Evidence map›Paper›PMID 34281296›Full record

ArticleCancer research and treatment2022

Incidence Patterns and Outcomes of Ewing Sarcoma in South Korea (1999-2017): A Retrospective Analysis Using Korea Central Cancer Registry Data.

Jun Ah Lee, Jiwon Lim, Dayeon Park, Hye Young Jin, Meerim Park, Hyeon Jin Park, Jong Woong Park, June Hyuk Kim, Hyun Guy Kang, Young-Joo Won

Open access · diamondAbstract read
In one paragraph

Article in Cancer research and treatment, 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
0.4field-weighted citation impact, top 35% 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, 7 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Jun Ah LeeDepartment of Pediatrics, Center for Pediatric Center, National Cancer Center, Goyang, Korea.
Jiwon LimDivision of Cancer Registration and Surveillance, National Cancer Center, Goyang, Korea.
Dayeon ParkDivision of Cancer Registration and Surveillance, National Cancer Center, Goyang, Korea.
Hye Young JinDepartment of Pediatrics, Center for Pediatric Center, National Cancer Center, Goyang, Korea.
Meerim ParkDepartment of Pediatrics, Center for Pediatric Center, National Cancer Center, Goyang, Korea.
Hyeon Jin ParkDepartment of Pediatrics, Center for Pediatric Center, National Cancer Center, Goyang, Korea.
Jong Woong ParkOrthopaedic Oncology Clinic, Center for Rare Cancer, National Cancer Center, Goyang, Korea.
June Hyuk KimOrthopaedic Oncology Clinic, Center for Rare Cancer, National Cancer Center, Goyang, Korea.
Hyun Guy KangOrthopaedic Oncology Clinic, Center for Rare Cancer, National Cancer Center, Goyang, Korea.
Young-Joo WonDivision of Cancer Registration and Surveillance, National Cancer Center, Goyang, Korea.
National Cancer Center · KR

Funding

National Cancer Center 1910132-3
6 · The paper itself

Abstract

purposeDue to low incidence, epidemiologic data of Ewing sarcoma in the Asian population are scarce. We aimed to examine the incidence pattern and outcome of patients with Ewing sarcoma in the Republic of Korea. MATERIALS AND

methodsData of patients with Ewing sarcoma diagnosed between 1999 and 2017 were obtained from the Korea Central Cancer Registry (KCCR). Incidence, clinical characteristics, and survival rates were analyzed and compared between different age groups.

resultsThere were 788 cases (459 males, 329 females), with a median age at diagnosis of 20 years. The age-standardized rate of Ewing sarcoma was 1.01. The number of cases and incidence rates in each age group were as follows: children, 1.6; adolescents and young adults (AYA), 0.93; adults, 0.44; and elderly, 0.53. There were more male cases in children and the AYA group (p < 0.001). Extraskeletal tumors (p < 0.001), primary sites other than extremity (p=0.007), and presence of metastasis at diagnosis (p=0.031) were more frequent in the adults and elderly group. With a median survival time of 78 months, the 5-year overall survival (OS) rate of the entire cohort was 52%. Children fared best (5-year OS, 75%), and the 5-year OS of AYA patients (51%) approximated the OS of the entire cohort. A two-fold difference of 5-year OS was observed between adults and elderly patients (42% vs. 19%). On univariate and multivariate analyses, age ≥ 15 years and presence of metastasis were adverse prognostic factors.

conclusionThis was the first epidemiologic study of Ewing sarcoma using the KCCR data. With a similar incidence to other Asian countries, the survival rate was slightly lower than that of Euro-American cases. Collaborative clinical studies are necessary to improve the outcome of Ewing sarcoma in low-incidence populations.

Indexed as

Bone NeoplasmsSarcoma, EwingAdolescentAgedChildFemaleHumansIncidenceMaleRegistriesRetrospective StudiesSurvival RateYoung AdultEpidemiologyEwing sarcomaKoreaLow-incidence

Identifiers

PMID34281296
PMCPMC9016312
OpenAlexW3186442623

What OpenQuestion holds

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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.