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dc.contributor.authorMuruganandan, S.
dc.contributor.authorAlfonso, Helman
dc.contributor.authorFranklin, P.
dc.contributor.authorShilkin, K.
dc.contributor.authorSegal, A.
dc.contributor.authorOlsen, N.
dc.contributor.authorReid, Alison
dc.contributor.authorde Klerk, N.
dc.contributor.authorMusk, A.
dc.contributor.authorBrims, F.
dc.date.accessioned2017-03-15T22:24:01Z
dc.date.available2017-03-15T22:24:01Z
dc.date.created2017-03-08T06:39:33Z
dc.date.issued2017
dc.identifier.citationMuruganandan, S. and Alfonso, H. and Franklin, P. and Shilkin, K. and Segal, A. and Olsen, N. and Reid, A. et al. 2017. Comparison of outcomes following a cytological or histological diagnosis of malignant mesothelioma. British Journal of Cancer. 116: pp. 703-708.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/50395
dc.identifier.doi10.1038/bjc.2017.20
dc.description.abstract

Background: Survival with the epithelioid subtype of malignant mesothelioma (MM) is longer than the biphasic or sarcomatoid subtypes. There is concern that cytology-diagnosed epithelioid MM may underdiagnose the biphasic subtype. This study examines survival differences between patients with epithelioid MM diagnosed by cytology only and other subtypes diagnosed by histology. Methods: Demographics, diagnosis method, MM subtype and survival were extracted from the Western Australia (WA) Mesothelioma Registry, which records details of all MM cases occurring in WA. Results: A total of 2024 MM cases were identified over 42 years. One thousand seven hundred forty-four (86.2%) were male, median (IQR) age was 68.6 (60.4–77.0) years. A total of 1212 (59.9%) cases were identified as epithelioid subtype of which 499 (41.2%) were diagnosed using fluid cytology only. Those with a cytology-only diagnosis were older than the histology group (median 70.2 vs 67.6 years, P<0.001), but median survival was similar (cytology 10.6 (5.5–19.2) vs histology 11.1 (4.8–19.8) months, P=0.727) and Cox regression modelling adjusting for age, sex, site and time since first exposure showed no difference in survival between the different diagnostic approaches. Conclusions: Survival of cytologically and histologically diagnosed epithelioid MM cases does not differ. A diagnostic tap should be considered adequate to diagnose epithelioid MM without need for further invasive testing.

dc.publisherNature Publishing Group
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.titleComparison of outcomes following a cytological or histological diagnosis of malignant mesothelioma
dc.typeJournal Article
dcterms.source.issn0007-0920
dcterms.source.titleBritish Journal of Cancer
curtin.departmentEpidemiology and Biostatistics
curtin.accessStatusOpen access


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