Evidence map›Paper›PMID 21374084›Full record

ArticleClinical & experimental metastasis2011

Effect of zoledronic acid and amputation on bone invasion and lung metastasis of canine osteosarcoma in nude mice.

Tobie D Wolfe, Smitha Pankajavally Somanathan Pillai, Blake Eason Hildreth, Lisa G Lanigan, Chelsea K Martin, Jillian L Werbeck, Thomas J Rosol

Abstract read
In one paragraph

Article in Clinical & experimental metastasis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  9. Downregulated Long Non-Coding RNA MSC-AS1 Inhibits Osteosarcoma Progression and Increases Sensitivity to Cisplatin by Binding to MicroRNA-142.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  10. Evaluation of effects of radiation therapy combined with either pamidronate or zoledronate on canine osteosarcoma cells.Canadian journal of veterinary research = Revue canadienne de recherche veterinaire · 2019
    Article
  11. Article
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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

7 authors at 1 institution in 1 country.

Tobie D WolfeDepartment of Veterinary Biosciences, The Ohio State University, Columbus, 43210, USA.
Smitha Pankajavally Somanathan Pillai
Blake Eason Hildreth
Lisa G Lanigan
Chelsea K Martin
Jillian L Werbeck
Thomas J Rosol
The Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Effects of nuclear PTHrP on bone formation and the skeletal microenvironmentF32AR057597 · NIAMS · OHIO STATE UNIVERSITY · PI HILDRETH, BLAKE EASON · 2009 to 2011
$190k
NCI NIH HHS P30 CA016058NIAMS NIH HHS F32 AR057597
6 · The paper itself

Abstract

Osteosarcoma (OSA) is an aggressive, highly metastatic and lytic primary bone neoplasm commonly affecting the appendicular skeleton of dogs and children. Current treatment options include amputation of the afflicted limb, limb-sparing procedures, or palliative radiation with or without adjunct chemotherapy. Therapies that inhibit bone resorption, such as the bisphosphonates, may be an effective palliative therapy by limiting the local progression of OSA in those patients that are not viable candidates for amputation. We have developed a mouse model of canine skeletal OSA following intratibial inoculation of OSCA40 cells that spontaneously metastasized to the lungs. We demonstrated that therapy with a nitrogen-containing bisphosphonate, zoledronic acid (Zol), reduced OSA-induced bone lysis; however, Zol monotherapy or in combination with amputation was not effective at inhibiting pulmonary metastasis. While not reaching statistical significance, amputation of the tumor-bearing limb reduced the average incidence of lung metastases; however, this effect was nullified when Zol was added to the treatment protocol. In untreated mice, the magnitude of proximal tibial lysis was significantly correlated with the incidence of metastasis. The data support amputation alone for the management of appendicular OSA rather than combining amputation with Zol. However, in patients that are not viable candidates for amputation, Zol may be a useful palliative therapy for OSA by reducing the magnitude of lysis and therefore bone pain, despite the risk of increased pulmonary metastasis.

Indexed as

Amputation, SurgicalDog DiseasesAnimalsAntineoplastic AgentsBone NeoplasmsDiphosphonatesDogsFemaleImidazolesLung NeoplasmsMiceMice, NudeNeoplasm InvasivenessOsteosarcomaTumor Cells, CulturedXenograft Model Antitumor AssaysAntineoplastic AgentsDiphosphonatesImidazolesZoledronic Acid

Identifiers

PMID21374084
PMCPMC4284437
OpenAlexW1988957044

What OpenQuestion holds

Textmetadata
LicenceTDM
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.