Evidence map›Paper›PMID 33714528›Full record

ArticleInternational journal of radiation oncology, biology, physics2021

Ultrasound-Mediated Gemcitabine Delivery Reduces the Normal-Tissue Toxicity of Chemoradiation Therapy in a Muscle-Invasive Bladder Cancer Model.

Jia-Ling Ruan, Richard J Browning, Yesna O Yildiz, Michael Gray, Luca Bau, Sukanta Kamila, James Thompson, Amy Elliott, Sean Smart, Anthony P McHale and 4 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 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
2.9field-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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Application of Ultrasound Combined with Microbubbles for Cancer Therapy.International journal of molecular sciences · 2022
    Review
  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

14 authors at 3 institutions in 1 country.

Jia-Ling RuanDepartment of Oncology, Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.
Richard J BrowningInstitute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.
Yesna O YildizDepartment of Oncology, Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.
Michael GrayInstitute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.
Luca BauInstitute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.
Sukanta KamilaBiomedical Sciences Research Institute, University of Ulster, Coleraine, Northern Ireland, United Kingdom.
James ThompsonDepartment of Oncology, Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.
Amy ElliottDepartment of Oncology, Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.
Sean SmartDepartment of Oncology, Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.
Anthony P McHaleBiomedical Sciences Research Institute, University of Ulster, Coleraine, Northern Ireland, United Kingdom.
John F CallanBiomedical Sciences Research Institute, University of Ulster, Coleraine, Northern Ireland, United Kingdom.
Borivoj VojnovicDepartment of Oncology, Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.
Eleanor StrideInstitute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.
Anne E KiltieDepartment of Oncology, Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom. Electronic address: anne.kiltie@oncology.ox.ac.uk.
University of Oxford · GBCRUK/MRC Oxford Institute for Radiation Oncology · GBUniversity of Ulster · GB

Funding

Cancer Research UK 19817Cancer Research UK C15140/A19817
6 · The paper itself

Abstract

purposeChemoradiation therapy is the standard of care in muscle-invasive bladder cancer (MIBC). Although agents such as gemcitabine can enhance tumor radiosensitivity, their side effects can limit patient eligibility and treatment efficacy. This study investigates ultrasound and microbubbles for targeting gemcitabine delivery to reduce normal-tissue toxicity in a murine orthotopic MIBC model. MATERIALS AND

methodsCD1-nude mice were injected orthotopically with RT112 bladder tumor cells. Conventional chemoradiation involved injecting gemcitabine (10 mg/kg) before 6 Gy targeted irradiation of the bladder area using the Small Animal Radiation Research Platform (SARRP). Ultrasound-mediated gemcitabine delivery (10 mg/kg gemcitabine) involved either coadministration of microbubbles with gemcitabine or conjugating gemcitabine onto microbubbles followed by exposure to ultrasound (1.1 MHz center frequency, 1 MPa peak negative pressure, 1% duty cycle, and 0.5 Hz pulse repetition frequency) before SARRP irradiation. The effect of ultrasound and microbubbles alone was also tested. Tumor volumes were measured by 3D ultrasound imaging. Acute normal-tissue toxicity from 12 Gy to the lower bowel area was assessed using an intestinal crypt assay in mice culled 3.75 days posttreatment.

resultsA significant delay in tumor growth was observed with conventional chemoradiation therapy and both microbubble groups (P < .05 compared with the radiation-only group). Transient weight loss was seen in the microbubble groups, which resolved within 10 days posttreatment. A positive correlation was found between weight loss on day 3 posttreatment and tumor growth delay (P < .05; R

conclusionsUltrasound and microbubbles offer a promising new approach for improving chemoradiation therapy for muscle-invasive bladder cancer, maintaining a delay in tumor growth but with reduced acute intestinal toxicity compared with conventional chemoradiation therapy.

Indexed as

AnimalsAntimetabolites, AntineoplasticBiotinylationCell Line, TumorChemoradiotherapyContrast MediaDeoxycytidineFemaleGemcitabineHumansIntestinesMiceMice, NudeMicrobubblesNeoplasm InvasivenessOrgans at RiskAntimetabolites, AntineoplasticContrast MediaDeoxycytidineGemcitabine

Identifiers

PMID33714528
PMCPMC7955285
OpenAlexW3128754424

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.