Somatic Disease in Survivors of Childhood Malignant Bone Tumors in the Nordic Countries

Survivors of malignant bone tumors in childhood are at risk of long-term adverse health effects. We comprehensively reviewed cases of somatic diseases that required a hospital contact in survivors of osteosarcoma and Ewing sarcoma. In a population-based cohort study, 620 five-year survivors of osteo...

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Published in:Cancers
Main Authors: Camilla Pedersen, Catherine Rechnitzer, Elisabeth Anne Wreford Andersen, Line Kenborg, Filippa Nyboe Norsker, Andrea Bautz, Thomas Baad-Hansen, Laufey Tryggvadottir, Laura-Maria Madanat-Harjuoja, Anna Sällfors Holmqvist, Lars Hjorth, Henrik Hasle, Jeanette Falck Winther, on behalf of the ALiCCS Study Group on behalf of the ALiCCS Study Group
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2021
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Online Access:https://doi.org/10.3390/cancers13184505
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spelling ftmdpi:oai:mdpi.com:/2072-6694/13/18/4505/ 2023-08-20T04:07:30+02:00 Somatic Disease in Survivors of Childhood Malignant Bone Tumors in the Nordic Countries Camilla Pedersen Catherine Rechnitzer Elisabeth Anne Wreford Andersen Line Kenborg Filippa Nyboe Norsker Andrea Bautz Thomas Baad-Hansen Laufey Tryggvadottir Laura-Maria Madanat-Harjuoja Anna Sällfors Holmqvist Lars Hjorth Henrik Hasle Jeanette Falck Winther on behalf of the ALiCCS Study Group on behalf of the ALiCCS Study Group 2021-09-07 application/pdf https://doi.org/10.3390/cancers13184505 EN eng Multidisciplinary Digital Publishing Institute Pediatric Oncology https://dx.doi.org/10.3390/cancers13184505 https://creativecommons.org/licenses/by/4.0/ Cancers; Volume 13; Issue 18; Pages: 4505 childhood malignant bone tumors survivorship late effects somatic disease cohort study Text 2021 ftmdpi https://doi.org/10.3390/cancers13184505 2023-08-01T02:38:30Z Survivors of malignant bone tumors in childhood are at risk of long-term adverse health effects. We comprehensively reviewed cases of somatic diseases that required a hospital contact in survivors of osteosarcoma and Ewing sarcoma. In a population-based cohort study, 620 five-year survivors of osteosarcoma (n = 440) or Ewing sarcoma (n = 180), diagnosed before the age of 20 years in Denmark, Finland, Iceland, and Sweden during 1943–2008, were followed in the national hospital registers. Overall rates of hospital contacts for any somatic disease and for 12 main diagnostic groups and 120 specific disease categories were compared with those in a matched comparison cohort (n = 3049) randomly selected from the national population registers. The rate of hospital contact for any somatic disease was 80% higher in survivors of malignant bone tumors than in comparisons and remained elevated up to 30 years after diagnosis. The rate of hospital contacts was higher after Ewing sarcoma (rate ratio (RR) 2.24; 95% confidence interval (CI) 1.76–2.85) than after osteosarcoma (RR 1.67; 95% CI 1.41–1.98). Elevated rates were observed for 11 main diagnostic groups, including infections, second malignant neoplasms, and diseases of the skin, bones, and circulatory, digestive, endocrine, and urinary systems. Survivors of malignant bone tumors in childhood are at increased risk of somatic diseases many years after diagnosis. This comprehensive study contributes new insight into the risk of late effects in survivors of osteosarcoma and Ewing sarcoma, which is an essential basis for optimal patient counseling and follow-up care. Text Iceland MDPI Open Access Publishing Ewing ENVELOPE(-61.257,-61.257,-69.924,-69.924) Cancers 13 18 4505
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic childhood malignant bone tumors
survivorship
late effects
somatic disease
cohort study
spellingShingle childhood malignant bone tumors
survivorship
late effects
somatic disease
cohort study
Camilla Pedersen
Catherine Rechnitzer
Elisabeth Anne Wreford Andersen
Line Kenborg
Filippa Nyboe Norsker
Andrea Bautz
Thomas Baad-Hansen
Laufey Tryggvadottir
Laura-Maria Madanat-Harjuoja
Anna Sällfors Holmqvist
Lars Hjorth
Henrik Hasle
Jeanette Falck Winther
on behalf of the ALiCCS Study Group on behalf of the ALiCCS Study Group
Somatic Disease in Survivors of Childhood Malignant Bone Tumors in the Nordic Countries
topic_facet childhood malignant bone tumors
survivorship
late effects
somatic disease
cohort study
description Survivors of malignant bone tumors in childhood are at risk of long-term adverse health effects. We comprehensively reviewed cases of somatic diseases that required a hospital contact in survivors of osteosarcoma and Ewing sarcoma. In a population-based cohort study, 620 five-year survivors of osteosarcoma (n = 440) or Ewing sarcoma (n = 180), diagnosed before the age of 20 years in Denmark, Finland, Iceland, and Sweden during 1943–2008, were followed in the national hospital registers. Overall rates of hospital contacts for any somatic disease and for 12 main diagnostic groups and 120 specific disease categories were compared with those in a matched comparison cohort (n = 3049) randomly selected from the national population registers. The rate of hospital contact for any somatic disease was 80% higher in survivors of malignant bone tumors than in comparisons and remained elevated up to 30 years after diagnosis. The rate of hospital contacts was higher after Ewing sarcoma (rate ratio (RR) 2.24; 95% confidence interval (CI) 1.76–2.85) than after osteosarcoma (RR 1.67; 95% CI 1.41–1.98). Elevated rates were observed for 11 main diagnostic groups, including infections, second malignant neoplasms, and diseases of the skin, bones, and circulatory, digestive, endocrine, and urinary systems. Survivors of malignant bone tumors in childhood are at increased risk of somatic diseases many years after diagnosis. This comprehensive study contributes new insight into the risk of late effects in survivors of osteosarcoma and Ewing sarcoma, which is an essential basis for optimal patient counseling and follow-up care.
format Text
author Camilla Pedersen
Catherine Rechnitzer
Elisabeth Anne Wreford Andersen
Line Kenborg
Filippa Nyboe Norsker
Andrea Bautz
Thomas Baad-Hansen
Laufey Tryggvadottir
Laura-Maria Madanat-Harjuoja
Anna Sällfors Holmqvist
Lars Hjorth
Henrik Hasle
Jeanette Falck Winther
on behalf of the ALiCCS Study Group on behalf of the ALiCCS Study Group
author_facet Camilla Pedersen
Catherine Rechnitzer
Elisabeth Anne Wreford Andersen
Line Kenborg
Filippa Nyboe Norsker
Andrea Bautz
Thomas Baad-Hansen
Laufey Tryggvadottir
Laura-Maria Madanat-Harjuoja
Anna Sällfors Holmqvist
Lars Hjorth
Henrik Hasle
Jeanette Falck Winther
on behalf of the ALiCCS Study Group on behalf of the ALiCCS Study Group
author_sort Camilla Pedersen
title Somatic Disease in Survivors of Childhood Malignant Bone Tumors in the Nordic Countries
title_short Somatic Disease in Survivors of Childhood Malignant Bone Tumors in the Nordic Countries
title_full Somatic Disease in Survivors of Childhood Malignant Bone Tumors in the Nordic Countries
title_fullStr Somatic Disease in Survivors of Childhood Malignant Bone Tumors in the Nordic Countries
title_full_unstemmed Somatic Disease in Survivors of Childhood Malignant Bone Tumors in the Nordic Countries
title_sort somatic disease in survivors of childhood malignant bone tumors in the nordic countries
publisher Multidisciplinary Digital Publishing Institute
publishDate 2021
url https://doi.org/10.3390/cancers13184505
long_lat ENVELOPE(-61.257,-61.257,-69.924,-69.924)
geographic Ewing
geographic_facet Ewing
genre Iceland
genre_facet Iceland
op_source Cancers; Volume 13; Issue 18; Pages: 4505
op_relation Pediatric Oncology
https://dx.doi.org/10.3390/cancers13184505
op_rights https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.3390/cancers13184505
container_title Cancers
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