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. 2016 Apr 15;8:53–59. doi: 10.2147/CLEP.S100779

Table 3.

Incidence or mortality rate (per 1,000 person-years) of heart failure and cardiac death among soft tissue sarcoma (STS) patients in Denmark (national cohort), 2000–2009

Characteristics Heart failure
Cardiac death
Total N Number of events % Person- years Incidence rate (95% confidence interval) Number of events % Person- years Mortality rate (95% confidence interval)
Total 1,187 40 3.4 5,449.2 7.3 (5.4–10.0) 15 1.3 5,510.6 2.7 (1.6–4.5)
Age, years
 <40 226 1 0.4 1,217.0 0.8 (0.1–5.8) 0 0.0 1,219.2
 40–59 379 6 1.6 2,095.9 2.9 (1.3–6.4) 0 0.0 2,104.4
 60–79 461 21 4.6 1,795.2 11.7 (7.6–17.9) 9 2.0 1,835.4 4.9 (2.6–9.4)
 ≥80 121 12 9.9 341.1 35.2 (20.0–61.9) 6 5.0 351.6 17.1 (7.7–38.0)
Sex
 Female 535 20 3.7 2,410.9 8.3 (5.4–12.9) 5 0.9 2,445.6 2.0 (0.9–4.9)
 Male 652 20 3.1 3,038.4 6.6 (4.2–10.2) 10 1.5 3,065.0 3.3 (1.8–6.1)
STS subtype
 Liposarcoma 392 14 3.6 2,112.5 6.6 (3.9–11.2) 3 0.8 2,149.2 1.4 (0.5–4.3)
 Leiomyosarcoma 381 13 3.4 1,661.6 7.8 (4.5–13.5) 8 2.1 1,675.3 4.8 (2.4–9.5)
 Fibrosarcoma 92 3 3.3 390.1 7.7 (2.5–23.8) 2 2.2 391.9 5.1 (1.3–20.4)
 Synovial 84 2 2.4 322.5 6.2 (1.6–24.8) 0 0 322.6
 Hemangiosarcoma 78 5 6.4 235.7 21.2 (8.8–51.0) 1 1.3 240.5 4.2 (0.6–29.5)
 Rhabdomyosarcoma 74 0 0 298.3 0 0 298.3
 Kaposi’s 66 3 4.5 363.4 8.3 (2.7–25.6) 1 1.5 367.7 2.7 (0.4–19.3)
 Neurofibrosarcoma 18 0 0 58.7 0 0 58.7
 Lymphangiosarcoma 2 0 0 6.4 0 0 6.4
Event timing after
STS diagnosis, years 1,187
 <1 13 1.1 1,076.1 12.1 (7.0–20.8) 6 0.5 1,079.4 5.6 (2.5–12.4)
 <2 20 1.7 2,001.5 10.0 (6.4–15.5) 9 0.8 2,012.8 4.5 (2.3–8.6)
 <5 33 2.8 3,995.8 8.3 (5.9–11.6) 13 1.1 4,034.6 3.2 (1.9–5.5)

Abbreviations: –, not available; STS, soft tissue sarcoma.