Liver resection for malignant tumors should respect oncological margins while ensuring safety and improving the quality of life, therefore tumor staging, underlying liver disease and performance status should all be attentively assessed in the decision process. The concept of parenchyma-sparing liver surgery is nowadays used as an alternative to major hepatectomies to address deeply located lesions with intricate topography by means of complex multiplanar parenchyma-sparing liver resections, preferably under the guidance of intraoperative ultrasound. Regenerative liver surgery evolved as a liver growth induction method to increase resectability by stimulating the hypertrophy of the parenchyma intended to remain after resection (referred to as future liver remnant), achievable by portal vein embolization and liver venous deprivation as interventional approaches, and portal vein ligation and associating liver partition and portal vein ligation for staged hepatectomy as surgical techniques. Interestingly, although both strategies have the same conceptual origin, they eventually became caught in the never-ending parenchyma-sparing liver surgery vs. regenerative liver surgery debate. However, these strategies are both valid and must both be mastered and used to increase resectability.
Regenerative surgery (RS) evolved as a method to increase resectability by stimulating the hypertrophy of the parenchyma intended to remain after resection, which is referred to as future liver remnant (FLR) [29][30]. This liver growth induction can be achieved by portal vein embolization (PVE) and liver venous deprivation (LVD) as interventional approaches, and portal vein ligation (PVL) and associating liver partition and portal vein ligation for staged hepatectomy (ALPPS) as surgical techniques.
PVE was conceived by Makuuchi et al. in 1990 as a tool to induce hypertrophy of the FLR and decrease the risk of liver failure after major hepatectomy, enabling major anatomical LR, which would otherwise not be feasible [30][31]. The mechanism behind this approach is based on the redirection of the portal flow, that stimulates the contralateral hypertrophy. PVE is associated with a low morbidity and mortality. However, the growth of FLR is limited to a volume by 40% at best, for most cases within a period of around 2 months [31][32]. This may lead to insufficient FLR and/or tumor progression while waiting for hypertrophy. PVL (open or minimally invasive surgery) is a feasible alternative to PVE. For patients undergoing PVE, major hepatectomy becomes feasible in 2/3 of cases with a similar overall survival to those without PVE [32][33]. Chemotherapy after PVE decreases the tumor progression rate and has not been shown to decrease liver hypertrophy. In about 1/3 of patients, PVE fails and leads to canceling of the planned LR (drop-out rate) [33][34].
Recently, liver venous deprivation (LVD), consisting of embolization of both the PV and one or two HVs of the hemi-liver, has been proposed as a promising way for improved regeneration (1–2 weeks) [35,36]. Several studies comparing LVD to PVE reported improved FLR volume growth following LVD [34][35][36][37,38,39], as well as better FLR functional regeneration [37][40]. In particular, one study has shown a more than 75% increase in the kinetic growth rate of the FLR after LVD compared to PVE [35]. Moreover, a 54% functional increase in the FLR 7 days after LVD has been reported [37][40]. However, literature data on LVD of a cirrhotic liver are lacking [38][41].
The two-stage hepatectomy (TSH) was introduced in 2000 as two successive surgical steps for removing multiple bilobar tumors that cannot be removed by a sole hepatectomy [39][42]. Usually, the response to neoadjuvant chemotherapy was used to select candi- dates with favorable tumor biology. TSH can be used by itself or combined with PVE or portal vein ligation (PVL) [40][43]. It usually has resection rates of up to 70–75%; the main reason for non-completion is disease progression between the two stages (around 90% of cases) [39][41][42,44]. The postoperative morbidity rate is around 20% after the 1st stage and 40% after the 2nd stage, with an overall mortality below 5% [42][45].
In 2012, Schnitzbauer et al. proposed combining PVL with in situ liver partition to obtain rapid FLR hypertrophy (in 7–10 days) as a new strategy to increase resectability [43][46], which was subsequently termed ALPPS [44][47]. One mechanism behind this technique is thought to trigger an inflammatory response that induces a growth rate of 22–35 mL daily, significantly superior to PVE (3–5 mL daily) [45][48]. However, this volume growth does not automatically equal an increase in liver function [46][49]. This strategy results in a FLR increase of up to 80% and above (compared to 40% in PVE/PVL), while shortening the interstage period to 1–2 weeks [47][50]. Moreover, ALPPS enables resection rates to increase to more than 90% [48][49][50][51,52,53], now being feasible even when using a minimally invasive approach [51][54].
Of note, although relatively easy to perform, tourniquet ALPPS [64] mighortt be as- sociated with a higher risk of operative events during the second stage due to severe adhesions/perihilar fibrosis.
Short-term results after ALPPS, that were initially a major concern, have been con- tinuously improved over time, now reaching 90-day mortality rates below 5% [61][65] and a relatively low major morbidity (21%) in high-volume centers.
To further increase resectability while reducing morbidity, scholarswe proposed a new techni- cal variant of ALPPS—parenchyma-sparing ALPPS (psALPPS)—that involves shifting the transection plane through segment 4 using IOUS guidance, preserving part of this segment along with the left lateral section [66]. Besides avoiding S4 necrosis, that is a source of complication when performing conventional ALPPS, a significant advantage of psALPPS lies in preventing major bile leaks at the transection surface by avoiding complete exclusion of S4 from the biliary system (as in conventional ALPPS). Parenchyma-sparing ALPPS offers the advantage of maximizing FLR while simultaneously reducing ischemic injury of S4 compared to conventional ALPPS (Figures 1 and 2). Moreover, when compared to stan- dard ALPPS, partitioning through segment 4, away from the umbilical portion of the left portal pedicle, protects against potential injuries of the vascular and biliary structures for segments 2 and 3. This new technical variant also embeds some of the main modifications already proposed, such as partial ALPPS, avoiding the transection beyond the middle HV, and delayed ALPSS [62][66]. It also adapts the concept of avoiding hilar dissection by adopt- ing a minimal hilar dissection (right side approach only) [62][66]. Using an extra-Glissonean approach to complete the hepatectomy during the second step further increases safety by avoiding re-dissection of the liver hilum.
Figure 1. Intraoperative aspects of parenchymal sparing ALPPS in a 67-year-old male patient, for a large HCC located in segments 4, 5, 6, 7 and 8, with satellites in segment 4, on HBV chronic hepatitis. Stage 1: (A) intraoperative aspect at exploration; (B) ultrasound-guided partitioning of the liver through segment 4, adding the non-tumoral parenchyma of segment 4 to the FLR. Stage 2 after an interstage interval of 14 days; (C) remnant liver after completion of right hemi-hepatectomy non-anatomically extended to segment 4; (D) surgical specimen. No intraoperative adverse events were encountered during both operations, and only minor ascites after stage 2 were recorded as complications.
Figure 2. (A). Preoperative CT showing the large HCC located in segments 5 and 8 with extension to segments 6, 7, 4, compressing the middle hepatic vein; volumetry: volume of segments 2 and 3, 16.8% of total functional liver volume, volume of FLR 27.8%. (B) Interstage CT showing the liver partitioning, absence of contrast in the right portal vein (due to ligation), and sufficient growth of FLR (38.5% of total functional liver volume). (C) Postoperative CT with well-perfused, non-dilated bile ducts, and tumor-free remnant liver.
Besides being the best available tool for identifying and mapping the focal liver lesions in real time, IOUS increases the safety of ALPPS and its variants by identifying the anatomic
variants of the portal vein bifurcation and guiding the right portal vein ligation and the liver transection.
PsALPPS combines both concepts of complex liver surgery, RS and PSS, which syn- ergistically achieve resectability, which would otherwise not be possible with either approach [66].
The minimally invasive approach is feasible for both PSS and RS. However, for com- plex bilobar deeply located liver tumors, PSS is often not feasible due to technical limitations of this approach, making the RS approach, even ALPPS, a technical alternative. Nevertheless, the type of approach should not change the indication for a certain resection strategy. Therefore, if complex PSS is indicated, this should be carried out even if it is feasible only by open approach, and not switched to major two-stage LR only to perform laparoscopic surgery.
3.5. Other Focal Liver Lesions
Indications for surgical resection of GIST include limited disease, progression refrac- tory to TKI and locally advanced or previously unresectable tumors that manifest favorable response to neoadjuvant therapy with TKI [119].
In the case of NELM, LR is the treatment of choice whenever feasible, since patient outcomes after resection have been reported to be favorable compared to those with unresectable tumors [120]. Repeat hepatectomy, if feasible, can be a good option for intra- hepatic recurrence and can provide long-term survival [121].
Regarding hemangiomas, as complications are rare, observation is justified in the absence of symptoms. LR is indicated in patients with abdominal (mechanical) complaints or complications or when diagnosis remains inconclusive. Enucleation is the preferred surgical method according to existing literature [122].
ALPPS may be also deployed in neuroendocrine liver metastases (NELMs) [123], and other rare indications, such as lymphoma [124]. In NELM, 2-year overall survival rates of 95.2% were reported [123].