Evidence map›Paper›PMID 42192992›Full record

ArticleCancers2026

Beyond the 5-Year Window: Late-Onset Ocular Morbidity and a Proposed 10-Year Functional Survivorship Protocol for Pediatric Orbital Rhabdomyosarcoma.

Hadeel Halalsheh, Yacoub A Yousef, Mona Mohammad, Ahmad Kh Ibrahimi, Iyad Sultan

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Hadeel HalalshehDepartment of Pediatrics, King Hussein Cancer Center, Queen Rania Street, Amman 11941, Jordan.ORCID 0000-0003-4803-1976
Yacoub A YousefDepartment of Surgery (Ophthalmology), King Hussein Cancer Center, Amman 11941, Jordan.ORCID 0000-0001-7750-6454
Mona MohammadDepartment of Surgery (Ophthalmology), King Hussein Cancer Center, Amman 11941, Jordan.ORCID 0000-0002-8318-1171
Ahmad Kh IbrahimiDepartment of Radiation Oncology, King Hussein Cancer Center, Amman 11941, Jordan.ORCID 0000-0001-6256-861X
Iyad SultanDepartment of Pediatrics, King Hussein Cancer Center, Queen Rania Street, Amman 11941, Jordan.ORCID 0000-0002-2664-1565

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOrbital rhabdomyosarcoma (RMS) is the most common primary pediatric malignant orbital tumor, typically curable with chemotherapy and radiation. Data regarding MRI chemotherapy response and long-term ophthalmologic outcomes remain limited in non-cooperative-group settings.

methodsWe retrospectively reviewed children with primary orbital RMS treated at King Hussein Cancer Center (2002-2025) with vincristine, actinomycin-D, and cyclophosphamide (VAC). Pre-local-control MRI responses were classified as complete (CR), partial (PR), stable/minor (SD/MR), or progressive disease (PD). Survival and ophthalmologic outcomes were analyzed.

resultsTwenty-two patients (median age 5.6 years) were included. All had localized disease (77% low-risk). All received VAC; 20 (91%) received radiotherapy (median 45 Gy). Pre-radiotherapy MRI showed 8 (36%) CR and 11 (50%) PR. Four patients (18%) died. Five-year event-free survival (EFS) and overall survival (OS) were 73% and 84%, respectively. Cataracts developed in 45% of the cohort (50% of irradiated patients) at a median of 39.1 months (range 9.4-95.1). At last assessment, visual acuity was good in 60%, moderate in 25%, and severely impaired in 15%.

conclusionsExcellent survival in orbital RMS is achievable in resource-stratified settings. Induction MRI progressive disease (PD) was associated with poor outcomes in this cohort and may represent an early prognostic signal warranting further validation in larger studies. Furthermore, the documented maximum cataract latency of 95 months suggests that the standard 5-year surveillance window is insufficient. These findings support extending ophthalmologic surveillance beyond the standard 5-year window. We propose, based on our retrospective institutional data, a 10-year functional survivorship framework.

Indexed as

childrenEBRTJordanMRI responseophthalmologic late effectsorbitoutcomesrhabdomyosarcoma

Identifiers

PMID42192992
PMCPMC13204557

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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.