Evidence map›Paper›PMID 35982807›Full record

ArticleIndian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India

Role of 18-Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography in Predicting Residual Disease Posttreatment Completion in Retinoblastoma Patients.

Abdul Wajid Moothedath, Kanwaljeet Kaur Chopra, Rachna Seth, Jagdish Prasad Meena, Aditya Kumar Gupta, Rakesh Kumar, Manisha Jana, Sreedharan Thankarajan ArunRaj

Open access · greenAbstract read
In one paragraph

Article in Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Retinoblastoma: present scenario and future challenges.Cell communication and signaling : CCS · 2023
    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

8 authors at 1 institution in 1 country.

Abdul Wajid MoothedathDepartment of Pediatrics, Division of Pediatric Oncology, All India Institute of Medical Sciences, New Delhi, India.
Kanwaljeet Kaur ChopraDepartment of Pediatrics, Division of Pediatric Oncology, All India Institute of Medical Sciences, New Delhi, India.
Rachna SethDepartment of Pediatrics, Division of Pediatric Oncology, All India Institute of Medical Sciences, New Delhi, India.
Jagdish Prasad MeenaDepartment of Pediatrics, Division of Pediatric Oncology, All India Institute of Medical Sciences, New Delhi, India.
Aditya Kumar GuptaDepartment of Pediatrics, Division of Pediatric Oncology, All India Institute of Medical Sciences, New Delhi, India.
Rakesh KumarDepartment Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, India.
Manisha JanaDepartment of Radiodiagnosis, All India Institute of Medical Sciences, New Delhi, India.
Sreedharan Thankarajan ArunRajDepartment Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, India.
All India Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Retinoblastoma (RB) is the most common primary intraocular malignancy of childhood. Magnetic resonance imaging (MRI) of the orbit and brain is the preferred imaging modality to diagnose and define extent of disease as well as to assess response to therapy. Sometimes, it may be difficult to differentiate the presence of active residual disease from therapy-related changes based on posttreatment completion MRI. Materials and Methods: RB patients who completed treatment between January 2017 and October 2019 were retrospectively analyzed. We evaluated the utility of F-18-fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET-CT) to predict active disease in RB patients who continued to have residual disease on MRI at completion of treatment. Results: Out of the 89 patients who completed treatment, dilemma regarding remission status was present in 11 children. All 11 patients underwent FDG-PET-CT. None of them had evidence of metabolically active disease in the orbit, optic nerve, brain, or rest of the body. After a median follow-up of 24 months, no children developed any evidence of disease progression in the form of local or distant relapse. Conclusion: Our results showed that in MRI doubtful cases, a nonavid FDG-PET is reassuring in avoiding further therapy as long as close follow-up can be ensured. FDG-PET-CT may emerge as a useful functional modality to predict disease activity in RB.

Indexed as

Fluorodeoxyglucose positron emission tomography/computed tomographymagnetic resonance imagingresidual diseaseretinoblastoma

Identifiers

PMID35982807
PMCPMC9380795
OpenAlexW4285309077

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.