| Literature DB >> 30465187 |
Kristina Hasselgren1, Per Sandström1, Bård Ingvald Røsok2, Ernesto Sparrelid3, Gert Lindell4, Peter Nørgaard Larsen5, Anna Lindhoff Larsson1, Nicolai A Schultz5, Bjorn Atle Björnbeth2, Bengt Isaksson6, Magnus Rizell7, Bergthor Björnsson8.
Abstract
BACKGROUND: Portal vein occlusion (PVO) is an established method to increase the volume of the future liver remnant (FLR). The main reasons for not proceeding to radical hepatectomy are lack of volume increase and tumor progression due to a wait-time interval of up to 8 weeks. The hypothesis was that the increase in FLR volume is not linear and is largest during the first weeks.Entities:
Keywords: Colorectal liver metastases; Future liver remnant; Liver surgery; Portal vein embolization; Portal vein ligation
Mesh:
Year: 2018 PMID: 30465187 PMCID: PMC6414468 DOI: 10.1007/s11605-018-4031-3
Source DB: PubMed Journal: J Gastrointest Surg ISSN: 1091-255X Impact factor: 3.452
Clinical variables and preoperative data
| Number of patients | 48 |
|---|---|
| Male/female | 36/12 |
| Age (mean ± 1 SD) | 65 ± 12 |
| BMI (mean ± 1 SD) | 26 ± 4 |
| ASA (median, range) | 2 (1–3) |
| ECOG (median, range) | 0 (0–1) |
| Cortisone treatment | 1 (2%) |
| Diabetes mellitus | 6 (13%) |
| Primary tumor resected/not resected | 30/18 |
| Chemotherapy cycles (mean ± 1 SD) | 7 ± 4 |
| Response to chemotherapy/stable disease | 37/9* |
| Time (days) between last dose of chemotherapy and first intervention (median, range) | 35 (7–412) |
| Liver metastases at time of surgery (median, range) | 8 (1–23) |
| Size (mm) of the largest liver metastasis (mean ± 1 SD) | 48 ± 38 |
| Metastases in the FLR | 30 (63%) |
| Extra hepatic disease | 7 (15%) |
| Local lymph node enlargement | 2 (4%) |
| Complications after PVO | 8 (17%)** |
*One patient did not receive chemotherapy and for one patient, the response to given chemotherapy was difficult to evaluate. ** Data are lacking for one patient. Complications were grade 1 or 2 according to the Clavien-Dindo classification
Fig. 1Temporal increase of the FLR, expressed as KGR, from PVO to the first evaluation and between the first and second CT. The KGR was 5.4 (± 4), compared to 1.5 (± 2) between the first and second CT. The difference was statistically significant (p < 0.05). The interval between the first and second CT was between 7 to 35 days
Fig. 2Temporal course of the increase of FLR, with the intervals 1 to 7 days between stage1/PVE and the first CT, and 1 to 21 and 22 days or more between the first and second CT. The KGR was 5.4 (± 4), 3.8 (± 2), 1.8 (± 2), and 0.9 (± 1). The difference between KGR values for the interval of 1 to 7 days compared to the intervals of 1 to 21 days and 22 days or more between the first and second CT evaluation was statistically significant at p < 0.005
Volumetry for the entire cohort and analysis of the subgroups success, failure, and tumor progression
| Volumetry | Entire PVO cohort ( | Treated with radical hepatectomy ( | Failure to achieve sufficient volume ( | Tumor progression ( | |
|---|---|---|---|---|---|
| sFLR pre-PVO (percent of standardized FLR) | 21 ± 5 | 23 ± 4 | 17 ± 5 | 22 ± 5 | < 0.05* |
| FLR pre-PVO (ml) | 365 ± 105 | 415 ± 95 | 281 ± 77 | 331 ± 52 | < 0.05* |
| KGR day 1–7 after PVO (%/week) | 5.4 ± 4 | 7 ± 4 | 4.3 ± 2 | 2.6 ± 0.8 | Ns |
| KGR between the first and second CT (%/week) | 1.5 ± 2 | 2.2 ± 2 | 0.1 ± 0.8 | 2.4 ± 1 | 0.017* |
| Increase in ml from PVO to the last evaluation (ml) | 156 ± 118 | 217 ± 123 | 79 ± 41 | 77 ± 39 | < 0.05* |
| Increase in percent from PVO to the last evaluation (%) | 43 ± 30 | 55 ± 33 | 31 ± 21 | 24 ± 13 | 0.044* |
| sFLR at last volume assessment (percent of standardized FLR) | 30 ± 10 | 35 ± 9 | 21 ± 5 | 27 ± 6 | < 0.05* |
| Days between PVO and the first CT evaluation | 10 ± 8 | 11 ± 9 | 9 ± 8 | 8 ± 3 | Ns |
| Days between the first and second CT evaluation | 22 ± 9 | 23 ± 12 | 23 ± 6 | 17 ± 5 | Ns |
*Comparison of success and failure. **Comparison between success and progress. Data are presented as the mean ± 1 SD