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
INTR
ODUCTION
I
n the era of total mesorectal excision (TME) surgery, preoperative radiotherapy (RT) reduces local recurrence (LR) and can be adminis­tered either as long-course RT (LCRT) with a 5-uorouracil (5-FU)– based regimen or as short-course RT (SCRT). For patients with a positive circumferential resection margin (CRM) at TME, tumor downstaging is highly desirable. In these circumstances, SCRT is not as eective as LCRT in preventing LR. To reduce radiation-related toxicity, eld adjustments and new targeted radiation modalities should be explored.
Radiation therapy was initially introduced as part of the treatment regimen of rectal cancer to improve local control in conjunction with surgery for patients with locally advanced disease. During the past two decades, neoadjuvant (NA) therapy has evolved signicantly, not only through its application in serial randomized clinical trials (RCTs) but also as a result of advances in technology that include introduction of computerized imaging techniques. Currently, the treatment of patients with rectal cancer centers around a TME along with NA therapy. Locally advanced rectal cancers are those that are stage III and some that are stage II with extensive local tumor spread. Such patients are treated with similar strategies based on National Comprehensive Cancer Network recommendations (http://www.nc
cn.org/clinical.asp). However, in the era of modern tumor imaging,
rectal magnetic resonance imaging (MRI) in particular facilitates the precise estimation of involvement of the CRM, which is the most important factor predicting LR and systemic disease. e Mercury Trial investigators reported that for patients with a positive CRM on preoperative MRI, the risks of LR and systemic spread were signi­cantly higher than for patients with a negative CRM. 
Vuong,
e LR rate was 5% in the patients receiving NA SCRT and 12% in
 patients undergoing surgery alone (P <.001), demonstrating that selective postoperative CT-LCRT is not able to provide the same results as preoperative treatment.
It has been established that NA RT (either SCRT alone or CT­LCRT) provides signicantly better local control than does postop­erative CT-LCRT, and LR rates are signicantly improved in patients receiving NA SCRT. In this study, the benets of NA SCRT were observed at all tumor levels, including upper third tumors, and were signicant even for patients with specimens obtained within the mesorectal plane. us far no survival benet has been demonstrated for patients who received RT and underwent surgery with the TME technique. In the Dutch TME trial, NA SCRT had no eect on OS or cancer-specic survival when all randomized patients were included in the analyses. However, in patients with a negative CRM who under­went surgery, RT signicantly improved cancer-specic survival. Unfortunately, this benet was oset by an increase in other causes of death, resulting in an equal OS rate compared with the group that underwent surgery only. A subgroup analysis demonstrated that for patients with TNM stage III cancer who had a negative CRM, 10-year survival was 50% in the NA SCRT group versus 40% in the surgery­alone group (P = .032). In most studies, the LR rate was reduced from greater than 10% for patients treated with surgery only to 5% for patients treated with NA RT and surgery.
NA RT, in conjunction with TME, improves local control but does not improve OS. 
R
Aurélie Garant,
and Tamim Niazi
OLE OF CIRCUMFERENTIAL
RESECTION MARGIN
RADIO
urgery remains the cornerstone of rectal cancer treatment for locally
S advanced (T3/T4) tumors. To further improve local control (LC) in rectal cancer, NA RT has been added to surgical treatment. e ben­et of NA SCRT was rst shown by the Swedish Rectal Cancer Group in the pre-TME era. Aer a median follow-up of 5 years, the LR risk was 11% in the group that underwent radiation and 27% in the group that did not undergo radiation, and the overall survival (OS) rates were 58% and 48%, respectively. In spite of these excellent results, the role of RT was questioned aer the introduction of TME. In a Dutch TME study, the benet of SCRT followed by immediate TME was demonstrated, with a 10-year LR rate of 11% for patients treated with TME alone versus 5% for patients treated with SCRT followed by TME. In the MRC-CR07 study, which has a comparable design, patients with resectable rectal cancer were randomized between NA SCRT followed immediately by surgery versus surgery alone. e patients in the group that underwent surgery alone received post­operative chemotherapy (CT)-LCRT when the CRM was involved.
THERAPY TRIALS
I
n the Dutch TME trial, patients with a positive CRM who had not undergone RT had an LR rate of 23.3%, whereas those who received RT showed a drop in LR to 15.5% (P = .16). e MRC-CR07 trial showed an LR of 13.8% in patients receiving NA SCRT with 5 × 5 Gy and an LR of 20.7% in patients receiving postoperative CT-LCRT.
In patients with a positive CRM, NA SCRT is not as eective in
reducing LR. 
TIMODALITY TREATMENT
MUL APPROACHES
Several Northern European RCTs have demonstrated a signicant reduction in the LR rate aer SCRT. Optimal treatment for the dierent stages of rectal cancer and prioritization of treatment modal­ities are controversial. In Northern Europe, SCRT is the standard of care for most patients with stage II and III rectal cancer, whereas CT-LCRT is reserved for more advanced cases with a positive CRM. On the other hand, in America and southern Europe, most patients are treated with NA LCRT (LCRT, 45 to 50 Gy) in combination
141
142
CanCer of
reCtum: neo
the
adjuvant
therapy
ith CT. Furthermore, because the EORTC-22921 and FFCD-9203
w studies demonstrated that the addition of CT to preoperative LCRT enhances local control in locally advanced (T3/T4) tumors, with this nding recently conrmed by a recent Cochrane review, patients are now treated with CT-LCRT, followed by TME. 
RANDOMIZED TRIALS
COMPARING NEOADJUVANT SHORT­COURSE RADIOTHERAPY WITH CHEMOTHERAPY–LONG-COURSE RADIOTHERAPY
T
wo RCTs compared SCRT to CT-LCRT: a Polish trial, with 312 patients, and an Australian trial, with 326 patients. Both studies had a similar design, and sample size was calculated to demonstrate a dierence of 15% in the rate of sphincter preservation and 10% in LR, respectively. Both trials showed higher rates of early radiation toxicity in the CT-LCRT arm when compared with the SCRT group; grade III to IV acute toxicity rates were 18% versus 3% (P = .001) in the Polish trial and 28% versus 1.9% (P = .001) in the Australian study. In the Polish trial, the sphincter preservation rate did not dier between the groups, with 61% in the SCRT group and 58% in the CT-LCRT (P = .57). In this trial, the LR rate was slightly lower in the SCRT group than in the CT-LCRT group at 10.6% versus 15.6% (P = .21), whereas the opposite tendency was seen in the Australian study at 7.5% versus 4.4% (P = 0.24). In this latter trial, a dierence was observed in the group of tumors at or below 5 cm from the anal verge, with 6 of 48 patients in the SCRT arm versus 1 of 31 patients aer CT-LCRT (not statistically signicant). In the Polish study, severe late toxicity was observed in 10.1% of patients aer SCRT and in 7.1% of patients aer CT-LCRT compared with 5.8% of patients aer SCRT and 8.2% of patients aer CT-LCRT (P = .53) in the Australian trial (Table 29-1).
At present, because no consensus has been reached regarding the superiority of one radiation schedule over another, standard RT can be dened as either SCRT or CT-LCRT.
Five contemporary RCTs have been performed to test the oxali­platin-based CT regimen: STAR-0145, ACCORD 12/0405-Prodige 246, NSABP R-0447, CAO/ARO/AIO-0448, and the PETACC-6 trial, which compared standard NA 5-FU–based CT and LCRT (CT-RT) with oxaliplatin and 5-FU CT and NA LCRT. Patients with T3 or T4 rectal cancer were recruited sequentially. All but the CAO/ARO/AIO-0448 investigators reported higher morbidity without any improvement in early endpoints such as pathologic complete response (pCR) rate (Table 29-2). Therefore, it can be concluded that the 5-FU–based CT regimen remains standard when LCRT is used. 
RADIA
ME provides optimal tumor bed resection together with the peri-
T rectal nodes within the mesorectal fascia, but it does not address the pelvic nodes. e Dutch CKVO 95-04 study is unique in that it has an arm with more than 908 patients who were treated with TME alone. In this trial, the LR rate was 5% versus 11% aer a median follow-up of 12 years. Most of the recurrences were located below the S2-S3 interspace in patients with negative nodes and a negative CRM and were therefore consistent with the Swedish experience reporting on the level of S1-S2 interspace. e addition of RT reduced mostly the central recurrence.
In North America, the denition of clinical target volume for the treatment of rectal cancer has been based on consensus by a panel of experts to include coverage of the tumor bed, entire mesorectum, and perirectal, presacral, and internal iliac nodes, which is supported by the literature on patterns of LR. It is imperative to note that most of
TION TREATMENT VOLUMES
hese data were derived before the implementation of quality imaging
t such as pelvic MRI and the introduction of TME. 

RADIATION-RELATED TOXICITIES

A
lthough the value of RT is now well established, cumulative data on long-term toxicities associated with external beam RT (EBRT) raise concerns. In a meta-analysis, Camma etal reported an increased risk of septic complications in patients who had undergone RT compared with patients who had not undergone RT: 21% versus 15.2% (P .001). Moreover, the group that had undergone RT had an increased risk of overall complications: 21% versus 5.2% (P <.003). Postoper­ative adverse events were also higher in the RT group: 57.4% ver­sus 42.3% (P <.02). Finally, patients who underwent RT had a 15% higher risk of death from vascular or infectious causes compared with patients who had not undergone RT (P = .02). In 2007, Wong et al performed a Cochrane Database Systematic Review in which they assessed the eect of preoperative RT versus surgery alone for patients with rectal cancer and conrmed the benets of preoperative RT in reducing LC (hazard ratio [HR], 0.71; 95% condence interval [CI], 0.64-0.78), with borderline signicance with respect to cancer­specic and OS (HR, 0.93; 95% CI, 0.87-1.0). Late toxicities includ­ing pelvic fractures, venothrombosis events, intestinal obstruction, postoperative stula, cardiovascular death, bowel obstruction, anal sphincter, and sexual dysfunction were all increased.
us, if NA EBRT has been eective in decreasing LR, the number of patients requiring treatment will need to be weighed against the substantial morbidity risks and long-term adverse eects related to EBRT. Reducing treatment volumes to the level of S1/S2 might be the most eective and simple means of improving the therapeutic index. 
THER PERIOPERATIVE RADIATION
O TREATMENT OPTIONS
Boosting the Dose
ost patients with rectal cancer do well with current management,
M but less favorable cases with a positive CRM or recurrent tumors aer previous pelvic RT remain a clinical management challenge. In these situations, other radiation modalities, apart from EBRT, could be considered.
e likelihood of achieving tumor downstaging and/or R0 improves as a function of the dose. Wiltshire etal investigated the value of dose escalation with 5-FU CT in a phase II trial for patients with operable rectal cancer. e three dose levels were 40 Gy in 20 fractions, 46 Gy in 23 fractions, and 50 Gy in 25 fractions and included 46, 52, and 36 patients, respectively. e pCR rates were 15%, 23%, and 33% (P = .07), respectively, and the 2-year relapse-free survival rate was 72%, 90%, and 89%, respectively (P = .02). In the Lyon RCT study, R96-0256 NA RT alone using 39 Gy in 13 fractions was compared with the same RT with boost (85 Gy in 3 fractions) using contact x-ray for 88 patients with low rectal cancer (5 cm or less from the anal verge). A signicant improvement in pCR rate was seen in the contact x-ray boost arm (2% vs. 24%), along with a complete or near complete sterilization of the operative specimen (34% vs. 57%), resulting in a signicant increase in sphincter-preserving surgery in the boost group (44% vs. 76%, P = .04). At a median follow-up time of 152 months, although there was no dierence in OS and LC, the rate of colostomy-free survival was 37% versus 71% (P = .001) in favor of the boost arm. Using modern preoperative staging imaging, Jakobsen etal conducted a recent randomized controlled trial on T3/T4 tumors with dose escalation, comparing CT-LCRT delivering 50.4 Gy in 28 fractions versus a dose escalation to 60 Gy with the same regimen (50.4 Gy/28 fractions) and high-dose-rate endorectal brachytherapy (HDREBT) as a boost modality to deliver 10 Gy. A negative CRM rate
RECTAL AND PARARECTAL REGION
143
TABLE 29-1: Five-Year Local Control and Overall Survival Rate Results from Selected Randomized Clinical
Trials Using Preoperative 5-Fluorouracil–Based Chemotherapy and Long-Course/Short-Course Radiotherapy
RCT T/S Status No
erman trial: preop-
G
T1-T4 405 62 6 76 1.9
erative
. of Patients Median Age, yr LR Rate at 5 yr, % OS at 5 yr, % pCR Rate, %
German trial: postop-
T1-T4 394 62 13 74 0 (P < .001)
erative
Dutch trial TME alone S1-S4 908 66 10.9 63.5 0
Dutch trial NA SCRT +
S1-S4 897 65 5.6 64.2 0
TME
MRC-CR07 NA SCRT S1-S4 674 65 4.7 70.3 N/A
MRC-CR07 postopera-
S1-S4 676 65 11.5 67.9 N/A
tive
CT-LCRT
Polish trial SCRT T3-T4 155 60 9 67.2 (4 yr) 0.7
Polish trial CT-LCRT T3-T4 157 59 14.2 66.2 (4 yr) 16.1
(P N/A)
Trans Tasman SCRT T3 162 63 7.5 (3 yr) 74 0
Trans Tasman CT-
LCRT
T3 161 64 4.4 (3 yr) 70 12.4
(P N/A)
FFCD-9203 NA LCRT T3-4 367 63 16.5 67.9 3.6
FFCD-9203 NA CT-
T3-4 375 64 8.1 67.4 11.4 (P < .0001)
LCRT
-LCRT, Chemotherapy–long-course radiation therapy; LR, local recurrence; N/A, not available; NA, neoadjuvant; OS, overall survival; pCR, pathologic
CT complete response; RCT, randomized controlled trial; S, stage; SCRT, short-course radiation therapy; T, tumor; TME, total mesorectal excision.
ABLE 29-2: Tumor Pathologic Complete Response Rate from Published Randomized Clinical Trials Using
T
eoperative Oxaliplatin and 5-Fluorouracil–Based Chemotherapy and Long-Course Radiotherapy
Pr
RCT T/S Status No
CCORD 12: capecitabine + LCRT T2-T4 293 63 13.9
A
ACCORD 12: capecitabine + oxaliplatin +
T2-T4 291 61 19.2 (P = .09)
. of Patients Median Age, yr pCR rate, %
LCRT
STAR-01: 5-FU + LCRT T1-T4 377 63 16
STAR-01: 5-FU + oxaliplatin + LCRT T1-T4 362 62 16 (P = .904)
NSABP R-04: 5-FU + LCRT SII-SIII 804 N/A 19.1
NSABP R-04: 5-FU + oxaliplatin + LCRT SII-SIII 804 N/A 20.9 (P = .46)
CAO/ARO/AIO-04: 5-FU + LCRT T1-T4 623 63 13
CAO/ARO/AIO-04: 5-FU + oxaliplatin +
T1-T4 613 64 17 (P = .038)
LCRT
PETACC-6: capecitabine + LCRT T3-T4 547 N/A 11.3
PETACC-6: capecitabine + oxaliplatin +
T3-T4 547 N/A 13.3 (P = .31)
LCRT
5-FU, 5-Fl S, stage; T, tu mor.
uorouracil; LC RT, long-course radiation therapy; N/A, not available; pCR, pathologic complete response; RC T, randomized controlled trial;
144
CanCer of
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the
adjuvant
therapy
f 90% versus 99%, respectively, was observed (P = .03) for T3 tumors
o only in favor of the boost arm. 
INTRA
OPERATIVE RADIATION
THERAPY
Intraoperative radiation therapy (IORT) has been developed to further optimize local control, especially in this unfavorable tumor group (T3 or T4 or N+ and M0). Most studies have investigated IORT in combination with EBRT. is regimen delivers a higher radiation dose to the clinical target volume (CTV) at the time of surgical explo­ration with the advantage of accurate treatment delivery to the area of maximum concern, with adjacent normal structures displaced from the irradiation eld. Because it is administered at the time of surgery, IORT can only be delivered in a single dose, usually varying from 10 to 20 Gy, with the peripheral nerve dened as principal dose-limiting normal tissue. e benets of IORT as a means of delivering higher doses and improving LC have been reported, and some data were quite compelling despite being small retrospectives series as a result of the limited access to IORT equipment worldwide. e results are most benecial in patients undergoing complete resection. e IORT literature includes a large spectrum of tumors because the selection criteria varied from one center to another, making the evidence of benets dicult to ascertain. However, Dubois etal reported on a unique IORT RCT with 142 patients who had T3/T4 primary and/ or recurrent tumors in which EBRT using 40 Gy alone was compared with the same EBRT with an IORT boost (an additional 18 Gy). No disease-free survival benets (P = .7808) were identied from the addition of IORT. In this series, it is possible that the composite pop­ulation of T3 and T4 tumors contributed to these negative results. 
e. At the Jewish General Hospital (McGill University), in the less
dos favorable T4 tumors for which optimal tumor downstaging is highly desirable, IMRT was explored as a means of dose escalation with 60 Gy in 25 fractions during neoadjuvant treatment for 60 patients iden­tied by pelvic MRI as having a positive CRM. e R0 rate was 90% and a multivisceral resection rate was 29.5%. e overall acute toxic­ity prole was acceptable, with a distribution of a grade 3 or greater rate of 16.6% for GI, 18% for skin, and 10% for bone marrow.
e role of IMRT requires further demonstration of meaningful clinical benets in patient outcomes to further substantiate its routine application in the treatment of rectal cancer. 

HIGH-DOSE-RATE ENDORECTAL BRACHYTHERAPY

At the Jewish General Hospital (McGill University), image-guided HDREBT was developed as a highly targeted RT NA modality for persons with low T2 with a positive CRM and selected T3 rectal can­cer. e treatment consists of 26 Gy in four consecutive fractions pre­scribed to the deepest aspect of the tumor bed. It is performed in the ambulatory setting, without CT. Acute proctitis was the only toxicity observed with 1% grade 3 toxicity. In more than 500 patients treated, at a median follow-up time of 5 years, the LR rate was 4.5%, which compared favorably to NA CT-LCRT. In contrast to EBRT, HDREBT allows lower normal tissue exposure to radiation and is given without CT, and thus it is less costly and less toxic. An important observa­tion from this institutional experience remains the excellent LC rate despite the absence of an attempt to treat pelvic nodes and signi­cantly smaller MRI-based treatment volume when compared with the standard volume used with EBRT. 
INTENSITY
-MODULATED RADIATION
THERAPY
T was initially based on two-dimensional planning with standard
R treatment elds using anatomic bony landmarks. In the early 1990s, three-dimensional (3D) imaging radiation planning systems were introduced that permitted 3D denition of the target and normal tissues by using a thin-section computed tomography (CT) scan. A decade later, the new generation of linear accelerators were equipped with dynamic multileaf collimators (MLCs) capable of following the projection of the target as the accelerator gantry arcs around the patient. As a result of MLC delivery and accurate tumor localization of areas at risk, a safe dose to targets in a variety of areas has led to an improvement in local tumor control while reducing the radiation dose to normal structures. is technology has signicantly contrib­uted to the therapeutic index of RT of head and neck cancer. Subse­quently, intensity-modulated RT (IMRT) was tested for treatment of pelvic tumors, in particular anal canal cancer, and was shown to be of value in reducing skin and gastrointestinal (GI) toxicities. However, in rectal cancer, few preliminary studies have been performed, and the benet of IMRT has not been demonstrated. e acute toxicity data from the multi-institutional radiation therapy oncology group (RTOG)-0822 study was not signicantly convincing, with 51% of grade 2 or greater GI toxicity versus 58% (P = .31) in the conventional 3D-based RTOG-0247 study. Major dierences in the CTVs contrib­uted to inconsistent results. In gynecologic and anal canal cancer, external iliac and inguinal nodes are routinely included, whereas in rectal cancer, the CTV is posterior. Because radiation is currently administered in the context of an NA setting, it is unusual that small bowel loops are close, unlike in the era of adjuvant treatment. Con­sequently, even with use of the conventional 3D technique, the inci­dence of grave GI toxicity is unusual, especially if the CTV superior limit is adjusted to the S1-S2 level.
IMRT has interesting virtues and allows superior dose conforma-
tion within the CTV with the ability to limit normal tissue radiation
SUMMAR
n the era of TME, preoperative RT reduces LR and can be given either
I
Y
as LCRT with a 5-FU–based regimen or as SCRT. For patients with a positive CRM, tumor downstaging is highly desirable, and SCRT is not as eective to prevent LR. Contemporary patterns of recurrence suggest that it is possible to lower the upper limit of the treatment eld level. In an eort to reduce RT-related toxicity, eld adjustments along with exploration of new radiation options are desirable.
g g e
u
S
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intensity modulated radiation therapy (IMRT) and concurrent chemo­therapy for patients with advanced rectal cancer and magnetic resonant imaging (MRI) dened positive circumferential radial margins (CRM+). Int J Radiat Oncol Biol Phys. 2011;81(2): abstract 252.
Vuong T, Belliveau PJ, Michel RP, etal. Conformal preoperative endorectal
brachytherapy treatment for locally advanced rectal cancer: early results of a phase I/II study. Dis Colon Rectum. 2002;45:1486–1493. discussion 1493–1495.
Vuong T, Richard C, Niazi T, et al. High dose rate endorectal brachy-
therapy for patients with curable rectal cancer. Semin Colon Rect Surg. 2010;21:115–119.
Wiltshire KL, Ward IG, Swallow C, etal. Preoperative radiation with concur-
rent chemotherapy for resectable rectal cancer: eect of dose escalation on pathologic complete response, local recurrence-free survival, disease-free survival, and overall survival. Int J Radiat Oncol Biol Phys. 2006;64:709–
716.
Wong RKS, Tandan V, De Silva S, etal. Pre-operative radiotherapy and cura-
tive surgery for the management of localized rectal carcinoma. Cochrane Database Syst Rev. 2007;(2). CD002102.
C
   R:

O M
Kn
ut Magne Augestad, Benjamin Crawshaw, and Conor P. Delaney
INTR
ODUCTION
T
wo decades ago, surgery for rectal cancer was associated with local recurrence rates as high as 30% and poor long-term overall survival. However, during the past 10 years, survival has signicantly improved and the local recurrence rate has decreased. Several important fac­tors have contributed to this increase in overall survival for patients with rectal cancer, including new regimens for radiotherapy/che­motherapy, centralization of surgical practice, and multidisciplinary treatment. However, the most important single factor for increased survival has been the paradigm shi related to surgical technique.
In the early 1980s, attention was focused on the “holy plane” between the fascia propria of the rectum and the presacral fascia, and a dissection technique within this plane was proposed that would keep the mesorectal fascia intact. is total mesorectal excision dra­matically reduced local recurrence rates to 5% to 10% and increased the overall 5-year survival among patients with rectal cancer to about 71%. is signicant improvement in outcomes has led to widespread acceptance of total mesorectal excision as the standard technique for surgical treatment of rectal cancer.
e second technical issue aecting rectal cancer surgery has been the evolution of minimally invasive surgery. During the past decade, laparoscopic rectal cancer surgery has been associated with less post­operative pain, shorter hospital length of stay, and lower readmission rates. Laparoscopic surgery has increasingly been accepted as the standard approach to rectal cancer resection. Oncologic outcomes appear to be similar to those of open surgery, although data from some newer trials are pending.
is chapter outlines the principles of radical surgery for rectal cancer based on our experience and publications. Transanal excision is covered in a separate chapter. Important surgical decision-making choices will be highlighted, and a stepwise approach to the operative management of rectal cancer will be described. 
he IMV, allows well vascularized descending colon to reach the anus
t for anastomosis. e le ureter lies in the retroperitoneum, behind the sigmoid mesentery and lateral to the gonadal vessels. It can be identied posterolaterally as it crosses over the internal iliac artery and vein, posterior to Toldt’s fascia, to run around the pelvic side wall on its way to the bladder. e inferior hypogastric plexus lies behind the IMA at the pelvic brim, receiving the hypogastric nerves and con­tributing sympathetic bers to the pelvic plexus. e pelvic plexus is composed of these sympathetic bers and parasympathetic nerves from L2 and L3. It lies on the pelvic sidewall like a fan, buried below the endopelvic fascia and safe from harm except anteriorly, where the terminal bers pass to the seminal vesicles and prostate and penis, deep to Denonvilliers fascia. e risk of damage to this plexus is low, unless the endopelvic fascia or Denonvilliers fascia is breached dur­ing the pelvic dissection.
e mesorectum is a distinct anatomic unit composed of the rectum, perirectal fat, blood vessels, nerves, and lymphatic ves­sels. A layer of broareolar tissue called the mesorectal fascia surrounds the mesorectum, and dissection along the surface of mesorectal fascia is the key to successful surgical treatment of rectal cancer. Staying in the loose areolar tissue between the mesorectal and endopelvic fascia minimizes blood loss and protects the sur­rounding neurovascular anatomy. Anteriorly, the posterior vaginal venous system in females lies close, as do the seminal vesicles and prostate in men. ese structures can be a source of bleeding dur­ing dissection of the low rectum; however, if dissection stays on the rectal side of Denonvilliers fascia, no bleeding occurs at all. Because dissection anterior to Denonvilliers fascia increases bleeding and places the neurovascular bundles at risk, it is only performed for locally invasive anterior tumors. 
PRESURGIC
AL PATIENT PREPARATION
AND EVALUATION
KEY ANA
n intimate working knowledge of the anatomy of the rectum is a
A prerequisite to safe, eective proctectomy.
e inferior mesenteric artery (IMA) supplies blood to the descending colon, sigmoid colon, and upper rectum. It arises from the anterior aspect of the aorta and passes downward at the base of the sigmoid mesentery to the le iliac fossa. e IMA crosses the pel­vic brim and then descends within the mesorectum as the superior hemorrhoidal artery. e other branches of the IMA are the le colic artery, which is the most proximal branch, and the sigmoid arteries. e inferior mesenteric vein (IMV) runs parallel to the IMA but con­tinues cephalad to the origin of the IMA up to and behind the tail of the pancreas. High ligation of the IMA preserves the collateral arte­rial arcade to the le colon and, in combination with high ligation of
146
TOMIC POINTS
1. Preoperative cancer staging and planning for neoadjuvant radio­therapy/chemotherapy are performed in a multidisciplinary set­ting. e methods of staging and preoperative patient examina­tion are described in another chapter; however, we favor staging with pelvic magnetic resonance imaging (MRI) using a standard­ized rectal cancer protocol.
2. F
unctional sphincter status and defecation pattern: Preoperative
e
valuation of continence is an important predictor of postoperative results. Patients should be informed about expected postoperative changes in defecation and the possibility of soiling, especially with intersphincteric resection. e history should include assessment of preoperative fecal continence including nighttime soiling and incontinence relating to liquids, solids, or gas.
reoperative anesthesia and cardiac and pulmonary assess
3. P m
ent is performed, including blood typing and complete blood
-
unt. We tend to cross-match only patients with antibodies
co or those undergoing extended resections, because transfusion rates are low.
reoperative bowel preparation: We use mechanical bowel prepa
4. P ra
tion for patients undergoing rectal cancer surgery, especially
when a diversion procedure will be used.
5. r
ombosis prevention: Subcutaneous low-dose molecular hepa
r
in is administered prior to the induction of anesthesia, in con-
junction with use of pneumatic compression devices.
ntibiotics: For patients undergoing colorectal resection, we use
6. A
mbination of oral neomycin and metronidazole, as well as in-
a co travenous antibiotic prophylaxis against both anaerobes and aer­obes, which is not continued aer surgery.
7. 
e duration of preoperative fasting should be 2 hours for liquids
a
nd 6 hours for solids. Patients undergo carbohydrate loading
preoperatively.
8. Marking for patients requiring a permanent or temporary ostomy
s performed preoperatively. 
i
PREOPERA
S
urgery is planned aer careful review of preoperative imaging. For most cases, review by a multidisciplinary team is required. Any tumor extension seen on the preoperative and prechemotherapy/ radiotherapy MRI is an indication for neoadjuvant therapy and may require surgery outside the total mesorectal excision (TME) plane.
Deciding Betw
TIVE DECISION MAKING
een an Open or Laparoscopic
Approach
A l
aparoscopic approach follows the same oncologic principles as an open surgical procedure. Patients who have a locally advanced tumor with unquestionable radiologic signs of neighboring organ invasion generally undergo an open procedure. An open approach may be considered for certain other patients with extensive prior abdominal surgery (such as a previous cystectomy or prostatectomy), particu­larly for obese patients. However, obesity is very rarely an indication for open surgery in women. In men with a body mass index greater than 40, an initial laparoscopy is performed and a nal decision is made about whether to proceed laparoscopically. It is very challeng­ing to perform laparoscopic procedures for men with a body mass index greater than 50. 
Should a Sta
pled or Hand-Sewn Restorative
Procedure Be Performed?
F
or rectal cancers with an inferior border more than 5 cm from the anal verge, low anterior resection (LAR) and primary anastomosis generally can be used. Anastomosis also may be suitable for patients with lower tumors, depending on the distance between the distal part of the tumor and the dentate line using the preradiation measure­ment. If the tumor is within 2 cm of the dentate line, a stapled anasto­mosis is generally not possible, particularly in obese males who may have a long anal canal and in whom it is dicult to place a transverse stapler close to the dentate line. For these lesions, a transanal inter­sphincteric dissection is performed with a hand-sewn anastomosis. Abdominoperineal resection of the anus and rectum is indicated in patients with preexisting or likely postoperative incontinence or invasion of the anal sphincters or the pelvic oor. When the pelvic oor is invaded, an extralevator dissection is routinely performed. Inexperience with low rectal dissection, intersphincteric dissection, and hand-sewn anastomosis, or with radical perineal dissection, is an indication for referral of the patient to a surgeon and hospital with the necessary expertise. 
RECTAL AND PARARECTAL REGION
SURGIC
-
Total Mesorectal Excision
TME is performed by sharp dissection within the plane that sepa-
-
rates the visceral from the parietal layers of the perirectal pelvic fascia, enabling radical removal of the rectum with its surrounding mesorectum intact. e intent of TME is to remove completely the mesenteric lymph nodes and any nodules of cancer that are pres­ent within the mesorectum but are contained by the fascia propria. TME is based on embryology and anatomy and the concept that cancer spread will stay conned within the embryologic mesorec­tal envelope during most stages of the disease. TME achieves a radical resection along avascular planes without compromising bladder or sexual function. If the tumor approaches or breaches the mesorectal fascia, neoadjuvant chemoradiation is indicated, and the resection should include the aected neighboring organs where possible, which may mean taking nerves, ureters, the blad­der, the prostate, the uterus or vagina, and, in very rare cases, even the sacrum or iliac vessels. e goal is complete removal with negative margins. 
AL PRINCIPLES
Ligation of the Inferior Mesenteric Artery
e level of ligation of the IMA has been debated. A recent inter-
 national survey showed that 69% of rectal cancer surgeons perform high ligation of the IMA. Some evidence indicates that a high ligation of the IMA improves overall survival. We perform a high ligation of the IMA (proximal to the le colic artery), resulting in a D3 lymph node dissection. A high ligation of the IMA is important in achiev­ing a tension-free, well-vascularized colorectal or coloanal anastomo­sis, because when the IMV is ligated close to the tail of the pancreas, mobility of the descending colon is improved. 
Distal Resection Margins
e principal goal in surgical treatment of rectal cancer is to achieve an R0 resection. It is important that cancer-free margins be achieved both circumferentially and distally. Perforation of the tumor or of a rectal segment close to the tumor increases local recurrence threefold. Special care must be taken when dissecting in the perianal area during abdominoperineal resection (APR). When a tumor is located in the upper part of rectum, there is no need to remove the entire mesorectum, and a partial mesorectal excision can be performed. A clear 5-cm distal resection margin (of both rectum and mesorectum) is important when resecting upper and mid rectal cancers, because lymph node metastases can be found in the mesentery distal to the cancer. In persons with low rectal cancers, when the entire mesorectum is removed, a distal resection margin of 1 cm is adequate. 
Choice of Anastomotic Configuration
lorectal or coloanal anastomosis may be performed in several ways.
A co A coloanal anastomosis can be end to end or side to end, with a 6-cm­long coloanal J pouch or a coloplasty. Creation of a J-pouch above a coloanal anastomosis will improve functional results for the rst 2 years, compared with coloplasty or straight anastomosis. is option is per­formed for patients in whom a J pouch can both reach the pelvis and can t. Although a side-to-end anastomosis is less well studied, it appears that the functional results may be equivalent to a J pouch. An end-to­end reconstruction is generally performed when the anastomosis is hand sewn or a pouch or side-to-end anastomosis will not t. 
147
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Drainage
hether routine drainage of the pelvis reduces the frequency of
W anastomotic leakage aer LAR is unclear. We do not routinely use drains. 
Div
erting Stoma
A di
verting ileostomy helps reduce the clinical manifestations of anastomotic leak. Moreover, in two recent meta-analyses, a divert­ing stoma was shown to reduce the frequency of anastomotic leakage and the need for a second surgery. We recommend use of a diverting stoma when the anastomosis is lower than 7 cm from the anal verge, in very elderly or frail patients who might not tolerate a leak, and in patients who have undergone preoperative chemoradiation. We per­form diversion with a loop ileostomy, which is used as the specimen extraction site in laparoscopic cases. 
KEY STEPS OF SURGIC
AL
PROCEDURES
Lo
w Anterior Resection
C
ases involving LAR are generally performed laparoscopically. e
setup we perform is identical for laparoscopic and open cases.
Positioning and Equipment
e patient is positioned on a beanbag to achieve a steep Tren­delenburg position. e patient’s legs are placed in stirrups, and the perineum should be at or below the break of the table. Straps are used rarely and only for obese patients whose abdominal pannus may op to one side or the other during lateral rotation. An oro­gastric tube and Foley catheter are inserted. For laparoscopic cases, we prefer using atraumatic 5-mm bowel graspers, which also can be used as pelvic retractors. Dissection is performed with scissors cautery, but hook cautery may be required, especially at the right lower pelvic sidewall to avoid electrical short circuiting. Energy­based devices are not usually required because the dissection plane in the pelvis is avascular, but they are used to divide the primary vessels, based on data from our randomized trials. We do not use hand-assist and robotic devices. 
Trocar Placement
A 10-mm open cutdown is made for the camera trocar in the umbi­licus, and a 12-mm port is placed in the right lower quadrant. For higher anterior resections, this port is usually placed 2 to 3 cm medial and superior to anterior superior iliac spine, but when performing a low pelvic dissection, the right side of the pelvic brim limits access to the low pelvis, particularly in tall men. For this reason, the right lower quadrant trocar is moved medially in those patients. When an ileostomy is planned, the site is used for a trocar except for patients who have such a high body mass index that the stoma site has been marked in the right upper quadrant. Further 5-mm trocars are placed in the right upper and le lower quadrants. 
Exposure of the Operating Field
e abdominal cavity is inspected for metastatic or other concomi­tant disease. e patient is placed in the Trendelenburg position and tilted to the right. e greater omentum is placed in the upper abdominal cavity, and the loops of the small intestine are carefully moved upward to expose the retroperitoneum from the pelvis up to the ligament of Treitz. In obese patients, a 5-mm grasper may be
required through an additional right upper quadrant trocar to help keep the small bowel out of the operating eld. A medial-to-lateral or lateral-to-medial approach is chosen according to the preference of the surgeon; both approaches should be mastered. Toldt fascia, the correct dissection plane, is most easily found with the medial-to-lat­eral approach as described in the next section. 
Identification of Inferior Mesenteric Vessels and Left Ureter
e sigmoid colon should be lied toward the anterior abdominal wall to visualize the contours of the IMA pedicle at the level of the pelvic inlet. e peritoneum is incised beneath the IMA groove. Care must be taken to preserve the hypogastric nerve plexus by staying anterior to the Toldt fascia. e dissection plane should display the posterior surface of the capsule of the IMA, entering into the pel­vis in the avascular presacral space. Carbon dioxide rushes into this space, clearly demonstrating the planes, which keeps the hypogastric nerves in a posterior position and the ureter in a posterolateral posi­tion, safe from injury. If smooth fascial surfaces are not seen or if the le ureter cannot be found, the dissection may be too deep in the retroperitoneum. If any uncertainty exists about plane of dissection, a lateral-to-medial approach can be performed. Starting slightly distal to the sacral promontory usually helps identify the correct plane. In very obese patients (particularly males) and some others, the plane is not easily seen. Before compromising oncologic planes or potentially damaging any structures, a lateral approach is performed and the lat­eral side of the mesentery is followed and dissected until the presacral space is entered. When using an open approach, a lateral-to-medial approach is preferred. e remainder of the technique is performed using 5-mm laparoscopic instruments or an open approach, with no procedural dierences. 
Division of the Vessels and Splenic Flexure Mobilization
e dissection continues on the posterior surface of the “mesorectal package,” up toward the origin of the IMA. A high ligation—that is, division above the le colic artery—is performed. e laparoscopic vascular division may be performed with an endovascular stapler, with clips, or with a laparoscopic electromechanical device, or if an open procedure is used, it may be performed with absorbable ties. For the IMV, the dissection continues proximally, and the peritoneum is incised along its right side up to the ligament of Treitz. e IMV is divided at this level to ensure optimal mobilization of the le colon. With gentle dissection, the le mesocolon can easily be lied o the retroperitoneum from a medial approach. is dissection continues laterally until the lateral attachments are reached. Finally, the le colic artery is divided o the IMA, proximal to its bifurcation, to preserve collateral ow. e lateral side of the colon is then visualized and the remaining peritoneal attachment is divided with cautery scissors. e splenocolic and gastrocolic ligaments are divided with scissors cau­tery, mobilizing the splenic exure as far medially as needed to avoid tension on the anastomosis. 
Mobilization and Division of the Rectum
A 5-mm grasper is used to elevate the uterus or bladder, optimizing access to the pelvis. In some cases the uterus can be suspended from the anterior abdominal wall by a suture passed through it on a Keith needle.
e initial posterior dissection has already been performed while mobilizing and dening the IMA. Now the right lateral mesorectal peritoneum is incised by cautery, exposing the avascular loose con­nective tissue around the mesorectal fascia, which is then dissected down to the pelvic oor. e key to this dissection is having adequate upward traction while drawing the mesorectum away from the pel­vic sidewall, which keeps the loose areolar tissue demonstrated, and it becomes the line of dissection. e mid pelvic dissection on the
ight and le sides can be where the plane is most dicult to see, and
r
reat attention must be directed toward staying in the plane, thereby
g protecting the “erigent pillars” and surrounding anatomy. A useful trick can be to start the anterior dissection and then work back, join­ing this with the posterior dissection. By alternately dissecting pos­teriorly, laterally, and anteriorly, adequate traction can be maintained on the least dissected side to display the planes. Dissection continues down to the upper anal canal, at which stage the mesorectum has tapered and thinned to almost nothing. It is crucial to avoid coning into the mesorectum below the level of the tumor, as well as to avoid going too laterally, thereby damaging the pelvic parasympathetic gan­glia close to the anterolateral surface of the mesorectum. e ante­rior incision is made a few millimeters anterior to the apex of the pouch of Douglas, allowing the plane between Denonvilliers fascia and the mesorectum to be displayed easily. Complete hemostasis can be maintained during the entire dissection, and the entire dissection is oen performed with only 1 or 2 mL of blood loss.
e exact distal margin of the tumor must be veried before the distal line of resection can be determined. If there is any doubt, a rigid proctoscopy should be performed intraoperatively. If the veri­ed correct distal resection site is in the upper or mid rectum, a tun­nel is made between the posterior rectal wall and the mesorectum, using a 5-mm dissector or an atraumatic grasper. For low transection at the anorectal junction, the stapler can be immediately applied to the bare bowel. In open cases this maneuver is performed with a PI­type stapler, and for laparoscopic cases, it is performed with an Endo GIA–type device. More than one ring is sometimes required, and it is important to have a straight and smooth nal distal staple line. To place the laparoscopic stapler, the rectum may be drawn to the le, opening the angle to insert the stapler low on the right side. If this maneuver does not create enough space, pressure can be applied to the perineum to elevate the anal canal and pelvic oor. 
Exteriorization of the Specimen
For upper rectal cancers not requiring a temporary stoma, a 4- to 6-cm le lower quadrant incision is made through the 5-mm port site. e exteriorization of the specimen should always be performed through a wound protector to reduce the risk of tumor implantation. e specimen is removed to a nearby table and examined to conrm an adequate distal margin and document the completeness of the mesorectal specimen.
For lower tumors, the specimen is removed through the tempo­rary ileostomy site, extending it into a “keyhole” incision if necessary. Aer returning the J pouch to the abdomen, any ostomy site exten­sion is closed with absorbable sutures, and the port is reinserted for anastomosis. 
Creation of the Anastomosis
When performing a stapled coloanal or low colorectal anastomosis, a 6-cm colonic J pouch is favored and made with a single ring of a linear stapler. is option is possible when the J pouch can t into the pelvis and when there is enough reach. e open end of the colon with the anvil tied in place is delivered into the abdominal cavity and the wound is closed or the wound protector is twisted and clamped before the abdominal cavity is reinsuated. e colonic mesentery must be oriented to avoid twisting. e circular stapler is inserted through the anal opening and carefully maneuvered up to the rectal remnant resection line. e anastomosis is made under direct vision. A side-to-end anastomosis is less well studied but appears to be an equally eective option that is becoming a popular alternative. 
Desufflation and Closure of Trocar Incisions
e abdominal cavity should be desuated through open trocars. e wound made for specimen extraction is closed in two layers. All trocar incisions larger than 5 mm are closed with fascial sutures. Placement of pelvic drains is usually not necessary. 
RECTAL AND PARARECTAL REGION
149
Abdominoperineal Resection
AP
Rs are usually performed by laparoscopic TME, division of the sigmoid, creation of an end colostomy, and use of a “cylindrical” peri­neal resection. We tend to use a high lithotomy position and reserve the eort of changing to a prone position for patients who have anal tumors that extend further posteriorly and cannot be seen well in lithotomy. APR is used for low tumors, when a restorative resection cannot be performed because of invasion of the anal canal, the anal sphincters, or the pelvic oor. Care is required when removing these low tumors because historically there is an increased tendency for tumor perforation during dissection. In addition, R1 resections are more common with APR compared with LAR. Keeping the pelvic dissection wide on the levators is important and is increasingly rec­ognized as helping to lower local recurrence rates.
Closure of the Anal Opening
e rst step of an APR is closure of the anus with a 2-0 nylon suture. Long thread ends are kept to help with traction during the perianal dissection. In laparoscopic cases we do not perform this step until we go down to perform the perineal portion, to enable digital examina­tion during the pelvic dissection. Steps 2 to 6 follow the same surgical principles as described for LAR:
2. P
ositioning, equipment and trocar placement
3. E
xposure of the operating eld
4. I
dentication of le ureter
5. Identication and division of the IMA
dentication and division of the IMV
6. I
e mesosigmoid and its lateral attachments are mobilized suf­ciently to give adequate length to the colonic stoma. It is not usually necessary to take down the splenic exure. 
Mobilization of the Rectum
Mobilization of the rectum is similar to the technique described for LAR. It is important to stop the dissection at the level of the coccyg­eus posteriorly. e anterior dissection can continue distally as far as possible, which facilitates the dissection from below. 
Proximal Division of the Left Colon
e level of division of the le colon is selected to secure a healthy and well-functioning stoma. e mesocolon is divided, and then the colon is divided with a laparoscopic linear stapler. e proximal divi­sion is performed before the perineal dissection from below is com­pleted because the pneumoperitoneum disappears at the time the perineal dissection reaches the abdominal cavity. 
Perineal Dissection and Exteriorization
An oval incision is made around the closed anus with diathermy. e dis­section plane should be outside the external anal sphincter. If necessary, the puborectalis muscle or even the coccygeus should be removed with the specimen to secure a safe resection margin. e most technically demanding dissection is anterior, which is why the dissection should go as low as possible during the abdominal dissection. e posterior vaginal wall in women and the urethra in men must not be injured. However, when the vagina is invaded by tumor, a posterior vaginectomy must be performed. Once the perineal dissection is completed circumferentially, the specimen can be removed through the perineal opening. 
Closure of Pelvic Wound and Trocar Incisions and Creation of the Colostomy
e perineal opening is rinsed with warmed saline solution. Pelvic and perineal hemostasis is secured before the wound is closed in layers.
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nlike some surgeons, we do not favor the use of mesh. All trocar inci-
U sions larger than 5 mm are sutured at the fascial level. e le lower quadrant trocar incision is excised and a colostomy aperture is cre­ated. e colostomy is sutured with absorbable sutures. Vertical rectus abdominis myocutaneous aps are reserved for cases with a very wide perineal resection, such as a large or recurrent anal cancer. 
VIC EXENTERATION
PEL
Surgical Appr
s dened by the Beyond TME Collaborative (see suggested reading),
A an exenteration entails a pelvic dissection beyond the fascia propria. It involves the removal of some or all of the pelvic organs, including the bladder, prostate, seminal vesicles, urethra, vagina, uterus, part of the sacrum, and/or the lateral pelvic vasculature. 
Assessment Bef
ptimizing the patient’s preoperative function before multivisceral
O resection is important to minimize perioperative complications. A preoperative multidisciplinary team assessment is mandatory. For­mal cardiopulmonary testing assesses tness and identies areas for potential improvement. General preoperative surgical principles include perioperative stoma counseling/marking, discretionary ure­teric stenting, the availability of hemostatic agents during pelvic dis­section, and intensive postoperative monitoring. 
Signs of Ir
S
igns of a nonresectable cancer are debated. e Beyond TME Col­laborative recommends that encasement of external or common iliac vessels are a relative contraindication. Streamlined referral pathways should exist to allow all patients equal access to centers with high expertise in pelvic exentration. 
oaches
ore Exenteration
resectability
ysterectomy, bilateral salpingo-oophorectomy, and a vaginectomy
h with or without preservation of the anterior vaginal wall. When the bladder is involved, a partial cystectomy may be carried out, although trigone involvement requires a total cystectomy with uri­nary diversion. 
Central Recur
solated central recurrences have the best prognosis of all pelvic
I recurrences. Abdominoperineal excision can be performed, or a restorative anterior resection can be performed if the tumor is suf­ciently high, although planes are oen distorted and dissection is outside of the conventional TME plane. 
der Reconstruction
Blad
e role of bladder reconstruction instead of cystectomy and urinary
 diversion is unresolved. An intestinal neobladder may be formed if urethra and its sphincters are preserved. e risk of stulation is however high, especially with a concomitant low rectal anastomosis. Another option is to make a continent catheterizable reservoir in the upper abdomen. e functional results of these reservoirs are usually good, with up to a 98% rate of continence. 
erineal Reconstruction
P
urgeons who are experienced in the use of free-ap rotations or
S transfer should perform reconstruction of perineal defects. Com­monly used reconstruction techniques include the myocutaneous oblique or vertical rectus abdominis muscle (VRAM) ap, gracilis muscle ap, gluteal rotation ap, inferior gluteal artery perforator ap, free ap, or biologic gra with omentoplasty. ere is no estab­lished evidence as to which of these techniques is superior; however, we generally favor a VRAM, which provides bulky healthy muscle with overlying skin that nicely lls the pelvis. A heavily irradiated eld is associated with an increased complication rate. 
rence
ectomy
Sacr
R0 a
bdominosacral resection for primary rectal cancer beyond total mesorectal planes and locally recurrent rectal cancer prolongs sur­vival, has an acceptable postoperative morbidity prole, and is associ­ated with acceptable quality of life. Although involvement of S1 or S2 was earlier considered a contraindication to surgery, with appropriate surgical expertise, there may be a role for resection in highly selected patients. A sacrectomy distal to S2 is a major procedure but is man­ageable with experience and a supportive multidisciplinary team. 
elvic Sidewall Disease
P
ecurrent cancer in the pelvic sidewall is associated with reduced rate
A r of R0 resections, especially when the iliac vessels or ureters are involved. Strategies that are likely to improve the R0 resection rate include an anatomical dissection of the lymphoid tissues around the nerves and vessels, targeted radiation, and en bloc removal of iliac vessels. ereaf­ter a reconstruction must be performed with embolization and/or dis­section of internal iliac vessels and necessary bony resections. 
Anterior Compar
hen only the vagina is involved, a posterior exenteration is pos-
W sible. is means surgical resection of the rectum, anus, a total
tment/Urogenital Disease
OUTCOMES:
SURVIVAL AND LOCAL
RECURRENCE
e improved management of patients with primary rectal cancer,
 including the adoption of TME and neoadjuvant chemoradiation, has substantially reduced the proportion of patients in whom local recur­rence develops from 31% to 9% and improved the survival rate from 55% to 69%. However, fewer data are available for the application of laparoscopy for rectal cancer. Several single-institution reports support the feasibility and equivalent long-term outcomes of lapa­roscopic LAR, and the Conventional versus Laparoscopic-Assisted Surgery in Colorectal Cancer (CLASICC) study provides the highest level of evidence to date. e 5-year local recurrence rate for LAR was
9.4% for laparoscopy and 7.6% for open surgery (P = .740). Overall, the distant recurrence rate in 111 cases at 5 years was 20.9%. No sig-
21%; open, 20.6%; P = .820). Overall survival was also equivalent for laparoscopic and open resection of rectal cancer (laparoscopic,
60.3%; open, 52.9%; P = .132). is nding suggests that no dier­ence exists in overall survival at 5 years between treatment arms for any stage of rectal cancer. In the ongoing COlorectal cancer Laparo­scopic or Open Resection (COLOR II) trial, preliminary data show that in selected patients with rectal cancer treated by skilled surgeons, laparoscopic surgery can result in similar complication rates, similar resection margins, and equivalent completeness of resection when compared with open surgery. In the laparoscopic group, bowel func­tion returned sooner and hospital stay was shorter.