Evidence map›Paper›PMID 28405782›Full record

ArticleFamilial cancer2017

Importance of updating family cancer history in childhood cancer survivors.

Selena Russo, Meera Warby, Katherine M Tucker, Claire E Wakefield, Richard J Cohn

Open access · greenAbstract readLetter
PubMed Publisher
In one paragraph

Article in Familial cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Selena RussoBehavioural Sciences Unit, Sydney Children's Hospital, Kids Cancer Centre, Level 1 South, Sydney Children's Hospital, High Street, Randwick, NSW, 2031, Australia. s.russo@unsw.edu.au.ORCID http://orcid.org/0000-0002-3024-3316
Meera WarbyDepartment of Medical Oncology, Hereditary Cancer Clinic, Prince of Wales Hospital, Randwick, Australia.
Katherine M TuckerDepartment of Medical Oncology, Hereditary Cancer Clinic, Prince of Wales Hospital, Randwick, Australia.
Claire E WakefieldBehavioural Sciences Unit, Sydney Children's Hospital, Kids Cancer Centre, Level 1 South, Sydney Children's Hospital, High Street, Randwick, NSW, 2031, Australia.
Richard J CohnBehavioural Sciences Unit, Sydney Children's Hospital, Kids Cancer Centre, Level 1 South, Sydney Children's Hospital, High Street, Randwick, NSW, 2031, Australia.
UNSW Sydney · AUPrince of Wales Hospital · AU

Funding

the National Health and Medical Research Council of Australia APP1067501
6 · The paper itself

Abstract

Estimates of the number of childhood cancers with a genetic basis range from 5-8.5% found in germline samples to 29% based on clinical criteria. Family history-taking practice is a fundamental first step in detecting at risk individuals and families. This study focused on Li-Fraumeni Syndrome (LFS), a highly penetrant cancer syndrome. Reported family history in a cohort of 648 of cancer survivor cohort (CCS) was examined. Eligible CCS were: (i) aged up to 14 years at diagnosis; (ii) more than 5 years postdiagnosis; (iii) treated for a childhood cancer at the study hospitals in NSW, Australia; (iv) in remission for more than 3 years. CCS completed self-administered questionnaires. Medical records confirmed diagnosis and treatment-related information. Our findings reveal an increased cancer risk among sibling and relatives of CCS. 91% of siblings diagnosed with cancer were diagnosed under the age of 40 and about 30% diagnosed under the aged of 15 revealing a 5- (RR = 5.1; 95% CI, 3.3-7.9) and 44-fold (RR = 44.6; 95% CI, 18.4-108.3) increased risked of cancer compared with the Australian population, respectively. About 2% of CCS reported that they had been diagnosed with a genetic cancer syndrome. However, 11% of survivors described a family history pattern which met Chompret criteria for screening for TP53 mutations associated with LFS. Our data suggests that familial cancer predispositions may be initially overlooked. Aperiodic and accurate ascertainment of family cancer history of childhood cancer patients and survivors is therefore recommended.

Indexed as

Cancer SurvivorsPedigreeAdolescentAdultAgedAustraliaChildChild, PreschoolFemaleGenetic Predisposition to DiseaseHumansInfantInfant, NewbornMaleMiddle AgedNeoplastic Syndromes, HereditaryCancerCancer family historyCancer syndromeChildhood cancer survivorsGeneticOncologyPediatric

Identifiers

PMID28405782
OpenAlexW2606376578

What OpenQuestion holds

Textmetadata
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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.