Pancreatic cancer survival by stage and age in seven high-income countries (ICBP SURVMARK-2): a population-based study.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
06 2022
Historique:
received: 21 06 2021
accepted: 09 02 2022
revised: 25 01 2022
pubmed: 4 3 2022
medline: 10 6 2022
entrez: 3 3 2022
Statut: ppublish

Résumé

The global burden of pancreatic cancer has steadily increased, while the prognosis after pancreatic cancer diagnosis remains poor. This study aims to compare the stage- and age-specific pancreatic cancer net survival (NS) for seven high-income countries: Australia, Canada, Denmark, Ireland, New Zealand, Norway, and United Kingdom. The study included over 35,000 pancreatic cancer cases diagnosed during 2012-2014, followed through 31 December 2015. The stage- and age-specific NS were calculated using the Pohar-Perme estimator. Pancreatic cancer survival estimates were low across all 7 countries, with 1-year NS ranging from 21.1% in New Zealand to 30.9% in Australia, and 3-year NS from 6.6% in the UK to 10.9% in Australia. Most pancreatic cancers were diagnosed with distant stage, ranging from 53.9% in Ireland to 83.3% in New Zealand. While survival differences were evident between countries across all stage categories at one year after diagnosis, this survival advantage diminished, particularly in cases with distant stage. This study demonstrated the importance of stage and age at diagnosis in pancreatic cancer survival. Although progress has been made in improving pancreatic cancer prognosis, the disease is highly fatal and will remain so without major breakthroughs in the early diagnosis and management.

Sections du résumé

BACKGROUND
The global burden of pancreatic cancer has steadily increased, while the prognosis after pancreatic cancer diagnosis remains poor. This study aims to compare the stage- and age-specific pancreatic cancer net survival (NS) for seven high-income countries: Australia, Canada, Denmark, Ireland, New Zealand, Norway, and United Kingdom.
METHODS
The study included over 35,000 pancreatic cancer cases diagnosed during 2012-2014, followed through 31 December 2015. The stage- and age-specific NS were calculated using the Pohar-Perme estimator.
RESULTS
Pancreatic cancer survival estimates were low across all 7 countries, with 1-year NS ranging from 21.1% in New Zealand to 30.9% in Australia, and 3-year NS from 6.6% in the UK to 10.9% in Australia. Most pancreatic cancers were diagnosed with distant stage, ranging from 53.9% in Ireland to 83.3% in New Zealand. While survival differences were evident between countries across all stage categories at one year after diagnosis, this survival advantage diminished, particularly in cases with distant stage.
CONCLUSION
This study demonstrated the importance of stage and age at diagnosis in pancreatic cancer survival. Although progress has been made in improving pancreatic cancer prognosis, the disease is highly fatal and will remain so without major breakthroughs in the early diagnosis and management.

Identifiants

pubmed: 35236937
doi: 10.1038/s41416-022-01752-3
pii: 10.1038/s41416-022-01752-3
pmc: PMC9174285
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1774-1782

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

Citadel J Cabasag (CJ)

Cancer Surveillance Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France. CabasagC@fellows.iarc.fr.

Melina Arnold (M)

Cancer Surveillance Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France.

Mark Rutherford (M)

Biostatistics Research Group, Department of Health Sciences, University of Leicester, University Road, Leicester, UK.

Aude Bardot (A)

Cancer Surveillance Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France.

Jacques Ferlay (J)

Cancer Surveillance Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France.

Eileen Morgan (E)

Cancer Surveillance Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France.

Alana Little (A)

Cancer Institute New South Wales, Sydney, NSW, Australia.

Prithwish De (P)

Surveillance and Cancer Registry, Ontario Health (Cancer Care Ontario), Toronto, ON, Canada.

Elijah Dixon (E)

Department of Surgery, University of Calgary, Calgary, AB, Canada.

Ryan R Woods (RR)

Cancer Control Research, BC Cancer, Vancouver, BC, Canada.

Nathalie Saint-Jacques (N)

Nova Scotia Health Cancer Care Program, Registry & Analytics, Halifax, NS, Canada.

Sue Evans (S)

Victorian Cancer Registry Division, Cancer Council Victoria, Melbourne, VIC, Australia.

Gerda Engholm (G)

Cancer Surveillance and Pharmacoepidemiology, Danish Cancer Society Research Center, Strandboulevarden, Copenhagen, Denmark.

Mark Elwood (M)

School of Population Health, University of Auckland, Auckland, New Zealand.

Neil Merrett (N)

Department of Upper Gastrointestinal Surgery, Bankstown-Lidcombe Hospital and School of Medicine, Western Sydney University, Sydney, NSW, Australia.

David Ransom (D)

Fiona Stanley Hospital and Western Australian Department of Health, Perth, WA, Australia.

Dianne L O'Connell (DL)

The Daffodil Centre, The University of Sydney, a joint venture with Cancer Council NSW, Sydney, NSW, Australia.

Freddie Bray (F)

Cancer Surveillance Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France.

Isabelle Soerjomataram (I)

Cancer Surveillance Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France.

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