Steady survival improvements in soft tissue and bone sarcoma in the Nordic countries through 50 years

Sarcomas are rare cancers with many subtypes in soft tissues, bone and cartilage. International survival trends in these cancers are not well known. We present 50-year survival trends for soft tissue sarcoma (STS) and bone sarcoma (BS) in Denmark (DK), Finland (FI), Norway (NO) and Sweden (SE). Rela...

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Veröffentlicht in:Cancer epidemiology 2024-10, Vol.92, p.102449, Article 102449
Hauptverfasser: Tichanek, Filip, Försti, Asta, Hemminki, Otto, Hemminki, Akseli, Hemminki, Kari
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container_start_page 102449
container_title Cancer epidemiology
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creator Tichanek, Filip
Försti, Asta
Hemminki, Otto
Hemminki, Akseli
Hemminki, Kari
description Sarcomas are rare cancers with many subtypes in soft tissues, bone and cartilage. International survival trends in these cancers are not well known. We present 50-year survival trends for soft tissue sarcoma (STS) and bone sarcoma (BS) in Denmark (DK), Finland (FI), Norway (NO) and Sweden (SE). Relative 1-, 5/1 conditional- and 5-year survival data were obtained from the NORDCAN database for years 1971–20. We additionally estimated annual changes in survival rates and determined significant break points. In the last period, 2016–20, 5-year survival in STS was best for NO men (74.6%) and FI women (71.1%). For the rarer BS, survival rates for SE men (72.0%) and DK women (71.1%) were best. Survival in BS was lower than that in STS in 1971–75 and the difference remained in 2016–20 for men, but for women the rates were almost equal. Sex- and country-specific differences in survival in STS were small. The 50-year improvement in 5-year survival in STS was highest in NO men, 34.0 % units and FI women, 30.0 % units. The highest improvements in BS were in SE men 26.2 % units and in FI women 29.2 % units. The steady development in survival over the half century suggests contribution by stepwise improvements in diagnostics, treatment and care. The 10–15% mortality in the first year probably indicates diagnostic delays which could be improved by organizing patient pathways for aggressive rare diseases. Early diagnosis would also reduce metastatic disease and breakthroughs in treatment are a current challenge. •Survival in bone (BS) and soft tissue sarcoma (STS) has increased, as documented.•5-year survival reached 70% in these cancers but male BS remained at over 60%.•Steady survival development suggests contributions by stepwise improvements in care.•Over 10% mortality in the first year is a challenge for survival improvements.•Achieving this would require vigilance and ready care pathways to experts.
doi_str_mv 10.1016/j.canep.2023.102449
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International survival trends in these cancers are not well known. We present 50-year survival trends for soft tissue sarcoma (STS) and bone sarcoma (BS) in Denmark (DK), Finland (FI), Norway (NO) and Sweden (SE). Relative 1-, 5/1 conditional- and 5-year survival data were obtained from the NORDCAN database for years 1971–20. We additionally estimated annual changes in survival rates and determined significant break points. In the last period, 2016–20, 5-year survival in STS was best for NO men (74.6%) and FI women (71.1%). For the rarer BS, survival rates for SE men (72.0%) and DK women (71.1%) were best. Survival in BS was lower than that in STS in 1971–75 and the difference remained in 2016–20 for men, but for women the rates were almost equal. Sex- and country-specific differences in survival in STS were small. The 50-year improvement in 5-year survival in STS was highest in NO men, 34.0 % units and FI women, 30.0 % units. The highest improvements in BS were in SE men 26.2 % units and in FI women 29.2 % units. The steady development in survival over the half century suggests contribution by stepwise improvements in diagnostics, treatment and care. The 10–15% mortality in the first year probably indicates diagnostic delays which could be improved by organizing patient pathways for aggressive rare diseases. Early diagnosis would also reduce metastatic disease and breakthroughs in treatment are a current challenge. •Survival in bone (BS) and soft tissue sarcoma (STS) has increased, as documented.•5-year survival reached 70% in these cancers but male BS remained at over 60%.•Steady survival development suggests contributions by stepwise improvements in care.•Over 10% mortality in the first year is a challenge for survival improvements.•Achieving this would require vigilance and ready care pathways to experts.</description><identifier>ISSN: 1877-7821</identifier><identifier>ISSN: 1877-783X</identifier><identifier>EISSN: 1877-783X</identifier><identifier>DOI: 10.1016/j.canep.2023.102449</identifier><identifier>PMID: 37679266</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Age ; Aged ; Bone cancer ; Bone Neoplasms - epidemiology ; Bone Neoplasms - mortality ; Bone Neoplasms - pathology ; Bone tumors ; Cancer therapies ; Chemotherapy ; Chromosomes ; Conditional survival ; Diagnostics ; Ewings sarcoma ; Female ; Females ; Finland - epidemiology ; Humans ; Incidence ; Male ; Metastases ; Middle Aged ; Mortality ; Osteosarcoma - epidemiology ; Osteosarcoma - mortality ; Osteosarcoma - pathology ; Osteosarcoma - therapy ; Radiation therapy ; Rare diseases ; Registries ; Relative survival ; Risk factors ; Sarcoma - epidemiology ; Sarcoma - mortality ; Sarcoma - pathology ; Sarcoma - therapy ; Scandinavian and Nordic Countries - epidemiology ; Soft Tissue Neoplasms - epidemiology ; Soft Tissue Neoplasms - mortality ; Soft Tissue Neoplasms - pathology ; Soft tissue sarcoma ; Soft tissues ; Software ; Survival ; Survival Rate ; Treatment ; Tumors ; Young Adult</subject><ispartof>Cancer epidemiology, 2024-10, Vol.92, p.102449, Article 102449</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. 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International survival trends in these cancers are not well known. We present 50-year survival trends for soft tissue sarcoma (STS) and bone sarcoma (BS) in Denmark (DK), Finland (FI), Norway (NO) and Sweden (SE). Relative 1-, 5/1 conditional- and 5-year survival data were obtained from the NORDCAN database for years 1971–20. We additionally estimated annual changes in survival rates and determined significant break points. In the last period, 2016–20, 5-year survival in STS was best for NO men (74.6%) and FI women (71.1%). For the rarer BS, survival rates for SE men (72.0%) and DK women (71.1%) were best. Survival in BS was lower than that in STS in 1971–75 and the difference remained in 2016–20 for men, but for women the rates were almost equal. Sex- and country-specific differences in survival in STS were small. The 50-year improvement in 5-year survival in STS was highest in NO men, 34.0 % units and FI women, 30.0 % units. The highest improvements in BS were in SE men 26.2 % units and in FI women 29.2 % units. The steady development in survival over the half century suggests contribution by stepwise improvements in diagnostics, treatment and care. The 10–15% mortality in the first year probably indicates diagnostic delays which could be improved by organizing patient pathways for aggressive rare diseases. 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International survival trends in these cancers are not well known. We present 50-year survival trends for soft tissue sarcoma (STS) and bone sarcoma (BS) in Denmark (DK), Finland (FI), Norway (NO) and Sweden (SE). Relative 1-, 5/1 conditional- and 5-year survival data were obtained from the NORDCAN database for years 1971–20. We additionally estimated annual changes in survival rates and determined significant break points. In the last period, 2016–20, 5-year survival in STS was best for NO men (74.6%) and FI women (71.1%). For the rarer BS, survival rates for SE men (72.0%) and DK women (71.1%) were best. Survival in BS was lower than that in STS in 1971–75 and the difference remained in 2016–20 for men, but for women the rates were almost equal. Sex- and country-specific differences in survival in STS were small. The 50-year improvement in 5-year survival in STS was highest in NO men, 34.0 % units and FI women, 30.0 % units. The highest improvements in BS were in SE men 26.2 % units and in FI women 29.2 % units. The steady development in survival over the half century suggests contribution by stepwise improvements in diagnostics, treatment and care. The 10–15% mortality in the first year probably indicates diagnostic delays which could be improved by organizing patient pathways for aggressive rare diseases. Early diagnosis would also reduce metastatic disease and breakthroughs in treatment are a current challenge. •Survival in bone (BS) and soft tissue sarcoma (STS) has increased, as documented.•5-year survival reached 70% in these cancers but male BS remained at over 60%.•Steady survival development suggests contributions by stepwise improvements in care.•Over 10% mortality in the first year is a challenge for survival improvements.•Achieving this would require vigilance and ready care pathways to experts.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>37679266</pmid><doi>10.1016/j.canep.2023.102449</doi><orcidid>https://orcid.org/0000-0002-2769-3316</orcidid><orcidid>https://orcid.org/0000-0002-9857-4728</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Age
Aged
Bone cancer
Bone Neoplasms - epidemiology
Bone Neoplasms - mortality
Bone Neoplasms - pathology
Bone tumors
Cancer therapies
Chemotherapy
Chromosomes
Conditional survival
Diagnostics
Ewings sarcoma
Female
Females
Finland - epidemiology
Humans
Incidence
Male
Metastases
Middle Aged
Mortality
Osteosarcoma - epidemiology
Osteosarcoma - mortality
Osteosarcoma - pathology
Osteosarcoma - therapy
Radiation therapy
Rare diseases
Registries
Relative survival
Risk factors
Sarcoma - epidemiology
Sarcoma - mortality
Sarcoma - pathology
Sarcoma - therapy
Scandinavian and Nordic Countries - epidemiology
Soft Tissue Neoplasms - epidemiology
Soft Tissue Neoplasms - mortality
Soft Tissue Neoplasms - pathology
Soft tissue sarcoma
Soft tissues
Software
Survival
Survival Rate
Treatment
Tumors
Young Adult
title Steady survival improvements in soft tissue and bone sarcoma in the Nordic countries through 50 years
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