TABLE 1

Baseline Clinical Characteristics of HD and Control Enrolled Patients

CharacteristicHDControlP
Age (y)39 ± 13 (range, 19–58)41 ± 8 (range, 20–72)NS
Male sex37/69 (53%)35/69 (50%)NS
Weight (kg)67.1 ± 1276.5 ± 7<0.05
Glycemia at 18F-FDG injection (mg/dL)79 ± 7 (range, 61–101)83 ± 11 (range, 62–94)NS
Cardiovascular risk profile
 Hypertension6/69 (8%)15/69 (21%)<0.01
 Tobacco use19/69 (27%)30/69 (43%)<0.05
 Total cholesterol183.7 ± 30188 ± 53NS
 Low-density lipoprotein114.5 ± 32120 ± 25NS
 Triglycerides121.3 ± 49129.7 ± 57NS
 Creatinine0.8 ± 0.10.85 ± 0.2NS
 Family history of CAD7/69 (10%)5/69 (7%)NS
Time intervals between PET studies
 PET1–PET2 (d)73.7 ± 2199 ± 90<0.05
 PET2–PET3 (d)148 ± 70167 ± 98NS
 PET3–PET4 (d)195 ± 92229 ± 100NS
 Overall PET1–PET4 (d)427 ± 198448 ± 141NS
Baseline Ann-Arbor staging
 I stage7/69 (10%)
 II stage42/69 (60%)
 III stage8/69 (12%)
 IV stage12/69 (17%)
 B symptoms10/69 (14%)
 Mediastinal radiotherapy35/69 (55%)
 Total administered doxorubicin dose (mg)456.6 ± 103
  • NS = not statistically significant; CAD = coronary artery disease.

  • Qualitative data are expressed as numbers followed by percentages in parentheses; continuous data are expressed as mean ± SD.