Evidence map›Paper›PMID 35969241›Full record

ArticleJournal of surgical oncology2022

Surgical management of pediatric salivary malignant tumors-A single-center cohort study.

Joseph Lopez, Yu Han Chen, Alana Eagan, Conall Fitzgerald, Robbie Woods, Richard Wong, Jatin Shah, Ian Ganly

Abstract read
In one paragraph

Article in Journal of surgical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Joseph LopezDepartment of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.ORCID https://orcid.org/0000-0003-3001-1109
Yu Han ChenDepartment of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
Alana EaganDepartment of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
Conall FitzgeraldDepartment of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
Robbie WoodsDepartment of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
Richard WongDepartment of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
Jatin ShahDepartment of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.ORCID http://orcid.org/0000-0002-6444-6592
Ian GanlyDepartment of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundThe purpose of this study was to report incidence, clinicopathologic behavior, management, and outcome of pediatric patients treated surgically for salivary gland (SG) malignancies.

methodsPatients who underwent surgery for SG malignancies from 1985 to 2015 were identified. Clinical, pathological, treatment and outcomes data were collected. Disease-specific survival (DSS), recurrence-free survival (RFS), and overall survival (OS) were calculated using Kaplan-Meier method.

resultsTwenty-eight pediatric patients were included. The most common histopathological types were mucoepidermoid (n = 18, 64.3%), acinic cell (n = 7, 25.0%), adenoid cystic (n = 2, 7.1%), and adenocarcinoma (n = 1, 3.6%). Surgical approach varied and ranged from superficial parotidectomy (n = 11, 39.3%) to partial maxillectomy (n = 6, 21.4%). Nine patients (32%) required postoperative radiotherapy. DSS, OS, and RFS probability at 5 years were 96.4%, 96.4%, and 89.3%, respectively.

conclusionPediatric SG malignancies are rare and have favorable outcome at 5 years. Larger, multi-institutional studies are required to better understand the natural history of these rare tumors.

Indexed as

AdenocarcinomaCarcinoma, MucoepidermoidSalivary Gland NeoplasmsChildCohort StudiesHumansRetrospective Studiespediatric salivary gland malignanciessurvival outcomes

Identifiers

PMID35969241
PMCPMC10251410

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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.