Evidence map›Paper›PMID 32585321›Full record

ReviewBone2020

Targeting anti-cancer agents to bone using bisphosphonates.

Lianping Xing, Frank H Ebetino, Robert K Boeckman, Venkat Srinivasan, Jianguo Tao, Tomi K Sawyer, Jinbo Li, Zhenqiang Yao, Brendan F Boyce

Open access · greenAbstract readReview
In one paragraph

Review in Bone, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 47 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

9 authors at 3 institutions in 1 country.

Lianping XingDepartment of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA; Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY 14642, USA.
Frank H EbetinoDepartment of Chemistry, University of Rochester, Rochester, NY 14627, USA; BioVinc, Pasadena, CA 91107, USA.
Robert K BoeckmanDepartment of Chemistry, University of Rochester, Rochester, NY 14627, USA.
Venkat SrinivasanDepartment of Chemistry, University of Rochester, Rochester, NY 14627, USA.
Jianguo TaoDepartment of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA.
Tomi K SawyerMaestro Therapeutics, Southborough, MA 01772, USA.
Jinbo LiDepartment of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA.
Zhenqiang YaoDepartment of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA.
Brendan F BoyceDepartment of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA; Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY 14642, USA. Electronic address: Brendan_Boyce@urmc.rochester.edu.
University of Rochester Medical Center · USUniversity of Rochester · USBioVinc (United States) · US

Funding

Studies on the fate of the OsteoclastR01AR043510 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI BOYCE, BRENDAN F · 1995 to 2025
$8.4M
Bone targeted delivery of an antimicrobial drug for osteomyelitis therapyR44AI125060 · NIAID · BIOVINC, LLC · PI EBETINO, FRANK H. · 2020 to 2022
$3.0M
Synovial lymphatics and osteoarthritis in agingR01AG059775 · NIA · UNIVERSITY OF ROCHESTER · PI XING, LIANPING · 2020 to 2024
$1.9M
Studies of TRAF3 in age-related low-level chronic inflammation and osteoporosisR01AG049994 · NIA · UNIVERSITY OF ROCHESTER · PI BOYCE, BRENDAN F, YAO, ZHENQIANG · 2016 to 2020
$1.6M
Bone targeted antimicrobials for biofilm-mediated osteolytic infection treatmentR42DE025789 · NIDCR · BIOVINC, LLC · PI EBETINO, FRANK H., SEDGHIZADEH, PARISH PAYMON · 2017 to 2018
$1.5M
Study of osteoblast regulation in TNF-mediated bone lossR01AR063650 · NIAMS · UNIVERSITY OF ROCHESTER · PI XING, LIANPING · 2013 to 2016
$1.4M
Development of novel bone-targeted chloroquine conjugates to prevent bone resorption.R21AR070984 · NIAMS · UNIVERSITY OF ROCHESTER · PI BOECKMAN, ROBERT K, BOYCE, BRENDAN F · 2016 to 2017
$372k
Protein modification in bone cell regulationR21AR069789 · NIAMS · UNIVERSITY OF ROCHESTER · PI BOECKMAN, ROBERT K, XING, LIANPING · 2016 to 2017
$372k
Bone targeted antimicrobials for the treatment of diabetic foot related infections and osteomyelitisR43AR073727 · NIAMS · BIOVINC, LLC · PI EBETINO, FRANK H. · 2018 to 2018
$225k
NIAID NIH HHS R44 AI125060NIAMS NIH HHS R01 AR043510NIAMS NIH HHS R01 AR063650NIAMS NIH HHS R21 AR069789NIAMS NIH HHS R21 AR070984NIAMS NIH HHS R43 AR073727NIA NIH HHS R01 AG049994NIA NIH HHS R01 AG059775NIDCR NIH HHS R42 DE025789
6 · The paper itself

Abstract

The skeleton is affected by numerous primary and metastatic solid and hematopoietic malignant tumors, which can cause localized sites of osteolysis or osteosclerosis that can weaken bones and increase the risk of fractures in affected patients. Chemotherapeutic drugs can eliminate some tumors in bones or reduce their volume and skeletal-related events, but adverse effects on non-target organs can significantly limit the amount of drug that can be administered to patients. In these circumstances, it may be impossible to deliver therapeutic drug concentrations to tumor sites in bones. One attractive mechanism to approach this challenge is to conjugate drugs to bisphosphonates, which can target them to bone where they can be released at diseased sites. Multiple attempts have been made to do this since the 1990s with limited degrees of success. Here, we review the results of pre-clinical and clinical studies made to target FDA-approved drugs and other antineoplastic small molecules to bone to treat diseases affecting the skeleton, including osteoporosis, metastatic bone disease, multiple myeloma and osteosarcoma. Results to date are encouraging and indicate that drug efficacy can be increased and side effects reduced using these approaches. Despite these successes, challenges remain: no drugs have gone beyond small phase 2 clinical trials, and major pharmaceutical companies have shown little interest in the approach to repurpose any of their drugs or to embrace the technology. Nevertheless, interest shown by smaller biotechnology companies in the technology suggests that bone-targeting of drugs with bisphosphonates has a viable future.

Indexed as

Antineoplastic AgentsBone NeoplasmsOsteolysisOsteoporosisBone and BonesDiphosphonatesHumansAntineoplastic AgentsDiphosphonatesBisphosphonateBone metastasisBone-targetingBortezomibChloroquineDrug conjugate

Identifiers

PMID32585321
PMCPMC8485333
OpenAlexW3036448610

What OpenQuestion holds

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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.