Evidence map›Paper›PMID 26885619›Full record

ArticleOncotarget2016

MR imaging biomarkers for evaluating therapeutic effects shortly after near infrared photoimmunotherapy.

Yuko Nakamura, Marcelino Bernardo, Tadanobu Nagaya, Kazuhide Sato, Toshiko Harada, Peter L Choyke, Hisataka Kobayashi

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

7 authors at 3 institutions in 1 country.

Yuko NakamuraMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Marcelino BernardoResearch Technology Program, SAIC-Frederick Inc., National Cancer Institute, Bethesda, MD, USA.
Tadanobu NagayaMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Kazuhide SatoMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Toshiko HaradaMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Peter L ChoykeMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Hisataka KobayashiMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
National Cancer Institute · USCenter for Cancer Research · USScience Applications International Corporation (United States) · US

Funding

Cancer-cell specific therapy: photo-immunotherapyZIABC011513 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KOBAYASHI, HISATAKA · 2013 to 2025
$15.5M
6 · The paper itself

Abstract

Near infrared photoimmunotherapy (NIR-PIT) is a new cancer treatment that combines the specificity of antibodies for targeting tumors with the toxicity induced by photon absorbers after irradiation with NIR light. The purpose of this study was to determine if MR imaging can detect changes in the MR properties of tumor within several hours of NIR-PIT. A431 cells were injected subcutaneously in the right and left dorsi of 12 mice. Six days later, the mice were injected with a photon absorber, IR700, conjugated to panitumumab, an antibody targeting epidermal growth factor receptor. One day later, only right sided tumor was exposed to NIR light (treated tumor). MRI was performed 1 day before and 1-2 hours after NIR-PIT using gadofosveset for six mice and gadopentetate dimeglumine for another six mice. T2 relaxation times, the apparent diffusion coefficient (ADC) for the following combinations of b-values: 0-1000, 200-1000 and 500-1000 s/mm2 and enhancement indices were compared before and after NIR-PIT using a two-sided paired t-test. For treated tumors, T2 relaxation time increased after NIR-PIT (p < 0.01) and all three ADC values decreased after NIR-PIT (p < 0.01). Moreover, the enhancement area under the curve (AUC) using gadofosveset increased after NIR-PIT (p = 0.02). In conclusion, prolongation of T2, reductions in ADC and increased enhancement using gadofosveset are seen within 2 hours of NIR-PIT treatment of tumors. Thus, MRI can be a useful imaging biomarker for detecting early therapeutic changes after NIR-PIT.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorContrast MediaFemaleGadoliniumGadolinium DTPAHumansImmunoconjugatesImmunotherapyInfrared RaysMagnetic Resonance ImagingMiceMice, NudeNeoplasms, ExperimentalOrganometallic CompoundsAntineoplastic AgentsContrast Mediagadofosveset trisodiumGadoliniumGadolinium DTPAImmunoconjugatesOrganometallic CompoundsPhotosensitizing Agentsdiffusion weighted imagegadofosvesetMRInear infrared photoimmunotherapyT2 relaxation time

Identifiers

PMID26885619
PMCPMC4941385
OpenAlexW2292515774

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.