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@ARTICLE{Thong:143985,
author = {M. Thong$^*$ and L. Koch-Gallenkamp$^*$ and L. Jansen$^*$
and H. Bertram and A. Eberle and B. Holleczek and M.
Waldeyer-Sauerland and A. Waldmann and S. R. Zeissig and H.
Brenner$^*$ and V. Arndt$^*$},
title = {{A}ge-specific health-related quality of life in long-term
and very long-term colorectal cancer survivors versus
population controls - a population-based study.},
journal = {Acta oncologica},
volume = {58},
number = {5},
issn = {0001-6926},
address = {Abingdon},
publisher = {Taylor $\&$ Francis Group},
reportid = {DKFZ-2019-01542},
pages = {801 - 810},
year = {2019},
abstract = {Background: Previous research suggests an age differential
in health-related quality of life (HRQOL) among long-term
(5-10 years post-diagnosis, LTS) colorectal cancer (CRC)
survivors. Few studies have specifically addressed the
association of age differentials with HRQOL for very
long-term CRC survivors (>10 years post-diagnosis, VLTS)
and non-cancer population controls. We aimed to assess
possible deficits in HRQOL of disease-free CRC-LTS and
CRC-VLTS in comparison with non-cancer population controls,
and whether the observed pattern varies by age and time
since diagnosis. Methods: We used data from the CAncEr
Survivorship - A multi-Regional (CAESAR+) study in
collaboration with five population-based German cancer
registries. HRQOL from controls was accessed from the
Lebensqualität in DEeutschland (LinDE) study. All
respondents completed the European Organization for Research
and Treatment of Cancer Quality of Life Core-30
questionnaire. We calculated least square means of HRQOL
scores. Analyses were adjusted for age, sex, and education,
where appropriate. Results: The sample included 862 CRC-LTS,
400 CRC-VLTS and 1689 controls. CRC survivors reported
overall good HRQOL but significantly poorer social
functioning and more problems with dyspnea, constipation,
diarrhea and finances than controls. When stratified by age,
deficits in functioning and global health, and more problems
with symptoms and finances were noted mainly among younger
CRC survivors. Further stratification by time since
diagnosis showed that similar deficits in HRQOL and symptoms
were noted mainly among the younger CRC-LTS group when
compared with controls. Generally, CRC-VLTS reported
comparable HRQOL to controls. An exception was noted for
diarrhea, whereby CRC survivors, regardless of age and time
since diagnosis, reported significantly more problems with
this symptom than controls. Conclusions: In comparison with
non-cancer controls, disease-free CRC survivors reported
overall good HRQOL but experience persistent specific
detriments in HRQOL many years after diagnosis. In age
stratified analyses, HRQOL deficits were noted mainly among
younger CRC-LTS.},
cin = {C071 / C070 / L101},
ddc = {610},
cid = {I:(DE-He78)C071-20160331 / I:(DE-He78)C070-20160331 /
I:(DE-He78)L101-20160331},
pnm = {313 - Cancer risk factors and prevention (POF3-313)},
pid = {G:(DE-HGF)POF3-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30736716},
doi = {10.1080/0284186X.2018.1557340},
url = {https://inrepo02.dkfz.de/record/143985},
}