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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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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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. Published by Elsevier Ltd.. All rights reserved.</rights><rights>2023. The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c382t-962e503c01f6f719116a776f55768e73e717a450de3e15decda2c9c3ccaa87b23</cites><orcidid>0000-0002-2769-3316 ; 0000-0002-9857-4728</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/3104452489?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997,64387,64389,64391,72471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37679266$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tichanek, Filip</creatorcontrib><creatorcontrib>Försti, Asta</creatorcontrib><creatorcontrib>Hemminki, Otto</creatorcontrib><creatorcontrib>Hemminki, Akseli</creatorcontrib><creatorcontrib>Hemminki, Kari</creatorcontrib><title>Steady survival improvements in soft tissue and bone sarcoma in the Nordic countries through 50 years</title><title>Cancer epidemiology</title><addtitle>Cancer Epidemiol</addtitle><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.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age</subject><subject>Aged</subject><subject>Bone cancer</subject><subject>Bone Neoplasms - epidemiology</subject><subject>Bone Neoplasms - mortality</subject><subject>Bone Neoplasms - pathology</subject><subject>Bone tumors</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Chromosomes</subject><subject>Conditional survival</subject><subject>Diagnostics</subject><subject>Ewings sarcoma</subject><subject>Female</subject><subject>Females</subject><subject>Finland - epidemiology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Male</subject><subject>Metastases</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Osteosarcoma - epidemiology</subject><subject>Osteosarcoma - mortality</subject><subject>Osteosarcoma - pathology</subject><subject>Osteosarcoma - therapy</subject><subject>Radiation therapy</subject><subject>Rare diseases</subject><subject>Registries</subject><subject>Relative survival</subject><subject>Risk factors</subject><subject>Sarcoma - epidemiology</subject><subject>Sarcoma - mortality</subject><subject>Sarcoma - pathology</subject><subject>Sarcoma - therapy</subject><subject>Scandinavian and Nordic Countries - epidemiology</subject><subject>Soft Tissue Neoplasms - epidemiology</subject><subject>Soft Tissue Neoplasms - mortality</subject><subject>Soft Tissue Neoplasms - pathology</subject><subject>Soft tissue sarcoma</subject><subject>Soft tissues</subject><subject>Software</subject><subject>Survival</subject><subject>Survival Rate</subject><subject>Treatment</subject><subject>Tumors</subject><subject>Young Adult</subject><issn>1877-7821</issn><issn>1877-783X</issn><issn>1877-783X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kU1PGzEQhi3Uiq_yC5CQpV64JPhjbe8eeqgQpUgIDrRSb5Zjz4Kj7Dr1eCPl39dpKIceONkaP-_M-H0JOedszhnXV8u5dyOs54IJWSuiaboDcsxbY2amlb8-vN0FPyIniEvGtOZcHZIjabTphNbHBJ4KuLClOOVN3LgVjcM6pw0MMBakcaSY-kJLRJyAujHQRRqBoss-DW73Xl6APqQcoqc-TWPJEbAWc5qeX6hidAsu4yfysXcrhLPX85T8_Hbz4_r77P7x9u766_3My1aUWacFKCY9473uDe84184Y3StldAtGguHGNYoFkMBVAB-c8J2X3jvXmoWQp-Ry37f-4fcEWOwQ0cNqVY1KE1rRaikZb4Sq6Of_0GWa8li3s5KzplGiabtKyT3lc0LM0Nt1joPLW8uZ3aVgl_ZvCnaXgt2nUFUXr72nxQDhTfPP9gp82QNQzdhEyBZ9hNFDiBl8sSHFdwf8Ab6OmVc</recordid><startdate>20241001</startdate><enddate>20241001</enddate><creator>Tichanek, Filip</creator><creator>Försti, Asta</creator><creator>Hemminki, Otto</creator><creator>Hemminki, Akseli</creator><creator>Hemminki, Kari</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2769-3316</orcidid><orcidid>https://orcid.org/0000-0002-9857-4728</orcidid></search><sort><creationdate>20241001</creationdate><title>Steady survival improvements in soft tissue and bone sarcoma in the Nordic countries through 50 years</title><author>Tichanek, Filip ; Försti, Asta ; Hemminki, Otto ; Hemminki, Akseli ; Hemminki, Kari</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-962e503c01f6f719116a776f55768e73e717a450de3e15decda2c9c3ccaa87b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age</topic><topic>Aged</topic><topic>Bone cancer</topic><topic>Bone Neoplasms - epidemiology</topic><topic>Bone Neoplasms - mortality</topic><topic>Bone Neoplasms - pathology</topic><topic>Bone tumors</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Chromosomes</topic><topic>Conditional survival</topic><topic>Diagnostics</topic><topic>Ewings sarcoma</topic><topic>Female</topic><topic>Females</topic><topic>Finland - epidemiology</topic><topic>Humans</topic><topic>Incidence</topic><topic>Male</topic><topic>Metastases</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Osteosarcoma - epidemiology</topic><topic>Osteosarcoma - mortality</topic><topic>Osteosarcoma - pathology</topic><topic>Osteosarcoma - therapy</topic><topic>Radiation therapy</topic><topic>Rare diseases</topic><topic>Registries</topic><topic>Relative survival</topic><topic>Risk factors</topic><topic>Sarcoma - epidemiology</topic><topic>Sarcoma - mortality</topic><topic>Sarcoma - pathology</topic><topic>Sarcoma - therapy</topic><topic>Scandinavian and Nordic Countries - epidemiology</topic><topic>Soft Tissue Neoplasms - epidemiology</topic><topic>Soft Tissue Neoplasms - mortality</topic><topic>Soft Tissue Neoplasms - pathology</topic><topic>Soft tissue sarcoma</topic><topic>Soft tissues</topic><topic>Software</topic><topic>Survival</topic><topic>Survival Rate</topic><topic>Treatment</topic><topic>Tumors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tichanek, Filip</creatorcontrib><creatorcontrib>Försti, Asta</creatorcontrib><creatorcontrib>Hemminki, Otto</creatorcontrib><creatorcontrib>Hemminki, Akseli</creatorcontrib><creatorcontrib>Hemminki, Kari</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tichanek, Filip</au><au>Försti, Asta</au><au>Hemminki, Otto</au><au>Hemminki, Akseli</au><au>Hemminki, Kari</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Steady survival improvements in soft tissue and bone sarcoma in the Nordic countries through 50 years</atitle><jtitle>Cancer epidemiology</jtitle><addtitle>Cancer Epidemiol</addtitle><date>2024-10-01</date><risdate>2024</risdate><volume>92</volume><spage>102449</spage><pages>102449-</pages><artnum>102449</artnum><issn>1877-7821</issn><issn>1877-783X</issn><eissn>1877-783X</eissn><abstract>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.</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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