Evidence map›Paper›PMID 36345911›Full record

ArticleCancer science2023

Incidence of second primary cancers among survivors of childhood cancer: A population-based study, Osaka, Japan, 1975-2015.

Satomi Odani, Kayo Nakata, Masami Inoue, Mizuki Kato, Mari Kajiwara Saito, Toshitaka Morishima, Yoshiko Hashii, Junich Hara, Keisei Kawa, Isao Miyashiro

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2023. 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
1.9field-weighted citation impact, top 13% 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, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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 3 institutions in 1 country.

Satomi OdaniCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID https://orcid.org/0000-0002-6263-4952
Kayo NakataCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID https://orcid.org/0000-0001-9782-8637
Masami InoueDepartment of Hematology/Oncology, Osaka Women's and Children's Hospital, Osaka, Japan.
Mizuki KatoCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.
Mari Kajiwara SaitoCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.
Toshitaka MorishimaCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID https://orcid.org/0000-0002-0747-3287
Yoshiko HashiiDepartment of Pediatrics, Osaka International Cancer Institute, Osaka, Japan.
Junich HaraDepartment of Pediatric Hematology and Oncology, Osaka City General Hospital, Osaka, Japan.ORCID https://orcid.org/0000-0002-6798-1558
Keisei KawaDepartment of Hematology/Oncology, Osaka Women's and Children's Hospital, Osaka, Japan.
Isao MiyashiroCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.
Osaka International Cancer Institute · JPOsaka Women's and Children's Hospital · JPOsaka City General Hospital · JP

Funding

Japan Society for the Promotion of Science JP20K18952Japan Society for the Promotion of Science JP22K10548Ministry of Health, Labour and Welfare 20EA1026Ministry of Health, Labour and Welfare H30-Gantaisaku-Ippan-009
6 · The paper itself

Abstract

Second primary cancer (SPC) is one of the most life-threatening late effects of childhood cancers. We investigated the incidence and survival outcomes of SPC in childhood cancer patients in Japan. Data were obtained from the population-based Osaka Cancer Registry. Individuals diagnosed with cancer at age 0-14 years during 1975-2014 and survived 2 months or longer were followed through December 2015. The risk of developing SPC was assessed with standardized incidence ratio (SIR), excess absolute risk (EAR, per 100,000 person-years), and cumulative incidence. Multivariable Poisson regression analysis was carried out to assess relative risks of SPC by treatment method. Survival analysis was undertaken using the Kaplan-Meier method. Of 7229 childhood cancer survivors, 101 (1.4%) developed SPC after a median of 11.6 years. Overall SIR was 5.0, which corresponded with 84.3 EAR. The cumulative incidence was 0.9%, 2.1%, and 3.4% at 10, 20, and 30 years, respectively. Among all SPCs, the type that contributed most to the overall burden was cancers in the central nervous system (EAR = 28.0) followed by digestive system (EAR = 15.1), thyroid (EAR = 8.3), and bones and joints (EAR = 7.8); median latency ranged from 2.0 years (lymphomas) to 26.6 years (skin cancers). Patients treated with radiotherapy alone were at a 2.58-fold increased risk of developing SPC compared to those who received neither chemotherapy nor radiotherapy. Among patients who developed SPCs, 5-year and 10-year survival probabilities after SPC diagnosis were 61.7% and 52.0%, respectively. Risk-based long-term follow-up planning is essential to inform survivorship care and help reduce the burden of SPCs in childhood cancer survivors.

Indexed as

Cancer SurvivorsNeoplasms, Second PrimarySkin NeoplasmsAdolescentChildChild, PreschoolHumansIncidenceInfantInfant, NewbornJapanRegistriesRisk Factorscancer registrychildhood cancerpopulation-based analysissecond primary cancer

Identifiers

PMID36345911
PMCPMC9986077
OpenAlexW4308553943

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LicenceCC BY-NC-ND
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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.