Evidence map›Paper›PMID 34845852›Full record

ArticleCancer medicine2022

Incidence and relative risk of metachronous second primary cancers for 16 cancer sites, Osaka, Japan, 2000-2015: Population-based analysis.

Satomi Odani, Takahiro Tabuchi, Kayo Nakata, Toshitaka Morishima, Yoshihiro Kuwabara, Shihoko Koyama, Haruka Kudo, Mizuki Kato, Isao Miyashiro

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 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

9 authors at 2 institutions in 1 country.

Satomi OdaniCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0002-6263-4952
Takahiro TabuchiCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0002-1050-3125
Kayo NakataCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0001-9782-8637
Toshitaka MorishimaCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0002-0747-3287
Yoshihiro KuwabaraCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0003-4161-2970
Shihoko KoyamaCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0002-7786-4910
Haruka KudoCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0003-3816-8303
Mizuki KatoCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0002-7728-8853
Isao MiyashiroCancer Control Center, Osaka International Cancer Institute, Osaka, Japan.ORCID 0000-0002-2575-4971
Osaka International Cancer Institute · JPOsaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn increasing number of cancer survivors have developed multiple primaries. This study aims to describe the incidence and risk patterns of metachronous second primary cancers (SPCs) in Osaka, Japan.

methodsData were obtained from the Osaka Cancer Registry, a population-based database of all cancers diagnosed in Osaka. The study subjects were individuals who were first diagnosed with invasive cancers in 16 major cancer sites during 2000-2014, aged 15-79 years, survived at least 3 months, and were followed up for 10 years. We measured incidence rates, cumulative risks, and standardized incidence ratios (SIRs: with the Osaka general population as the referent) of developing SPCs during 3 months to 10 years after the first diagnosis.

resultsDuring 2000-2015, among 418,791 cancer survivors, 24,368 (5.8%) developed SPCs within 10 years of first diagnosis. Males had higher incidence rates than females except among young-onset survivors (aged 15-39 years). 10-year cumulative risks among survivors aged 70-79 years (the most dominant age group) were 24.0% (male) and 11.8% (female). 10-year SIRs were 1.38 (95% CI, 1.36-1.40; male) and 1.44 (95% CI, 1.41-1.48; female) with higher estimates among younger survivors in both sexes. Strong bidirectional associations were observed between oral/pharyngeal, esophageal, and laryngeal cancers. Survivors of any smoking-related cancers had elevated SIRs of developing smoking-related SPCs. Similar results were observed for alcohol-related cancers.

conclusionsCancer survivors are at excess risk of developing SPCs compared to the general population. Continued surveillance is warranted to inform survivorship care through risk-based long-term care planning and lifestyle-changing efforts to prevent new cancers.

Indexed as

AdolescentAdultAgedAge DistributionFemaleHumansIncidenceJapanMaleMiddle AgedNeoplasms, Second PrimaryRegistriesRetrospective StudiesRisk FactorsSex DistributionYoung Adultalcohol-related cancercumulative riskepidemiologyincidence ratemultiple primary cancerssmoking-related cancerstandardized incidence ratio

Identifiers

PMID34845852
PMCPMC8729047
OpenAlexW3217793083

What OpenQuestion holds

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LicenceCC BY
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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.