Table 1.
Study Cohort.
Parameter | Study Cohort |
---|---|
CCA patients | n = 75 |
Gender (%): | |
male | 53.3 (40) |
female | 46.7 (35) |
Age (years, median, and range) | 70 (30–87) |
BMI class (kg/m2, %) | |
BMI < 20 | 9.3 (7) |
BMI 20–25 | 45.3 (34) |
BMI 25–30 | 28 (21) |
BMI > 30 | 17.3 (13) |
Systemic therapy (%) | |
Yes | 85.3 (64) |
No | 14.7 (11) |
Chemotherapy regimen (%) | |
Gemcitabine + Cisplatin | 81.3 (52) |
Gemcitabine + Oxaliplatin | 4.7 (3) |
Carboplatin + Paclitaxel | 1.6 (1) |
Capecitabine Mono | 1.6 (1) |
Gemcitabine Mono | 10.9 (7) |
Tumor progression during follow-up? (%) | |
Yes | 28 (21) |
No | 72 (54) |
Localization of tumor metastasis (%) | |
Lymphatic | 20 (15) |
Vascular | 8 (6) |
Pulmonary | 18.7 (14) |
Bone | 10.7 (8) |
Suprarenal gland | 1.3 (1) |
Peritoneum | 22.7 (17) |
Other | 16 (12) |
Pre-existing medical conditions (%) | |
Preceded tumor disease | 24 (18) |
Preceded systemic chemotherapy | 1.3 (1) |
Diabetes mell. Typ 2 | 29.3 (22) |
Arterial hypertension | 58.7 (44) |
Hepatitis B | 6.7 (5) |
Hepatitis C | 5.3 (4) |
Alcohol abuse | 1.3 (1) |
Primary biliary cholangitis | 2.7 (2) |
Primary sclerosing cholangitis | 1.3 (1) |
Nonalcoholic steatohepatitis | 2.7 (2) |
Inflammatory bowel disease | 1.3 (1) |
Gastritis | 24 (18) |
Overall survival (days, median, and range) | 224 (3–1059) |
Progression-free survival (days, median, and range) | 132 (3–916) |
Bone mineral density (HU, median, and range) | 144 (57.65–258) |
AFP (mean, range) | 1025.5 (1.0–31,496) ng/mL (49) |
CEA (mean, range) | 38.8 (0.7–653.5) ng/mL (54) |
Ca19-9 (mean, range) | 1584.8 (0.6–10,000) U/mL (56) |
BMI: Body mass index; AFP: Alpha-fetoprotein; CEA: Carcinoembryonic antigen; CA19-9: Carbohydrate antigen 19-9; table modified after [4].