

Multiscale Modeling of Bone Environment Responses to Metastatic Prostate CancerU01CA202958 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI BASANTA GUTIERREZ, DAVID, LYNCH, CONOR C · 2016 to 2020
$3.3M
Predicting Prostate Cancer AggressivenessU01CA151924 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI ANDERSON, ALEXANDER ROBERTSON ALLAN, AYALA, GUSTAVO ENRIQUE · 2011 to 2015
$2.8M
Host MMP-mediated regulation of the vicious cycle of prostate to bone metastasesR01CA143094 · NCI · VANDERBILT UNIVERSITY · PI LYNCH, CONOR C · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA143094NCI NIH HHS R01CA143094NCI NIH HHS U01 CA151924NCI NIH HHS U01 CA202958
6 · The paper itself

Abstract

Metastatic castrate resistant prostate cancer (mCRPC) is responsible for the majority of prostate cancer deaths with the median survival after diagnosis being 2 years. The metastatic lesions often arise in the skeleton, and current treatment options are primarily palliative. Using guidelines set forth by the National Comprehensive Cancer Network (NCCN), the medical oncologist has a number of choices available to treat the metastases. However, the sequence of those treatments is largely dependent on the patient history, treatment response and preferences. We posit that the utilization of personalized computational models and treatment optimization algorithms based on patient specific parameters could significantly enhance the oncologist's ability to choose an optimized sequence of available therapies to maximize overall survival. In this perspective, we used an integrated team approach involving clinicians, researchers, and mathematicians, to generate an example of how computational models and genetic algorithms can be utilized to predict the response of heterogeneous mCRPCs in bone to varying sequences of standard and targeted therapies. The refinement and evolution of these powerful models will be critical for extending the overall survival of men diagnosed with mCRPC.

Indexed as

Computer SimulationModels, TheoreticalMolecular Targeted TherapyPrecision MedicineAlgorithmsBone NeoplasmsHumansMalePrognosisProstatic Neoplasms, Castration-ResistantSignal Transduction

Identifiers

PMID25173680
PMCPMC5399888

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.