Radiol Oncol 2018; 52(1): 42-53. doi: 10.1515/raon-2017-0047 42 research article Simultaneous pure laparoscopic resection of primary colorectal cancer and synchronous liver metastases: a single institution experience with propensity score matching analysis Arpad Ivanecz1,3, Bojan Krebs1 3, Andraz Stozer2, Tomaz Jagric1, Irena Plahuta1, Stojan Potrc1,3 1 Department of Abdominal and General Surgery, University Medical Center Maribor, Maribor, Slovenia 2 Institute of Physiology, Faculty of Medicine, University of Maribor, Maribor, Slovenia 3 Department of Surgery, Faculty of Medicine, University of Maribor, Maribor, Slovenia Radiol Oncol 2018; 52(1): 42-53. Received 8 September 2017 Accepted 8 October 2017 Correspondence to: Dr. Arpad Ivanecz, Department of Abdominal and General Surgery, University Medical Center Maribor, Ljubljanska ulica 5, 2000 Maribor, Slovenia. E-mail: arpad.ivanecz@ukc-mb.si Disclosure: No potential conflicts of interest were disclosed. Background. The aim of the study was to compare the outcome of pure laparoscopic and open simultaneous re- section of both the primary colorectal cancer and synchronous colorectal liver metastases (SCLM). Patients and methods. From 2000 to 2016 all patients treated by simultaneous resection were assessed for entry in this single center, clinically nonrandomized trial. A propensity score matching was used to compare the laparo- scopic group (LAP) to open surgery group (OPEN). Primary endpoints were perioperative and oncologic outcomes. Secondary endpoints were overall survival (OS) and disease-free survival (DFS). Results. Of the 82 patients identified who underwent simultaneous liver resection for SCLM, 10 patients underwent LAP. All these consecutive patients from LAP were matched to 10 comparable OPEN. LAP reduced the length of hospital stay (P = 0.044) and solid food oral intake was faster (P = 0.006) in this group. No patient undergoing the lapa- roscopic procedure experienced conversion to the open technique. No difference was observed in operative time, blood loss, transfusion rate, narcotics requirement, clinical risk score, resection margin, R0 resections rate, morbidity, mortality and incisional hernias rate. The two groups did not differ significantly in terms of the 3-year OS rate (90 vs. 75%; P = 0.842) and DFS rate (60 vs. 57%; P = 0.724). Conclusions. LAP reduced the length of hospital stay and offers faster solid food oral intake. Comparable oncologic and survival outcomes can be achieved. LAP is beneficial for well selected patients in high volume centers with ap- propriate expertise. Key words: colorectal cancer; synchronous liver metastases; laparoscopy; liver resection; colorectal resection Introduction Colorectal cancer is one of the most common caus- es of cancer related death in the Western world.1 At the time of diagnosis of the primary tumor, up to 25% of patients present with synchronous colorec- tal liver metastases (SCLM).2 Complete surgical re- section of both primary tumor and SCLM remains the only treatment option providing long-term sur- vival and chance for cure.3 Different oncological strategies have been de- scribed including traditional two-stage colon first approach,4 liver first procedure5 or a one-step surgical resection of both the primary tumor and Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases 43 SCLM.6 Several reports have shown the benefit of a simultaneous open resection of primary tumor and SCLM compared with a staged approach.7-8 Minimally invasive colorectal and liver surgery are both accepted worldwide.9-11 Technical refine- ments and the development of advanced laparo- scopic techniques has made simultaneous resection an attractive option. However, despite the increas- ing use of laparoscopy in colorectal and liver re- sections, simultaneous pure laparoscopic resection (SPLR) of the primary colorectal cancer and SCLM is still rarely performed. Sporadic case reports and single institution series have shown the feasibility and safety of si- multaneous laparoscopic resection of both primary CRC and SCLM.12-28 Recently, two large interna- tional multicenter retrospective studies, which were published from the same group of surgeons, confirmed that in selected patient’s laparoscopic surgery allowed similar outcomes compared with the traditional open approach.29-30 The aim of this study was to compare the surgi- cal and oncological outcomes of patients undergo- ing simultaneous resection of primary colorectal cancer and SCLM by laparoscopic or open surgery using propensity score matching. Patients and methods Patient selection and study design All patients with SCLM were discussed by the multidisciplinary team. Treatment decisions were based on location and complexity of resection of the primary tumor, extent of liver resection, liver function and physical condition of the patients. The policy of the institution is not to combine a simul- taneous major liver resection (≥ 3 segments) with complex colorectal procedure (e.g. total colectomy, low anterior resection). The most ideal candidates for combined laparoscopic liver resection were pa- tients with solitary, peripherally located metastasis in anterolateral segments. Study subjects were identified from a prospec- tively maintained database of patients who under- went liver resections for CLM from January 2000 to December 2016 at the Department of Abdominal and General Surgery, University Medical Centre Maribor. This institution is a tertiary referral center with more than 15 years’ experience in laparo- scopic colorectal and with 8 years’ experience in laparoscopic liver surgery. SCLM were defined as those identified at the time of diagnosis of the primary colorectal cancer. All patients gave their informed consent. Ethical approval for this study was obtained from the local institutional review board. Patient records were anonymized and de- identified prior to analysis. All patients in the database who submitted to si- multaneous laparoscopic resection of both the pri- mary tumor and SCLM were selected and included in the study. Those laparoscopic patients were com- pared to patients that underwent open simultane- ous liver and colorectal resection for stage IV colo- rectal cancer. A propensity score matching was ap- plied to identify the most comparable patients from the open surgery group. Primary endpoints of the study were perioperative and oncologic outcomes. Secondary endpoints of the study were overall sur- vival (OS) and disease-free survival (DFS). Neoadjuvant and adjuvant therapy Patients with rectal advanced local disease (≥ T3 and/or ≥ N1) and SCLM received short-course pre- operative radiotherapy (5 x 5 Gy) and neoadjuvant systemic chemotherapy (3–6 courses) as a standard treatment protocol. However, neoadjuvant sys- temic therapy was not administered routinely for patients with colon cancer and SCLM. Adjuvant systemic therapy was administered at the discre- tion of the medical oncologist. In general, chemotherapy included fluoropy- rimidine-based therapies in combination with ox- aliplatin or irinotecan. The different chemotherapy protocols included the FOLFOX (oxaliplatin, fluo- rouracil, and leucovorin), XELOX (capecitabin and oxaliplatin), XELIRI (capecitabin and irinotecan) and FOLFIRI (irinotecan, fluorouracil, and leuco- vorin) protocol, respectively. From year 2006, an- tiangiogenic agents (bevacizumab or cetuximab) were also added to these protocols. Simultaneous liver and colorectal surgery: surgical technique Surgical procedures were performed by one dedi- cated team and the liver resection was completed first. All liver resections (laparoscopic and open) were executed by at least one experienced senior HPB surgeon (SP or AI). A liver parenchymal spar- ing approach was applied in both groups. All lapa- roscopic colorectal resections were performed by one experienced senior colorectal surgeon (BK). Laparoscopic procedure Only pure laparoscopic liver and colorectal resec- tions were performed. Generally, patients were Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases44 placed in the supine position, except for resection of posterosuperior segments of the liver when the left lateral decubitus position was used. For rectal resections a split leg position was used. Four 12 mm ports were always used and additional 5 mm ports were placed as necessary. Laparoscopic ultra- sonography of the liver was routinely performed to complete staging, locate the metastases, and accu- rately assess its margins and also to locate any ad- jacent biliary/vascular structures. It was also used to mark the plane of transection. Carbon dioxide pressure for pneumoperitoneum was kept at 12–14 mmHg during hepatic parenchymal transection. Pressures higher than this are generally avoided to reduce the risk of gas embolism but a slight rise during bleeding can aid hemostasis. The surface of the hepatic parenchyma was precoagulated with a 1-cm surgical margin using monopolar coagula- tion. Liver transection was performed under low (<5 mmHg) central venous pressure. Pringle’s ma- neuver was used selectively. Hepatic transections were performed using different high energy devic- es according to surgeon’s preference (bipolar co- agulation, thermofusion, ultrasound section or ul- trasonic surgical aspirator). Larger structures were controlled with endoclips and endoscopic linear stapler devices were used selectively for division of portal pedicles and hepatic veins or their branches. The resected liver specimen was placed in a plastic bag and extracted after finishing the colorectal pro- cedure. It was retrieved either through a suprapu- bic, a prolonged 12mm port site or a short midline incision. Laparoscopic colorectal surgery was performed according to standard oncologic procedures. Open resection A long midline incision was routinely performed which was extended to right subcostal incision whenever needed to adequately expose the pos- terosuperior segments of the liver. Intraoperative ultrasonography was routinely performed to guide resection. Hepatic transection was performed un- der low central venous pressure and intermittent pedicle clamping was used only in case of bleed- ing. Abdominal drains for liver resection were se- lectively used. Colorectal resection routinely involved proxi- mal ligation of vessels (the inferior mesenteric ar- tery for the left colon and rectum, and the ileocolic artery for the right colon) and partial or total mes- orectal excision depending on the location of the rectal cancer. After right colon resection a recon- struction was a hand-sewn ileocolic anastomosis. For cancer located in the left colon and the rectum, reconstruction was a stapled colorectal anastomo- sis. A protective ileostomy was always performed for a low anastomosis. Abdominal drains were al- ways used for rectal resections. Follow up Patients were followed at outpatient clinics at peri- odic intervals. Follow-up included physical exami- nation, biochemical carcinoembryogenic antigen (CEA) test, thoracic X-ray or computed tomogra- phy (CT), and liver ultrasound, CT or magnetic res- onance imaging (MRI) evaluation every 3 months for the first 2 years, and every 6 months thereafter. Metastatic recurrence was diagnosed by CEA rise and CT or MRI. Positron emission tomography (PET) - CT scans were carried out in selected pa- tients. In any uncertainty, histology was required. Follow-up data were obtained from outpatient follow-up and from the National Cancer Register of Slovenia. Patient follow-up included details of dates of disease recurrence and death, site of recur- rence, further therapy (e.g. systemic therapy, sur- gery), and cause of death. Recurrences were classi- fied as hepatic, extrahepatic or combined. Recurrent disease was treated according to standard clinical practice and included surgery and/or chemothera- py whenever possible. The principles behind the se- lection criteria for resecting recurrent CRLM were the same as those for the initial hepatectomy. Follow up was fully completed for all patients included in this study. All patients were followed up until their death or until March 2017. Primary endpoints: variables selected for analysis of the perioperative and oncologic outcomes Several routinely available clinical variables were analyzed and were divided in four groups: • Preoperative clinical variables included baseline characteristics of patients, primary colorectal tu- mor and synchronous liver metastases. Herein any neoadjuvant therapy was included in the analysis; • Intraoperative - simultaneous liver and colorectal surgery related variables; • Postoperative oncological results after patohistol- ogy and clinical risk score (CRS); • Postoperative outcome: patient’s recovery, mor- bidity, mortality and incisional hernia rate. Performance status was defined according to the American Society of Anesthesiologists (ASA). Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases 45 Location of SCLM were defined as anterolateral (segments 2, 3, 4b, 5, 6) or posterosuperior (seg- ments 1, 4a, 7, 8). The liver anatomy and resection terminology were based on the Brisbane classifica- tion.31 Hepatic resections were considered major when at least three adjacent segments were re- moved and defined as minor if <3 liver segments were resected. Conversion to an open operation was defined as an abdominal incision larger than that needed for specimen retrieval. CRS (from 0 to 5) as defined by Fong was applied.32 Briefly, pa- tients with lower CRS tends to have a better prog- nosis. The histological surgical margin was defined as microscopically positive (<1 mm, R1) or negative (R0). R0 resection was defined as complete remov- al of the tumors with a clear microscopic margin and without residual tumors. Complication was defined as any deviation from the normal course of recovery with the need for pharmacological, surgical, radiological, or endoscopic intervention. Postoperative morbidity was classified according to the Clavien-Dindo classification.33 Morbidity and mortality were defined as complications or death occurring within 90 days of surgery, or at any time during the postoperative hospital stay. Secondary endpoint: survival analysis Overall survival (OS) was defined as the interval between the date of first therapy (the date of first cycle of neoadjuvant therapy; if it was not applied then the date of simultaneous resection) and the date of death or the date of the last follow-up in surviving patients. Disease-free survival (DFS) was calculated from the date of first therapy (neo- adjuvant therapy or simultaneous resection) to the date of intra- and/or extrahepatic recurrence or the date of the last follow-up in patients with no recur- rence. Statistical analysis SigmaPlot 11.0 for Windows (Systat Software, Inc, CA) was used for statistical computations. Because of the inherent bias between patients undergoing laparoscopic and open surgery in terms of pre- operative clinical characteristics, a 1:1 propensity score-matched analysis have been used to adjust for these differences.34 In this setting, propensity score adjustment was performed on the factors known to influence the choice of the approach. These factors included ASA score, primary tumor location (colon or rectal cancer), size, location, dis- tribution and number of liver metastases and ex- tent of liver surgery. Differences in the frequency distributions of preoperative, intraoperative and postoperative clinical variables in relation to open and laparo- scopic surgery were tested using the chi-squared test for categorical variables (Pearson’s or Fisher’s exact test when appropriate, two-tailed in all in- stances). Continuous variables were analyzed us- ing Student’s t-test for independent samples or the Mann-Whitney U test if the criteria for a paramet- ric testing were not met. The effects of open and laparoscopic surgery on overall and disease-free survival probabilities were estimated by using the Kaplan-Meier survival analysis and compared by using the log-rank test. A difference with a P value of < 0.05 was considered statistically significant. Results Study population and preoperative characteristics Of the 572 patients identified who underwent liver resections for CLM during the study period, simul- taneous resection of both the primary tumor and SCLM were performed in 82 patients. From these, 10 patients were submitted to simultaneous pure laparoscopic procedure. After propensity score matching, all these 10 patients operated laparo- scopically (LAP) were compared with 10 patients FIGURE 1. Study inclusion criteria and patient flow. Study subjects were identified from a prospectively maintained database of 572 patients who underwent liver resections for colorectal liver metastases (CLM) from January 2000 to December 2016 at the Department of Abdominal and General Surgery, University Medical Center Maribor. Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases46 treated by traditional open surgery (OPEN). Study inclusion criteria and patient flow are shown in Figure 1. The diagnosis of primary colorectal can- cer was confirmed preoperatively by histology in all patients of both groups. The diagnosis of SCLM was confirmed postoperatively by histology in both groups as well. The two groups were well matched and com- parable in terms of preoperative clinical charac- teristics of patients, primary colorectal tumor and SCLM. Results are shown in Table 1. Intraoperative results The patients from LAP and OPEN group were comparable in terms of intraoperative variables. Results are detailed in Table 2. Since extent of liver resection was one of the terms of propensity score matching, only minor liver resections were performed in both groups. A portal triad clamping (Pringle’s maneuver) was not routinely used and was applied selectively, only in the case of bleeding with no significant difference in both groups. All patients with rectal cancer had either stoma covering low anastomosis or terminal colostomy. Postoperative short term outcomes: oncological results, clinical risk score, patient’s recovery, morbidity and mortality There were no differences between LAP and OPEN group in terms of oncological results and CRS. All patients were found to have a CRS within the range of 1–4; no patients had a CRS 0 or 5 (Table 3). Results of patient’s recovery, morbidity and mor- tality are detailed in Table 4. No postoperative mortality occurred in either group. Fully descrip- tion of morbidity and hospitalization of studied population are shown in Table 5. Postoperative long term outcome: recurrence and survival Of the 10 patients from OPEN group submitted to potentially curative simultaneous resection of pri- mary colorectal cancer and SCLM four developed recurrent disease and, of these, all of them under- went repeat hepatic resection. Of the 10 patients from LAP two patients developed recurrence, which was both hepatic and extrahepatic and re- peat resection was not feasible. Patterns and time TABLE 1. Preoperative clinical characteristics of patients, primary colorectal tumor and synchronous colorectal liver metastases Variable Simultaneous Open(n = 10) Simultaneous Laparoscopy (n = 10) P Patients Gender (male/female) 6/4 6/4 1.00 Age [mean ± SD (years)] 65.4 ± 8.1 62.2 ± 7.9 0.39 BMI [median (IQR) (kg/m2)] 24.0 (23.1–25.5) 26.9 (23.6–32.1) 0.34 ASA (I /II/III) 4/3/3 5/3/2 0.86 Preoperative chemotherapy (y/n) 3/7 7/3 0.18 Preoperative radiotherapy (y/n) 3/7 4/6 1.00 CEA at diagnosis [mean ± SD (ng/mL)] 15.2 ± 12.5 7.7 ± 7.7 0.12 Colorectal tumor Right colon/ left colon/ rectum 3/3/4 2/2/6 0.67 Colorectal liver metastases Number of lesions [median (IQR)] 1 (1–2) 1 (1–2) 0.68 Larger diameter [mean ± SD (cm)] 2.9 ± 1.5 2.0 ± 1.2 0.17 Laterality (unilateral /bilateral) 9/1 9/1 1.00 Proximity of major vessel [(hilar or hepatic confluence) (y/n)] 0/10 0/10 1.00 Location (anterolateral / posterosuperior) 8/2 9/1 1.00 ASA = American Society of Anesthesiologist physical status score; BMI = body mass index; CEA = carcinoembryonic antigen; SD = standard deviation Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases 47 of recurrences, redo surgical procedures and long- term outcomes are shown in Table 5. The median follow-up for surviving patients in the OPEN and LAP was 78 (61–130) and 24 (1–63) months, respectively (P = 0.001). Among patients in OPEN OS/DFS was 100%/90% at 1 year, 90%/60% at 3 years, and 80%/60% at 5 years. Among patients in LAP OS/DFS was 100%/100% at 1 year, and 75%/57% at 3 years. Simultaneous laparoscopic re- section of the primary tumor and associated SCLM was first performed in this center in May 2012, thus the median follow-up period was too short to calculate the 5-year survival expectations for LAP group. There were no statistically significant dif- TABLE 2. Intraoperative - simultaneous liver and colorectal surgery related variables Variable Simultaneous Open (n = 10) Simultaneous Laparoscopy (n = 10) P Totally pure laparoscopic – 10 – Conversion to laparotomy – 0 – Liver surgery Minor/major resection 10/0 10/0 1.00 Atypical/ segmentectomy/LLS 6/2/2 5/3/2 0.87 Pringle’s maneuver (y/n) 2/8 3/7 1.00 Colorectal surgery Colon/rectal resection 6/4 5/5 1.00 Temporary stoma covering low anastomosis (y/n) 2*/8 3*/7 1.00 Terminal colostomy (Hartman or APE) 2/8 2/8 1.00 Operative time [mean ± SD (min)] 257 ± 66.8 261 ± 92.8 0.91 Blood loss Estimated [median (IQR) (mL)] 170 (70–230) 105 (30–180) 0.23 Hemoglobin drop** [median (IQR) (g/L)] 22.5 (9–28) 15.5 (9–17) 0.38 Transfusion required (y/n) 3/7 3/7 1.00 APE = abdominoperineal excision; LLS = left lateral sectionectomy; *in both groups one patient required ileostomy after anastomotic leak; **Hemoglobin drop = Hemoglobin preoperatively - Hemoglobin postoperatively (g/L) FIGURE 2. Kaplan-Meier estimates of overall survival between the simultaneous laparoscopy (blue line) and open surgery groups (red line). FIGURE 3. Kaplan-Meier estimates of disease-free survival between the simultaneous laparoscopy (blue line) and open surgery groups (red line). Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases48 ferences between OPEN and LAP either in OS (P = 0.842) and DFS (P = 0.724), respectively. Kaplan- Meier estimates of OS and DFS between the LAP and OPEN group are shown in Figures 2 and 3. Discussion The optimal strategy for resectable SCLM has not been established yet. In selected cases, the simul- taneous surgery approach gives the advantages to avoid two surgical procedures thus reducing risk for patients and provides for economic savings while keeping acceptable morbidity and adequate oncologic results.6-8 However, open resection of both primary tumor and SCLM often requires an extensive incision, especially if the location of the liver metastasis is opposite to the primary tumor location. Using laparoscopic approach exposure can be improved thus avoiding extensive laparoto- mies.20 Consequently, surgical stress and pain as- sociated with large incisions can be reduced and patient’s recovery enhanced. There is an ongo- ing effort to show the potential benefit of totally laparoscopic strategies for the radical treatment of stage IV colorectal cancer.12-30,35 The present study was designed to investigate the perioperative results, oncologic outcomes and survival of patients undergoing pure laparo- scopic simultaneous resection of both the primary colorectal cancer and SCLM. During this study period, the choice of intervention was subject to selection bias since simultaneous laparoscopic liver procedures were reserved for the most ideal candidates. Moreover, the laparoscopic treatment of patients with an extraperitoneal rectal cancer remains clinically challenging compared to upper rectal or colon cancer. To minimize these biases, the LAP group was compared to OPEN group by propensity score matching on the factors known to influence the choice of the approach. Importantly, there were no differences in patient demographics, tumor characteristics, or the extent of the opera- tion, so the present characteristics well identify the most ideal candidates to a combined laparoscopic liver and colorectal surgery. Patients selected for this approach were without severe comorbidi- ties (ASA I–II in majority of cases), with a solitary (median number: 1), small (median diameter: 2 cm), unilateral SCLM, located in accessible ante- rolateral segments and were mostly resectable by atypical wedge resections or left lateral sectionec- tomy. Consequently, only minor liver resections were performed. These results are consistent with previous studies showing well selected patients and demonstrating a high rate of minor (89%) and nonanatomical resections (60%).17-27,35 In this study colorectal cancer characteristics did not preclude the possibility to perform a laparoscopic surgery as well with majority of patients presenting a T3 primary tumor. There were no differences in N stage and importantly, the number of harvested lymph nodes was even higher in the LAP group. Half of the patients in the LAP group presented with rectal cancer. Surprisingly, previous studies have demonstrated that despite the high rate of rectal resections in some series, the number of the temporary ileostomies was low.25,27,35 The results of the present study contradict this: all of the rectal cancer patients had either temporary ileostomy TABLE 3. Postoperative oncological results after patohistology and clinical risk score Variable Simultaneous Open (n = 10) Simultaneous Laparoscopy (n = 10) P Colorectal tumor T (T1/T2/T3/T4) 0/1/8/1 0/1/9/0 1.00 N (N0/N+) 2/8 2/8 1.00 Number of harvested lymph nodes (mean ± SD) 9.5 ± 6.2 13.7 ± 6.9 0.17 Well/moderately/poorly differentiated 4/5/1 4/6/0 1.00 Negative surgical margin Liver (y/n) 10/0 10/0 1.00 Colorectal (y/n) 10/0 10/0 1.00 Liver resection margin [median (IQR) (mm)] 2.5 (2–5) 5.0 (1.8–8) 0.38 CRS (1/2/3/4) 2/5/2/1 2/4/3/1 0.96 CRS = clinical risk score (no patients with CRS 0 or 5 in any of the group) Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases 49 covering low anastomosis or terminal colostomy. This finding might have been due to a high rate of preoperative radiotherapy, which highlights that most rectal resections were performed for cancer in the lower rectum. Moreover, according to some reports simultaneous resection generally is consid- ered unsuitable for rectal cancer due to a high rate of anastomotic leakage.36 Another possible expla- nation is a concern regarding prolonged vascular clamping which is responsible for transient portal hypertension with edema of the intestinal mucosa that might be leading to colorectal anastomotic fail- ure.21,35 The feasibility of simultaneous laparoscopic op- erations was clearly demonstrated in the present study: no conversion to open surgery has been performed. This result reflects a findings of a re- cent review, where a conversion rate of only 0.7% has been reported.35 Similarly, Tranchart et al. re- ported a low conversion rate of 7% in their large multicenter study.30 It has been highlighted, that simultaneous resections executed by two different specialized teams allowing good results in terms of conversion rates and perioperative outcomes.35 Of note, the present study was performed at high-vol- ume tertiary referral center, where all procedures were performed by an expert surgical team, com- posed of experienced colorectal and hepatobiliary surgeons. Controversy still exist, which procedure should be carried out first and many authors re- ported colorectal resection was the first step of the simultaneous surgery.15-16,20,22,29-30 Instead, in the present study liver resection precede colorectal surgery and the same strategy has been reported by others.18-19,21,35 The underlying rationality is that the resection of liver metastases requires a low cen- tral venous pressure to minimize the blood loss and the preceding liver resection will not interfere with the subsequent fluid resuscitation in the pro- cess of colorectal resection. In addition, the choice of carrying out the liver resection as first step of treatment gives to the surgeon the opportunity to change surgical strategy from a simultaneous procedure to a “liver first” resection which has been showed to be another effective treatment of SCLM.5 Moreover, liver metastases are the main determinant of patient prognosis and the present authors believe, that SCLM are leading the deci- sion making process: if simultaneous strategies are not feasible, then the metastases should be man- aged first. However, no decisions were modified and all procedures were finished simultaneously. In terms of intraoperative measurements of out- come, the median operating time of 261 min after LAP is comparable with the time reported by Jung et al.25, and is shorter than the time reported by TABLE 4. Postoperative outcome: patient’s recovery, morbidity and mortality. No postoperative mortality occurred in either group. Adjuvant chemotherapy and incisional hernias Variable Simultaneous Open (n = 10) Simultaneous Laparoscopy (n = 10) P ICU stay 0 0 – HDU stay [median (IQR) (days)] 4 (2–6) 3 (2–5) 0.59 Solid food oral intake [median (IQR) (days)] 5.5 (4–6) 3 (3–4) 0.006 Stool passing [median (IQR) (days)] 4.5 (4–5) 4 (3–5) 0.46 Intravenous narcotics requirement [median (IQR) (days)] 6.5 (6–7) 4.5 (3–7) 0.08 Hospital stay [median (IQR) (days)] 11.5 (10–33) 8 (8–12) 0.044 Morbidity Overall (y/n) 5/5 3/7 0.65 Liver specific* (y/n) 2/8 0/10 0.47 CD < III (y/n) 2/8 2/8 1.00 CD IIIab (y/n) 3/7 1/9 0.58 CD > III (y/n) 0/10 0/10 1.00 Mortality (y/n) 0/10 0/10 1.00 Postoperative chemotherapy (y/n) 5/5 2/8 0.35 Incisional hernias (y/n) 3/7 0/10 0.21 HDU = high dependency unit; ICU = intensive care unit; *Liver specific complications included liver failure, bile leak, bile collection or liver hemorrhage; values in bold are significant at P < 0.05 Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases50 others, where it was more than 300 min.13-16,19,22-24,30 Nevertheless, operative time was not different be- tween OPEN and LAP group. This result is incon- sistent with some previous studies showing that the duration of operation was significantly longer in the laparoscopic groups.15,22,25 A possible expla- nation can be, that in contrast to present study, these reports included major liver resections as well, which are known to prolong operative time. However, several authors reported equivalent op- erative times for both groups.16,23,30 Intraoperative blood loss is a major concern especially in hepatic resection and perioperative transfusion has been associated with a poor prog- nosis.37 The findings of decreased blood loss with the laparoscopic approach have been reported in several studies, explained in part by the laparo- scopic magnification, and decreased venous ooz- ing from the cut surface under pneumoperito- neum.15-16,22-23 Results of present study contradicts this as laparoscopic approach did not allow dimin- ishing blood loss and transfusion rate. Contrast to prior studies, in this analysis blood loss was not based only on estimation but it has been objectiv- ized by measuring the volume of blood in the suc- tion canister and precisely weighing the absorbed blood in the sponges. Moreover, the pre- and post- operative hemoglobin levels were demonstrated exactly as well. The reason for this was to exclude the possibility of differences in preoperative hemo- globin levels which can contribute to the difference in blood loss and transfusion rate between two groups since it is well known that patients with SCLM can develop anemia. Moreover, it has been suggested that the blood loss can be underestimat- ed especially in the open surgery.38 Despite analyz- ing additional objective variable in this study, there were no differences between groups. It should be TABLE 5. Morbidity details, hospital stay, patterns and time of recurrence, redo procedures and long-term outcome Patients Morbidity Hospital stay (days) Recurrence location (years after first surgery) Redo Survival (years) Survival status (March 2017) OPEN 1 Wound infection(CD II) 12 1) Liver (2Y) 2) Liver (3Y) 1) Liver 2) / 3 DOD 2 Bile collection (CD IIIa) 36 Liver (1Y) Liver 7 NED 3 nil 9 1) Liver (1Y) 2) Colon (3Y) 3) Peritoneal carcinosis (4Y) 1) Liver 2) Colon 3) / 4 DOD 4 Anastomotic leak (CD IIIb) 54 Liver (1Y) Liver 5 NED 5 nil 10 no / 11 NED 6 Pneumonia (CD II) 12 no / 10 D - other 7 nil 11 no / 8 NED 8 nil 9 no / 8 NED 9 Bile collection (CD IIIa) 33 no / 7 NED 10 nil 10 no / 5 NED LAP 1 nil 8 no / 5 NED 2 Anastomotic leak (CD IIIb) 42 Liver and peritoneal carcinosis (1Y) / 2 DOD 3 nil 7 no / 4 NED 4 nil 7 Liver and peritoneal carcinosis (3Y) / 4 AWD 5 nil 8 no / 2 NED 6 nil 12 no / 2 NED 7 nil 8 no / 1 NED 8 Pulmonary embolism(CD II) 9 no / 1 NED 9 nil 8 no / <1 NED 10 Ictus cerebri (CD II) 21 no / <1 NED AWD = alive with disease; CD = Clavien Dindo classification of complication severity; D - other = death without recurrence of disease; DOD = dead of disease; LAP = simultaneous laparoscopic surgery; OPEN = simultaneous open surgery; NED = no evidence of disease; Y = years Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases 51 noted that outcome observed after open surgery was excellent as well (median estimated blood loss 170 ml). Similarly, several recent studies have sug- gested that there is no decreased blood loss and transfusion rate in the laparoscopic group.19,25,30 In respect to postoperative oncological results, a high CRS has been found to be an independent negative prognostic predictor in previous stud- ies.32,39 The impacts of CRS and colorectal tumor differentiation on survival analysis were eliminat- ed, since the OPEN and LAP groups were compa- rable in that terms as well. The risk of inadequate oncologic resection is the major concern for the use of laparoscopic resection for malignancy. A positive surgical margin has been shown to pre- dict worse DFS after resection.40 Castaing et al. emphasized that the increase in R1 resections did not affect OS and suggest it might reflect complex anatomic locations of metastases adjacent to major vascular structures.41 To avoid an inherent selec- tion bias with more difficult cases potentially being relegated to open approach, it is important to point out that the two groups of the present study were perfectly matched in term of SCLM proximity to major vessels (hilar or hepatic confluence) as well; there were no tumors with such characteristics in any of groups. Importantly, complete R0 resections of both the primary and SCLM were achieved in all patients confirming the reports of others, which reported a high rate of R0 resections of 100% and 90% as well.25,30 Surprisingly, the rate of R0 resec- tions has been not reported by many authors.14-16,22 The width of the surgical margin was not different between two groups and interestingly, the width was even larger in the LAP group. Moreover, a recent study failed to demonstrate that the width of negative margin correlated with recurrence or survival.42 Importantly, in this study neither peri- toneal carcinomatosis nor port site metastases after simultaneous resections of SCLM by laparoscopic means were found. These results suggest that lapa- roscopic procedure does not compromise oncolog- ic principles. The major findings in this study were lesser length of hospital stay and faster solid food oral in- take for LAP group. The median hospital stay of 8 days in the LAP group is similar to or shorter than the time reported by others, where it has been in a range from 7.4 to 16 days. The benefit of decreased hospital stay was recognized in these analyses as well.15-30 Interestingly, substantial geographical differences exist which depends on national health care systems. Takasu et al. confirmed the benefit of lesser length of hospital stay which were 16 days for the laparoscopy and 36 days for the open group.23 However, Tranchart et al. found no differences in the length of stay between laparoscopic and open groups, and noted that simultaneous resections still appear as difficult procedures for surgeons, which could have influence their decisions concerning patient’s hospital discharge.30 Patients undergoing laparoscopic procedure resumed solid food oral intake earlier, however it has no impact on earlier stool passing in this study, thus the benefit of this parameter remains questionable. Similarly, several authors reported a shorter time to resume a bowel movement and starting an oral intake.19,25 In terms of other postoperative measurements of outcome none of the patients required intensive care unit stay and the high dependency unit stay was comparable between groups. Ferretti et al. re- ported a median one-day intensive care unit stay.29 However, these relevant parameters were not re- ported in several previous analyses.15-28,35 Pain control is one of the potential advan- tage of laparoscopy and in this study, it was evaluated by intravenous narcotics requirement. Laparoscopy offered a benefit of less narcotic re- quirements, patients in the LAP group needed intravenous narcotics for 4.5 days compared with the OPEN group where these were necessary for 6.5 days. Notwithstanding, statistical significance was reached only marginally (P = 0.08). Hu et al. reported that patients having undergone laparo- scopic resection had less severe postoperative pain, but it is not clear how they asses this parameter.19 Surprisingly, in several other reports on this topic pain control was not investigated.13-18,20-30 Some sur- geons combined a laparoscopic colorectal resection with an open procedure for the liver, as reported by Hatwell et al.20 However, this technique also left a large incision in the upper abdomen, and the ad- vantage of laparoscopy was not realized fully. The present study found that LAP and OPEN were not significantly different in terms of post- operative morbidity and mortality. Of note, no liver specific morbidity was observed in the LAP group. Nevertheless, some bile collections which occurred in the OPEN group were easily managed by percutaneous drainage. Importantly, there were no organ failures and postoperative deaths in two groups either. Similarly, no differences in morbid- ity and zero mortality were reported in several oth- er analyses.15-16,19,22-23 Polignano et al. reported that the surgical morbidity was mainly related to the co- lonic surgery.18 Contrary, in the present series only one anastomotic leak occurred in OPEN and one in the LAP group, respectively. Jung et al. reported a Radiol Oncol 2018; 52(1): 42-53. Ivanecz A et al. / Laparoscopic resection of primary colorectal cancer and synchronous liver metastases52 higher rate of minor complications in the open sur- gery group (superficial surgical site infections and adhesive ileus), which seem to be strongly related to the presence of the bigger wound.25 However, the number of minor complications were equal in the present analysis. Interestingly, despite laparos- copy has the potential to reduce the incisional her- nia rates, none of the studies on the present topic investigated this parameter which is responsible for long-term morbidity.12-30,35 In the present study none of the LAP whereas three patients from the OPEN group developed incisional hernia, but the difference was not significant. In the present study, neither the 3-year OS nor the DFS was found to be different for LAP com- pared with the OPEN group. Similarly, no differ- ences were found between groups in terms of OS reported by others .15-16,19,22-23,30 After long and ad- equate median follow-up of 78 months this analy- sis revealed excellent long-term results among pa- tients in OPEN with 5-year OS/DFS of 80 and 60%, respectively. However, due to a shorter follow-up period, only mid-term results were available for the LAP group with 3-year OS of 75% and DFS of 57%, respectively. Similarly, in the current literature some of the authors reported the short- and mid- term results only and the 3-year OS rates ranged from 52 to 78%.15,30 Unfortunately, data regarding recurrence were inconsistently reported in several case-matched series on this topic.15-16,19,23,25 The present study is a subject to a number of limitations. First and foremost, only a small co- hort of patients from a single center were analyzed which were collected across a long interval of time. However, the majority of case-matched studies in the literature derived from a small single center se- ries, which included from 7 to 24 patients.15-16,19,22-23,25 Even in the largest multicenter analysis, which in- cluded 142 patients from 14 centers the average number of patients per hospital was ten.29 It dem- onstrates clearly the limited indications of simul- taneous laparoscopic procedures even in the most experienced centers worldwide. Second, given the retrospective nature of this study, selection bias may have been present. Although propensity score matching was performed to overcome po- tential bias and to make the two groups similar it is less effective than a prospective randomized trial. Notwithstanding, to conduct a randomized study on this topic is still an unresolved issue. Third, since laparoscopic simultaneous procedures started in 2012 the median follow-up data between groups differs and the excellent long-term survival results achieved with OPEN are still waiting to be proved by LAP. However, except for introduction of laparoscopy, the management of SCLM was ho- mogeneous over the study period and the same surgical team made the treatment decisions and performed the procedures. Indeed, the power of the present study is lim- ited, but importantly the two surgical approaches brought about similar outcomes in terms of post- operative morbidity, mortality, survival and recur- rence. 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