Impact of Body Mass Index on Surgical and Oncological Outcomes in Laparoscopic Total Mesorectal Excision for Locally Advanced Rectal Cancer after Neoadjuvant 5-Fluorouracil-Based Chemoradiotherapy.
Obesity is a major public health problem associated with numerous morbidities . Body mass index (BMI), the basis for the assessment of obesity, has been shown to be a risk factor for colorectal cancer incidence and death [1, 2]. It was recognized that higher BMI was associated with increased technical difficulties and postoperative morbidity during colorectal surgery [3-5]. In contrast, other studies reported no negative impact of obesity on surgical outcome after rectal surgery [6, 7].
The concept of total mesorectal excision (TME), introduced by Professor Bill Heald (father of TME) , significantly reduces the rate of local recurrence of rectal cancer. Recent randomized clinical trials (RCTs) have demonstrated better results for laparoscopic TME (laTME) in terms of short- and long-term oncological outcomes, when compared with open TME [9-11]. However, obesity presents both negative and positive challenges to laparoscopic rectal surgery: the laparoscopic procedure becomes more technically demanding; on the other hand, the laparoscopic approach may be particularly advantageous to obese patients, resulting in reduced postoperative pain, faster postoperative recovery, and shorter hospital stay .
The long-term results of the CAO/ARO/AIO-94 trial of the GRCSG have demonstrated the enormous effect of neoadjuvant chemoradiotherapy (nCRT) . Nowadays, nCRT followed by total mesorectal excision (TME) has become the standard of care for patients with locally advanced rectal cancer (LARC), clinically staged as UICC stages II and III (cUICC-II/III) [12, 13]. A phase 3 study (CAO/ARO/AIO-04), which integrated oxaliplatin into standard fluorouracil-based combined modality treatment, has reported that intensification of CRT was feasible and led to a higher pathologically complete (pCR) response [14-16]. Surgeons may encounter increased technical difficulties and surgical morbidity during laTME following nCRT . Therefore, implementation of laTME following nCRT in those obese patients requires a specific assessment of the impact of obesity on this invasive procedure. To date, however, there have been few studies looking at the impact of obesity on surgical outcomes in laTME for rectal cancer following nCRT.
This study was intended to evaluate the impact of obesity, as measured by BMI, on feasibility, safety, and oncological outcome of laTME for LARC patients after nCRT in a high-volume center. We also sought to identify factors associated with postoperative morbidity of laTME following nCRT in the present study.
2. Materials and Methods
2.1. Patient Population. This study was a retrospective and monocentric analyses. Between 2008 and 2014, 312 consecutive patients with LARC who underwent laTME were identified from our prospectively maintained database. The inclusion criteria were as follows: (1) clinically staged as UICC stages II and III, (2) within 12 cm above the anal verge, (3) a histologically proven adenocarcinoma, and (4) no evidence of distant metastasis. Patients with previous or concurrent malignancies and those who underwent emergent surgery, palliative resection, or local excision were excluded. Our institutional review board approved this study.
2.2. Neoadjuvant Chemoradiotherapy. Patients chose inclusion to the direct surgery or nCRT groups based on the current stage of their disease and after understanding the risks and benefits and without the influence of the surgeon. All patients underwent CT simulation of the three-field technique for conformal radiotherapy planning. Clinical target volume (CTV) included the primary tumor, the mesentery with vascular supply, and the perirectal, presacral, and internal iliac nodes up to the S1/S2 junction. Planning target volume (PTV) was formed by enlarging 10 to 15 mm on the basis of the clinical target volume. Preoperative radiotherapy was delivered in fractions of 1.8-2.0 Gy, 5 fractions per week for 5-6 consecutive weeks followed by a boost of 5.4 Gy to reach a dose of 45-50.5 Gy. The chemotherapeutic regimens with dosages were as follows: FOLFOX4: oxaliplatin 85 mg/[m.sup.2] IV, day 1, leucovorin 200mg/[m.sup.2] IV x 2 days, 5-FU 400 mg/[m.sup.2] IV bolus x 2 days, then 600 mg/[m.sup.2]/d x 2 days as a 22-hour continuous infusion. Repeat every 2 weeks to a total of 6 months of perioperative therapy [14, 15]. CapeOX: oxaliplatin 130 mg/[m.sup.2] IV, day 1, capecitabine 1000 mg/[m.sup.2] twice daily, days 1-14 every 3 weeks. Repeat every 3 weeks to a total of 6 months of perioperative therapy .
2.3. Surgical Procedure. Procedures were performed by the same surgical team. Our team has experience with more than 3000 cases of laparoscopic colorectal surgeries since September, 2000 . Surgery was performed 6-8 weeks after the end of radiation. Laparoscopic rectal surgery was standardized in our center, as presented in Figure 1. TME was performed for middle and low rectal cancers, and partial TME with a distal margin of 5 cm was performed for high rectal cancers. The inferior mesenteric artery (IMA) was ligated at the level of the root to ensure a tension-free anastomosis, and IMA lymph nodes were dissected to the IMA just below the bifurcation of the left colic artery. Pelvic autonomic nerves were identified and preserved. After the dissection was completed, the rectum was transected with an endoscopic linear stapler. A 5-6 cm Pfannenstiel incision was made for specimen extraction and proximal transection. An end-to-end anastomosis was constructed using a circular stapler, and the donuts were checked. Air leak test was used to identify mechanically insufficient anastomosis. Generally, protective diverting ileostomy was performed in an effort to protect low rectal anastomosis, taking into considerations the general health of the patient, nutritional status, diabetes, the distance of the anastomosis from the anal verge, and the use of nCRT. Starting approximately 3 to 4 weeks after surgery, patients received adjuvant chemotherapy for 6 months. Two different chemotherapy regimens were used, including FOLFOX or CapeOX.
2.4. Follow-Up. Follow-up evaluations were performed every 3 months for the first 3 years, then every 6 months for the next 2 years, and annually thereafter. At each visit, a physical examination, serum carcinoembryonic antigen (CEA) test, chest X-ray or computed tomography (CT) scans, and abdominopelvic magnetic resonance imaging (MRI) or CT scans were performed. A colonoscopy was performed annually after surgery. Positron emission tomography (PET) examination was added when needed.
2.5. Definitions. Using the proposed International Obesity Task Force (IOTF) classifications for obesity in Asians, BMI cut-off points were used to categorize patients into two groups: nonobese (BMI < 25.0 kg/[m.sup.2]) and obese (BMI [greater than or equal to] 25.0 kg/[m.sup.2]) . CRM was measured using a microscopic ruler, and CRM involvement was defined as a microscopic tumor <1 mm from the circumferential or radial resection margins . Tumor regression levels were graded according to the Rectal Cancer Regression Grade (RCRG) method by Wheeler et al.  as follows: RCRG 1, sterilization or only microscopic foci of adenocarcinoma remaining, with marked fibrosis; RCRG 2, marked fibrosis but macroscopic disease present; RCRG 3, little or no fibrosis, with abundant macroscopic disease. Postoperative morbidity was defined as any complication occurring within 30 days after surgery and was graded according to the Clavien-Dindo classification . Major morbidity was defined as any event that required endoscopic, radiological, surgical reoperations or intensive care unit treatment (Clavien-Dindo grades III-IV) and minor morbidity as Clavien-Dindo grades I-II. Perioperative mortality was defined as any death either within 30 days after surgery or during the hospitalization period.
2.6. Statistical Analysis. Statistical analysis was performed using SPSS version 20.0 (SPSS INC., Chicago). The categorical variables were expressed as numbers with percentages and compared using a chi-square test or Fisher's exact test when appropriate. Normally distributed data were described as the means [+ or -] standard deviations and analyzed with Student's t-tests. Nonnormally distributed data were presented with medians and ranges and analyzed with the Mann-Whitney U test. Univariate and multivariate logistic analysis were performed to identify risk factors of postoperative complications. Overall survival (OS) was measured from the date of surgery to the date of death from any cause [24, 25]. Local recurrence was defined as any tumor relapse within the pelvis, perineum, or anastomosis as diagnosed by pathological examination. Distant metastasis was identified as evidence of a tumor in any other area diagnosed by imagining or pathological examinations. Survival outcomes were assessed using the Kaplan-Meier method and log-rank test. Statistical significance was defined as P < 0.05.
3.1. Study Population. A total of 312 LARC patients who underwent laTME after nCRT were included in our study (nonobese, 249; obese, 63). The median BMI of the nonobese patients was 21.7kg/[m.sup.2], significantly lower than 26.9kg/[m.sup.2] in the obese group (P <0.001). No significant differences were observed in clinical characteristics between two groups, as summarized in Table 1.
3.2. Technical Feasibility. Obese patients had significantly longer operative time (224.3 [+ or -] 38.8 min versus 207.9 [+ or -] 43.9 min, P = 0.004), as summarized in Table 2. A trend towards greater estimated blood loss was observed among obese patients (73.6 [+ or -] 59.1ml versus 63.2 [+ or -] 87.6 ml), but it was not statistically significant (P = 0.265). Conversion to open procedure occurred in 9 nonobese patients and 4 obese patients, and the difference was not significant (3.6% versus 6.3%, P = 0.332). Conversions in nonobese patients were due to severe intra-abdominal adhesions (three), abdominal bleeding (one), bowel injury (one), fixed tumor (two), and a narrow pelvis (two). The reasons for conversion in obese patients were severe intraabdominal adhesions (two) and a narrow pelvis (two).
3.3. Postoperative Recovery. No significant differences were found between two groups in terms of time to first flatus, time to faeces, time to off bed activities, time to liquid diet, and time to soft diet (P > 0.05). Similarly, postoperative hospital stay did not differ between two groups (P = 0.900).
3.4. Postoperative Complications. Postoperative morbidities were similar in both groups (nonobese versus obese, 23.3% versus 23.8%, P = 0.931), as shown in Table 2. Obese patients seemed to experience more anastomotic leakage (6.3% versus 5.2%, P = 0.724), ileus (7.9% versus 6.0%, P = 0.580), and wound infection (7.9% versus 4.0%, P = 0.194), but this trend was not significant. Regarding the severity and degree of postoperative morbidity, major and minor complication rates were comparable between both groups (P = 0.133, P = 0.540).
Univariate analysis showed that age (P = 0.040), American Society of Anesthesiologists (ASA) score (P = 0.002), surgical type (P <0.001), and diverting stoma (P = 0.002) were risk factors for postoperative complication (Table 3). Multivariate analysis demonstrated that higher ASA score (ASA 2: OR = 2.755, P = 0.012; ASA 3: OR =6.274, P = 0.036) and abdominoperineal resection (OR = 4.972, P < 0.001) were independently associated with postoperative complications, and diverting stoma was a protective factor for postoperative complications (OR = 0.527, P = 0.037).
3.5. Oncological Safety. The proximal and distal lengths of the resection specimen (nonobese versus obese: proximal: 14.9 [+ or -] 3.5 cm versus 14.8 [+ or -] 1.9 cm, distal: 3.2 [+ or -] 1.2 cm versus 3.0 [+ or -] 1.1cm) were not significantly different (P >0.05), as shown in Table 4. Positive CRM rates for obese and nonobese patients were 1.2% and 3.2%, but the difference was not significant. The number of lymph node retrieved was comparable for both groups (P = 0.107). With respect to the tumor response to nCRT, no differences were found among the two groups regarding pathological TNM stage, pCR, and rectal cancer regression grade (P >0.05).
With a median follow-up time of 55 months (ranging 20-102 months), no significant difference was found in the 5-year overall survival rate between the two groups (nonobese versus obese: 85.9% versus 77.4%; P = 0.904), as presented in Figure 2. The 5-year local recurrence rate (nonobese versus obese: 3.5% versus 3.9%; P = 0.207) was similar in the two groups. The 5-year distant metastasis rate was slightly higher in the obese group, but the difference was not significant (nonobese versus obese: 23.4% versus 29.4%; P = 0.110).
The present study is the first to compare the surgical outcomes of laTME after nCRT in relation to obesity, using the Asian definition (BMI [greater than or equal to] 25kg/[m.sup.2]). The result demonstrates that obesity does not increase surgical morbidity or mortality during laTME and does not jeopardize short- and long-term oncological outcomes.
During rectal resection after CRT, the downsizing and downstaging of large tumor can improve exposure of the surgical field in the narrow pelvic cavity; however, tissue edema and vascularity associated with nCRT may hamper dissection of the tissue [10, 26]. The technical complexity of laTME is exacerbated in obese patients due to poor exposure of the operation field, difficulties in dissection, mobilization and ligation, more operative time required, and difficulties in maneuvering instruments in a restricted intraabdominal space [3, 5, 27]. It remains unclear whether these negative factors are capable of counteracting the advantages of laparoscopic surgery. In a meta-analysis of 8 studies including 2181 rectal cancer patients, laparoscopic procedure was more difficult in obese patients, together with an increase in the conversion rate and operative time . When performing laTME after CRT, we often experienced difficulties in dissecting while recognizing a right plane of TME and were hampered by edema and exudates when utilizing ultrasonic dissectors, which contributed to a longer operative time. Obese patients did not suffer from increased estimated blood loss. The conversion rate in the current study (nonobese versus obese, 3.1% versus 6.3%) was comparable with 2.8% to 15.5% in the literature [29-31]. It was reported that tumor fixation, obesity, and intra-abdominal adhesions were the most common reasons for conversion during laparoscopic rectal resection . In our series, procedures were performed by the same surgical team, which has experience with more than 3000 cases of laparoscopic colorectal surgeries since September, 2000 . Our low conversion rate can be attributed to the high volume and extensive surgical experience of our specialized center. In our experience, laTME in obese patients with LARC after nCRT is feasible when performed by specialist surgeons.
In laparoscopic rectal surgery, there were some additional tricks in our center. The most important point was fully exposing the operation field. The patient was positioned at a 30-degree Trendelenburg and 15-degree right lateral tilt position. Gravity was utilized to handle the intestinal loops out of the operative field. Gauze was folded to protect the small bowel loops, especially when IMA high ligation was performed. We preferred to use fenestrated nontraumatic Babcock forceps to manipulate the bulky bowel mesentery, which was vulnerable to laceration and bleeding. In female patients, anterior exposure was achieved by hanging the uterus with a percutaneously inserted silk suture with a straight needle. Circumferential sharp dissection within the "holy plane" is fundamental to rectal cancer resection . In our experience, maintaining good and constant tension contributes to reach the extremes of the pelvis. Furthermore, the pelvic autonomic nerve preservation is improved laparoscopically because of a magnified view of laparoscopic surgery . Unfortunately, sexual and urinary functional data in our series were incomplete and thus could not be assessed in this study.
There is a concern regarding whether laparoscopic rectal resection can achieve adequate oncological clearance in obese patients. It was reported that higher BMI was an obstacle to perform proper lymph node dissection and the number of retrieved lymph nodes could be affected by obesity . Additionally, the most significant reduction of mean retrieved lymph node numbers in rectal cancer was observed in obese patients with a short specimen length . Nevertheless, considering the current recommendation of 12 lymph nodes or more for accurate staging , the average lymph nodes retrieved in the present study were acceptable, and no significant difference in specimen length was found between two groups. Additionally, significant prognostic factors in rectal cancer surgery, such as distal and circumferential resection margin involvement, were comparable, when compared with nonobese patients.
A phase 3 study (CAO/ARO/AIO-04), which integrated oxaliplatin into standard fluorouracil-based combined modality treatment, has reported that intensification of CRT was feasible and led to a higher pCR rate [14-16]. It has been noted that nCRT may result in significant morbidity, such as anastomotic leakage and wound infection [13, 37, 38]. Whether obesity will increase the risk of postoperative morbidity during laparoscopic resection after nCRT remains unanswered. In a recent meta-analysis, obese patients had a higher rate of minor complications after laparoscopic colorectal surgery, including ileus, wound infection, and respiratory events and comparable major complications, such as anastomotic leakage, which required surgical and endoscopic interventions . Our study did not demonstrate an increase in overall morbidity in obese patients compared with nonobese patients. Also, the individual complication rate, including anastomotic leakage, ileus, and wound infection, did not differ between the two groups. Previous study found male sex, obesity, and preoperative radiation to be associated with postoperative complications after laparoscopic surgery for rectal cancer [31, 39]. In the current study, no association between BMI and postoperative morbidity was identified. Multivariate analysis showed that higher ASA score and abdominoperineal resection were independently associated with postoperative complications. These results suggested that obesity does not affect surgical safety in laparoscopic rectal resection for LARC patients following nCRT.
Transanal total mesorectal excision (taTME), an emerging surgical technique, has been described as a good solution for a male, with a narrow pelvis, obese patient with rectal cancer [40, 41]. However, whether taTME could achieve the standard of TME in the medium rectal cancer and part of low rectal cancer remains controversial, when compared with conventional laTME . Additionally, comparable technical success of taTME might not be achieved in low-volume centers until this technique is fully accepted by surgeons .
There are several limitations in our study. First, because BMI is relatively lower in Asians than in non-Asians , obesity in this study was defined using IOTF classification for Asians (BMI [greater than or equal to] 25 kg/[m.sup.2]). Second, Asian populations have greater visceral adiposity, and the impact of visceral fat in the field of colorectal surgery has been discussed mainly in Asian populations. BMI may be an imperfect marker for visceral obesity. Unfortunately, due to the retrospective nature of our study, the impact of visceral fat was not evaluated. We intended to evaluate the impact of visceral fat on surgical outcome of laparoscopic TME in LARC patients following nCRT in further studies. Third, this study is based on a single institutional retrospective analysis and subject to an inherent selection bias. Another limitation is that we did not conduct subgroup analysis of underweight patients owing to an insufficient number of samples in our series. We intend to explore these questions in the coming future studies.
Obesity does not affect the surgical and oncological outcomes of laparoscopic rectal resection after nCRT. LaTME may be feasible and safe to obese patients with LARC after nCRT in a high-volume center with sufficient experience. Further studies are needed to confirm the above findings.
Conflicts of Interest
The authors declare that they have no competing interests.
Yanwu Sun performed the conception and design. Yanwu Sun and Pan Chi performed the acquisition and analysis. All authors performed the interpretation, drafting, and revision and approved the final manuscript.
This study was supported by the National Clinical Key Specialty Construction Project (General Surgery) of China (no. 2012-649).
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Yanwu Sun and Pan Chi
Department of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, Fujian, China
Correspondence should be addressed to Pan Chi; email@example.com
Received 11 May 2017; Accepted 23 August 2017; Published 14 September 2017
Academic Editor: Riccardo Casadei
Caption: FIGURE 1: Pictures from laparoscopic surgery in obese patients with locally advanced rectal cancer. (a) A medial to lateral dissection was performed, the IMA was skeletonized and ligated, the inferior mesenteric plexus was identified and protected; (b) the anterior space of rectum was well exposed, and the anterior layer of Denonvilliers' fascia was dissected below the seminal vesicle; (c) the left "holy plane" was well exposed, the left NVB and pelvic autonomic nerve were identified and protected; (d) the right "holy plane" was well exposed, the right NVB and pelvic autonomic nerve were identified and protected; (e) the specimen with an intact mesorectum fascia; (f) the tumor was downsized after nCRT (tumor size: pre-CRT 2.5 cm, post-CRT 1.5 cm) with a distal resection margin of more than 2 cm; IMA: inferior mesenteric artery; NVB: neurovascular bundle.
Caption: FIGURE 2: (a) Overall survival, (b) cumulative local recurrence, and (c) cumulative distant metastasis rate between nonobese and obese groups.
TABLE 1: Clinicopathological characteristics between nonobese and obese groups in locally advanced rectal cancer patients following nCRT. Characteristics BMI < 25 BMI [greater than P (n = 249) or equal to] 25 value (n = 63) Sex 0.085 Male 157 (63.1) 47 (74.6) Female 92 (36.9) 16 (25.4) Age (years) 54.9 [+ or -] 12.0 54.7 [+ or -] 9.1 0.861 BMI (kg/[m.sup.2]) 21.7 [+ or -] 2.2 26.9 [+ or -] 2.8 <0.001 ASA score 0.658 1 164 (65.9) 45 (71.4) 2 78 (31.3) 17 (27.0) 3 7 (2.8) 1 (1.6) Distance from 5.9 [+ or -] 2.1 5.9 [+ or -] 1.8 0.948 the anal verge (cm) Gross type 0.843 Expanding 56 (22.5) 16 (25.4) Ulcering 178 (71.5) 44 (69.8) Infiltrating 15 (6.0) 3 (4.8) Histopathology 0.100 Adenocarcinoma 227 (91.2) 53 (84.1) Mucinous or signet 22 (8.8) 10 (15.9) ring adenocarcinoma Tumor 0.196 differentiation Well or moderately 214 (85.9) 50 (79.4) differentiated Poorly 35 (14.1) 13 (20.6) differentiated and others (a) Clinical T stage 0.230 T3 57 (22.9) 19 (30.2) T4 192 (77.1) 44 (69.8) Clinical N stage 0.580 N0 15 (6.0) 5 (7.9) N+ 234 (94.0) 58 (92.1) Preoperative CEA 0.650 level (ng/ml) <5 216 (86.7) 56 (88.9) [greater than or 33 (13.3) 7(11.1) equal to] 5 Data are expressed as number (%) or as median [+ or -] standard deviation, where appropriate. (a) including mucinous and signet cell carcinoma. nCRT: neoadjuvant chemoradiotherapy; BMI: body mass index; ASA: American Society of Anesthesiology; CEA: carcinoembryonic antigen. TABLE 2: Perioperative outcomes between nonobese and obese groups in locally advanced rectal cancer patients following nCRT. Variables BMI < 25 (n = 249) Operative time (min) 207.9 [+ or -] 43.9 Estimated blood loss (ml) 63.2 [+ or -] 87.6 Conversion 9 (3.6) Surgical procedure Sphincter-preserving 222 (89.2) surgery Abdominoperineal resection 27 (10.8) Diverting stoma 127 (51.0) Postoperative hospital stay 9.0 [+ or -] 6.1 Time to flatus (days) 1.9 [+ or -] 0.9 Time to faeces (days) 3.1 [+ or -] 1.7 Time to off bed activities (days) 1.9 [+ or -] 0.8 Time to liquid diet (days) 1.9 [+ or -] 1.0 Time to soft diet (days) 4.5 [+ or -] 2.2 Overall morbidity 58 (23.3) Postoperative complications (a) Anastomotic leakage 13 (5.2) Ileus 15 (6.0) Wound infection 10 (4.0) Sepsis 3 (1.2) Acute urinary retention 5 (1.6) Respiratory complications 10 (4.0) Others (b) 9 (3.6) Reoperation 2 (0.8) Grade of morbidity Minor 46 (18.5) Major 25 (10.0) Variables BMI [greater P value than or equal to] 25 (n = 63) Operative time (min) 224.3 0.004 [+ or -] 38.8 Estimated blood loss (ml) 73.6 [+ or -] 59.1 0.265 Conversion 4 (6.3) 0.332 Surgical procedure 0.497 Sphincter-preserving 58 (92.1) surgery Abdominoperineal resection 5 (7.9) Diverting stoma 34 (54.0) 0.674 Postoperative hospital stay 8.9 [+ or -] 6.7 0.900 Time to flatus (days) 1.9 [+ or -] 0.7 0.751 Time to faeces (days) 2.9 [+ or -] 1.5 0.412 Time to off bed activities (days) 1.9 [+ or -] 0.9 0.829 Time to liquid diet (days) 1.8 [+ or -] 0.9 0.297 Time to soft diet (days) 4.3 [+ or -] 1.7 0.463 Overall morbidity 15 (23.8) 0.931 Postoperative complications (a) Anastomotic leakage 4 (6.3) 0.724 Ileus 5 (7.9) 0.580 Wound infection 5 (7.9) 0.194 Sepsis 1 (1.6) 0.809 Acute urinary retention 2 (3.2) 0.576 Respiratory complications 4 (6.3) 0.424 Others (b) 4 (6.3) 0.332 Reoperation 1 (1.6) 0.569 Grade of morbidity Minor 17 (27.0) 0.133 Major 8 (12.5) 0.540 (a) Some patients experienced more than one complication. (b) Including cardiovascular events, cerebrovascular events, deep vein thrombosis, and chyle leakage. Data are expressed as number (%) or as median [+ or -] standard deviation, where appropriate. nCRT: neoadjuvant chemoradiotherapy. TABLE 3: Univariate and multivariate analysis of perioperative complications for patients with locally advanced rectal cancer after nCRT. Variables Complication (-) n = 239 Age (year) 54. 1 [+ or -] 11.0 Gender Male 156 (65.3) Female 83 (34.7) BMI (kg/[m.sup.2]) <25 191 (79.9) [greater than 48 (20.1) or equal to] 25 ASA score 1 172 (72.0) 2 63 (26.4) 3 4(1.7) Previous laparotomy 25 (10.5) history Tumor distance from 6.0 [+ or -] 1.9 the anal verge (cm) Tumor diameter (cm) 2.9 [+ or -] 1.0 Radiation dose (cGy) 4869.8 [+ or -] 443.2 Interval to surgery (weeks) 8.0 [+ or -] 2.0 Surgical type Sphincter-preserving surgery 226 (94.6) Abdominoperineal resection 13 (5.4) Diverting stoma 135 (56.4) Conversion 10 (4.2) Operative time (min) 209.0 [+ or -] 41.1 Estimated blood loss (ml) 64.0 [+ or -] 88.3 Pathological TNM stage 0 40 (16.7) I 61 (25.5) II 72 (30.1) III 66 (27.6) Rectal cancer regression grade 1 126 (52.7) 2 91 (38.1) 3 22 (9.2) Variables Complication (+) Univariate n = 73 P value Age (year) 57.5 [+ or -] 12.5 0.040 Gender 0.529 Male 48 (65.8) Female 25 (34.2) BMI (kg/[m.sup.2]) 0.525 <25 58 (79.5) [greater than 15 (20.5) or equal to] 25 ASA score 0.002 1 37 (50.7) 2 32 (43.8) 3 4 (5.5) Previous laparotomy 7 (9.6) 0.829 history Tumor distance from 5.6 [+ or -] 2.2 0.129 the anal verge (cm) Tumor diameter (cm) 2.9 [+ or -] 1.1 0.491 Radiation dose (cGy) 4908.5 [+ or -] 336.5 0.426 Interval to surgery (weeks) 8.4 [+ or -] 2.4 0.229 Surgical type <0.001 Sphincter-preserving surgery 54 (74.0) Abdominoperineal resection 19 (26.0) Diverting stoma 26 (35.6) 0.002 Conversion 3 (4.1) 0.639 Operative time (min) 218.5 [+ or -] 49.6 0.143 Estimated blood loss (ml) 69.7 [+ or -] 60.1 0.606 Pathological TNM stage 0.299 0 18 (24.7) I 15 (20.5) II 17 (23.3) III 23 (31.5) Rectal cancer regression grade 0.967 1 39 (53.4) 2 28 (38.4) 3 6 (8.2) Variables OR Multivariate P 95% CI value Age (year) 0.268 0.963-1.030 0.136 Gender Male Female BMI (kg/[m.sup.2]) <25 [greater than or equal to] 25 ASA score 1 1 2 2.755 1.253-6.060 0.012 3 6.274 1.123-35.039 0.036 Previous laparotomy history Tumor distance from the anal verge (cm) Tumor diameter (cm) Radiation dose (cGy) Interval to surgery (weeks) Surgical type Sphincter-preserving surgery 1 Abdominoperineal resection 4.972 2.178-11.349 <0.001 Diverting stoma 0.527 0.289-0.963 0.037 Conversion Operative time (min) Estimated blood loss (ml) Pathological TNM stage 0 I II III Rectal cancer regression grade 1 2 3 Data are expressed as number (%) or as median [+ or -] standard deviation, where appropriate. OR: odds ratio; CI: confidential interval; BMI: body mass index; ASA: American Society of Anesthesiologists. including mucinous and signet cell carcinoma. TABLE 4: Oncological clearance between nonobese and obese groups in locally advanced rectal cancer patients after nCRT. Characteristics BMI < 25 BMI [greater than P or equal to] 25 (n = 249) (n = 63) value Length of resection margin (cm) Proximal 14.9 [+ or -] 3.5 14.8 [+ or -] 1.9 0.864 Distal 3.2 [+ or -] 1.2 3.0 [+ or -] 1.1 0.172 CRM involvement 3 (1.2) 2 (3.2) 0.266 Tumor clearance 0.382 R0 242 (97.2) 59 (93.7) R1 4 (1.6) 2 (3.2) R2 3 (1.2) 2 (3.2) No. of lymph node 12.7 [+ or -] 8.2 11.4 [+ or -] 4.8 0.107 retrieved Lymph node ratio * 0.08 (0-0.86) 0.04 (0-0.47) 0.278 ypUICC stages 0.617 0 48 (18.3) 10 (15.9) I 59 (23.7) 17 (27.0) II 68 (27.3) 21 (33.3) III 74 (29.7) 15 (23.8) Tumor grade 0.196 G1 + G2 214 (85.9) 50 (79.4) G3 + GX 35 (14.1) 13 (20.6) pCR 48 (19.3) 10 (15.9) 0.535 RCRG 0.221 I 137 (55.0) 28 (44.4) II 89 (35.7) 30 (47.6) III 23 (9.2) 5 (7.9) Data are expressed as number (%) or as median [+ or -] standard deviation, where appropriate. * Data are expressed as median (range) and analyzed with the Mann-Whitney U test. nCRT: neoadjuvant chemoradiotherapy; CRM: circumferential resection margin; pCR: pathological complete response; RCRG: rectal cancer regression grade: RCRG 1, sterilization or only microscopic foci of adenocarcinoma remaining, with marked fibrosis; RCRG 2, marked fibrosis but macroscopic disease present; RCRG 3, little or no fibrosis, with abundant macroscopic disease.
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|Title Annotation:||Clinical Study|
|Author:||Sun, Yanwu; Chi, Pan|
|Publication:||Gastroenterology Research and Practice|
|Date:||Jan 1, 2017|
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