Abstract
Background
The surgical resection of the splenic flexure carcinoma (SFC) is challenging and the optimal surgical procedure for SFCs remains a matter of debate. The present study aimed to compare in a multicenter European sample of patients the short- and long-term outcomes of extended right (ERC) vs. left (LC) vs. segmental left colectomy (SLC) for SFCs.
Methods
This retrospective multicenter study analyzed the surgical and oncological outcomes of SFC patients undergoing elective curative intent surgery between 2000 and 2018. Descriptive and exploratory analyses were first conducted on the whole sample. Outcomes of the different procedures (ERC vs. LC vs. SLC) were then compared using propensity score matching for multilevel treatment. Overall (OS) and disease-free survival (DFS) were evaluated by Kaplan–Meier method.
Results
From a total of 399 SFC patients, 143 (35.8%) underwent ERC, 131 (32.8%) underwent LC, and 125 (31.4%) underwent SLC. Overall, 297 (74.4%) were laparoscopic procedures. An increase in operative time, time to flatus, time to regular diet, and hospital stay was observed with the progressive extension of SFC resection. ERC was associated with significantly increased risk of postoperative ileus compared to both LC and SLC. A significantly greater number of lymph nodes were retrieved by ERC, but the objective of at least 12 retrieved lymph nodes was achieved in 85% of patients, without procedure-related differences. No differences were observed in OS or DFS between ERC, LC, and SLC.
Conclusion
The present study supports the resection of SFCs by colon-sparing surgical techniques, such as SLC.
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Splenic flexure carcinomas (SFCs) have traditionally been defined as the tumors arising from the portion between the distal third of the transverse colon and the proximal part of the descending colon [1, 2]. More recently, some authors limited the definition to tumors located within 10 cm of the splenic flexure edge [3, 4]. SFCs represent less than 10% of all colorectal cancers [2, 5], but they have been associated with a poorer prognosis compared to other colonic locations due to the high risks of presentation as an emergency or at an advanced stage [2, 6].
Achieving a complete tumor resection with free margins and adequate lymph node retrieval can be challenging for cancers located at the splenic flexure [7]. Nonetheless, SFCs have been systematically excluded from the main randomized clinical trials (RCTs) that evaluated the use of laparoscopy for colon cancer resection [8].
In this scenario, studies specifically focusing on the surgical outcomes of SFC patients are scarce, and no clear evidence exists on the gold standard surgical approach and extent of resection [3, 4, 8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31]. Overall, three main types of surgical procedures have been described: the extended right colectomy (ERC), the left colectomy (LC) and the segmental left colectomy (SLC) [8]. Evidence-based criteria for assisting surgeons’ decisions are lacking, and previous comparisons between ERC, LC and SLC procedures found inconclusive results. Some authors advocate for extended resections of SFCs due to the highly heterogeneous blood supply and lymphatic drainage of the splenic flexure [1], whereas others support colon-sparing options to avoid an unnecessary resection of the middle colic artery and to preserve colonic length [24, 32].
The present study aims to evaluate and compare the short- and long-term outcomes of three different surgical procedures (i.e., ERC, LC, and SLC) performed for the elective treatment of SFCs in a large, multicenter European sample of SFC patients.
Materials and Methods
Study design
The SFC Study Group was established in March 2017 with the aim of building a European multicenter database of SFC patients who underwent surgical resection between January 2000 and January 2018. The SFC study group comprised 11 surgical units from tertiary care centers in 6 European countries. Each participating center contributed data retrieved from prospectively maintained local databases that were input into a single common database used for the statistical analyses in the present study. Patients signed an informed consent for the use of their personal data for scientific purposes. Due to the retrospective design of the project, which was conducted exclusively on anonymous patients’ records, no institutional review board was required. All personal data were treated in conformity to the principles declared to the National Commission for Data Protection and Liberties and the study was reported following the recommendations listed in the STROBE checklist for cohort and case–control studies [33].
Study population
Patients’ records were selected to be included in the SFC database and were further extracted for the present statistical analyses if they met the following criteria: adults aged > 18 years; radiologically (by total body computed tomography [CT] and positron emission tomography [PET] in cases of suspected lymphatic packets), clinically, and histologically proven colon cancer located at the splenic flexure or up to 10 cm proximal towards the transverse colon or 10 cm distal towards the descending colon (as assessed on the preoperative CT scan) [4, 8, 17]; SFCs graded as AJCC TNM stage I to IV [34]; curative intent surgical resection; elective surgery setting; and one- or two-stage surgery (via temporary stoma). Patients with more than one carcinoma of the colon and polyposis coli were excluded.
Three types of surgical procedures were considered: ERC, LC, and SLC [8]. The ERC procedure consists of the resection of the terminal ileum and the right, transverse, and proximal descending colon, in which the ileocolic, right colic, middle colic, and left colic arteries are ligated, and an anastomosis between the ileum and the colon is performed [17, 20]. The LC procedure consists of the resection of the colonic segment between the left third of the transverse colon and the colorectal juncture (i.e., left half of the colon). The inferior mesenteric artery and the left branch of the middle colic artery are ligated at their origins, and a colorectal anastomosis is performed [4, 13, 20]. The SLC procedure consists of the resection of the distal part of the transverse colon, the splenic flexure and the proximal descending colon. The left colic artery and left branches of the middle colic vessels are ligated, and a colo-colonic anastomosis is performed between the transverse and descending sigmoid colon [9, 35].
Two types of surgical approaches were considered: laparoscopy and open surgery.
All patients were operated on by experienced colorectal surgeons. The perioperative care and follow-up was guided by the local multidisciplinary team in all participating centers. Adjuvant chemotherapy was considered for patients with AJCC TNM stage III/IV disease and unfavorable tumor characteristics. Follow-up was continued for at least 5 years, including blood tests (e.g., CEA levels), abdominal and chest CT scans, full colonoscopy and selective use of biopsies in case of suspected recurrence.
Study outcomes
Study outcomes included: intraoperative variables (e.g., operative time, blood loss), postoperative variables (e.g., postoperative morbidity and mortality, length of hospital stay), quality of the surgical resection (e.g., resection margin status, number of retrieved lymph nodes) and overall (OS) and disease-free survival (DFS) up to 5 years.
Conversion was defined as a premature interruption of the laparoscopic approach before the resection phase was concluded [36]. Postoperative morbidity and mortality were defined as events that occurred during the hospital stay or within 90 days after surgery. Postoperative complications were graded according to the Dindo-Clavien classification; complications graded as Dindo-Clavien III or higher were considered as severe postoperative complications [37]. Postoperative ileus was defined as the absence of bowel movements or flatus associated with intolerance of oral intake lasting more than 3 days postoperatively [38]. An R0 resection was defined as macroscopically complete removal of the tumor with a microscopically free resection margin and no peritoneal spread.
Statistical analysis
Descriptive and exploratory analyses
Statistical analyses were performed using R 3.5.1 [39]. For descriptive analyses, means (sd) and counts (%) were provided for continuous and categorical variables, respectively, and for each group of surgical procedures (ERC, LC, SLC). The first comparisons were carried out by applying Chi-squared tests for categorical variables and ANOVA tests for continuous variables. For this preliminary descriptive step, p values were given without any adjustment for multiple testing. In order to highlight graphical differences within the 3 groups of surgical procedures, a principle component analysis was also conducted on the continuous variables of interest.
Propensity score matching
In order to minimize the selection bias inherent in a retrospective study design, and to compare the three groups by taking into account covariates that may have potentially influenced the selection of ERC, LC or SLC procedures, we applied the propensity score matching (PSM) method for three groups, as described in Bryer et al. [40] For each group (ERC, LC, SLC), propensity scores were calculated by running logistic regression models that included the following covariates: age, gender, body mass index (BMI), American Society of Anesthesiologists (ASA) score, comorbidity > 1, tumor size on preoperative CT scan, tumor category (pT), node category (pN), metastasis category (pM), surgical approach (laparoscopic vs. open surgery), and year of surgery. The type of surgical procedure (LC vs. ERC, SLC vs. ERC and LC vs. SLC) was entered into the regression model as the dependent variable. Caliper matching method was used to minimize the number of retained triplets (i.e., to reduce the number of duplicate treatments units). The three matched groups were then evaluated with respect to the study endpoints. Global (respectively, Two-by-Two) comparisons between ERC, LC and SLC groups were performed using ANOVA (respectively, paired T-tests) for continuous variables and Chi-squared (respectively, McNemar) tests for categorical variables. All p values were adjusted for multiple comparisons using the Benjamini & Yekutieli correction [41]. In addition, for categorical variables that reached statistical significance, Odds ratios (OR) were calculated and provided with their 95% confidence interval (CI).
Survival analyses
As pointed by several authors [42,43,44,45,46], cox regression models applied to the entire cohort could be often more powerful tools in detecting treatment effects as compared with matched studies. Therefore, survival analyses were carried out on the whole sample. Overall Survival (OS) was defined as the time from surgery to death and was censored at the last follow-up date if no events occurred. Disease-Free Survival (DFS) was defined as the time from surgery to disease recurrence and was censored at the last follow-up date if no events occurred. First, Kaplan–Meier curves were provided for OS and DFS, with a log rank (Mantel–Cox) test for group comparisons. Then, a stepwise variable selection procedure (with iterations between the 'forward' and 'backward' steps and a control of variance inflating factors values) was used to obtain the best candidates final regression models for both OS and DFS. Adjusted HR for both best candidates was given with their 95% confidence intervals. For both models, proportional hazards assumptions were tested using the scaled Schoenfeld residuals.
Results
The present study population comprised 399 SFC patients who met the selection criteria. According to the type of surgical procedure, 143 (35.8%) patients underwent ERC, 131 (32.8%) underwent LC, and 125 (31.3%) underwent SLC. No difference in tumor location was observed between the three groups. No preemptive diversion or endoscopic stenting was performed. Overall, 297 (74.4%) patients were operated on via laparoscopic surgery.
Demographic, clinical and oncological variables of the whole study population and by surgical procedure are presented in Table 1. Compared to the other surgical procedures, ERC was most commonly performed in patients with a weight loss > 10% and presenting with more than one comorbidity. Conversely, in patients who had undergone previous abdominal surgery, SLC was performed more frequently compared to the other approaches. No significant group differences were observed for tumor characteristics, size, and differentiation and AJCC stage.
Explorative data analysis by Principal Component Analysis (Fig. 1) showed that ERC patients formed a larger cluster to the top and right as compared with others. Looking at the first two axes (that explained 68.5% of the total variability), showed that ERC are characterized by higher values for hospital stay, time to regular diet and time to flatus (x axis), and also higher values for operative blood loss and operative time (y axis). These exploratory findings were confirmed with significant within-group differences after PSM (Table 2).
By applying PSM, the final matched sample was composed by 110 patients per group. No demographic, clinical and oncological variables showed a significant imbalance between the 3 groups after PSM. In addition, the multiple covariate balance plot of absolute standardized effect sizes before and after propensity score adjustment (Fig. 2) suggested reasonable balance has been achieved across all covariates and across three models since effect sizes were smaller than the unadjusted in most cases and relatively small.
Overall, conversion from laparoscopy to open surgery occurred in 32 (9.9%) patients, without procedure-related difference. Reasons for conversion included: uncontrollable bleeding during vascular pedicle dissection (n = 4, 12.5%), impossible adhesiolysis (n = 5, 15.6%), technical difficulties due to tumor invasion of an adjacent organ (n = 5, 15.6%), and difficult exposure or inadequate visualization due to tumor fixation (n = 18, 56.3%).
The rate of postoperative complications was higher among ERC patients (58.2%) compared to the SLC group (33.6%; p < 0.001) and the LC group (43.6%; p = 0.043), but there were no group differences in terms of severity (Dindo-Clavien classification) (p = 0.548). Anastomotic leakage occurred in 29 (8.8%) patients, with no differences between groups. In total, 7 (6.4%) ERC patients, 12 (10.9%) LC patients, and 10 (9.1%) SLC patients presented with an anastomotic leakage. Of these, 19/29 (66%) required reoperation. Conversely, postoperative ileus was more frequently observed in ERC patients, who presented an increased risk by 8.43 times compared to the SLC group and by 3.97 times compared to the LC group. A faster recovery (time to flatus, time to regular diet and hospital stay) was observed for patients in the SLC group compared to the ERC group, with a mean difference of -1.7 days for time to flatus, -3.3 days for return to regular diet, and -5.7 days for hospital stay. No group differences were observed regarding 90 days mortality. An R0 resection was observed in 99.7% of the patients and in more than 80% of the patients at least 12 lymph nodes were retrieved during the operation, without procedure-related differences. However, a significantly higher mean number of retrieved lymph nodes was associated with the ERC procedure (Table 2).
Over a mean follow-up time of 41.74 (37.27) months, no group differences were observed in the OS or DFS rates, which are shown in Figs. 3 and 4, respectively. Disease recurrence over the entire follow-up period was observed in 77 (20%) patients: 29 (21.3%) in the ERC group, 25 (19.4%) in the LC group, and 23 (19.2%) in the SLC group (p = 0.89). Overall, distant metastases were observed in 71 (18.4%) patients and local recurrence was observed in 10 (2.6%) patients, with no differences among the groups (p = 0.94 and p = 0.95, respectively). Distant recurrences included: isolated liver metastasis (n = 33, 46.5%), isolated pulmonary metastasis (n = 9, 12.7%), isolated spleen metastasis (n = 1, 1.4%), liver and pulmonary metastasis (n = 3, 4.2%), peritoneal carcinomatosis (n = 13, 18.3%) and systemic metastatic disease (n = 12, 16.9%), with no differences among the three groups (p = 0.222).
Cox regression best predictors for OS and DFS are given in Table 3. Proportional hazards were assumed for both models (p = 0.472 for OS and p = 0.10 for DFS) and no collinearity issues were detected, as variance-inflating factors were lower to 1.5 for all predictors included in both models. Synchronous metastasis was identified as a strong predictor of both OS and DFS. Neither the type of resection (ERC, SLC, LC) nor the type of surgical approach (open vs. laparoscopy) were found to have a significant effect on OS or DFS rates.
Discussion
The present results, which are based on a large multicenter European sample of SFC patients, showed an increase in operating time, time to flatus, time to resumption of oral diet, and length of hospital stay with the progressive extension of SFC resection. Moreover, patients undergone ERC procedures showed an increased incidence of postoperative complications, particularly a significant higher risk of postoperative ileus compared to both LC and SLC. Despite ERC being associated with an average greater number of retrieved lymph nodes, no group differences was observed in the rate of retrieving at least 12 lymph nodes. Concerning the long-term outcomes, no procedure-related difference was found for OS and DFS.
The published literature about the surgical treatment of SFCs is limited and heterogeneous [8, 25, 31, 47], as splenic flexure is a less common location for colon cancers, and its definition has not yet been standardized. Most of the previous studies provided pooled analyses of elective and emergency surgeries for SFCs, which makes direct comparisons difficult [4, 20, 21, 27, 29]. Odermatt et al. [29] compared 38 ERC vs. 30 LC patients, whereas Gravante et al. [21] compared 64 ERC vs. 34 LC patients. Both studies included fewer than 15% of cases operated on by laparoscopy, as well as a high rate of emergency procedures (50% and 36.7%, respectively), which were more likely in the ERC patients. Nonetheless, no procedure-related differences were observed in regard to short- or long-term outcomes [21, 29]. Similarly, a matched case–control study by de’Angelis et al. [20] comparing 27 patients undergoing elective laparoscopic ERC vs. 27 patients undergoing elective laparoscopic LC demonstrated similar postoperative outcomes and survival in the absence of metastatic disease. However, the ERC procedure was associated with a significantly longer operative time [20]. The observational multicenter study by Beisani et al. [4] compared 68 elective subtotal colectomy (STC) vs. 76 elective LC patients and found a higher rate of overall morbidity, particularly postoperative ileus, in STC patients, but there were no differences in patient recovery, hospital stay, need for reoperation, or survival. More recently, Binda et al. [25] compared 158 ERC and 166 LC, of which 16.6% were performed in emergency settings. The authors found no significant difference concerning 30-day mortality and need for reoperation, concluding that the optimal procedure for SFC remains debatable as ERC and LC appear to achieve comparable short-term outcomes. Only a previous study, in our knowledge, considered the three surgical procedures for the treatment of SFCs, namely, ERC, LC and SLC [27]. Martin Arevalo et al. [27], however, performed only two-by-two comparisons by using PSM on 170 patients; of these, 72.4% were operated on in an elective surgery setting, and 15% via laparoscopy [27]. The results showed no pairwise differences between the surgical techniques for any of the variables being evaluated.
The present study, which represents the largest sample analyzed so far composed of only elective surgery for SFCs, demonstrates significant procedure-related differences. Indeed, the present findings suggest that the progressively extending the surgical resection has a significant impact on intraoperative and postoperative outcomes. Major differences are observed when comparing ERC to SLC, with longer operative time, more overall postoperative complications and postoperative ileus, longer time to flatus, time to regular diet and hospital stay for ERC patients. These differences may be explained by the extent of the surgical resection, considering that the larger dissection related to the ERC procedure likely requires a longer operative time and is more likely associated with a slower recovery. However, no significant difference was noted on OS or DFS up to 5 years. This was confirmed in the Cox regression models, where the type of surgery was not a significant predictor of OS and DFS. Conversely, the age at surgery > 75 years, the tumor stage (pT4), and the presence of synchronous metastasis (pM +) impact on OS, as the pT4 and the pM + predicted DFS.
In accordance with previous studies [4, 20, 21, 27, 29], the present analyses show that ERC is associated with an average greater number of lymph nodes retrieved with the surgical specimen, although all 3 procedures appear to achieve the goal of harvesting at least 12 lymph nodes at similar rates. For many authors, the number of harvested lymph nodes is essential for correct tumor staging, adjuvant chemotherapy indication, and consequently, long-term survival [17, 48]. In the case of SFCs, extensive resection of the terminal ileum and the right, transverse, and proximal descending colon is related to the vascular anatomy of the splenic flexure, which is marked by the binding, through different and variable arterial archways (i.e., Riolan’s arch, Drummond and Moskowitz arteries), between the superior and inferior mesenteric vascular systems [49]. This singular area shows a triple lymphatic drainage to both mesenteric drainways with potential extramesocolic spread. The majority of lymph node metastases of SFCs are located along the para-colic arcade and the left colic artery [13, 24]. However, several reports have suggested the existence of alternative routes of lymphatic dissemination toward the root of the inferior mesenteric vein, the middle colic and superior mesenteric arteries, the spleen, the greater omentum, and the lower border of the pancreas [17, 32, 50]. Particularly, Manceau et al. [17] recently reported a single institution series of 65 patients in which nearly 10% of SFC cases had the involvement of distal lymph nodes along the right colic artery. The authors conclude that ERC is a valid oncologic procedure for SFC patients, particularly for those with synchronous resectable or potentially resectable liver metastasis. However, this justification may be debatable in light of only anecdotal evidence of middle colic and superior mesenteric artery involvement and similar oncologic outcomes and long-term survival between ERC, LC and SLC procedures. It should be considered that distal lymph node involvement could be interpreted as metastatic disease and the systemic dissemination of the primary SFC tumor [27, 32].
It is interesting to note that the rate of laparoscopy observed in the present study (74.4%) is higher than in previous ones, representing the current trends of applying minimally invasive approaches in colorectal cancer surgery. All laparoscopic procedures were safely performed, as deemed by a similar rate of conversion to laparotomy and similar rate of R0 resection. These results are in accordance with the findings of a recent systematic review and meta-analysis by Martínez-Pérez et al. [8] and support the clear trend of increasing application of laparoscopy to perform all three surgical procedures for SFCs.
The present study has the strength to analyze a large homogeneous sample of SFC patients undergoing only elective curative-intent SFC resections. The exclusion of emergency procedures is essential to correctly compare and interpret the outcomes of the 3 different surgical techniques for SFC. Moreover, we matched the 3 groups by PSM in order to minimize the selection bias related to the choice of the type of surgical procedure. As it is unlikely that a randomized controlled trial would be feasible in this area given the relative rarity of SFCs, the use of TriMatch PSM may represent the best available method to analyze and interpret the present short- and long-term data. However, due to the retrospective design, other potential selection bias, such as the exact tumor distance (cm) from the splenic flexure as assess intra-operatively, cannot be excluded. Moreover, the present study, as the current literature, did not evaluate important patient-centered outcome measures, as the quality of life, which may be drastically affected by the type of surgical resection (e.g., risk of defecatory anomalies) [8] and which need to be considered in future research to implement the evidence-based choice of the surgical procedure in case of SFCs.
In conclusion, the present findings, based on a large multlicentric experience in SFC surgical treatments, support the tendency to resect SFCs with more conservative and minimally invasive surgical techniques (e.g., SLC).
References
Fukuoka A, Sasaki T, Tsukikawa S, Miyajima N, Ostubo T (2017) Evaluating distribution of the left branch of the middle colic artery and the left colic artery by CT angiography and colonography to classify blood supply to the splenic flexure. Asian J Endosc Surg 10(2):148–153
Nakagoe T, Sawa T, Tsuji T, Jibiki M, Nanashima A, Yamaguchi H, Yasutake T, Ayabe H, Ishikawa H (2000) Carcinoma of the splenic flexure: multivariate analysis of predictive factors for clinicopathological characteristics and outcome after surgery. J Gastroenterol 35(7):528–535
Kim MK, Lee IK, Kang WK, Cho HM, Kye BH, Jalloun HE, Kim JG (2017) Long-term oncologic outcomes of laparoscopic surgery for splenic flexure colon cancer are comparable to conventional open surgery. Ann Surg Treat Res 93(1):35–42
Beisani M, Vallribera F, Garcia A, Mora L, Biondo S, Lopez-Borao J, Farres R, Gil J, Espin E (2017) Subtotal colectomy versus left hemicolectomy for the elective treatment of splenic flexure colonic neoplasia. Am J Surg 216(2):251–254
Shaikh IA, Suttie SA, Urquhart M, Amin AI, Daniel T, Yalamarthi S (2012) Does the outcome of colonic flexure cancers differ from the other colonic sites? Int J Colorectal Dis 27(1):89–93
Benedix F, Schmidt U, Mroczkowski P, Gastinger I, Lippert H, Kube R, Study Group "Colon/Rectum C (2011) Colon carcinoma–classification into right and left sided cancer or according to colonic subsite?—Analysis of 29,568 patients. Eur J Surg Oncol 37(2):134–139
Akiyoshi T, Kuroyanagi H, Oya M, Ueno M, Fujimoto Y, Konishi T, Yamaguchi T (2010) Factors affecting difficulty of laparoscopic surgery for left-sided colon cancer. Surg Endosc 24(11):2749–2754
Martinez-Perez A, Brunetti F, Vitali GC, Abdalla S, Ris F, de'Angelis N (2017) Surgical treatment of colon cancer of the splenic flexure: a systematic review and meta-analysis. Surg Laparosc Endosc Percutan Tech 27(5):318–327
Ceccarelli G, Biancafarina A, Patriti A, Spaziani A, Bartoli A, Bellochi R, Pisanelli MC, Casciola L (2010) Laparoscopic resection with intracorporeal anastomosis for colon carcinoma located in the splenic flexure. Surg Endosc 24(7):1784–1788
Carlini M, Spoletini D, Castaldi F, Giovannini C, Passaro U (2016) Laparoscopic resection of splenic flexure tumors. Updates Surg 68(1):77–83
Fiscon V, Portale G, Migliorini G, Frigo F (2015) Splenic flexure colon cancers: minimally invasive treatment. Updates Surg 67(1):55–59
Matsuda T, Sumi Y, Yamashita K, Hasegawa H, Yamamoto M, Matsuda Y, Kanaji S, Oshikiri T, Nakamura T, Suzuki S, Kakeji Y (2018) Anatomical and embryological perspectives in laparoscopic complete mesocoloic excision of splenic flexure cancers. Surg Endosc 32(3):1202–1208
Nakagoe T, Sawai T, Tsuji T, Jibiki M, Ohbatake M, Nanashima A, Yamaguchi H, Yasutake T, Kurosaki N, Ayabe H, Ishikawa H (2001) Surgical treatment and subsequent outcome of patients with carcinoma of the splenic flexure. Surg Today 31(3):204–209
Pisani Ceretti A, Maroni N, Sacchi M, Bona S, Angiolini MR, Bianchi P, Opocher E, Montorsi M (2015) Laparoscopic colonic resection for splenic flexure cancer: our experience. BMC Gastroenterol 15(1):76
Roscio F, Bertoglio C, De Luca A, Frattini P, Clerici F, Scandroglio I (2012) Totally laparoscopic resection of the splenic flexure for tumor. Updates Surg 64(3):185–190
Grieco M, Cassini D, Spoletini D, Soligo E, Grattarola E, Baldazzi G, Testa S, Carlini M (2018) Laparoscopic resection of splenic flexure colon cancers: a retrospective multi-center study with 117 cases. Updates Surg 71(2):349–357
Manceau G, Mori A, Bardier A, Augustin J, Breton S, Vaillant JC, Karoui M (2018) Lymph node metastases in splenic flexure colon cancer: is subtotal colectomy warranted? J Surg Oncol 118(6):1027–1033
Panaccio P, Grottola T, Ricciardiello M, di Sebastiano P, di Mola FF (2018) How we do it: totally laparoscopic complete mesocolon excision for splenic flexure cancer. Langenbecks Arch Surg 403(6):769–775
Watanabe J, Ota M, Suwa Y, Ishibe A, Masui H, Nagahori K (2017) Evaluation of lymph flow patterns in splenic flexural colon cancers using laparoscopic real-time indocyanine green fluorescence imaging. Int J Colorectal Dis 32(2):201–207
de'Angelis N, Hain E, Disabato M, Cordun C, Carra MC, Azoulay D, Brunetti F (2016) Laparoscopic extended right colectomy versus laparoscopic left colectomy for carcinoma of the splenic flexure: a matched case-control study. Int J Colorectal Dis 31(3):623–630
Gravante G, Elshaer M, Parker R, Mogekwu AC, Drake B, Aboelkassem A, Rahman EU, Sorge R, Alhammali T, Gardiner K, Al-Hamali S, Rashed M, Kelkar A, Agarwal R, El-Rabaa S (2016) Extended right hemicolectomy and left hemicolectomy for colorectal cancers between the distal transverse and proximal descending colon. Ann R Coll Surg Engl 98(5):303–307
Han KS, Choi GS, Park JS, Kim HJ, Park SY, Jun SH (2010) Short-term outcomes of a laparoscopic left hemicolectomy for descending colon cancer: retrospective comparison with an open left hemicolectomy. J Korean Soc Coloproctol 26(5):347–353
Nakashima M, Akiyoshi T, Ueno M, Fukunaga Y, Nagayama S, Fujimoto Y, Konishi T, Noaki R, Yamakawa K, Nagasue Y, Kuroyanagi H, Yamaguchi T (2011) Colon cancer in the splenic flexure: comparison of short-term outcomes of laparoscopic and open colectomy. Surg Laparosc Endosc Percutan Tech 21(6):415–418
Vasey CE, Rajaratnam S, O'Grady G, Hulme-Moir M (2018) Lymphatic drainage of the splenic flexure defined by intraoperative scintigraphic mapping. Dis Colon Rectum 61(4):441–446
Binda GA, Amato A, Alberton G, Bruzzone M, Secondo P, Lopez-Borao J, Giudicissi R, Falato A, Fucini C, Bianco F, Biondo S (2019) Surgical treatment of the colon neoplasm of the splenic flexure: a multicentric study of short-term outcomes. Colorectal Dis. https://doi.org/10.1111/codi.14832
Chi Z, Li Z, Cheng L, Wang C (2018) Comparison of long-term outcomes after laparoscopic-assisted and open colectomy for splenic flexure cancer. J BUON 23(2):322–328
Martin Arevalo J, Moro-Valdezate D, Garcia-Botello SA, Pla-Marti V, Garces-Albir M, Perez Santiago L, Vargas-Duran A, Espi-Macias A (2018) Propensity score analysis of postoperative and oncological outcomes after surgical treatment for splenic flexure colon cancer. Int J Colorectal Dis 33(9):1201–1213
Milone M, Angelini P, Berardi G, Burati M, Corcione F, Delrio P, Elmore U, Lemma M, Manigrasso M, Mellano A, Muratore A, Pace U, Rega D, Rosati R, Tartaglia E, De Palma GD (2018) Intracorporeal versus extracorporeal anastomosis after laparoscopic left colectomy for splenic flexure cancer: results from a multi-institutional audit on 181 consecutive patients. Surg Endosc Surg Endosc 32(8):3467–3473
Odermatt M, Siddiqi N, Johns R, Miskovic D, Khan O, Khan J, Parvaiz A (2014) Short- and long-term outcomes for patients with splenic flexure tumours treated by left versus extended right colectomy are comparable: a retrospective analysis. Surg Today 44(11):2045–2051
Okuda J, Yamamoto M, Tanaka K, Masubuchi S, Uchiyama K (2016) Laparoscopic resection of transverse colon cancer at splenic flexure: technical aspects and results. Updates Surg 68(1):71–75
Rega D, Pace U, Scala D, Chiodini P, Granata V, Fares Bucci A, Pecori B, Delrio P (2019) Treatment of splenic flexure colon cancer: a comparison of three different surgical procedures: experience of a high volume cancer center. Sci Rep 9(1):10953
Kim CW, Shin US, Yu CS, Kim JC (2010) Clinicopathologic characteristics, surgical treatment and outcomes for splenic flexure colon cancer. Cancer Res Treat 42(2):69–76
von Elm E, Altman DG, Egger M, Pocock SJ, Gotzsche PC, Vandenbroucke JP, Initiative S (2008) The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. J Clin Epidemiol 61(4):344–349
Weiser MR (2018) AJCC 8th edition: colorectal cancer. Ann Surg Oncol 25(6):1454–1455
Kim JC, Lee JL, Yoon YS, Kim CW, Park IJ, Lim SB (2018) Robotic left colectomy with complete mesocolectomy for splenic flexure and descending colon cancer, compared with a laparoscopic procedure. Int J Med Robot 14(5):e1918
Petrucciani N, Memeo R, Genova P, Le Roy B, Courtot L, Voron T, Aprodu R, Tabchouri N, Saleh NB, Berger A, Ouaissi M, Pezet D, Mutter D, Brunetti F, de'Angelis N (2019) Impact of conversion from laparoscopy to open surgery in patients with right colon cancer. Am Surg 85(2):177–182
Dindo D, Demartines N, Clavien PA (2004) Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg 240(2):205–213
Chapuis PH, Bokey L, Keshava A, Rickard MJ, Stewart P, Young CJ, Dent OF (2013) Risk factors for prolonged ileus after resection of colorectal cancer: an observational study of 2400 consecutive patients. Ann Surg 257(5):909–915
Team RC (2017) R: A language and environment for statistical computing. In: Computing RFfS (ed), Vienna, Austria
Bryer JM (2013) TriMatch: an R package for propensity score matching of Non-binary treatments.
Benjamini Y, Yekutieli D (2001) The control of the false discovery rate in multiple testing under dependency. Ann Statis 29(4):1165–1188
Austin PC (2007) The performance of different propensity score methods for estimating marginal odds ratios. Stat Med 26(16):3078–3094
Austin PC (2013) The performance of different propensity score methods for estimating marginal hazard ratios. Stat Med 32(16):2837–2849
Biondi-Zoccai G, Romagnoli E, Agostoni P, Capodanno D, Castagno D, D'Ascenzo F, Sangiorgi G, Modena MG (2011) Are propensity scores really superior to standard multivariable analysis? Contemp Clin Trials 32(5):731–740
Brazauskas R, Logan BR (2016) Observational studies: matching or regression? Biol Blood Marrow Transplant 22(3):557–563
Elze MC, Gregson J, Baber U, Williamson E, Sartori S, Mehran R, Nichols M, Stone GW, Pocock SJ (2017) Comparison of propensity score methods and covariate adjustment: evaluation in 4 cardiovascular studies. J Am Coll Cardiol 69(3):345–357
Martínez-Perez A, Reitano E, Gavriilidis P, Genova P, Moroni P, Memeo R, Brunetti F, de'Angelis N (2019) What is the best surgical option for the resection of transverse colon cancer? Ann Laparosc Endosc Surg 4:69–80
Chen SL, Bilchik AJ (2006) More extensive nodal dissection improves survival for stages I to III of colon cancer: a population-based study. Ann Surg 244(4):602–610
Garcia-Granero A, Sanchez-Guillen L, Carreno O, Sancho Muriel J, Alvarez Sarrado E, Fletcher Sanfeliu D, Flor Lorente B, Frasson M, Martinez Soriano F, Garcia-Granero E (2017) Importance of the Moskowitz artery in the laparoscopic medial approach to splenic flexure mobilization: a cadaveric study. Tech Coloproctol 21(7):567–572
Stelzner S, Hohenberger W, Weber K, West NP, Witzigmann H, Wedel T (2016) Anatomy of the transverse colon revisited with respect to complete mesocolic excision and possible pathways of aberrant lymphatic tumor spread. Int J Colorectal Dis 31(2):377–384
Acknowledgements
The authors would like to thank Dr Clotilde Carra for her valuable support in manuscript revisions. SFC Study Group collaborators who participated in the study providing cares for the study patients and collecting the data: Giorgio Bianchi, Julie Pham, Pietro Genova, Iradj Sobhani (Unit of Digestive, Hepato-Pancreato-Biliary Surgery, Henri Mondor Hospital, AP-HP, University of Paris Est, UPEC, Créteil, France). Segundo A. Gómez, M. Teresa Torres, Carmen Payá, Paula Gonzálvez (Unit of Colorectal Surgery, Department of General and Digestive Surgery, Hospital Universitario Doctor Peset, Valencia, Spain). Aine Stakelum, Alexandra Zaborowski (Department of Surgery, St. Vincent’s Hospital, Elm Park, Dublin 4, Ireland). Albert Sueiras-Gil, Ramiro Hevia (Department of General Surgery, Viladecans Hospital, Barcelona, Spain). Michela Assalino (Service of Abdominal Surgery, Geneva University Hospitals and Medical School, Geneva, Switzerland). Denis Pezet, Mourad Abdallah (Department of Digestive and Hepato-biliary Surgery, Hospital Estaing, CHU Clermont-Ferrand, France). Luca Ansaloni (General, Emergency and Trauma Surgery Department, Bufalini Hospital of Cesena, Italy), Arianna Birindelli (Cambridge University Hospitals NHS Foundation Trust, Addenbrooke’s Hospital, Cambridge Biomedical Campus, Cambridge, UK), Christine Denet (Department of Digestive Oncologic and Metabolic Surgery, Institut Mutualiste Montsouris, Paris Descartes University, Paris France), Alejandro Solis, Miquel Kraft (Unit of Colorectal Surgery, Department of General and Digestive Surgery, University Hospital Vall d’Hebron, Barcelona, Universitat Autonoma de Barcelona, Spain).
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Drs Nicola de’Angelis, Aleix Martínez-Pérez, Des C. Winter, Filippo Landi, Giulio C. Vitali, Bertrand Le Roy, Federico Coccolini, Francesco Brunetti, Valerio Celentano, Salomone Di Saverio, Frederic Ris, David Fuks, and Eloy Espin have no conflicts of interest or financial ties to disclose.
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The SFC Study Group collaborators who participated in the study providing cares for the study patients and collecting the data has been included in ‘Acknowledgements’ section.
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de’Angelis, N., Martínez-Pérez, A., Winter, D.C. et al. Extended right colectomy, left colectomy, or segmental left colectomy for splenic flexure carcinomas: a European multicenter propensity score matching analysis. Surg Endosc 35, 661–672 (2021). https://doi.org/10.1007/s00464-020-07431-9
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DOI: https://doi.org/10.1007/s00464-020-07431-9