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LIVER 379
BC
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A
FIG. 3 (A) Division of the inferior vena cava ligament. (B) This ligament may contain liver parenchyma and/or a short hepatic vein and is therefore most
safely transected with a stapler. (C) Transection will allow exposure and control of the right hepatic vein. (From Blumgart LH, editor. Surgery of the liver, biliary
tract, and pancreas. 4th ed. Philadelphia: Elsevier; 2007:1354.)
HEPATECTOMY
Right Hepatic Lobectomy
If a right hepatectomy is planned, further dissection of the falciform ligament is carried up to expose the hepatic venous outflow, par­ticularly the right hepatic vein. The right coronary and triangular ligaments are divided, exposing the bare area of the liver. The right liver is mobilized and rotated to the patient’s left. The short hepatic veins draining directly into the retrohepatic IVC are controlled with a combination of clips, ties, and firings of a vascular stapler for any larger branches. The retrocaval ligament (Makuuchi’s ligament) is identified and transected with a vascular stapler (Fig. 3). Further dissection between the liver and the IVC will isolate the right hepatic vein, which is encircled with a vessel loop.
Attention is turned to the hilum, where the right hepatic artery and right portal vein are dissected and divided. A clear line of demarcation should be visible. The right hepatic vein, which was previously controlled with a vessel loop, is divided with a vascular stapler (Fig. 4). The transection plane follows the area of vascular demarcation. The right hepatic duct can be divided with a stapler or between ties.
For large right-sided tumors, an anterior approach can be used in which the parenchyma is divided before liver mobilization. Inflow control is obtained, and the parenchyma is transected until the ante­rior surface of the IVC is exposed. The right hepatic vein and short hepatic veins are identified and ligated. The hanging maneuver, ele­vation of the liver by an umbilical tape passed between the anterior surface of the IVC and the liver, can facilitate an anterior approach. The space between the right and middle hepatic veins is dissected, and a long clamp is gently passed along the anterior surface of the vena cava to emerge between the right and middle hepatic veins. An umbilical tape is then passed behind the liver and used to gently elevate the liver, serving as a guide to the transection plane.
Right Trisectionectomy
This includes extension of the right parenchymal transection to include segment IV. The initial hepatic mobilization is as described
FIG. 4 Division of the right hepatic vein. With the liver retracted to the
left, the right hepatic vein may be rapidly and safely divided using an Endo GIA stapler (Covidien) with a vascular load. (From Blumgart LH, editor.
Surgery of the liver, biliary tract, and pancreas. 4th ed. Philadelphia: Elsevier; 2007:364.)
for a right hepatectomy. The transection plane is along the falciform ligament, from the groove separating the middle and left hepatic veins cranially to the right side of the umbilical fissure caudally, directed toward the medial aspect of the right hilar plate while avoiding the confluence of the left and right hepatic ducts. Inflow to segment IV is controlled during the transection, as is the middle hepatic vein as the surgeon follows the transection caudally.
380 HEPATIC MALIGNANCY: RESECTION VERSUS TRANSPLANTATION
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Left Hepatic Lobectomy
For a left hepatectomy, the triangular ligament is divided, exposing the IVC and left hepatic vein. The round ligament is elevated and the parenchymal bridge between segments II and IVB is divided, expos­ing the left hilum at the base of the umbilical fissure. The left hepatic artery, portal vein, and hepatic duct are ligated individually. The left lateral segment is rotated to the patient’s right and the gastrohepatic ligament is divided. Exposure of the left hepatic vein is facilitated by dividing the ligamentum venosum at its insertion. The common trunk of the middle and left hepatic veins is encircled. Depending on the location of the pathology and the anatomy of the venous outflow, the middle and left hepatic vein may be divided together as a com­mon trunk or the middle hepatic vein may be spared. The outflow can usually be divided extrahepatically with a vascular stapler before proceeding with the parenchymal transection. If this is not feasible, the left hepatic vein can be divided intraparenchymally. The liver parenchyma is transected along the line of vascular demarcation. If oncologically feasible, the transection plane should run horizontally, approximately 1 cm above the hilum, from the area of transection of the left hilar plate to the left side of the gallbladder fossa, thus avoid­ing transection of an aberrant right anterior or posterior duct, and then turning vertical, parallel to Cantle’s line.
Left Trisectionectomy
When indicated, the right anterior section (segments V and VIII) may be transected along with the left hemiliver. The initial steps are the same as for a left hepatectomy. The main challenge is to define
the transection plane, which is horizontal, extending from the right of the gallbladder fossa and anterior to the right hepatic vein toward the base of segment IV without injuring the inflow to the posterior sector. The right anterior pedicle is identified and ligated as the parenchymal transection approaches the hilum.
S u g g e S t e d R e a d i n g S
Jarnagin WR. Hepatic resection: general considerations. In: Jarnagin WR, ed.
Surgery of the Liver, Biliary Tract, and Pancreas: Elsevier; 2017:1520–1521.
Kemeny N, Niedzwiecki D, Hollis D, etal. Hepatic arterial infusion versus
systemic therapy for hepatic metastases from colorectal cancer: a ran­domized trial of efficacy, quality of life, and molecular markers (CALGB
9481). J Clin Oncol. 2006;24:1395.
Memeo R, de Blasi V, Adam R, etal. Parenchymal-sparing hepatectomies
(PSH) for bilobar colorectal liver metastases are associated with lower morbidity and similar oncological results: a propensity score matching analysis. HPB. 2016;18:781–790.
Nordlinger B, Sorbye H, Glimelius B, etal. Perioperative FOLFOX4 chemo-
therapy and surgery versus surgery alone for resectable liver metastases from colorectal cancer (EORTC 40983): long-term results of a random­ized, controlled phase 3 trial. Lancet Oncol. 2013;14:1208–1215.
Primrose J, Fox R, Palmer D, etal. Capecitabine compared with observation
in resected biliary tract cancer (BILCAP): a randomised, controlled, mul­ticentre, phase 3 study. Lancet Oncol. 2019;20(5):663–673.
Sandstrom P, Rosok C, Sparrelid E, et al. ALPPS improves resectabil-
ity compared with conventional two-stage hepatectomy in patients with advanced colorectal liver metastasis. Results from a Scandinavian Multicenter Randomized Controlled Trial (LIGRO Trial). Ann Surg. 2018;267(5):833–840.
Hepatic Malignancy: Resection Versus Transplantation
Sharon R. Weeks, MD, and Shane E. Ottmann, MD
INTRODUCTION
Hepatocellular carcinoma (HCC) is the most common primary malignant tumor in the liver and the fifth most common cause of malignancy worldwide. It develops most commonly in the setting of hepatic injury or chronic liver disease. Prevalence of HCC is higher in populations and geographic regions with higher rates of hepatitis infection; the highest HCC rates are seen in Asia and sub-Saharan Africa. Worldwide, the most common risk factor for HCC is hepatitis B virus infection or carrier status, whereas in the United States, hepa­titis C is the most critical risk factor. Although the rates of many can­cers in the United States have been decreasing over the last decade, the incidence of HCC and resultant mortality have been on the rise. HCC remains the third most common indication for transplant in the United States, comprising 14% of liver transplants performed in 2019.
The prognosis for HCC is poor if left untreated, with a 5-year overall survival of less than 10% and a median survival less than 6 months. For patients with a resectable tumor without underly­ing liver disease, resection is the treatment of choice. However, as the majority of patients with HCC have concomitant chronic liver disease, resection options can be limited due to concern for post­operative liver failure from inadequate remnant volume. Although
transplantation for well-selected HCC patients has excellent out­comes and should be the treatment of choice in patients with decom­pensated cirrhosis, the limited donor pool prevents widespread application of this treatment modality for all patients. The patient with a resectable HCC in the setting of well-compensated cirrhosis presents a treatment dilemma: who should be resected and who would be better served with transplant? The answer for any given patient depends on local resources, including the availability of transplant, severity of underlying liver disease, and the technical resectability of the tumor, while weighing the risks associated with remnant liver recurrence and dropout on the transplant waitlist from tumor progression. Finally, while surgical intervention is the mainstay of treatment for HCC, many patients present at advanced stages that are not amenable to resection or do not meet criteria for transplant. For these patients, multiple locoregional therapies have been developed in the last few decades, including ablation, embo­lization, and radiation therapy; these interventions can be used as monotherapy or as a bridge to surgical therapy.
PATIENT EVALUATION
Risk factors for development of HCC include hepatitis B and C, alco­hol consumption, genetic hemochromatosis, nonalcoholic fatty liver disease (NAFLD), primary biliary cirrhosis, alpha-1 antitrypsin defi­ciency, and other causes of cirrhosis. Patients with HCC are typically asymptomatic until advanced stages of the disease. When patients do have symptoms, they are typically due to mass effect of the tumor and may include abdominal pain, early satiety, weight loss, or a pal­pable mass. As cirrhosis is present in more than 90% of patients with HCC, cirrhotic symptomatology may be present, including weak­ness, fatigue, jaundice, pruritis, and hepatic encephalopathy. Patients may also manifest features of liver decompensation such as ascites
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or variceal bleeding. Finally, liver decompensating events may result from tumor extension into the hepatic or portal veins.
Ideally, patients at high risk for HCC are followed via a surveil­lance protocol with ultrasound and alpha fetoprotein (AFP). The National Comprehensive Cancer Network (NCCN) recommends surveillance ultrasound every 6 months in all patients with chronic hepatitis B (including those without cirrhosis) as well as patients with cirrhosis due to any cause. Cross-sectional imaging with multiphasic CT or MRI is a more sensitive but less cost-effective approach to HCC screening; these modalities may be used as alternatives to ultra­sound if visualization is poor. Unfortunately, adherence to these rec­ommendations is low and patients often present at advanced stages of disease. Whether identified on surveillance, incidental, or for cause imaging, the diagnosis of HCC can typically be made radiograph­ically without need for liver biopsy. Abdominal multiphasic CT or MRI with contrast should be performed to confirm the diagnosis and the extent of tumor burden. All patients with diagnosis of HCC war­rant oncologic staging; NCCN guidelines recommend evaluation for distant metastases with chest CT and complete imaging of the abdo­men and pelvis if not previously performed. The most common sites of metastasis are lungs, bone, and lymph nodes; less common sites include adrenal and peritoneal metastases. Consequently, selective use of bone scan in patients with skeletal symptoms may be consid­ered. Laboratory evaluation should include hepatitis panel, biliru­bin, transaminases, alkaline phosphatase, coagulation factors, basic chemistry and blood counts, and AFP if not previously performed.
The differential diagnosis for a presumed HCC on imaging includes cholangiocarcinoma, metastases, and benign liver masses, but typically imaging is diagnostic, particularly in high-risk patients. Patients at high risk for HCC are also at risk for intrahepatic chol­angiocarcinoma and combined HCC-cholangiocarcinoma; these diagnoses should be considered in patients without sufficiently diag­nostic imaging characteristics and in those with elevated CA 19-9 or carcinoembryonic antigen (CEA). In these patients or in other cases of diagnostic dilemma, such as patients with concern for metastasis or those with a low risk history, biopsy is warranted to confirm the diagnosis and guide treatment decisions.
Once diagnosis is confirmed, further treatment is guided by underlying liver function, resectability of tumor, and availability of treatment modalities, including transplantation.
ASSESSMENT OF LIVER FUNCTION
Of primary concern for choosing a treatment course is determina­tion of the patient’s underlying liver function. Multiple schemas have been developed for this purpose, the most well-known of which are the Child-Pugh classification (shown in Table 1) and the Model for End-Stage Liver Disease (MELD) score. Both predict mortality in cirrhotic patients, including postoperative mortality. Child class C cirrhotic patients, with up to 80% risk of mortality after surgery, are not generally considered candidates for nontransplant surgery. The
TABLE 1 Child-Pugh Classification
1 point 2 points 3 points
Albumin (g/dL) >3.5 2.8–3.5 <2.8 Bilirubin (mg/dL) <2 2–3 >3 INR <1.7 1.7–2.3 >2.3 Ascites None Slight Moderate Encephalopathy None 1–2 3–4
Child-Pugh classification is calculated by summing the points per parameter. Class A = 5–6; Class B = 7–9; Class C = 10–15.
MELD score, most recently modified to include sodium, includes bilirubin, international normalized ratio, and creatinine, and is used for prioritization of patients on the liver transplant waitlist. It has also been shown to predict 30-day mortality after surgery, with a 1% increase in mortality per MELD point in patients with MELD scores less than 20 and an additional 2% increase per MELD point greater than 20.
In recent years, other scoring systems have been evaluated as predictors of mortality in cirrhotic patients. The Mayo postoperative mortality risk calculator attempts to provide more specific results for a patient given their comorbidities; it calculates probability of mor­tality using age, American Society of Anesthesiologists(ASA) score, bilirubin, creatinine, International Normalized Ratio (INR), and the etiology of cirrhosis. This calculator provides predicted mortality at 7, 30, and 90 days postoperatively as well as at 1 and 5 years. Recently, use of the hepatic venous pressure gradient (HVPG) has been used to predict 1-year mortality in cirrhotic patients undergoing elective surgery. HVPG values higher than 16 mm Hg have been shown to be independently associated with higher mortality, and values greater than 20 mm Hg were associated with a very high risk of death, up to 44%. Notably, HVPG values <10 mm Hg have been shown to be protective against postoperative decompensating liver events.
In evaluating the specific question of the risk of postresection liver failure in patients with HCC, the albumin-bilirubin (ALBI) grade was found to effectively predict outcomes and importantly does not rely on the subjective scoring of the Child-Pugh classifi­cation. The ALBI grade performed as well as the Child-Pugh clas­sification in predicting mortality in cirrhotic patients with HCC. Three grades, corresponding to three separate prognostic groups, were identified: ALBI grade I (score ≤−2.60), grade II (score >−2.60 to ≤−1.39), and grade III (>−1.39). The three grades also predicted 1-year survival after hepatic resection, with rates of 100%, 81.9%, and
62.9%, respectively.
The most commonly used staging classification for HCC that incorporates both tumor characteristics as well as underlying liver function is the Barcelona Clinic Liver Cancer (BCLC) staging system (Fig. 1). It classifies patients based on Child-Pugh classification and performance status, in addition to tumor size, nodal and metastatic disease, and local invasion characteristics. It also provides recom­mended treatment modalities for patients based on these charac­teristics. Studies of its prognostication outcomes have been mixed, with some evidence that it outperforms many models (including the American Joint Committee on Cancer [AJCC] TNM staging system) but underperformed in other settings. Importantly, several studies have shown that treatment outside Barcelona guidelines can be effective, and surgical resection has potential beyond the limited scope detailed in BCLC guidelines.
RESECTION FOR HEPATOCELLULAR
CARCINOMA
Surgical resection remains the mainstay of treatment for HCC patients without underlying liver disease. Additionally, in many areas where access to transplantation is low, it remains standard therapy for HCC patients with well-compensated cirrhosis without evidence of portal hypertension. Well-selected patients in this group have an overall 5-year survival as high as 60% to 70%. However, recurrence rates in the remnant liver are quite high, with most large studies reporting only 25% to 45% disease-free survival at 5 years. Further­more, as many patients present with advanced disease, only 20% to 30% present as initially resectable on surgical evaluation.
Careful preoperative evaluation of these patients to determine candidacy for resection is critical. Imaging studies can determine resectability in regard to location, vascular involvement, and absence of distant metastases. Volumetrics, using CT, MRI, or scintigraphy, can be obtained to estimate the size of the remnant liver; 20% to 30% is considered adequate for a healthy liver. Larger remnants, 30% for the steatotic or chronic hepatitis liver and 40% for the cirrhotic liver,
382 HEPATIC MALIGNANCY: RESECTION VERSUS TRANSPLANTATION
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HCC
Stage 0 Stage D
PS 0,
Child-Pugh A
Very early
stage (0)
Single <
carcinoma in situ
2 cm,
Single
Portal pressure /
bilirubin
Increased
Normal No Yes
Single or 3 nodules
Early
stage (A)
PS 0
3 nodules
Associated
diseases
3 cm,
3 cm
Stage A–C
PS 0–2,
Child-Pugh A–B
Intermediate
stage (B)
Multinodular,
PS 0
Advanced
stage (C)
Portal invasion, N1, M1, PS 1–2
2,
PS >
Child-Pugh C
Terminal
stage (D)
Liver
transplantation
/ LDLT)
(CLT
FIG. 1 Barcelona Clinic Liver Cancer staging system for hepatocellular carcinoma. (From Khorsandi SE, Heaton N. Contemporary strategies in the management of
hepatocellular carcinoma.HPB Surg. 2012;2012:154056.)
are recommended for the diseased liver. Preoperative assessment of liver function is also critical to prevent postoperative liver failure and decompensating liver events. Patients with Child class A cirrhosis, no evidence of portal hypertension, and well-preserved synthetic liver function can be considered as resection candidates. Patients without evidence of portal hypertension include those with HVPG <10, normal platelet count, normal appearing spleen, and lack of ascites and esophageal varices. In these patients, however, the risk of recurrence in the liver remnant and time at risk (with respect to patient age and other comorbidities) must be considered. Risk factors independently associated with tumor recurrence include tumor size greater than 5 cm and vascular invasion. Most studies have failed to identify a significant benefit to recommend anatomic over nonanatomic resection in preventing recurrence or mortality. Some have advocated for anatomic resection based on the theoret­ical risk of intrahepatic metastases via portal vein tributaries, but this recommendation has not yet been supported by evidence of improved outcomes. Regardless of planned approach, intraoperative ultrasound should be used liberally to best define the tumor burden intraoperatively and ensure an oncologically sound resection mar­gin. It is the most sensitive imaging modality for identifying intrahe­patic metastases and tumor margins, and it may clarify or expand on findings from preoperative imaging.
RF
/ PEI
In patients in whom the remnant liver volume is of concern, portal vein embolization and the two-staged associating liver partition and portal vein ligation for staged hepatectomy (ALPPS) procedure are available modalities to facilitate resection. Preoper­ative portal vein embolization utilizes any of a number of emboli­zation agents injected in percutaneous fashion via a transjugular or transhepatic approach to obliterate the portal blood flow to the ipsilateral side of the liver as the tumor (Fig. 2). This insult elicits hypertrophy of the contralateral side to augment volume of the future liver remnant and is performed 2 to 8 weeks in advance of a planned hepatic resection. Repeat imaging before surgery can determine effectiveness of the procedure. In a large clinical series of 358 patients, median regeneration of the future liver remnant was 50.3% at a median of 32 days postprocedure. Harnessing sim­ilar pathophysiology, the ALPPS procedure has been developed to accelerate hypertrophy of the liver remnant. The first stage involves operative portal vein ligation and in situ parenchymal transection of the resection plane. The second stage, at postoperative week one or two, involves completion of the resection and removal of the specimen. Published studies report liver remnant growth of 40% to 160% in only 6 to 9 days, a period in which significant tumor progression is less likely than the longer regenerative time period needed for portal vein embolization. Currently, ALPPS remains
SorafenibResection TACE
Best
supportive
care
FIG. 2 Portal vein embolization. Right portal vein embolization from the
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contralateral approach. (From Jarnagin: Blumgart’s Surgery of the Liver, Biliary Tract and Pancreas, 6th ed. Elsevier; 2017.)
limited to high-volume centers due to concerns regarding high rates of morbidity and mortality. However, a recent randomized trial showed higher resection rates for the ALPPS group compared with patients undergoing two-stage hepatectomy with portal vein embolization. Additionally, the vast majority of patients who fail to reach a sufficient future liver remnant with embolization were able to be rescued with ALPPS. With these improved outcomes and increasing experience with the procedure, ALPPS may play a larger role as a treatment modality in the future for patients with an insufficient future liver remnant.
LIVER TRANSPLANTATION IN HEPATOCELLULAR CARCINOMA
Excellent data exist to support transplantation of patients with cir­rhosis and HCC tumors with early stage HCC; 5-year survival rates after transplant exceed 70%. The Milan criteria were developed in 1996 and remain the most commonly used and accepted criteria for listing of liver transplant candidates with HCC. Patients meet Milan criteria if they have a single nodule ≤5 cm or up to three nodules, each ≤3 cm; additionally, they must be free of macroscopic vascular invasion or distant disease. Overall survival after transplantation within Milan criteria is over 75% at 5 years. In the decades following Milan, the criteria received criticism for being unnecessarily narrow and excluding patients who would benefit from transplant. Multi­ple other extended criteria were proposed, with the University of California San Francisco (UCSF) criteria being the most commonly utilized. Patients qualify by UCSF parameters if they have a single nodule ≤6.5 cm or up to three nodules, each ≤4.5 cm, with a total tumor diameter ≤8 cm. Five-year overall survival using these criteria is 70% to 80%; conversely, transplantation outside these criteria was quite poor with less than 50% 1-year survival.
In patients with cirrhosis, multiple studies have shown clear benefits in disease-free and overall survival in those undergoing transplantation compared with resection. In a retrospective study of 1765 patients with HCC and concomitant cirrhosis who met Milan criteria, patients undergoing transplantation had significantly improved survival at 5 (74% vs. 53%) and 10 years (54% vs. 22%), as well as increased disease-free survival (72% vs 30% at 5 years; 53% vs 12% at 10 years) compared with transplant eligible patients who underwent liver resection. However, in the same large series, only about 10% of patients presenting with HCC and cirrhosis were eligi­ble for transplant based on Milan criteria.
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Given the threat to life from malignancy not captured by the degree of liver dysfunction, HCC patients in the United States who fall within the Milan criteria are given exception points on the liver transplant waitlist after a 6-month waiting period that correlates with the region’s mean MELD at transplant. Thus, while transplantation is the most oncologically sound treatment for patients with HCC, drastically reducing the risk of recurrence compared with resection, the choice to proceed with transplant must be weighed against the risk of tumor progression on the waitlist. Living donor liver trans­plantation, which has been growing in safety and availability through the United States, may prove to reduce this risk. Some studies have shown that living donor liver transplantation significantly decreases risk of death from time of listing due to lower dropout rates.
FUTURE DIRECTIONS
Adjunctive and palliative treatments for HCC patients who are not resection or transplant candidates at presentation deserve special mention. These include transarterial chemoembolization, radiof­requency ablation, and other local therapies; they may serve as adjuvant or palliative therapy, as well as a bridge to definitive ther­apy. Ablative therapies for recurrences limited to the liver have also shown promising results. The long-term outcomes of these treat­ments and their use as a bridge to transplant or resection remain to be well defined, but these modalities are becoming more widespread, and indications are expanding.
Resection is the mainstay of therapy for cholangiocarcinoma, but the majority of patients are deemed unresectable at presentation. The Mayo protocol for unresectable cholangiocarcinoma treated with preoperative chemoradiotherapy followed by transplantation reported impressive results with a 5-year survival rate of 82%. These results have been questioned as many patients included in the study were found to be without viable tumor in the hepatectomy specimen. Multiinstitutional studies using similar protocols showed improved outcome for transplant over resection for hilar cholangiocarcinoma. Transplantation for cholangiocarcinoma remains controversial and is an area for further investigation.
SUMMARY
Any discussion of resection versus transplantation for HCC must include the degree of liver disfunction, tumor stage, availability of transplant, potential of recurrence in the remnant, and magnitude of the liver resection required to render the patient disease free. Retrospective analysis of resection versus transplantation is difficult to generalize given the obvious selection bias; patients who undergo resection are more likely to have less severe liver disease and patients without liver disease rarely undergo transplantation. These studies also necessarily exclude those patients on the waitlist who did not receive a transplant due to tumor progression. Although definitive data are lacking, most studies and observational experience support improved disease-free and overall survival in patients undergoing transplantation compared with resection. Over the past 30 years, there have been substantial advances in operative techniques of both liver transplantation and complex hepatic surgery, leading to improved selection and survival in both groups. There is little debate that resection can benefit many with isolated liver disease regardless of tumor size in a noncirrhotic patient. Liver resection offers the additional advantage of typically being immediately available and not dependent on the organ donor population. Similarly, HCC patients with liver failure and obvious decompensation clearly benefit from transplant provided there is a route to transplantation and the tumor is within acceptable criteria. The patient with well-compensated cir­rhosis and early-stage tumors within transplantable criteria presents a treatment challenge; the risk of delayed intervention while awaiting a suitable organ must be weighed against the inferior survival and disease-free survival rates seen after hepatic resection. When these patients present early enough to fall within transplantable criteria,
384 MANAGEMENT OF COLORECTAL LIVER METASTASES
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we believe they should be referred to a transplant program to discuss the options of resection versus transplant. Important considerations for all HCC patients include the risk of disease progression while on the transplant waitlist, options for living donor liver transplant, risk of HCC recurrence in the remnant liver, liver failure following hepa­tectomy, and liver transplant outcomes in the modern era.
S u g g e S t e d R e a d i n g S
Chapman WC, Klintmalm G, Hemming A, et al. Surgical Treatment of
Hepatocellular Carcinoma in North America: Can Hepatic Resection Still Be Justified? J Am Coll Surg. 220(4):628–637.
Management of Colorectal Liver Metastases
Jordan M. Cloyd, MD, and Timothy M. Pawlik, MD, MPH, PhD
INTRODUCTION
Colorectal cancer (CRC) is a leading cause of cancer-related deaths throughout the world with up to 50% of patients developing colorec­tal liver metastases (CRLM) during the course of their disease. For patients with CRLM, surgical resection provides the only opportunity for potentially curative therapy. Although improvements in modern systemic chemotherapy have expanded the number of patients eli­gible for curative-intent surgery, advances in operative techniques and perioperative care have simultaneously improved the outcomes following liver surgery. Given the therapeutic complexity, the man­agement of CRLM requires expert multidisciplinary care by an experienced oncology team. This chapter provides an overview of contemporary management of CRLM with an emphasis on surgical approaches.
EVALUATION
The diagnosis of CRLM is usually based on cross-sectional imaging obtained during the staging evaluation of patients recently diag­nosed with CRC or during surveillance of patients with a history of treated CRC. A thorough history and physical examination, an elevated carcinoembryonic antigen (CEA) level, and characteristic imaging of a liver lesion are generally sufficient to make a diagnosis of CRLM. When necessary, the diagnosis may be confirmed via percutaneous image-guided biopsy. Surgical planning for CRLM requires high-quality imaging. On contrast-enhanced multidetector computed tomography (CT), CRLMs typically appear as hypoatten­uating lesions best visualized on portal venous phases. Arterial phase images can be helpful to distinguish metastases from benign vascular lesions, to clarify vascular anatomy for operative planning, and/or if placement of a hepatic arterial infusion pump is being considered. Although CT is advantageous given its widespread availability and ease of use, magnetic resonance imaging (MRI) provides enhanced sensitivity of smaller tumors and better characterization of indeter­minate lesions (Fig. 1).
An evaluation of candidacy for liver resection involves a compre-
hensive assessment along three domains: physical, oncologic, and
Ethun CG, Lopez-Aguiar AG, Anderson DJ, et al. Transplantation
Versus Resection for Hilar Cholangiocarcinoma: An Argument for Shifting Treatment Paradigms for Resectable Disease. Ann Surg. 2018;267(5):797.
Rea DJ, Heimbach JK, Rosen CB, etal. Liver transplantation with neoadjuvant
chemoradiation is more effective than resection for hilar cholangiocarci­noma. Ann Surg. 2005;242(3):451.
Schadde E, Ardiles V, Robles-Campos R, etal. Early survival and safety of
ALPPS. Ann Surg. 2014;260(5):829–838.
Shindoh J, Tzeng CD, Aloia TA, etal. Safety and efficacy of portal vein embo-
lization before planned major or extended hepatectomy: an institutional experience of 359 patients. J Gastrointest Surg. 204;18(1):45–51.
technical. First, patients must be healthy enough and have appropri­ate functional status to undergo major liver surgery. For patients with prohibitive comorbidities or poor performance status, nonoperative therapies should be considered. Oncologic resectability refers to the selection of patients for surgery based on underlying tumor biology. Relevant factors may include the number or size of metastases, the presence of extrahepatic disease, the disease-free interval for meta­chronous tumors, tumor mutation status, and/or the response to neoadjuvant therapy. Technical resectability refers to the ability to perform a margin-negative resection while preserving an appropriate future liver remnant (FLR). In general, the minimum FLR must con­sist of at least two contiguous segments with intact vascular inflow, outflow, and biliary drainage. In addition, the estimated FLR volume should be calculated using liver volumetry to minimize the risk of posthepatectomy liver failure (PHLF). Although patients with nor­mal hepatic function can safely tolerate resection with a planned FLR size of >20%, individuals with compromised liver function (obesity, receipt of chemotherapy for greater than 12 weeks, diabetes mellitus) should have an FLR >30%, and those with fibrosis/cirrhosis require an FLR >40% to 50% of total liver volume.
ROLE OF CHEMOTHERAPY
A major contributor to improved survival among patients with advanced CRC, and a driving factor in expanding the role of surgery for CRLM, has been the advent of improved systemic therapies. Contemporary first-line chemotherapy for metastatic CRC primar­ily consists of fluorouracil-based regimens containing oxaliplatin and/or irinotecan, namely FOLFOX (fluorouracil, leucovorin, and oxaliplatin), FOLFIRI (fluorouracil, leucovorin, and irinotecan), XELOX (capecitabine and oxaliplatin), or FOLFOXIRI (fluorouracil, leucovorin, oxaliplatin, and irinotecan). Biologic agents, such as bev­acizumab or cetuximab, can be added to increase response rates. The choice of regimen largely depends on the patient’s performance sta­tus, prior receipt of chemotherapy, and the presence of RAS or BRAF mutations. Tumors with evidence of mismatch repair deficiency are more likely to respond to immunotherapy.
For patients with resectable CRLM, neoadjuvant therapy is controversial. In the European Organisation for Research and Treatment of Cancer (EORTC) intergroup 40983 trial, patients with resectable CRLM were randomized to either upfront surgical resection or perioperative FOLFOX chemotherapy. Neoadjuvant therapy led to a 9% absolute improvement in progression-free survival but no difference in overall survival (OS) (Fig. 2). There­fore, neoadjuvant chemotherapy continues to be used selectively for patients with high-risk features or unclear resectability. How­ever, prolonged chemotherapy may lead to chemotherapy-associ­ated liver injury (CALI). Specifically, irinotecan-based treatment
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FIG. 1 Imaging of colorectal liver metastases. (A)Portal venous phase contrast-enhanced liver CT: necrotic mass, with fibrous enhancement centered
on segments 2–4 (arrow).(B)A second hypodense lesion on CT scan is visible in segment 7 (thin arrow).(C)MRI shows peripheral enhancement of both lesions (arrows).(D)Both lesions are hypermetabolic on PET-CT (arrows).(E)Discovery of an additional lesion on portal venous phase contrast enhanced MRI (circle).(F)This third lesion was not seen on CT or PET-CT (circle). (From Rahnemai-Azar A, Dillhoff M, Schmidt C, Pawlik T. Colorectal Liver Metastases. In:
Hepatobiliary and Pancreatic Surger y: A Companion to Specialist Surgical Practice, 6, 104–120.)
is associated with steatohepatitis, whereas oxaliplatin-based che­motherapy is associated with sinusoidal congestion (Fig. 3). In general, if preoperative chemotherapy is used, the duration should be limited to 4 to 6 cycles (i.e., 2–3 months). In addition, neoad­juvant chemotherapy may lead to disappearing liver metastases, especially for small (<2 cm), centrally located tumors. If not
surgically resected, these lesions will recur in up to 50% to 80% of patients.
Similarly, the role of adjuvant chemotherapy following resec­tion of CRLM also remains controversial. Given that data from randomized controlled trials have produced mixed results, adju­vant chemotherapy is most often used selectively in patients with
386 MANAGEMENT OF COLORECTAL LIVER METASTASES
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A
Number at risk
chemotherapy
Number at risk
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All randomly assigned patients
100
90 80 70 60 50 40
Overall survival (%)
30 20 10
Overall log-rank test: p=0.34
0
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Surgery only Perioperative chemotherap
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Surgery only 182 167 138 116 94 79 72 58
chemotherapy
182 165 145 120 107 88 72 66Perioperative
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FIG. 2 Long-term overall survival of patients
with resectable colorectal liver metastases randomized to perioperative chemotherapy versus upfront surgery in the EORTC 40983 trial. All randomly assigned patients (A) and all eligible patients (B). (From Nordlinger B, Sorbye H, Glimelius B,
etal. Perioperative FOLFOX4 chemotherapy and surgery versus surgery alone for resectable liver metastases from colorectal cancer (EORTC 40983): long-term results of
Surgery only 171 159 133 111
a randomised, controlled, phase 3 trial. Lancet Oncol. 2013;14(12):1208–1215.)
high-risk disease (e.g., number of tumors, margin status, initial CEA level, etc.). Several nomograms or clinical risk scores have been developed to aid in prognostication and use of adjuvant ther­apy however, the use of these tools in the real-world clinical setting has been variable.
40
Overall survival (%)
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avoided given the potential for compromising margins and/or inad­vertent injury to biliovascular pedicles. Intermittent hepatoduodenal ligament clamping (i.e., Pringle’s maneuver) can help minimize blood loss. Enhanced recovery after surgery protocols can reduce postoperative length of stay and morbidity after liver surgery.
SURGICAL RESECTION
Surgical Technique
While there are several different techniques to divide the liver parenchyma, the universal goal of resection for CRLM is complete resection of all metastases with microscopic negative margins. A comprehensive understanding of liver anatomy is mandatory when performing hepatic resection of CRLM, as is adept use of intraoper­ative ultrasound for identifying all tumors, guiding planned surgical margins, and targeting intraoperative ablation (Fig. 4). Given its importance to perioperative and oncologic outcomes, strategies to minimize operative blood loss are paramount. A low central venous pressure (CVP) maintained by an experienced anesthesiologist is one of the most important steps. Although numerous parenchymal transection techniques are available, with none consistently demon­strating superiority over others, excessive use of staplers should be
Margin Status
Although an R0 resection consists of surgical margins >1 mm, the optimal margin width at the time of liver resection for CRLM remains controversial. In a seminal study, R1 margin status was asso­ciated with worse OS following liver resection for CRLM, but greater margin widths were not associated with improved outcomes (Fig. 5). Other studies have demonstrated that wider margins >1 mm are not advantageous; however, even submillimeter margin widths have been associated with improved OS compared with microscopically positive margins. Increasing evidence suggests that margin status may be more reflective of a biological effect. For example, patients with RAS mutations are more likely to have positive margins, and the prognostic significance of R1 margin status is lessened among patients who respond to neoadjuvant therapy. Therefore the objec­tive of any resection for CRLM should remain a microscopically negative margin ≥1 mm, yet the direct association between margin
LIVER 387
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FIG. 3 Chemotherapy-associated liver injury. (A)Intraoperative gross photograph of a fatty liver. Note the hepatomegaly, yellow appearance, and rounded
edges.(B)Intraoperative photograph of a liver with sinusoidal obstructive syndrome. Note the patchy blue mottled appearance. (From Srinevas K. Reddy S, Geller D. Hepatic steatosis, steatohepatitis, and chemotherapy-related liver injury. In: Blumgart’s Surgery of the Liver, Biliary Tract and Pancreas, Philadelphia: Elsevier;
2007)..
status and patient outcomes is likely influenced by a myriad of clini­cal and biological factors.
Parenchymal-Sparing Techniques
A parenchymal-sparing approach is increasingly advocated in the surgical management of CRLM. The goals of parenchymal-sparing hepatectomy (PSH) are to achieve the oncologic principles of margin-negative resection while preserving maximal uninvolved liver parenchyma. PSH not only leads to improved perioperative outcomes and reduced incidence of PHLF, but the preservation of normal liver is also associated with improved odds of salvageability in the case of liver recurrence. Although some anatomic resec­tions, such as segmentectomy or sectionectomy, can be considered parenchymal-sparing approaches, PSHs are more commonly nonan­atomic resections, occasionally termed wedge resections. An exam­ple of a PSH might be several nonanatomic resections of superficial tumors in the right liver instead of a formal right hepatectomy.
Minimally Invasive Approaches
While minimally invasive approaches to liver surgery have had slower widespread adoption than in other areas of surgery, minimally invasive liver resection (MILR) is now considered an acceptable approach to the management of CRLM by experienced surgeons. Numerous retrospective and institutional studies have demonstrated its safety and appropriate oncologic outcomes. More recently, the OSLO-COMET trial randomized patients with resectable CRLM to either open or laparoscopic PSH. In this study, patients who under­went MILR experienced improved perioperative outcomes with no differences in margin status or long-term outcomes. Increasingly, robotic surgery is employed to extend the benefits of MILR to patients with CRLM, and robotic approaches appear to result in similar short- and long-term outcomes compared with laparoscopic liver surgery. Several society guidelines have recommended MILR as the standard of care for metastases in favorable locations (e.g., left lateral sectionectomy, nonanatomic resections in anterosuperior segments), and MILR is increasingly used at experienced centers for major hepatectomy.
LOCOREGIONAL THERAPIES
Ablation
For oligometastatic disease that is not amenable to resection, thermal ablation is an alternative locoregional therapy for select
patients (Fig. 6). For small tumors, thermal ablation is a potentially curative-intent treatment with only marginally increased local recur­rence rates compared with resection when performed by experienced providers. Intraoperative ablation can also be used at the time of surgical resection to address multifocal or bilateral disease in a parenchymal-sparing approach, especially for central tumors that would otherwise have required a hemihepatectomy. Cryoablation and radiofrequency ablation (RFA) are less commonly used now in place of microwave ablation (MWA), which offers advantages in ther­mal spread and efficiency of use. Ideal metastases are <3 cm that are separate from major blood vessels and other vital structures. Ablation can generally be performed open, laparoscopic, or percutaneous.
Hepatic Artery Infusion Therapy
The primary rationale for hepatic artery infusion (HAI) therapy is that liver metastases derive their blood supply predominantly from the hepatic artery, while normal hepatocytes are primarily supplied by portal venous blood. HAI therapy involves delivering chemo­therapy directly to the liver via a catheter surgically placed into the gastroduodenal artery and connected to a subcutaneous port that can be accessed percutaneously. HAI therapy is generally well toler­ated, although hepatic artery thrombosis, biliary toxicity, incomplete perfusion of the liver, and toxicity from inadvertent perfusion to the stomach or duodenum can occur. In general, the primary tumor should be resected and there should be minimal or no extrahepatic disease. Floxuridine (FUDR) is the most commonly utilized drug for HAI therapy and is especially ideal given its short half-life and high hepatic extraction.
There are two current indications for HAI therapy: unresectable CRLM and adjuvant therapy following resection of CRLM. For patients with initially unresectable CRLM, the use of HAI therapy, with or without simultaneous systemic chemotherapy, has been shown to increase response rates compared with systemic therapy alone in some studies. A limitation of the current evidence is that most trials of HAI therapy were not compared with patients receiv­ing contemporary multiagent chemotherapy with biologic agents. Although further randomized controlled trials are needed, HAI therapy can be considered for patients with isolated unresectable CRLM to increase the odds of successfully downstaging to surgical resection. Similarly, a few randomized controlled trials, primary performed at a single high-volume institution, have suggested improved outcomes with adjuvant HAI therapy typically combined with systemic therapy versus systemic chemotherapy alone following resection of CRLM. Given the single institution nature of this evi­dence, the potential toxicity associated with HAI therapy, challenges
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A
FIG. 4 Functional division of the liver into
eight segments as described by Coinaud:(A) as observed in the anatomical position in the patient;(B) as observed ex vivo. (From Vincent
S. Yip V, Fenwick S. Hepatic, biliary and pancreatic anatomy. In: Hepatobiliary and Pancreatic Surgery: A Companion to Specialist Surgical Practice, 2 , 17–40.)
with maintaining a pump program, and the improved effectiveness of modern chemotherapy, adjuvant HAI therapy has not gained universal acceptance.
Other hepatic-artery based therapeutic strategies, includ­ing yttrium-90 transarterial radioembolization ( transarterial chemoembolization (TACE) have also been studied, particularly in the management of unresectable CRLM. An important study is the SIRFLOX trial that randomized 549 patients with unre­sectable CRLM to first-line chemotherapy with or without Although there was no difference in OS, the TARE group experi­enced increased adverse events. Although TARE should not be used as a first-line treatment, it is still occasionally considered in patients with isolated unresectable CRLM following induction systemic
B
90
Y TARE) and
90
Y TARE.
chemotherapy. TACE and drug-eluting bead (DEB)-TACE are not commonly used in the current management of unresectable CRLM.
SPECIFIC CLINICAL SCENARIOS
Initially Unresectable Disease
A substantial proportion of patients with metastatic CRC will present with unresectable bilateral or locally advanced CRLM. Given the effectiveness of systemic chemotherapy, neoadjuvant chemother­apy has the potential to downsize unresectable CRLM and convert initially inoperable lesions to resectable disease in up to 40% of patients. FOLFOX or FOLFIRI with or without a biologic agent are