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Oncology Letters logoLink to Oncology Letters
. 2017 Apr 13;13(6):4953–4958. doi: 10.3892/ol.2017.6035

Comparison of hand-assisted laparoscopic surgery (HALS) and conventional laparotomy in patients with colorectal cancer: Final results from a single center

Takayuki Tajima 1,, Masaya Mukai 2, Daiki Yokoyama 2, Shigeo Higami 2, Shuji Uda 2, Sayuri Hasegawa 1, Eiji Nomura 2, Sotaro Sadahiro 1, Seiei Yasuda 1, Hiroyasu Makuuchi 1,2
PMCID: PMC5452917  PMID: 28588735

Abstract

In recent years, the use of laparoscopic surgery has been expanded to include radical curative resection. In a previous study, 212 patients with primary colorectal cancer (stages I–III) underwent radical curative resection by hand-assisted laparoscopic surgery (HALS) (n=98) or conventional laparotomy (CL) (n=114) and were compared with respect to 3-year relapse-free survival (3Y-RFS) and 3-year overall survival (3Y-OS). The study included 210/212 patients who were followed up to 5 years, including 96 patients who underwent HALS and 114 treated with CL. The two groups were matched for stage, clinical background, and postoperative management. Patient characteristics were compared and the 5Y-RFS and 5Y-OS were determined. The 5-year follow-up rate was 97.6%. In stage I–III patients, 5Y-RFS and 5Y-OS showed no significant differences between HALS and CL. The patients with stage I disease accounted for 41.7% (40/96) of the patients undergoing HALS, while stage I patients only accounted for 23.7% (27/114) of the patients undergoing CL, and the difference was significant (P=0.005). Stage II patients undergoing CL were older than those treated with HALS (P=0.017). However, there were no differences in the characteristics of stage III patients undergoing HALS or CL. In conclusion, HALS achieved a similar survival to CL in patients with stage I to III colorectal cancer. Compared with CL, HALS was performed more safely and achieved superior cosmetic results.

Keywords: colorectal cancer, hand-assisted laparoscopic surgery, conventional laparotomy, laparoscopy-assisted colorectal surgery, laparoscopic surgery

Introduction

In recent years, the indications for laparoscopic surgery have been expanded to include radical curative resection of early to advanced colorectal cancer and palliative surgery for stage IV disease (16). In Japan, laparoscopy-assisted colorectal surgery (pure LACS) is widely used. However, pure LACS has several disadvantages, such as requiring at least 2 physicians who are familiar with the procedure and prolonging the operating time, as well as needing more staff and limiting the availability of operating theaters. Previously, it was reported that pure LACS achieves the same or better outcomes as conventional laparotomy (CL) with regard to wound infection, hospital stay, and survival, together with superior cosmetic results (710). In Europe and the USA, hand-assisted laparoscopic surgery (HALS) (HH) is more widely used than pure LACS. HH is characterized by: i) Providing the operator with palpation/tactile sensation, and allowing full grasping manipulation with the left hand and the possibility of smoothly removing even large and heavy tumors; ii) a shorter operating time than for pure LACS; and iii) a more rapid learning curve than for pure LACS (8,9,1117).

In Japan, various surgical procedures are employed for colorectal cancer, including pure LACS (30–40%), CL (~50%), and other methods such as HALS and microincisional surgery (18). HALS is often regarded as being an optimal medium between CL and pure LACS (8,9,1823). In Japan, HALS initially became popular for a short period of time during the introduction of pure LACS in 2000, possibly as a method of training for other procedures, prior to showing a marked decline in this function. Consequently, at present, single-center reviews of HALS are performed in countries other than Japan (9,24). Previously, 212 patients with primary colorectal cancer (stages I–III) underwent radical curative resection by hand-assisted laparoscopic surgery (HALS) (n=98) or conventional laparotomy (CL) (n=114) and were compared with respect to 3-year relapse-free survival (3Y-RFS) and 3-year overall survival (3Y-OS) (25). However this type of surgery has limitations. In the present study, 5-year data on the clinical outcomes of HALS and CL for colorectal cancer were analyzed at a single institution in Japan.

Patients and methods

Patients

In total, 850 patients underwent radical curative resection of primary colorectal cancer between April 2002 and December 2012. Aggressive introduction of HALS colorectal cancer surgery commenced in July 2007. Of the patients that were followed up over a period of 5 years, 114 patients (stage I, 27; stage II, 44; and stage III, 43) who received radical curative resection via CL prior to the introduction of HALS in July 2007, were carefully selected as historical controls (CL group), and were compared with 96 patients (stage I, 40; stage II, 28; and stage III, 28) who underwent resection by HALS (HALS group). The two groups were matched for stage and received the same postoperative adjuvant chemotherapy regimen and follow-up protocol. HALS and CL were performed in patients with a performance status of 0–2, and who exhibited no serious cardiopulmonary disease, no obvious preoperative lateral lymph node metastasis or multiple organ involvement, and no pelvic cavity disease (4,2427).

In the CL group, standard midline laparotomy was performed with a ≥30 cm incision, while 2-port HALS (colon, 5 mm/5 mm) or 3-port HALS (rectum and sigmoid colon, 5 mm/12 mm/5 mm) was performed in conjunction with a 45–55 mm longitudinal midline upper umbilical (colon)/umbilical (rectum/sigmoid colon) incision (4,26,27). At least 12 lymph nodes were collected from patients in the two groups following D2 or D3 resection according to the Japanese classification (2830). The postoperative adjuvant chemotherapy regimens were as follows: No chemotherapy in stage I, only oral anticancer agents (UFT/PSK) in stage II, and modified 5-fluorouracil (5-FU)/leucovorin (LV) or modified FOLFIRI (5-FU/LV+CPT-11) for ≥6 months in stage III (25,3136). To detect metastasis/recurrence, ultrasound scan (US) and computed tomography (CT) were performed 3–4 times annually, and patients in whom US and CT simultaneously identified metastatic/recurrent disease were classified as positive for metastasis/recurrence (25,3136). The 5-year relapse-free survival (5Y-RFS) and 5-year overall survival (5Y-OS) were calculated for each group and the results were compared.

Statistical analysis

The Kaplan-Meier method was used to estimate 5Y-RFS and 5Y-OS, while the log-rank test and hazard ratio [95% confidence interval (CI)] were used for comparison between the two groups. The χ2 test and Mann-Whitney U test were employed for any other parameters. SPSS statistics 21.1 software (IBM Corp., Armonk, NY, USA) was used. P<0.05 was considered to indicate a significant difference in all the analyses.

Results

Prognosis

For patients in stage I (n=67), 5Y-RFS was 95.0% with HALS (n=40) vs. 92.4% with CL (n=27) [P=0.690; hazard ratio (HR), 0.829 (95% CI, 0.305–2.254)] (Fig. 1A), while 5Y-OS was 94.9% with HALS (n=40) vs. 92.3% with CL (n=27) [P=0.637; HR, 0.829 (95% CI, 0.305–2.254)] (Fig. 1B). For patients in stage II (n=72), 5Y-RFS was 89.0% with HALS (n=28) vs. 72.5% with CL (n=44) [P=0.097; HR, 0.456 (95% CI, 0.159–1.308)] (Fig. 2A), while 5Y-OS was 96.4% with HALS (n=28) vs. 79.5% with CL (n=44) [P=0.055; HR, 0.230 (95% CI, 0.035–1.506)] (Fig. 2B). For patients in stage III (n=71), 5Y-RFS was 64.3% with HALS (n=28) vs. 67.3% with CL (n=43) [P=0.802; HR, 1.088 (95% CI, 0.599–1.975)] (Fig. 3A), while 5Y-OS was 78.4% with HALS (n=28) vs. 74.3% with CL (n=43) [P=0.645; HR, 0.866 (95% CI, 0.422–1.779)] (Fig. 3B).

Figure 1.

Figure 1.

(A) The 5-year relapse-free survival rate (5Y-RFS) and (B) 5-year overall survival rate (5Y-OS) of stage I patients in the hand-assisted laparoscopic surgery (HALS) and conventional laparotomy (CL) groups. The Kaplan-Meier method was employed, followed by comparison with the log-rank test and hazard ratio (HR) [95% confidence interval (CI)].

Figure 2.

Figure 2.

(A) 5-year relapse-free survival rate (5Y-RFS) and (B) 5-year overall survival rate (5Y-OS) of stage II patients in the hand-assisted laparoscopic surgery (HALS) and conventional laparotomy (CL) groups. The Kaplan-Meier method was employed, followed by comparison with the log-rank test and and hazard ratio (HR) [95% confidence interval (CI)].

Figure 3.

Figure 3.

(A) The 5-year relapse-free survival rate (5Y-RFS) and (B) 5-year overall survival rate (5Y-OS) of stage III patients in the hand-assisted laparoscopic surgery (HALS) and conventional laparotomy (CL) groups. The Kaplan-Meier method was employed, followed by comparison with the log-rank test and hazard ratio (HR) [95% confidence interval (CI)].

For all the patients in stages I–III (n=210), 5Y-RFS was 84.2% with HALS (n=96) vs. 75.2% with CL (n=114) [P=0.110; HR, 0.719 (95% CI, 0.464–1.114)] (Fig. 4A), while 5Y-OS was 90.5% with HALS (n=96) vs. 80.5% with CL (n=114) [P=0.042; HR, 0.597 (95% CI, 0.338–1.057)] (Fig. 4B).

Figure 4.

Figure 4.

(A) The 5-year relapse-free survival rate (5Y-RFS) and (B) 5-year overall survival rate (5Y-OS) of all the patients (stages I/II/III) in the hand-assisted laparoscopic surgery (HALS) and conventional laparotomy (CL) groups. The Kaplan-Meier method was employed, followed by comparison with the log-rank test and hazard ratio (HR) [95% confidence interval (CI)].

Patient characteristics

There were 67 patients with stage I disease. Forty stage I patients underwent HALS, accounting for 41.7% of the HALS group, while 27 stage I patients underwent CL, accounting for only 23.7% of the CL group, indicating a significant difference (P=0.005). Of the 72 patients in stage II, 28 patients underwent HALS (29.2% of the HALS group) and 44 patients were treated by CL (38.6% of the CL group), showing no significant difference (P=0.152). Of the 71 stage III patients, 28 patients underwent HALS (29.1% of the HALS group) and 43 patients received CL (37.7% of the CL group), also showing no significant difference (P=0.192; Table I). These results indicated that HALS was performed significantly more often than CL for stage I disease (Table I).

Table I.

Comparison of stage between the HALS group (n=96) and the CL group (n=114).

Stage HALS CL P-value (χ2)
1 41.7% (40/96) 23.7% (27/114) 0.005
2 29.2% (28/96) 38.6% (44/114) 0.152
3 29.1% (28/96) 37.7% (43/114) 0.192

HALS, hand-assisted laparoscopic surgery; CL, conventional laparotomy.

Regarding tumor site, the tumor was located in the colon in 53 patients undergoing HALS (55.2% of the HALS group) and 77 patients undergoing CL (67.5% of the CL group), while the tumor was located in the rectum in 43 patients undergoing HALS (44.8% of the HALS group) and 37 patients undergoing CL (32.5% of the CL group), and no significant difference was observed (P=0.067) (Table IIA).

Table II.

Tumor site and stage distribution of patients.

A, Comparison of tumor site between the HALS group (n=96) and the CL group (n=114)

Tumor site HALS CL P-value (χ2)
Colon 55.2% (53/96) 67.5% (77/114) 0.067
Rectum 44.8% (43/96) 32.5% (37/114)

B, Stage distribution of patients with colon cancer (n=130) and rectal cancer (n=80)

Stage Colon Rectum P-value (χ2)

1 30.8% (40/130) 33.8% (27/80) 0.653
2 38.5% (50/130) 27.5% (22/80) 0.104
3 30.8% (40/130) 38.8% (31/80) 0.235

HALS, hand-assisted laparoscopic surgery; CL, conventional laparotomy.

Patients in stage I (n=40) accounted for 30.8% of all the colon cancer patients, while stage I rectal cancer patients (n=27) comprised 33.8% of all rectal cancer patients (P=0.653). There were 50 patients with stage II colon cancer, accounting for 38.5% of all colon cancer patients, and there were 22 patients with stage II rectal cancer, accounting for 27.5% of all rectal cancer patients (P=0.104). There were 40 patients with stage III colon cancer, accounting for 30.8% of all colon cancer patients, and there were 31 patients with stage III rectal cancer, accounting for 38.8% of all rectal cancer patients (P=0.235). There were no significant differences in stages I–III (Table IIB).

Regarding the age distribution, the mean age was 62.4 (median, 62) years in the HALS group and 65.6 (median, 66) years in the CL group (Table IIIA).

Table III.

Comparison of age between the HALS group (n=96) and the CL group (n=114).

A, All patients, n=210

Characteristics HALS, n=96 CL, n=114 P-value, Mann-Whitney U test
Age, years 0.010
  Average 62.4 65.6
  Median 62 (36–81) 66 (42–87)

B, Stage I patients, n=67

Colon and rectum HALS, n=40 CL, n=27 P-value, Mann-Whitney U test

Age, years 0.090
  Average 64.5 68.3
  Median 64.5 (42–81) 71.0 (42–87)

C, Stage II patients, n=72

Colon and rectum HALS, n=28 CL, n=44 P-value, Mann-Whitney U test

Age, years 0.017
  Average 60.7 66.1
  Median 61.0 (40–75) 66.5 (45–81)

D, Stage III patients, n=71

Colon and rectum HALS, n=28 CL, n=43 P-value, Mann-Whitney U test

Age, years 0.207
  Average 60.9 63.5
  Median 60.0 (36–72) 64.0 (45–76)

HALS, hand-assisted laparoscopic surgery; CL, conventional laparotomy.

The mean age of the stage I patients was 64.5 years (median, 64.5) years and 68.3 (median, 71.0) years in the HALS and CL groups, respectively (P=0.090) (Table IIIB). In addition, the mean age of stage II patients was 60.7 (median, 61.0) years and 66.1 (median, 66.5) years in the HALS and laparotomy groups, respectively (P=0.017) (Table IIIC), while that of stage III patients was 60.9 (median, 60.0) years and 63.5 (median, 64.0) years, respectively (P=0.207; Table IIID).

Discussion

Due to its rapid utilization in recent years, a number of studies have reported on pure LACS in comparison with CL and HALS (8,9,1923). When surgical procedures are reviewed at a single center, CL is often selected as the control. However, it is difficult to exclude bias from the clinical background of the control group in relation to both pure LACS and HALS. In addition, problems with the standardization of subsequent treatment are likely to occur, such as the postoperative chemotherapy or radiotherapy regimens and the methods of handling recurrence. In the present study, we used historical controls treated prior to the utilization of HALS. The controls were matched for stage and for the postoperative adjuvant chemotherapy regimen, and were compared (410). The HALS and CL procedures were performed by Mukai et al (4,27); thus, the management of stage I/II/III colorectal cancer was standardized in the study population. Patients in stages II and III from the two groups received standardized chemotherapy and the ≥6-month completion rate was >80% in the two groups (data not shown) (25). The results of the 5-year follow up were also analyzed in the present study.

A comparison of pure LACS with CL has identified problems with human resources, surgical skill, a prolonged operating time, and higher cost in relation to LACS, although there have also been reports of a shorter hospital stay and a decrease in the total analgesic dose (710). Previous findings showed that the conversion rate of HALS was much lower than that of pure LACS (15). The rate for HALS in the present study was 4.2% (4/98 patients) in our study. There were significant differences of blood loss for stages I and II and in the length of hospital stay for stage III (25). However, stage III patients with multiple organ infiltration accounted for 18.6% (8/43 patients) in the CL group vs. 3.6% in the HALS group (1/28, P=0.063, data not shown) (25). There were no significant differences between the two groups with respect to complications.

Blood loss was obviously lower in stage I and II patients from the HALS group, suggesting that this method is safe when based on strict indications (25).

The present study also involved rectal cancer patients. Findings of studies conducted in Europe and America suggest that HALS does not show non-inferiority versus pure LACS and CL for the resection of rectal cancer (37,38). However, results of those studies, which included rectal cancer patients showed no significant difference between CL and HALS. Based on those findings, HALS is a safe and reliable technique for patients with colorectal cancer that achieves the same 5Y-RFS and 5Y-OS as CL, suggesting that it is a reasonable procedure to employ and is positioned between pure LACS and CL. Since HALS is easy to perform and is a cost-effective method, it is considered to be a superior technique that deserves to be reconsidered in the current medical environment where availability of surgeons and anesthesiologists is on the decrease at small and medium-sized hospitals in Japan.

Acknowledgements

The present study was supported by grants from the Hand-Assisted Laparoscopic Surgery Research Group (no. 2010–5007; Tokai University Hachioji Hospital, Hachioji, Tokyo, Japan) and the Research and Study Program of Tokai University Educational System General Research Organization (Tokai University Hospital, Isehara, Kanagawa, Japan).

Glossary

Abbreviations

HALS

hand-assisted laparoscopic surgery

CRC

colorectal cancer

CL

conventional laparotomy

LACS

laparoscopy-assisted colorectal surgery

References

  • 1.Franklin ME, Jr, Rosenthal D, Abrego-Medina D, Dorman JP, Glass JL, Norem R, Diaz A. Prospective comparison of open vs. laparoscopic colon surgery for carcinoma. Five-year results. Dis Colon Rectum. 1996;39(Suppl 10):S35–S46. doi: 10.1007/BF02053804. [DOI] [PubMed] [Google Scholar]
  • 2.Yano H, Ohnishi T, Kanoh T, Monden T. Hand-assisted laparoscopic low anterior resection for rectal carcinoma. J Laparoendosc Adv Surg Tech A. 2005;15:611–614. doi: 10.1089/lap.2005.15.611. [DOI] [PubMed] [Google Scholar]
  • 3.Mukai M, Tanaka A, Tajima T, Fukasawa M, Yamagiwa T, Okada K, Sato K, Tobita K, Oida Y, Makuuchi H. Two-port hand-assisted laparoscopic surgery for the 2-stage treatment of a complete bowel obstruction by left colon cancer: A case report. Oncol Rep. 2008;19:875–879. [PubMed] [Google Scholar]
  • 4.Mukai M, Kishima K, Tajima T, Hoshikawa T, Yazawa N, Fukumitsu H, Okada K, Ogoshi K, Makuuchi H. Efficacy of hybrid 2-port hand-assisted laparoscopic surgery (Mukai's operation) for patients with primary colorectal cancer. Oncol Rep. 2009;22:893–899. doi: 10.3892/or_00000514. [DOI] [PubMed] [Google Scholar]
  • 5.Koh DC, Law CW, Kristian I, Cheong WK, Tsang CB. Hand-assisted laparoscopic abdomino-perineal resection utilizing the planned end colostomy site. Tech Coloproctol. 2010;14:201–206. doi: 10.1007/s10151-010-0581-4. [DOI] [PubMed] [Google Scholar]
  • 6.Guerrieri M, Campagnacci R, de Sanctis A, Lezoche G, Massucco P, Summa M, Gesuita R, Capussotti L, Spinoglio G, Lezoche E. Laparoscopic versus open colectomy for TNM stage III colon cancer: Results of a prospective multicenter study in Italy. Surg Today. 2012;42:1071–1077. doi: 10.1007/s00595-012-0292-8. [DOI] [PubMed] [Google Scholar]
  • 7.Chung CC, Ng DC, Tsang WW, Tang WL, Yau KK, Cheung HY, Wong JC, Li MK. Hand-assisted laparoscopic versus open right colectomy: A randomized controlled trial. Ann Surg. 2007;246:728–733. doi: 10.1097/SLA.0b013e318123fbdf. [DOI] [PubMed] [Google Scholar]
  • 8.Yin WY, Wei CK, Tseng KC, Lin SP, Lin CH, Chang CM, Hsu TW. Open colectomy versus laparoscopic-assisted colectomy supported by hand-assisted laparoscopic colectomy for resectable colorectal cancer: A comparative study with minimum follow-up of three years. Hepatogastroenterology. 2009;56:998–1006. [PubMed] [Google Scholar]
  • 9.Pendlimari R, Holubar SD, Pattan-Arun J, Larson DW, Dozois EJ, Pemberton JH, Cima RR. Hand-assisted laparoscopic colon and rectal cancer surgery: Feasibility, short-term, and oncological outcomes. Surgery. 2010;148:378–385. doi: 10.1016/j.surg.2010.05.019. [DOI] [PubMed] [Google Scholar]
  • 10.Aimaq R, Akopian G, Kaufman HS. Surgical site infection rates in laparoscopic versus open colorectal surgery. Am Surg. 2011;77:1290–1294. doi: 10.1177/000313481107701003. [DOI] [PubMed] [Google Scholar]
  • 11.Nakajima K, Lee SW, Cocilovo C, Foglia C, Sonoda T, Milsom JW. Laparoscopic total colectomy: Hand-assisted vs standard technique. Surg Endosc. 2004;18:582–586. doi: 10.1007/s00464-003-8135-8. [DOI] [PubMed] [Google Scholar]
  • 12.Kang JC, Chung MH, Chao PC, Yeh CC, Hsiao CW, Lee TY, Jao SW. Hand-assisted laparoscopic colectomy vs open colectomy: A prospective randomized study. Surg Endosc. 2004;18:577–581. doi: 10.1007/s00464-003-8148-3. [DOI] [PubMed] [Google Scholar]
  • 13.Ringley C, Lee YK, Iqbal A, Bocharev V, Sasson A, McBride CL, Thompson JS, Vitamvas ML, Oleynikov D. Comparison of conventional laparoscopic and hand-assisted oncologic segmental colonic resection. Surg Endosc. 2007;21:2137–2141. doi: 10.1007/s00464-007-9401-y. [DOI] [PubMed] [Google Scholar]
  • 14.Young-Fadok TM. Colon cancer: Trials, results, techniques (LAP and HALS), future. J Surg Oncol. 2007;96:651–659. doi: 10.1002/jso.20921. [DOI] [PubMed] [Google Scholar]
  • 15.Tjandra JJ, Chan MK, Yeh CH. Laparoscopic- vs. hand-assisted ultralow anterior resection: A prospective study. Dis Colon Rectum. 2008;51:26–31. doi: 10.1007/s10350-007-9107-1. [DOI] [PubMed] [Google Scholar]
  • 16.Pattana-arun J, Sahakitrungruang C, Atithansakul P, Tantiphlachiva K, Khomvilai S, Rojanasakul A. Multimedia article. Hand-assisted laparoscopic total mesorectal excision: A stepwise approach. Dis Colon Rectum. 2009;52:1787. doi: 10.1007/DCR.0b013e3181b618d5. [DOI] [PubMed] [Google Scholar]
  • 17.Oncel M, Akin T, Gezen FC, Alici A, Okkabaz N. Left inferior quadrant oblique incision: A new access for hand-assisted device during laparoscopic low anterior resection of rectal cancer. J Laparoendosc Adv Surg Tech A. 2009;19:663–666. doi: 10.1089/lap.2008.0375. [DOI] [PubMed] [Google Scholar]
  • 18.Kitano S, Yamashita N, Shiraishi N, et al. 11th Nationwide survey of endoscopic surgery in Japan. J Jpn Soc Endoscopic Surg. 2012;17:595–611. (In Japanese) [Google Scholar]
  • 19.Cima R, Pemberton JH. How a hand-assist can help in lap colectomy. Contemp Surg. 2007;63:19–23. [Google Scholar]
  • 20.Cima RR, Pattana-arun J, Larson DW, Dozois EJ, Wolff BG, Pemberton JH. Experience with 969 minimal access colectomies: The role of hand-assisted laparoscopy in expanding minimally invasive surgery for complex colectomies. J Am Coll Surg. 2008;206:946–950, discussion 950–952. doi: 10.1016/j.jamcollsurg.2007.12.021. [DOI] [PubMed] [Google Scholar]
  • 21.Sheng QS, Lin JJ, Chen WB, Liu FL, Xu XM, Lin CZ, Wang JH, Li YD. Hand-assisted laparoscopic versus open right hemicolectomy: Short-term outcomes in a single institution from China. Surg Laparosc Endosc Percutan Tech. 2012;22:267–271. doi: 10.1097/SLE.0b013e3182516577. [DOI] [PubMed] [Google Scholar]
  • 22.Ng LW, Tung LM, Cheung HY, Wong JC, Chung CC, Li MK. Hand-assisted laparoscopic versus total laparoscopic right colectomy: A randomized controlled trial. Colorectal Dis. 2012;14:e612–e617. doi: 10.1111/j.1463-1318.2012.03028.x. [DOI] [PubMed] [Google Scholar]
  • 23.Sim JH, Jung EJ, Ryu CG, Paik JH, Kim G, Kim SR, Hwang DY. Short-term outcomes of hand-assisted laparoscopic surgery vs. open surgery on right colon cancer: A case-controlled study. Ann Coloproctol. 2013;29:72–76. doi: 10.3393/ac.2013.29.2.72. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Meshikhes AW, El Tair M, Al Ghazal T. Hand-assisted laparoscopic colorectal surgery: Initial experience of a single surgeon. Saudi J Gastroenterol. 2011;17:16–19. doi: 10.4103/1319-3767.74444. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Tajima T, Mukai M, Yamazaki M, Higami S, Yamamoto S, Hasegawa S, Nomura E, Sadahiro S, Yasuda S, Makuuchi H. Comparison of hand-assisted laparoscopic surgery and conventional laparotomy for colorectal cancer: Interim results from a single institution. Oncol Lett. 2014;8:627–632. doi: 10.3892/ol.2014.2182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Mukai M, Fukasawa M, Kishima K, Iizuka S, Fukumitsu H, Yazawa N, Tajima T, Nakamura M, Makuuchi H. Trans-anal reinforcing sutures after double stapling for lower rectal cancer: Report of two cases. Oncol Rep. 2009;21:335–339. [PubMed] [Google Scholar]
  • 27.Mukai M, Sekido Y, Hoshikawa T, Yazawa N, Fukumitsu H, Okada K, Tajima T, Nakamura M, Ogoshi K. Two-stage treatment (Mukai's method) with hybrid 2-port HALS (Mukai's operation) for complete bowel obstruction by left colon cancer or rectal cancer. Oncol Rep. 2010;24:25–30. doi: 10.3892/or_00000824. [DOI] [PubMed] [Google Scholar]
  • 28.Mukai M, Ito I, Mukoyama S, Tajima T, Saito Y, Nakasaki H, Sato S, Makuuchi H. Improvement of 10-year survival by Japanese radical lymph node dissection in patients with Dukes' B and C colorectal cancer: A 17-year retrospective study. Oncol Rep. 2003;10:927–934. [PubMed] [Google Scholar]
  • 29.Japanese Society for Cancer of the Colon and Rectum (JSCCR), corp-author General rules for clinical and pathological studies on cancer of the colon, rectum and anus. 7th. Kanehara & Co., Ltd.; Tokyo: 2009. pp. 10–13. [Google Scholar]
  • 30.Japanese Society for Cancer of the Colon and Rectum (JSCCR), corp-author JSCCR Guidelines 2010 for the treatment of colorectal cancer. Kanehara & Co., Ltd.; Tokyo: 2010. pp. 10–15. [Google Scholar]
  • 31.Mukai M, Tajima T, Nakasaki H, Sato S, Ogoshi K, Makuuchi H. Efficacy of postoperative adjuvant oral immunochemotherapy in patients with Dukes' B colorectal cancer. Ann Cancer Res Therap. 2003;11:201–214. doi: 10.4993/acrt1992.11.201. [DOI] [Google Scholar]
  • 32.Mukai M, Tajima T, Nakasaki H, Sato S, Ogoshi K, Makuuchi H. Efficacy of postoperative adjuvant oral immunochemotherapy in patients with Dukes' C colorectal cancer. Ann Cancer Res Therap. 2003;11:215–229. doi: 10.4993/acrt1992.11.201. [DOI] [Google Scholar]
  • 33.Ito I, Mukai M, Ninomiya H, Kishima K, Tsuchiya K, Tajima T, Oida Y, Nakamura M, Makuuchi H. Comparison between intravenous and oral postoperative adjuvant immunochemotherapy in patients with stage II colorectal cancer. Oncol Rep. 2008;20:1189–1194. [PubMed] [Google Scholar]
  • 34.Ito I, Mukai M, Ninomiya H, Kishima K, Tsuchiya K, Tajima T, Nakamura M, Makuuchi H. Comparison between intravenous and oral postoperative adjuvant immunochemotherapy in patients with stage III colorectal cancer. Oncol Rep. 2008;20:1521–1526. [PubMed] [Google Scholar]
  • 35.Mukai M, Okada K, Fukumitsu H, Yazawa N, Hoshikawa T, Tajima T, Hirakawa H, Ogoshi K, Makuuchi H. Efficacy of 5-FU/LV plus CPT-11 as first-line adjuvant chemotherapy for stage IIIa colorectal cancer. Oncol Rep. 2009;22:621–629. doi: 10.3892/or_00000481. [DOI] [PubMed] [Google Scholar]
  • 36.Mukai M, Kishima K, Uchiumi F, Ishibashi E, Fukasawa M, Tajima T, Nakamura M, Makuuchi H. Clinical comparison of QOL and adverse events during postoperative adjuvant chemotherapy in outpatients with node-positive colorectal cancer or gastric cancer. Oncol Rep. 2009;21:1061–1066. doi: 10.3892/or_00000324. [DOI] [PubMed] [Google Scholar]
  • 37.Stevenson ARL, Solomon MJ, Lumley JW, Hewett P, Clouston AD, Gebski VJ, Davies L, Wilson K, Hague W, Simes J. ALaCaRT Investigators: Effect of laparoscopic-assisted resection vs open resection on pathological outcomes in rectal cancer: The ALaCaRT randomized clinical trial. JAMA. 2015;314:1356–1363. doi: 10.1001/jama.2015.12009. [DOI] [PubMed] [Google Scholar]
  • 38.Fleshman J, Branda M, Sargent DJ, Boller AM, George V, Abbas M, Peters WR, Jr, Maun D, Chang G, Herline A, et al. Effect of laparoscopic-assisted resection vs open resection of stage II or III rectal cancer on pathologic outcomes: The ACOSOG Z6051 randomized clinical trial. JAMA. 2015;314:1346–1355. doi: 10.1001/jama.2015.10529. [DOI] [PMC free article] [PubMed] [Google Scholar]

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