Literature DB >> 22179459

Clinical outcomes of laparoscopic surgery for advanced transverse and descending colon cancer: a single-center experience.

Masashi Yamamoto1, Junji Okuda, Keitaro Tanaka, Keisaku Kondo, Nobuhiko Tanigawa, Kazuhisa Uchiyama.   

Abstract

BACKGROUND: The role of laparoscopic surgery in management of transverse and descending colon cancer remains controversial. The aim of the present study is to investigate the short-term and oncologic long-term outcomes associated with laparoscopic surgery for transverse and descending colon cancer.
METHODS: This cohort study analyzed 245 patients (stage II disease, n = 70; stage III disease, n = 63) who underwent resection of transverse and descending colon cancers, including 200 laparoscopic surgeries (LAC) and 45 conventional open surgeries (OC) from December 1996 to December 2010. Short-term and oncologic long-term outcomes were recorded.
RESULTS: The operative time was longer in the LAC group than in the OC group. However, intraoperative blood loss was significantly lower and postoperative recovery time was significantly shorter in the LAC group than in the OC group. The 5-year overall and disease-free survival rates for patients with stage II were 84.9% and 84.9% in the OC group and 93.7% and 90.0% in the LAC group, respectively. The 5-year overall and disease-free survival rates for patients with stage III disease were 63.4% and 54.6% in the OC group and 66.7% and 56.9% in the LAC group, respectively.
CONCLUSION: Use of laparoscopic surgery resulted in acceptable short-term and oncologic outcomes in patients with advanced transverse and descending colon cancer.

Entities:  

Mesh:

Year:  2011        PMID: 22179459      PMCID: PMC3351590          DOI: 10.1007/s00464-011-2071-9

Source DB:  PubMed          Journal:  Surg Endosc        ISSN: 0930-2794            Impact factor:   4.584


Since publication of the first report of laparoscopic surgery for colon cancer in 1991 [1], utilization of the procedure has steadily increased. Benefits of laparoscopic surgery relative to open surgery include improved cosmesis, improved short-term outcomes, reduced surgical trauma, reduced requirements for narcotic analgesia, earlier return of bowel function, and shorter postoperative hospital stay [2-4]. However, due to an insufficient body of clinical evidence, laparoscopic surgery for colon cancer has not yet replaced the conventional open surgery as the standard of care. Although the safety and oncologic efficacy of laparoscopic surgery for treatment of colon cancer have been demonstrated in many randomized controlled trials [5-13], patients with transverse colon and descending colon cancer were excluded from many of these trials, mainly due to the difficulty in determining the appropriate operative procedure and the extent of lymphadenectomy [14]. Several recent studies have described the feasibility and safety of laparoscopic surgery for transverse and descending colon cancer [15-19]. However, there are few reports that describe the long-term outcomes associated with this management strategy. In our institution, laparoscopic surgery was performed in more than 1,000 patients with colon cancer up to December 2008. Thus, the goal of this study is to investigate the short-term and oncologic long-term outcomes associated with laparoscopic surgery for transverse and descending colon cancer.

Patients and methods

The first laparoscopic resection for colon cancer at our institution was performed in 1996. At that time, laparoscopic colectomy was indicated only for early-stage cancer. Gradually, the indication for this procedure was expanded to more advanced stages of cancer. Further, with standardization of the surgical system, more than 90% of colorectal resections were ultimately performed laparoscopically. Conversion to conventional open surgery was performed at surgeon discretion. Between December 1996 and December 2008, 1,236 patients underwent surgery for colon cancer (laparoscopic surgery, n = 1,009: conventional open surgery, n = 227). Of these, 245 resections were performed for cancers of the transverse and descending colon without synchronous double malignancies. All patients underwent comprehensive assessment with blood testing, serum carcinoembryonic antigen measurement, colonoscopy, pathologic confirmation, barium or air enema, computed tomography (CT), and chest X-ray before surgery. If tumor localization was unclear, preoperative colonoscopic India ink tattooing and clipping was performed. The procedure for lymphadenectomy was determined based on depth of tumor invasion according to the Japanese Classification of Colorectal Carcinoma [20]. The laparoscopic nontouch isolation technique (i.e., the median-to-lateral approach) was utilized whenever possible. The study was approved by the institutional ethics of research committee, and informed consent was obtained from each patient.

Study design

This cohort study analyzed 245 patients (stage II disease, n = 70; stage III disease, n = 63) who underwent resection of the transverse and descending colon cancer, including 200 laparoscopic surgeries (LAC) and 45 conventional open surgeries (OC) from December 1996 to December 2010. Short-term outcomes and oncologic long-term outcomes were assessed among patients with stage II (70 cases) and stage III (63 cases) disease.

Laparoscopic procedures

For transverse colon lesions, proximal ligations of the right or left branch or the root of the middle colic vessels were conducted, and lymphadenectomy was performed simultaneously using the median-to-lateral approach. Mobilization was performed from the hepatic and/or splenic flexures. For the hepatic side, if the root of the middle colic vessels was clearly identified, the vein was divided just before the point at which it drained into the gastrocolic trunk of Henle. For descending colon lesions, the left branch of the middle colic, left colic and sigmoid colic pedicles were identified, and lymphadenectomy was performed simultaneously with proximal ligations of the tumor-feeding vessels. The mesentery of the descending colon was gently mobilized from the ligament of Treitz by the median-to-lateral approach. The omental bursa was entered, and the mesentery of the transverse colon was dissected from the inferior border of the pancreas. The bowel loop of transverse or descending colon was delivered under a wound protector through a 3- to 5-cm incision and was divided from the marginal vessels. The anastomosis was performed extracorporeally using the functional end-to-end method.

Postoperative follow-up

For follow-up, patients with stage I and II disease underwent assessment of serum carcinoembryonic antigen levels (at 3-month intervals during the first year and at 6-month intervals thereafter), chest and abdominopelvic CT (at 6-month intervals), and colonoscopy (at 1-year intervals) in addition to routine outpatient visits. Patients with stage III disease underwent assessment of serum carcinoembryonic antigen levels (at 4-month intervals during the first 2 years and at 6-month intervals thereafter), chest and abdominopelvic CT and colonoscopy at the same interval in addition to routine outpatient visits. Patients with stage III disease received adjuvant chemotherapy with 5-fluorouracil plus leucovorin per standards of care.

Statistical analysis

Statistical analysis was performed using JMP 8 (SAS Institute Inc., Cary, NC, USA) for Windows. Student’s t test, Mann–Whitney U test and the χ2 test were used to compare continuous and categorical variables, respectively, with two-sided p < 0.050 indicating significance. Patient survival analysis was performed using Kaplan–Meier survival curves with log-rank statistics.

Results

Laparoscopic surgery versus conventional open surgery

Patient demographics and pathologic variables are summarized in Table 1. Gender, age, body mass index (BMI), and American Society of Anesthesiology (ASA) classification were not significantly different when comparing the OC group and the LAC group. According to the tumor–node–metastasis (TNM) classification, the proportion of patients with advanced stage was higher in the OC group than in the LAC group, mainly because LAC was initially used only for early-stage cancers. Therefore, short-term outcomes and oncologic long-term outcomes were investigated in patients with stage II (70 cases) and stage III (63 cases) disease. Patient demographics and pathologic variables of these cases are summarized in Table 2. Patients with stage II disease undergoing OC included 3 right hemicolectomies, 4 left hemicolectomies, and 8 transverse colectomies, while patients with stage III disease undergoing OC included 1 right hemicolectomy, 6 left colectomies, and 12 transverse colectomies. By contrast, patients with stage II disease undergoing LAC included 15 right hemicolectomies, 21 left hemicolectomies, and 19 transverse colectomies, while patients with stage III disease undergoing LAC included 11 right hemicolectomies, 23 left colectomies, and 10 transverse colectomies. Five (9.1%) patients with stage II disease required conversion to open surgery (bleeding, n = 3; surgical technique, n = 1; massive invasion, n = 1). Six (13.6%) patients with stage III disease required conversion to open surgery (adhesion, n = 2; massive invasion, n = 2; bleeding, n = 1; surgical technique, n = 1). All patients underwent D3 lymphadenectomy according to the Japanese Classification of Colorectal Carcinoma [20]. Gender, age, BMI, ASA classification, tumor size, number of dissected lymph nodes, and tumor differentiation were not significantly different when comparing the OC group and the LAC group. According to the TNM classification, the proportion of patients with pathologic T (pT) category was higher in the OC group than in the LAC group, likely because of the exclusion criteria utilized for this study. However, in terms of pathologic N (pN) category, there was no significant difference between the OC and the LAC group.
Table 1

Characteristics of patients (n = 245) with transverse or descending colon cancer

OC (n = 45)LAC (n = 200) p valuea
Gender (male/female)26:19110:900.734b
Age, years (mean, range)64 (29–84)65 (24–90)0.570
BMI, kg/m2 (mean, range)21 (16–34)22 (16–32)0.102
ASA classification0.034b
 I1570
 II20116
 III714
 IV20
Tumor classification<0.001b
 0220
 I265
 II1555
 III1944
 IV716

OC Conventional open surgery, LAC laparoscopic surgery, BMI body mass index, ASA American Society of Anesthesiologists

Clinical stage is classified by UICC-7 staging

aStudent’s t test

b χ 2 test

Table 2

Patient demographics and characteristics of transverse and descending colon cancer in patients with stage II or stage III disease

Stage IIStage III
OC (15)LAC (55) p valueb OC (19)LAC (44) p valueb
Gender (male/female)9:627:280.452c 9:1022:220.848c
Age, yearsa 67 (51–84)66 (24–90)0.65463 (29–81)65 (44–83)0.701
BMI, kg/m2a 21 (16–26)22 (16–32)0.97522 (16–29)21 (16–32)0.528
ASA classification0.353c 0.470c
 I522718
 II8291023
 III1413
 IV1010
Tumor size, cma 5.4 (2.5–7.6)4.8 (1.4–8.7)0.3165.0 (3.2–11.2)4.2 (1.0–10)0.119
Lymph nodesa 19 (7–27)15 (3–33)0.13214 (5–41)16 (5–35)0.711
pT category0.860c 0.008c
 T10002
 T20015
 T314521437
 T41340
pN category0.566c
 N0155500
 N1001737
 N20027
Tumor differentiation0.071c 0.098c
 Well837918
 Moderate517725
 Poor2031
 Mucinous0100

Clinical stage is classified by UICC-7 staging

OC Conventional open surgery, LAC laparoscopic surgery, BMI body mass index, ASA American Society of Anesthesiologists, Well well-differentiated adenocarcinoma, Moderate moderately differentiated adenocarcinoma, Poor poorly differentiated adenocarcinoma, Mucinous mucinous adenocarcinoma

Lymph nodes is number of lymph nodes removed

aValues expressed as median (range)

bMann–Whitney U test

c χ 2 test

Characteristics of patients (n = 245) with transverse or descending colon cancer OC Conventional open surgery, LAC laparoscopic surgery, BMI body mass index, ASA American Society of Anesthesiologists Clinical stage is classified by UICC-7 staging aStudent’s t test b χ 2 test Patient demographics and characteristics of transverse and descending colon cancer in patients with stage II or stage III disease Clinical stage is classified by UICC-7 staging OC Conventional open surgery, LAC laparoscopic surgery, BMI body mass index, ASA American Society of Anesthesiologists, Well well-differentiated adenocarcinoma, Moderate moderately differentiated adenocarcinoma, Poor poorly differentiated adenocarcinoma, Mucinous mucinous adenocarcinoma Lymph nodes is number of lymph nodes removed aValues expressed as median (range) bMann–Whitney U test c χ 2 test Table 3 presents the short-term outcomes of patients with stage II or stage III disease who underwent OC or LAC for transverse and descending colon cancer. The median operative time in patients with stage II disease was longer in the LAC group (230 min) than in the OC group (165 min; p = 0.012), and the median operative time in patients with stage III disease was also longer in the LAC group (245 min) than in the OC group (202 min; p = 0.038) with stage III. In patients with stage II disease, the median blood loss was significantly lower in the LAC group (10 ml) than in the OC group (100 ml; p < 0.001), and in patients with stage III disease, the median blood loss was also significantly lower in the LAC group (10 ml) than in the OC group (155 ml; p < 0.001). The duration until start of solid food after surgery was shorter in the LAC group (5 days) than in the OC group (7 days; p = 0.026) in patients with stage II disease and was also shorter in the LAC group (4 days) than in the OC group (7 days; p < 0.001) in patients with stage III disease. The median hospital stay after surgery was shorter in the LAC group (15 days) than in the OC group (29 days; p < 0.001) in patients with stage II disease and was also shorter in the LAC group (7 days) than in the OC group (31 days; p < 0.001) in patients with stage III disease.
Table 3

Intraoperative and postoperative results of surgeries for transverse or descending colon cancer

Stage IIStage III
OC (15)LAC (55) p valuea OC (19)LAC (44) p valuea
Operative time (min)165 (130–460)230 (130–525)0.012202 (105–305)245 (150–465)0.038
Blood loss (ml)100 (40–660)10 (10–1050)<0.001155 (10–660)10 (10–450)<0.001
Days to diet7 (5–34)5 (2–22)0.0267 (4–34)4 (3–36)<0.001
Hospital stay (day)29 (12–72)15 (8–53)<0.00131 (10–75)7 (14–156)<0.001

OC Conventional open surgery, LAC laparoscopic surgery

Values expressed as median (range)

aMann–Whitney U test

Intraoperative and postoperative results of surgeries for transverse or descending colon cancer OC Conventional open surgery, LAC laparoscopic surgery Values expressed as median (range) aMann–Whitney U test Table 4 summarizes the mortality and morbidity in each group. There were no perioperative deaths in patients with stage II disease. In patients with stage III disease, two patients died postoperatively: one from severe sepsis and septic shock in the LAC group, and one from liver failure with liver cirrhosis in the OC group. There was no significant difference in morbidity when comparing groups.
Table 4

Mortality and morbidity associated with surgery for transverse or descending colon cancer

Stage IIStage III
OC (15)LAC (55) p valuea OC (19)LAC (44) p valuea
Mortality00110.517
Morbidity5110.069670.163
 SSI2826
 Leakage1121
 Ileus2010
 Colitis0200
 Duodenal ulcer0010

OC conventional open surgery, LAC laparoscopic surgery, Mortality within 30 days after surgery, SSI surgical-site infection

a χ 2 test

Mortality and morbidity associated with surgery for transverse or descending colon cancer OC conventional open surgery, LAC laparoscopic surgery, Mortality within 30 days after surgery, SSI surgical-site infection a χ 2 test Table 5 summarizes the oncologic outcomes for the various groups. For patients with stage II disease, the median (range) follow-up period was 64 (10–154) months in the OC group and was 61 (12–128) months in the LAC group. For patients with stage III, the median (range) follow-up period was 53 (24–167) months in the OC group and 44 (9–145) months in the LAC group.
Table 5

Five-year oncologic outcomes of patients who underwent surgery for transverse or descending colon cancer

Stage IIStage III
OC (15)LAC (55) p valuea OC (19)LAC (44) p valuea
Overall survival (%)84.993.70.24063.466.70.819
Disease-free survival (%)84.990.00.48954.656.90.890
Recurrence rate (%)03.60.322b 37250.346b
Recurrence site027110.432b
Liver0027
Lung0121
Local0133

OC conventional open surgery, LAC laparoscopic surgery, Recurrence site site of first recurrence

aLog-rank statistics

b χ 2 test

Five-year oncologic outcomes of patients who underwent surgery for transverse or descending colon cancer OC conventional open surgery, LAC laparoscopic surgery, Recurrence site site of first recurrence aLog-rank statistics b χ 2 test The 5-year overall and disease-free survival rates in patients with stage II disease were 84.9% and 84.9% in the OC group and 93.7% and 90.0% in the LAC group, respectively (Fig. 1A, B). The 5-year overall and disease-free survival rates in patients with stage III disease were 63.4% and 54.6% in the OC group and 66.7% and 56.9% in the LAC group, respectively (Fig. 2A, B). The number of recurrences did not differ significantly between the LAC group and the OC group (2 versus 0; p = 0.322) in patients with stage II disease or between the LAC group and the OC group (11 versus 7; p = 0.346) in patients with stage III disease. There was no port-site recurrence or wound recurrence in either group, and there was no significant difference in the site of recurrence when comparing the groups.
Fig. 1

Kaplan–Meier curves of patients with stage II disease undergoing laparoscopic surgery or conventional open surgery: A overall survival rate and B disease-free survival rate. There was no statistically significant difference in survival between the two groups

Fig. 2

Kaplan–Meier curves of patients with stage II disease undergoing laparoscopic surgery or conventional open surgery: A overall survival rate and B disease-free survival rate. There was no statistically significant difference in survival between the two groups

Kaplan–Meier curves of patients with stage II disease undergoing laparoscopic surgery or conventional open surgery: A overall survival rate and B disease-free survival rate. There was no statistically significant difference in survival between the two groups Kaplan–Meier curves of patients with stage II disease undergoing laparoscopic surgery or conventional open surgery: A overall survival rate and B disease-free survival rate. There was no statistically significant difference in survival between the two groups

Discussion

Several randomized controlled trials have demonstrated that laparoscopic surgery for colon cancer (excluding those with transverse or descending colon cancer) can achieve favorable short-term outcomes and oncologic outcomes that are similar to open surgery [5-13]. Other recent studies of laparoscopic surgery have also demonstrated the feasibility and safety of the procedure for transverse and descending colon cancers [15-19]. However, the oncologic outcomes of patients undergoing laparoscopic resection of transverse and descending colon cancer have not yet been studied. Certainly, there are some difficulties when utilizing laparoscopic resection for transverse and descending colon cancer, as described in previous studies [15-19]; for example, mobilization, extent of resection, and details of lymphadenectomy may vary according to the precise location of the tumor in patients with transverse and descending colon cancer. In addition, resection of transverse and descending colon cancers that are adjacent to other critical structures, including the pancreas, duodenum, spleen, and the base of the mesenteric vessels, can result in major complications in case of dissection in the wrong plane. Therefore, thorough appreciation of the intricacies of venous anatomy at the gastrocolic trunk of Henle at the level of pancreas along the right plane is required when conducting this procedure. Jamali et al. [14] reported that a high-grade technique was required for splenic flexure mobilization, because of the requirement for extensive posterior dissection with simultaneous preservation of the vascular supply to the hind gut via the marginal artery as well as preservation of retroperitoneal structures, such as the ureters and the tail of pancreas. Further, surgeons may have comparatively less experience in dealing with this procedure because the incidence of transverse and descending colon cancer is low. Thus, laparoscopic transverse colectomy and left colectomy are more difficult than sigmoid colectomy and right colectomy, which often limits their use for cancers of the transverse and descending colon, especially for those with advanced cancer. In our institution, laparoscopic surgery has been utilized in more than 200 patients with transverse and descending colon cancer. The present study characterized the short-term outcomes and oncologic long-term outcomes after resection for advanced cancer of transverse and descending colon in patients with stage II or stage III disease undergoing OC or LAC. Gender, age, BMI, ASA, and tumor size were similar in both groups. Operative time was longer in the LAC group than in the OC group, likely because of anatomical and technical difficulties. However, blood loss was significantly lower and the postoperative course of recovery was significantly shorter in the LAC group than in the OC group. The morbidity and mortality were not significantly different when comparing the two groups. Further, the number of dissected lymph nodes and the incidence of intraoperative injury were not significantly different when comparing the two groups, nor were there differences in the number of recurrences, overall survival, or disease-free survival. These data indicate that laparoscopic surgery for advanced transverse and descending colon cancer resulted in favorable short-term outcomes (i.e., lower blood loss, shorter postoperative stay) and similar oncologic long-term outcomes when compared with conventional open surgery. Thus, laparoscopic surgery is an acceptable management strategy for advanced colon cancer regardless of tumor location. Successful laparoscopic surgery for transverse and descending colon cancer requires an advanced technique. Thus, acquisition of general laparoscopic skills is required to perform this fairly complex procedure. Since the number of patients requiring this specific procedure is relatively low, one way to gain this experience is through the development of laparoscopic skills when performing simpler, more common procedures, such as sigmoid colectomy and right colectomy. This experience may attenuate the otherwise steep learning curve needed to successfully achieve more complex laparoscopic procedures, thereby reducing the operative time, need for conversion to open procedures, and complication rate. In conclusion, laparoscopic resection for transverse and descending colon cancer appears safe and feasible and produces acceptable short-term and oncologic long-term outcomes. Curative resection for advanced transverse and descending colon cancer is technically possible; however, the present data were derived from single-institution experience and were not generated in a prospective manner. Laparoscopic surgery for colon cancer has not yet replaced conventional open surgery as the standard, mainly because there is insufficient clinical evidence. Further, there are also controversies regarding the level of difficulty of the individual procedure, the lack of data regarding oncological long-term outcomes after curative resection, and hospital costs. However, the favorable results seen in several randomized controlled trials of the safety and oncologic efficacy of this procedure for advanced colon cancer have resulted in increased utilization of the procedure. Confirmation of the value of laparoscopic surgery for colon cancer in prospective randomized controlled trials may result in increased demand for laparoscopic procedures from physicians and patients. In our institution, the chief and senior surgeons are actively trained in laparoscopic colon surgery. Indeed, with standardization of the surgical system and gradual expansion of the indications, more than 90% of colon surgeries in 2010 were performed laparoscopically at our institution. Since the demand for laparoscopic surgery for colon cancer is expected to increase, chief and senior surgeons as well as young surgeons starting will gradually increase. Regardless, we believe that laparoscopic surgery may become the gold standard for management of colon cancer, regardless of stage or tumor location.
  17 in total

1.  Five-year follow-up of the Medical Research Council CLASICC trial of laparoscopically assisted versus open surgery for colorectal cancer.

Authors:  D G Jayne; H C Thorpe; J Copeland; P Quirke; J M Brown; P J Guillou
Journal:  Br J Surg       Date:  2010-11       Impact factor: 6.939

2.  Laparoscopic vs. open colectomy in cancer patients: long-term complications, quality of life, and survival.

Authors:  Marco Braga; Matteo Frasson; Andrea Vignali; Walter Zuliani; Vittorio Civelli; Valerio Di Carlo
Journal:  Dis Colon Rectum       Date:  2005-12       Impact factor: 4.585

3.  Evaluating the degree of difficulty of laparoscopic colorectal surgery.

Authors:  Faek R Jamali; Asaad M Soweid; Hani Dimassi; Charles Bailey; Joel Leroy; Jacques Marescaux
Journal:  Arch Surg       Date:  2008-08

4.  Minimally invasive colon resection (laparoscopic colectomy).

Authors:  M Jacobs; J C Verdeja; H S Goldstein
Journal:  Surg Laparosc Endosc       Date:  1991-09

5.  Laparoscopic resection of rectosigmoid carcinoma: prospective randomised trial.

Authors:  Ka Lau Leung; Samuel P Y Kwok; Steve C W Lam; Janet F Y Lee; Raymond Y C Yiu; Simon S M Ng; Paul B S Lai; Wan Yee Lau
Journal:  Lancet       Date:  2004-04-10       Impact factor: 79.321

6.  A comparison of laparoscopically assisted and open colectomy for colon cancer.

Authors:  Heidi Nelson; Daniel J Sargent; H Sam Wieand; James Fleshman; Mehran Anvari; Steven J Stryker; Robert W Beart; Michael Hellinger; Richard Flanagan; Walter Peters; David Ota
Journal:  N Engl J Med       Date:  2004-05-13       Impact factor: 91.245

7.  Laparoscopic colectomy for cancer is not inferior to open surgery based on 5-year data from the COST Study Group trial.

Authors:  James Fleshman; Daniel J Sargent; Erin Green; Mehran Anvari; Steven J Stryker; Robert W Beart; Michael Hellinger; Richard Flanagan; Walter Peters; Heidi Nelson
Journal:  Ann Surg       Date:  2007-10       Impact factor: 12.969

8.  Randomized trial of laparoscopic-assisted resection of colorectal carcinoma: 3-year results of the UK MRC CLASICC Trial Group.

Authors:  David G Jayne; Pierre J Guillou; Helen Thorpe; Philip Quirke; Joanne Copeland; Adrian M H Smith; Richard M Heath; Julia M Brown
Journal:  J Clin Oncol       Date:  2007-07-20       Impact factor: 44.544

9.  Laparoscopic colectomy for transverse colon carcinoma.

Authors:  O Zmora; A Bar-Dayan; M Khaikin; A Lebeydev; M Shabtai; A Ayalon; D Rosin
Journal:  Tech Coloproctol       Date:  2009-12-23       Impact factor: 3.781

10.  Surgical and pathological outcomes of laparoscopic surgery for transverse colon cancer.

Authors:  Y S Lee; I K Lee; W K Kang; H M Cho; J K Park; S T Oh; J G Kim; Y H Kim
Journal:  Int J Colorectal Dis       Date:  2008-04-01       Impact factor: 2.571

View more
  20 in total

1.  Comparative study of oncologic outcomes for laparoscopic vs. open surgery in transverse colon cancer.

Authors:  Woo Ram Kim; Se Jin Baek; Chang Woo Kim; Hyun A Jang; Min Soo Cho; Sung Uk Bae; Hyuk Hur; Byung Soh Min; Seung Hyuk Baik; Kang Young Lee; Nam Kyu Kim; Seung Kuk Sohn
Journal:  Ann Surg Treat Res       Date:  2014-01-01       Impact factor: 1.859

2.  Perioperative and short-term oncological outcomes of single-port surgery for transverse colon cancer.

Authors:  Mitsuyoshi Tei; Yozo Suzuki; Masaki Wakasugi; Hiroki Akamatsu
Journal:  Surg Today       Date:  2016-10-03       Impact factor: 2.549

3.  Cranially approached radical lymph node dissection around the middle colic vessels in laparoscopic colon cancer surgery.

Authors:  Takeru Matsuda; Takeshi Iwasaki; Masaaki Mitsutsuji; Kenro Hirata; Yoko Maekawa; Daisuke Tsugawa; Yutaka Sugita; Yasuo Sumi; Etsuji Shimada; Yoshihiro Kakeji
Journal:  Langenbecks Arch Surg       Date:  2014-09-17       Impact factor: 3.445

4.  Long-term outcomes of laparoscopic surgery for advanced transverse colon cancer.

Authors:  Liying Zhao; Yanan Wang; Hao Liu; Hao Chen; Haijun Deng; Jiang Yu; Qi Xue; Guoxin Li
Journal:  J Gastrointest Surg       Date:  2014-01-22       Impact factor: 3.452

Review 5.  Laparoscopic Versus Open Transverse Colectomy: A Systematic Review and Meta-Analysis.

Authors:  Paschalis Gavriilidis; Konstantinos Katsanos
Journal:  World J Surg       Date:  2018-09       Impact factor: 3.352

6.  Laparoscopic colectomy for transverse colon cancer: comparative analysis of short- and long-term outcomes.

Authors:  Weizheng Sheng; Bo Zhang; Weifeng Chen; Dayong Gu; Weidong Gao
Journal:  Int J Clin Exp Med       Date:  2015-09-15

7.  Preoperative assessment of vascular anatomy by multidetector computed tomography before laparoscopic colectomy for transverse colon cancer: report of a case.

Authors:  Aya Kawamoto; Yasuhiro Inoue; Masato Okigami; Hiromi Yasuda; Yoshinaga Okugawa; Junichiro Hiro; Yuji Toiyama; Koji Tanaka; Keiichi Uchida; Yasuhiko Mohri; Masato Kusunoki
Journal:  Int Surg       Date:  2015-02

8.  A Transverse Colectomy is as Safe as an Extended Right or Left Colectomy for Mid-Transverse Colon Cancer.

Authors:  Lieve G J Leijssen; Anne M Dinaux; Ramzi Amri; Hiroko Kunitake; Liliana G Bordeianou; David L Berger
Journal:  World J Surg       Date:  2018-10       Impact factor: 3.352

Review 9.  A systematic review and meta-analysis evaluating the role of laparoscopic surgical resection of transverse colon tumours.

Authors:  M Chand; M R S Siddiqui; S Rasheed; G Brown; P Tekkis; A Parvaiz; T Qureshi
Journal:  Surg Endosc       Date:  2014-06-25       Impact factor: 4.584

Review 10.  Technologies for deriving primary tumor cells for use in personalized cancer therapy.

Authors:  Abhisek Mitra; Lopa Mishra; Shulin Li
Journal:  Trends Biotechnol       Date:  2013-04-16       Impact factor: 19.536

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.