Colorectal Cancer Survival in Multiple Sclerosis A Matched Cohort Study

被引:5
|
作者
Marrie, Ruth Ann [1 ,2 ]
Maxwell, Colleen [4 ,5 ,6 ]
Mahar, Alyson [2 ,3 ,7 ]
Ekuma, Okechukwu [3 ]
McClintock, Chad [7 ]
Seitz, Dallasl [7 ,9 ,10 ]
Groome, Patti [7 ,8 ]
机构
[1] Univ Manitoba, Rady Fac Hlth Sci, Dept Internal Med, Max Rady Coll Med, Winnipeg, MB, Canada
[2] Univ Manitoba, Rady Fac Hlth Sci, Dept Community Hlth Sci, Max Rady Coll Med, Winnipeg, MB, Canada
[3] Univ Manitoba, Rady Fac Hlth Sci, Manitoba Ctr Hlth Policy, Max Rady Coll Med, Winnipeg, MB, Canada
[4] ICES, Toronto, ON, Canada
[5] Univ Waterloo, Sch Pharm, Waterloo, ON, Canada
[6] Univ Waterloo, Sch Publ Hlth & Hlth Syst, Waterloo, ON, Canada
[7] Queens Univ, ICES Queens, Canc Res Inst, Kingston, ON, Canada
[8] Queens Univ, Div Canc Care & Epidemiol, Canc Res Inst, Kingston, ON, Canada
[9] Univ Calgary, Cumming Sch Med, Dept Psychiat, Calgary, AB, Canada
[10] Univ Calgary, Cumming Sch Med, Dept Community Hlth Sci, Calgary, AB, Canada
关键词
SENSITIVITY-ANALYSIS; BRITISH-COLUMBIA; OLDER-ADULTS; DEATH; COMORBIDITY; MORTALITY; DIAGNOSIS; PREVALENCE; PROGNOSIS; ADMISSION;
D O I
10.1212/WNL.0000000000012634
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Objectives We tested the hypothesis that overall and cancer-specific survival after a colorectal cancer diagnosis is lower in persons with multiple sclerosis (MS) than in those without MS using a retrospective matched cohort design. Methods Using population-based administrative data in Manitoba and Ontario, we identified persons with MS from a validated case definition and linked these cohorts to cancer registries to identify those with colorectal cancer. We selected persons with colorectal cancer and without MS, matching 4:1 on birth year, sex, cancer diagnosis year, and region. We used Cox proportional hazards regression to compare all-cause survival between cohorts, adjusting for age at cancer diagnosis, cancer diagnosis year, income, region, and Elixhauser comorbidity score. We compared cancer-specific survival between cohorts using a cause-specific hazards model. We pooled findings across provinces using random-effects meta-analysis. Complementary analyses using a subcohort from Ontario, adjusted for cancer stage and disability status, as measured from the use of home care or long-term care services. Results We included 338 MS cases and 1,352 controls with colorectal cancer. The mean (SD) age at cancer diagnosis was 64.7 (11.1) years. After adjustment, MS was associated with an increased hazard for all-cause death that was highest 6 months after diagnosis (hazard ratio [HR] 1.45, 95% confidence interval [CI] 1.19-1.76) and then declined over time (HR [95% CI] at 1 year 1.34 [1.09-1.63], 2 years 1.24 [0.99-1.56], 5 years 1.10 [0.80-1.50]). MS was associated with increased cancer-specific death at 6 months after diagnosis only (HR 1.29, 95% CI 1.04-1.61). After adjustment for cancer stage, MS was associated with an increased hazard of death due to any cause (1.60, 95% CI 1.16-2.21) and with cancer-specific death (HR 1.47, 95% CI 1.02-2.12). The association of MS and all-cause death was partially attenuated after adjustment for disability status (HR 1.37, 95% CI 0.97-1.92), as was the association with cancer-specific death (HR 1.34, 95% CI 0.91-1.97). Discussion Overall and cancer-specific survival was lower in persons with than without MS in the early period after colorectal cancer diagnosis. Further study is warranted to determine what factors underlie these worse outcomes.
引用
收藏
页码:E1447 / E1456
页数:10
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