Anatomical Versus Nonanatomical Resection of Colorectal Liver Metastases: Is There a Difference in Surgical and Oncological Outcome?
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- Lalmahomed, Z.S., Ayez, N., van der Pool, A.E.M. et al. World J Surg (2011) 35: 656. doi:10.1007/s00268-010-0890-9
The increased use of neoadjuvant chemotherapy and minimally invasive therapies for recurrence in patients with colorectal liver metastases (CLM) makes a surgical strategy to save as much liver volume as possible pivotal. In this study, we determined the difference in morbidity and mortality and the patterns of recurrence and survival in patients with CLM treated with anatomical (AR) and nonanatomical liver resection (NAR).
From January 2000 to June 2008, patients with CLM who underwent a resection were included and divided into two groups: patients who underwent AR, and patients who underwent NAR. Patients who underwent simultaneous radiofrequency ablation in addition to surgery and patients with extrahepatic metastasis were excluded. Patient, tumor, and treatment data, as well as disease-free and overall survival (OS) were compared.
Eighty-eight patients (44%) received AR and 113 patients (56%) underwent NAR. NAR were performed for significant smaller metastases (3 vs. 4 cm, P < 0.001). The Clinical Risk Score did not differ between the groups. After NAR, patients received significantly less blood transfusions (20% vs. 36%, P = 0.012), and the hospital stay was significantly shorter (7 vs. 8 days, P < 0.001). There were no significant differences in complications, positive resection margins, or recurrence. For the total study group, estimated 5-year disease-free and OS was 31 and 44%, respectively, with no difference between the groups.
Our study resulted in no significant difference in morbidity, mortality, recurrence rate, or survival according to resection type. NAR can be used as a save procedure to preserve liver parenchyma.
Colorectal cancer is the most common gastrointestinal malignancy worldwide, affecting nearly one million people each year . Half of these patients have or will develop hepatic metastases at some point during their life. Liver resection is considered to be the best treatment for colorectal liver metastases (CLM) with 5-year survival rates up to 60% in highly selected patients . Until recently, only 10–20% of patients were considered suitable for attempted curative resection [3, 4]. Due to improvements in surgical techniques, the acceptance of resection margins <1 cm, the introduction of more effective systemic chemotherapeutics, the use of portal vein embolization (VPE), the addition of radiofrequency ablation (RFA), and stereotactic body radiation (STBR) to surgery, more patients are eligible for liver surgery [5–13]. Moreover, the indications for liver resection have expanded during the past decade and there are only few limitations left, which include unresectable extrahepatic disease and insufficient future remnant liver. The question has shifted from “what can be resected” to “what will be left.”
During this period, a change in surgical approach can be observed by an increase of nonanatomical resections . A nonanatomical resection maximizes the amount of residual liver parenchyma, which is important, in particular for patients who received neoadjuvant chemotherapy. Although chemotherapy increases resectability, it is associated with hepatic changes, which might increase the risk of progressive hepatic failure and death after resection [15, 16]. Moreover, in case of intrahepatic recurrences after partial liver resection in patients with CLM, a sufficient liver residual can offer the opportunity for local treatment .
The purpose of this study was to investigate the influence of a nonanatomical liver resection (NAR) compared with an anatomical resection (AR) on morbidity, mortality, margin positivity, disease-free, and OS.
All patients who underwent partial hepatic resection for CLM at the Erasmus Medical Center from January 2000 to June 2008 were evaluated for inclusion in this study. Patients who underwent simultaneous AR and NAR or received additional RFA in addition to surgery as well as patients with extrahepatic metastasis were excluded.
Patients were divided into two groups: patients who underwent an AR, and patients who underwent a NAR. An AR was defined as resection of two or more hepatic segments as described by Couinaud . This includes bisegmentectomy, (extended) right hemihepatectomy, (extended) left hemihepatectomy, or a combination of these . NAR was defined as resection of the CLM, including a rim of microscopically normal tissue. The choice of resection type was made in a multidisciplinary hepatobiliary working group, based on tumor number, location, and patient status.
Information collected included demographic details, primary tumor stage (TNM-classification), maximum size, number and distribution of liver metastases on CT, plasma carcinoembryonic antigen (CEA) levels, neoadjuvant chemotherapy, Clinical Risk Score (CRS) , type of liver surgery, transfusion data, overall duration of hospital stay, perioperative complications, radicality, site, and treatment of recurrence.
Overall survival and disease-free survival (DFS) were calculated from the date of liver resection. Complications or death occurring within 30 days or before discharge were considered perioperative. We defined a positive surgical margin as the presence of vital tumor along the line of transection.
After partial hepatic resection, patients routinely underwent a physical examination and determination of CEA level, abdominal/chest CT, or ultrasonography every 4 months for the first year, every 6 months the second year and once per year thereafter.
Statistical analyses were conducted using SPSS (version 15, SPSS Inc., Chicago, IL). Categorical variables are presented as number (percentage). Continuous variables are presented as median (range). Categorical variables were compared with the chi-square test; continuous variables were compared with the Mann-Whitney U test. Actuarial survival was calculated using the Kaplan-Meier method from the date of resection of CLM, and differences in survival were examined using the log-rank test. P < 0.05 (two-sided) was considered significant.
(n = 88)
(n = 113)
No. of tumors
Size largest tumor (cm)a
Time to resection
Disease-free interval (mo)
Clinical risk scorea
Site primary tumor
Tumor stage primary tumor
Lymph node primary tumor
Type of resection
No. of resections
(N = 201)
Nonanatomical (n = 113)
Anatomical (n = 88)
Extended right hemihepatectomy
Extended left hemihepatectomy
Combination of anatomical resectionsa
(n = 88)
(n = 113)
Positive resection margins
Patterns of recurrence and treatment modality
(n = 88)
(n = 113)
Liver + lung
Liver + elsewhere
Therapy liver metastases
This study demonstrated no significant difference in outcome between patients with CLM after anatomical or NAR. The 5-year disease-free (AR 30% vs. NAR 32%) and OSs (AR 49% vs. NAR 39%) in our study is consistent with the literature [2, 24–28].
The major drawback is the retrospective nature of this study. Randomization would be difficult in this patient group, because the technique for liver resection is a tailor-made approach based on the size, number, location, and distribution of the metastases. In addition, the consideration between conservation of liver parenchyma, complete surgical tumor clearance, and complications is of importance in this decision. Although patients were not randomized, the basic characteristics were similar as shown in Table 1.
Liver parenchymal-sparing surgery is already frequently used for CLM for several reasons. Functional hepatic reserve must be considered for any liver resection; its significance increases in the context of neoadjuvant chemotherapy, which is used to downsize the tumor load, making more patients eligible for surgery . However, although chemotherapy increases resectability, it is associated with significant hepatic changes, such as hepatic sinusoidal obstruction, periportal inflammation, and steatohepatitis, which can affect patient outcome . Specifically, chemotherapy-associated steatohepatitis is associated with the risk of progressive hepatic failure and death after resection . Therefore, maximizing the amount of residual liver parenchyma is of considerable importance in patients who have had chemotherapy.
Moreover, surgical stress can be reduced by nonanatomical resections, which may affect perioperative morbidity and mortality [14, 25]. Several studies reported significant shorter operating times and significant less blood loss after NAR [25, 26, 28]. This also is seen in our study population. Patients who underwent AR received significant more blood transfusions than the patients after NAR (AR 36% vs. NAR 20%; P = 0.012). In our series, there were three deaths within 30 days of surgery: two in the AR group, and one in the NAR, which was not significantly different. There are studies suggesting more postoperative deaths in the AR group [2, 25, 26, 28]. It is important to note that postoperative mortality is a rare event and that these studies are not powered to compare this.
The possibility to treat recurrent CLM with local therapy, such as repeated hepatectomy , RFA , or STBR  is a great benefit of the parenchymal sparing method. In our study, disease recurrence in the liver was similar for both AR and NAR (51%). The reintervention rate for CLM was higher in the NAR group (AR 41% vs. NAR 60%). Although this number does not reach significance, probably due to the small numbers, our findings suggest that local treatment for intrahepatic recurrences is more often possible in the parenchymal-sparing method. Our findings are consisted with the literature, which states that reinterventions for CLM increases the survival after disease recurrence [31–33]. For this reason, close surveillance of patients after NAR is essential. One of the possible disadvantages of NAR reported in the literature by DeMatteo et al.  is the higher incidence of positive resection margins. In more recently published literature, it is advocated that a resection margin <1 cm is no longer a contraindication for curative resection. Moreover recent literature suggests that size of surgical margin does not correlate significantly with DFS or OS; even the need for R0 resections is being discussed [34, 35]. In a study by de Haas et al., the 5-year OS was similar for patients after a R0 or a R1 resection (61 vs. 57%; P = 0.27), although the recurrence was higher in the R1 group (28 vs. 17%; P = 0.004) . In our study, the R1 resection rate was 9% in the AR group and 11% in the NAR group, which is comparable to the literature [6, 27]. The concept of performing limited NAR with narrow margins is supported by the fact that micrometastases in the liver parenchyma surrounding CLM are rare and are primarily confined to the immediate surrounding area of the tumor border [36, 37].
The second possible drawback of NAR, which is postulated in the literature (), is the lack of vascular control. This is the opposite of what was published during the past years. Blood loss and blood transfusions are reported to be significantly less during and after NAR, which is confirmed by our results [25, 26, 28].
In contrast to CLM, some studies report AR to be superior to NAR in HCCs [18–20]. This difference may be explained by the variation in disease biology seen in primary versus metastatic liver tumors. Metastatic liver lesions develop from blood-borne tumor cells circulating throughout the body. AR may not offer the same advantage for these lesions as for HCC, which arise within a segment of the liver and might benefit from the removal of the complete functional liver unit.
Multiple studies have been conducted to investigate which resection is favorable for patients with CLM: anatomical or nonanatomical. Most authors similarly conclude that there is no significant difference between AR and NAR in disease-free and OSs. A disadvantage of the majority of studies is that the patient characteristics are not comparable between the two groups regarding tumor size and number, nodal status of the primary tumor, disease-free interval, and CEA blood levels [2, 14, 25, 26]. Our study contributes to this discussion due to the use of the CRS in which the previous described characteristics are incorporated. The CRS is the same for the AR and NAR, which indicates that the groups are comparable.
Furthermore, the use of different neoadjuvant chemotherapy regimens during the years makes it difficult to compare the results of the studies [2, 14, 26–28]. We started our patient selection after 2000, because Irinotecan and Oxaliplatin were added to the chemotherapeutic arsenal from this year forward, and all patients were treated with effective chemotherapeutics.
We conclude that with a comparable complication rate, less blood transfusions, a significantly shorter hospital, and comparable disease-free and OS rates, a NAR is a safe technique for the resection of CLM.
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