Table 2. Intraoperative and postoperative data of patients in the two groups.
Index | Findings | P value | |
---|---|---|---|
ALPPS group | TACE + PVE group | ||
Data on first operation | |||
First operation/procedure | ALPPS stage-1 (n=38, 100%), Rt PVL (n=32, 84.2%), Lt PVL (n=6, 15.8%) | TACE (n=38, 100%), PVE (n=38, 100%), Rt PVE (n=28, 73.7%), Rt+ segment 4 PVE (n=8, 21.1%), Lt+ segment 5 8 PVE (n=2, 5.3%) | |
Intraoperative findings, median (range) | |||
Operating time (min) | 147.5 (55.0–255) | 140 (100.0–175) | 0.274 |
Pringle’s maneuver (min) | 15 (0–22.0) | 0 | |
Intraoperative blood loss (mL) | 200 (100.0–800) | 0 | |
Intraoperative blood transfusion (units) | 0 (0–4.0) | 0 | |
Postoperative complications* (Clavien Dindo) | |||
≥ Grade IIIa | n=6, 15.8%* | (n=1, 2.6%) | 0.108 |
Grade III | Ascites (n=1, 2.6%), pleural effusion (n=1, 2.6%), biliary obstruction (n=1, 2.6%), bile leakage (n=1, 2.6%), abdominal infection (n=2, 5.3%) | ||
Grade IV | n=0 | Liver failure (n=1, 2.6%) | 1.000 |
Data on second operation | |||
Second operation | ALPPS stage-2 (n=37, 97.4%) | Stage-2 hepatectomy (n=25, 65.8%) | <0.001 |
Reasons for not proceeding to stage-2 hepatectomy | Total: n=1 (2.6%), insufficient hypertrophy of FLR (n=1, 2.6%) | Total: n=13 (34.2%), tumor progression (n=5, 13.2%), insufficient hypertrophy of FLR (n=6, 15.8%), deranged LF (n=1, 2.6%), refused operation because of tumor necrosis (n=1, 2.6%) | |
Second operation time, min | 145 (105.0–380) | 210 (140.0–270) | <0.001 |
Intraoperative data | |||
Pringle maneuver duration, min | 12 (0–22.0) | 21 (0–47.0) | <0.001 |
Number of blood transfusion, n (%) | 18/37 (48.6%) | 14/25 (56.0%) | 0.570 |
Intraoperative bleeding volume, mL | 400 (100.0–4,700) | 800 (150.0–4,400) | 0.280 |
Type of hepatectomy | |||
Right hepatectomy | 22 (59.5%) | 17 (68.0%) | |
Left hepatectomy | 2 (5.4%) | 0 | |
Right trisectionectomy | 9 (24.3%) | 6 (24.0%) | |
Left trisectionectomy | 4 (10.8%) | 2 (8.0) | |
Complications, n (%) | 35/37 (94.6%) | 22/25 (88%) | 0.385 |
Major complications (≥ IIIa)† | 20/37 (54.1%) | 5/25 (20%) | 0.007 |
Grade III | n=18, 48.6% | n=4, 16.0% | |
Bile leakage ± ascites ± pleural effusion | 11 (29.7%) | 1 (4.0%) | |
Atelectasis + intra-abdominal infection | 1 (2.7%) | 0 | |
Pleural effusion + hemorrhage | 2 (5.4%) | 0 | |
Pleural effusion + disruption of wound | 1 (2.7%) | 0 | |
Pleural effusion | 1 (2.7%) | 2 (8.0%) | |
Hemorrhage | 0 | 1 (4.0%) | |
Ascites | 1 (2.7%) | 0 | |
Bile leakage | 1 (2.7%) | 0 | |
Grade IV | n=2, 5.4% | n=1, 4.0% | |
Liver failure | 2 (5.4%) | 1 (4.0%) | |
Resection margin (cm) | 1 (0.5–2.0) | 1 (0.5–2.2) | 0.602 |
Postoperative liver failure, n (%) | 13/37 (35.1%) | 6/25 (24.0%) | 0.351 |
Grade A | 5 | 3 | |
Grade B | 5 | 2 | |
Grade C | 3 | 1 | |
Death in 90 days, n (%) | 2/38 (5.3%) | 2/38 (5.3%) | 1.000 |
Cause of death: liver failure | 2 | 2 | |
HCC recurrence on follow-up | 19/37 (51.4%) | 13/25 (52.0%) | |
Treatment of recurrence | |||
Rehepatectomy | 1 (2.7%) | 1 (4.0%) | |
TACE | 2 (5.4%) | 5 (20.0%) | |
TACE + sorafenib | 5 (13.5%) | 0 | |
PMCT | 2 (5.4%) | 1 (4.0%) | |
PMCT + TACE | 0 | 1 (4.0%) | |
PMCT + radiotherapy | 2 (5.4%) | 0 | |
External radiation | 2 (5.4%) | 0 | |
Sorafenib | 3 (8.1%) | 3 (12.0%) | |
Supportive treatment | 2 (5.4%) | 2 (8.0%) |
*, all complications responded to drainage and conservative treatment; †, all complications were coped with conservative treatment, drainage or reoperation. PVL, portal vein ligation; deranged LF, deranged liver function; Lt, left portal trunk; Rt, right portal trunk; PMCT, percutaneous microwave coagulation therapy.