Evidence map›Paper›PMID 28673318›Full record

ArticlePopulation health metrics2017

Choice of relative or cause-specific approach to cancer survival analysis impacts estimates differentially by cancer type, population, and application: evidence from a Canadian population-based cohort study.

Diana R Withrow, Jason D Pole, E Diane Nishri, Michael Tjepkema, Loraine D Marrett

Open access · goldAbstract readComparative Study
In one paragraph

Article in Population health metrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  7. Choice of Survival Metric and Its Impacts on Cancer Survival Estimates for American Indian and Alaska Native People.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023
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  12. Differences in Cancer Survival with Relative versus Cause-Specific Approaches: An Update Using More Accurate Life Tables.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2019
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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

5 authors at 4 institutions in 2 countries.

Diana R WithrowRadiation Epidemiology Branch, National Cancer Institute, 9609 Medical Center Drive, Room 7E590, Bethesda, MD, 20892-9778, USA. diana.withrow@nih.gov.
Jason D PolePediatric Oncology Group of Ontario, 480 University Avenue, Suite 1014, Toronto, ON, M5G 1V2, Canada.
E Diane NishriPopulation Health and Prevention, Prevention and Cancer Control, Cancer Care Ontario, 505 University Ave, 14th Floor, Toronto, ON, M5G 1X3, Canada.
Michael TjepkemaHealth Analysis Division, Statistics Canada, 150 Tunney's Pasture Driveway, Ottawa, ON, K1A 0T6, Canada.
Loraine D MarrettAboriginal Cancer Control Unit, Prevention and Cancer Control, Cancer Care Ontario, 505 University Ave, 14th Floor, Toronto, ON, M5G 1X3, Canada.
Cancer Care Ontario · CANational Cancer Institute · USPediatric Oncology Group · CAStatistics Canada · CA

Funding

CIHR
6 · The paper itself

Abstract

backgroundCause-specific (CS) and net survival in a relative survival framework (RS) are two of the most common methods for estimating cancer survival. In this paper, we assess the differences in results produced by two permutations of cause-specific and relative survival applied to estimating cancer survival and disparities in cancer survival, using data from First Nations and non-Aboriginal populations in Canada.

methodsSubjects were members of the 1991 Canadian Census Mortality Cohort, a population-based cohort of adult respondents to the 1991 Long Form Census who have been followed up for incident cancers and death through linkage to administrative databases. We compared four methods: relative survival analyses with ethnicity-specific life tables (RS-ELT); relative survival with general population life tables (RS-GLT); cause-specific survival with a broad definition of cancer death (CS-Broad); and cause-specific survival with a narrow definition of cause of death (CS-Narrow) and applied these to the nine most common cancers among First Nations.

resultsApart from breast and prostate cancers, RS-ELT, RS-GLT, and CS-Broad tended to produce similar estimates of age-standardized five-year survival, whereas CS-Narrow yielded higher estimates of survival. CS-Narrow estimates were particularly unlike those based on the other methods for cancers of the digestive and respiratory tracts. Estimates of disparities in survival were generally comparable across the four methods except for breast and prostate cancers.

conclusionsCancer surveillance efforts in sub-populations defined by race, ethnicity, geography, socioeconomic status, or similar factors are necessary for identifying disparities and monitoring progress toward reducing them. In the absence of routine monitoring of cancer survival and cancer survival disparities in these populations, estimates generated by different methods will inevitably be compared over time and across populations. In this study, we demonstrate that caution should be exercised in making these comparisons, particularly in interpreting cause-specific survival rates with an unknown or narrow definition of cancer death and in estimates of breast and prostate cancer survival and/or disparities in survival generated by different methods.

Indexed as

Cause of DeathLife TablesSurvival AnalysisAdultAgedCanadaCensusesCohort StudiesEthnicityFemaleHealth Status DisparitiesHumansMaleMiddle AgedNeoplasmsRacial GroupsEpidemiologic methodsHealth status disparitiesIndian, north AmericanMinority healthNeoplasmsSurvival analysis

Identifiers

PMID28673318
PMCPMC5496357
OpenAlexW2730840605

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.