Evidence map›Paper›PMID 34280364›Full record

ArticleAmerican journal of ophthalmology2022

Frequency and Clinical Course of Residual Orbital Masses After Treatment of Orbital Rhabdomyosarcoma.

Rachel K Sobel, Joshua R Ford, Wenli Dong, Erin Shriver, Gregory J Griepentrog, J Matthew Debnam, Bita Esmaeli

Open access · greenAbstract read
In one paragraph

Article in American journal of ophthalmology, 2022. 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
0.6field-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, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Persistent mass after treatment for orbital rhabdomyosarcoma.American journal of ophthalmology case reports · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Rachel K SobelFrom the Department of Ophthalmology, Vanderbilt University Medical Center (R.K.S.), Nashville, Tennessee, USA.
Joshua R FordOrbital Oncology & Ophthalmic Plastic Surgery, Department of Plastic Surgery, University of Texas MD Anderson Cancer Center (J.R.F., B.E.), Houston, Texas, USA.
Wenli DongDepartment of Biostatistics, University of Texas MD Anderson Cancer Center (W.D.), Houston, Texas, USA; Department of Ophthalmology, University of Iowa (W.D.), Iowa City, Iowa, USA.
Erin ShriverDepartment of Ophthalmology, University of Iowa (W.D.), Iowa City, Iowa, USA.
Gregory J GriepentrogDepartment of Ophthalmology & Visual Sciences, Medical College of Wisconsin (G.J.G.), Milwaukee, Wisconsin, USA.
J Matthew DebnamDepartment of Neuroradiology, University of Texas MD Anderson Cancer Center (J.M.D.), Houston, Texas, USA.
Bita EsmaeliOrbital Oncology & Ophthalmic Plastic Surgery, Department of Plastic Surgery, University of Texas MD Anderson Cancer Center (J.R.F., B.E.), Houston, Texas, USA. Electronic address: besmaeli@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USUniversity of Iowa · USMedical College of Wisconsin · USVanderbilt University Medical Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

purposeTo evaluate the frequency and clinical course of residual orbital masses on imaging studies after multimodality treatment for orbital rhabdomyosarcoma.

designRetrospective case series.

methodsWe reviewed records of patients with primary orbital rhabdomyosarcoma who underwent chemotherapy and radiotherapy after surgical biopsy or debulking at 4 US centers during 1998-2019. Demographics, histologic subtype, tumor response 12 weeks after chemotherapy initiation and after completion of all treatment, and imaging findings were analyzed.

resultsThirty-two patients met inclusion criteria. Twenty-two were male, and 30 were younger than 18 years. Histologic subtype was embryonal in 22 patients, alveolar in 8, and mixed embryonal/alveolar in 2. Median follow-up time was 46 months (range, 4.9-199 months). Two patients died. Twenty-seven patients had reliable end-of-treatment imaging findings, of whom 9 had a residual mass. Three residual masses disappeared spontaneously (by 4, 32, and 53 months), 2 remained at last contact, at 2 and 7 years of follow-up, and 3 were excised; 1 progressed and underwent an exenteration. Complete response at 12 weeks was associated with complete response at the end of treatment (P < .001). Patients with T1 or T2 tumor at presentation were more likely to have complete response at last contact than were those with T3 or T4 tumor (P < .05). Biopsy type (incisional or excisional) was not associated with response to treatment at any time point.

conclusionA residual orbital mass on imaging may be present after multimodality treatment in approximately one-third of patients. Resolution without biopsy or excision varied from months to years.

Indexed as

Orbital NeoplasmsRhabdomyosarcomaCombined Modality TherapyHumansMaleRemission InductionRetrospective Studies

Identifiers

PMID34280364
PMCPMC12915236
OpenAlexW3183681233

What OpenQuestion holds

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Registered trials

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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.