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410 J.E. Efron and J.J. Nogueras
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37. Quirke P, Durdey P, Dixon MF, Williams NS. Local recurrence of rectal adenocarcinoma due to inadequate surgical resection: histopathological study of lateral tumor spread and surgical exci­sion. Lancet 1986;2:996–999.
38. Adam IJ, Mohamdee MO, et al. Role of circumferential margin involvement in the local recurrence of rectal cancer. Lancet 1994;344:707–711.
39. Hall NR, Finan PJ, et al. Circumferential margin involvement after mesorectal excision of rectal cancer with curative intent: predictor of survival but not local recurrence? Dis Colon Rectum 1998;41(8):979–983.
40. Nagtegaal ID, Marijnen CA, et al. Circumferential margin involvement is still an important predictor of local recurrence in rectal carcinoma: not one millimeter but two millimeters is the limit. Am J Surg Pathol 2002;26(3):350–357.
41. Marijnen CA, Nagtegaal ID, et al. Radiotherapy does not com­pensate for positive resection margins in rectal cancer patients: report of a multicenter randomized trial. Int J Radiat Oncol Biol Phys 2003;55(5):1311–1320.
42. Beets-Tan RG. MRI in rectal cancer: the T stage and circumfer­ential resection margin. Colorectal Dis 2003;5(5):392–395.
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44. Brown G, Daniels IR. Preoperative staging of rectal cancer: the MERCURY research project. Recent Results Cancer Res 2005; 165:58–74.
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49. Jochem RJ, Reading CC, Dozois RR, et al. Endorectal sono­graphic staging of rectal carcinoma. Mayo Clinic Proc 1990;65: 1571–1577.
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51. Orrom WJ, Wong WD, Rothenberger DA, et al. Endorectal ultra­sound in the preoperative staging of rectal tumors: a learning experience. Dis Colon Rectum 1990;33:654–659.
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30
Surgical Treatment of Rectal Cancer
Ronald Bleday and Julio Garcia-Aguilar
Approximately 42,000 patients each year are diagnosed with rectal cancer in the United States. Approximately 8500 die of this disease. Despite remarkable recent advances in new oncologic agents for the treatment of colon and rectal cancer, cure is almost never achieved without surgical resection. However, the current management of rectal cancer is now more varied and complex because of the new approaches with multimodality therapy and the refinements in surgical tech­niques. For example, small distal rectal cancers with minimal invasion can be treated with a local excision with or without adjuvant therapy. More proximal or more invasive tumors require a “radical” resection. The two most common pro­cedures are the low anterior resection (LAR) and the abdominoperineal resection (APR). Extended resections are occasionally required for patients with cancers that invade or adhere to adjoining structures such as the sacrum, pelvic sidewalls, prostate, or bladder.
This Chapter discusses the surgical management of rectal cancer including a basic review of the preoperative evaluation and how it pertains to surgical planning, the preoperative preparation, the surgical procedures, the biology of rectal cancer as it relates to surgery, the issue of margins, and the technical nuances that need to be appreciated for a successful resection.
Evaluation of the Patient with Rectal Cancer
History
The patient with rectal cancer usually presents to the sur­geon after a definitive endoscopic diagnosis. The patient’s initial complaint may have been rectal bleeding, a change in bowel habits, or a sense of rectal pressure. However, with the increase in surveillance colonoscopy, many patients are completely asymptomatic on presentation. During the initial history, the surgeon should ask about certain symptoms
because it will aid in selecting the best therapy for the patient. For example, tenesmus (the constant sensation of needing to move the bowels) is often indicative of a large cancer. Constant anal pain or pain with defecation suggests invasion of the anal sphincters or pelvic floor. Preemptive procedures such as a diverting colostomy may be required in patients with these distal painful cancers. Also, cancers growing into the anal sphincter are not candidates for a sphincter-sparing procedure. Questions concerning a patient’s fecal continence should also be discussed before any therapy. Sphincter-sparing procedures can put a tremen­dous stress on even the most normal of pelvic floors and anal sphincters. A history of significant continence prob­lems should prompt a discussion with the patient concerning quality of life issues. Sphincter-sparing surgery in these patients, even if technically possible, often leads to signifi­cant fecal soiling and the patient may be better served with a resection and permanent colostomy.
Physical Examination and Rigid Sigmoidoscopic Examination
A digital rectal examination (DRE) and a rigid sigmoi­doscopy are essential to the surgical decision-making process. Both a proper examination and rigid sigmoidoscopy should be performed on the initial patient visit unless the patient has a painful invasive lesion. On DRE, fixation of the lesion to the anal sphincter, its relationship to the anorectal ring (the col­lection of muscles that make up the sphincters), and possible fixation to both the rectal wall and the pelvic wall can be evaluated. For mid rectal or upper rectal lesions, the DRE and rigid sigmoidoscopy can help determine how much normal rectum lies distal to the lower border of the tumor. With the combination of DRE and sigmoidoscopy at the initial visit, the surgeon can often determine whether a patient is a candi­date for sphincter-sparing surgery, whether a temporary diverting ostomy is likely, and what anorectal function will be like post-treatment.
413
414 R. Bleday and J. Garcia-Aguilar
Colonoscopy
A colonoscopy should be performed before surgical resection of a rectal cancer. Colonoscopy allows for confirmation of a malignancy through biopsy and the diagnosis and possible removal of synchronous colonic lesions. Synchronous benign polyps have been reported in 13%–62% of cases and syn­chronous cancers have been reported in 2%–8% of cases.
1–6
Even if a colonoscopy has been recently performed on a patient, the surgeon should still perform a rigid sigmoi­doscopy because estimates of the location of the lesion are often misleading. For example, because of the flexibility of the colonoscope, a lesion that is described as 15 cm from the anal verge can sometimes be a close as 5 cm from the anal verge when evaluated with the rigid scope. Finally, both with a colonoscope and rigid sigmoidoscope, one should describe the distance from the lower border of the lesion to a standard distal landmark. The National Cancer Institute (NCI) consen­sus group recommends the use of the “anal verge” as the start­ing point for measuring distance; however, this anatomic landmark is variable. An alternative is to use the dentate line as the zero point and measure the distance from the lower bor­der of the lesion to the proximal border of the anorectal ring. This distance is essentially a measure of the maximal amount of rectum that one can resect before considering an APR.
Preoperative Staging
Preoperative staging of a patient with a rectal cancer is becoming essential in the decision-making process as adju­vant modalities become increasingly used preoperatively. Also, the range of surgical procedures that can be offered to a patient is in part dependent on the preoperative imaging. For a basic evaluation, all patients should receive a chest X-ray or chest computed tomography (CT) scan to exclude pulmonary metastases. One can obtain a carcinoembryonic antigen (CEA) level. If increased preoperatively, the CEA level should decrease to the normal range after treatment. CEA can then be followed postoperatively to detect a recurrence. Most other laboratory evaluations obtained preoperatively are use­ful for determining pertinent medical problems but are not very helpful in staging. By far, the most useful staging for rectal cancer is abdominal/pelvic imaging with CT, magnetic resonance imaging (MRI), or ultrasound (US)
Imaging for Rectal Cancer
Pretreatment abdominal and pelvic imaging of the patient with rectal cancer is necessary in this era because of the increasing value of preoperative adjuvant therapies. Therapy differs depending on stage, depth of invasion into the rectal wall within a stage, size of lesion, and location of the tumor. In particular, distal and mid rectal cancer treatment manage­ment will differ depending on the preoperative staging and
imaging. For upper rectal cancers, imaging to determine stage will often not influence the treatment plan. Many of these patients with upper rectal tumors will benefit from an LAR regardless of the stage and may not require neoadjuvant therapy as often as low and mid rectal cancers.
CT Scans
Differing opinions exist as to whether a CT scan is a useful routine assessment modality in a patient diagnosed with a rec­tal cancer. Some would argue that for routine, uncomplicated malignancies, a CT scan is generally not necessary, because the information obtained will not usually affect the treatment plan. This concept is probably more applicable to patients with colon cancers versus patients with rectal cancers. For rectal cancer, there may be some merit to a baseline preoper­ative CT scan for advanced lesions. CT scanning is quite accurate in assessing rectal tumors that have invaded adjacent organs. However, for assessment of small primary lesions, CT scanning has many limitations. CT scans do not effectively visualize the layers of the rectal wall and so do not help in evaluating the extent of rectal wall invasion of an early can­cer. The overall accuracy of CT scanning in determining depth of invasion is approximately 70%. Additionally, CT scanning is limited in its ability to determine the presence or absence of lymph node metastases. Overall accuracy with CT scanning for assessing lymph nodes in rectal cancer is only 45%.
7–11
The most current CT scanning, especially with dynamic contrast infusion, has a high accuracy rate in detecting liver metastases. However, abdominal US, similar to CT scan, can also detect occult liver metastases and should be used when the information obtained would alter therapeutic deci-
12
sions.
MRI is also very useful in evaluating the liver before
resection.
Endoluminal Imaging
Endoluminal imaging in the form of endoluminal US and endoluminal MRI has become extremely useful in the accu­rate preoperative staging of a rectal cancer. These modalities allow for more precise determination of the depth of invasion and the presence or absence of mesorectal lymph node metas­tasis. The knowledge of these factors is critical in determining the sequence and type of therapy for any given rectal cancer.
Endoscopic US is performed with a probe that is inserted into the rectum via the anus. The patient usually has taken a small preparation to clear the rectum of stool. A water-filled balloon is inflated and pressed against the rectal lesion. A 7.0­to 10.0-MHz transducer is then used to delineate the layers of the bowel wall into five distinct lines. Localized cancers involving only the mucosa and submucosa can therefore be distinguished from those tumors that penetrate the muscularis propria or extend through the rectal wall into the perirectal
13
fat.
A modified TNM classification has been proposed,
14,15
30. Surgical Treatment of Rectal Cancer 415
in which a US stage T1 lesion (uT1) denotes a malignancy confined to the mucosa and submucosa, a uT2 lesion implies penetration of the muscularis propria, but confinement to the rectal wall, a uT3 lesion indicates invasion into the perirectal fat, and a uT4 lesion denotes a primary rectal malignancy that invades an adjacent organ. Studies have compared endorectal US (ERUS)
16,17
to DRE17and have found the US much more accurate. In a recent metaanalysis review, endoluminal US was found to be 95% accurate in distinguishing whether a tumor was confined to the rectal wall (T1, T2) versus invasion into the perirectal fat (T3 or greater).
18
ERUS is less useful in predicting lymph node metastases
19
with 80%–85% accuracy.
Endosonographically identified malignant lymph nodes are generally more hypoechoic in perirectal tissues.
20
However, these results are only seen with
experienced operators.
Two methods of MRI can be used for the evaluation of rec­tal cancer. One can use the endorectal coil (ecMRI) or the sur­face coil MRI. The use of the MRI, either the endorectal or the surface coil, may offer some advantages compared with ERUS. First, it permits a larger field of view. Second, it may be less operator and technique dependent. And third, using the MRI may allow for the study of stenotic tumors.
21–24
Similar to ERUS, endorectal MRI (eMRI) can stage small­volume nodal disease and subtle transmural invasion. In gen­eral, eMRI has been more helpful in the assessment of perirectal nodal involvement than T stage. One reason is that MRI can identify involved nodes on the basis of characteris­tics other than size. nodal staging range from 50% to 95%.
25
Reported accuracy rates of MRI for
24-27
Several series have compared the preoperative staging accuracy of ecMRI to ERUS in patients with rectal can-
24,26–28
cer.
In a report of 89 patients, the overall accuracy for T staging was similar (81%) for ecMRI and ERUS compared with only 65% for CT.
29
The accuracy for N staging was equally poor among the three modalities (63%, 64%, and 57% for ecMRI, ERUS, and CT, respectively). Somewhat similar results were noted in a series of 49 patients.
28
Transmural pen­etration was predicted by ecMRI with equal sensitivity (89%), but higher specificity (65% versus 33%) than ERUS. With both techniques, the predicted N stage had a relatively low correlation with pathologic N stage (45% versus 53%). In one report of 21 patients, ERUS seemed to be superior to ecMRI for determination of pathologic T stage (accuracy 83% versus 40%) because of better differentiation between T1 and T2 tumors. The accuracy for detecting perirectal tumor infiltra­tion was 80% for ecMRI versus 100% for ERUS.
27
The ecMRI is less operator dependent and in answering the critical question of whether a patient has Stage I versus Stage II or Stage III disease, ecMRI was 88% accurate. Those patients who were not staged correctly were usually over­staged and not understaged.
Double contrast MRI may permit more accurate T staging of rectal cancer by allowing better distinction among mucosa, muscularis, and perirectal tissues.
30,31
The specificity and
sensitivity of ecMRI to predict infiltration of the anal sphinc­ter was 100% and 90%, respectively. However, N staging was not improved with this approach; the sensitivity and speci­ficity for nodal disease being 68% and 24%, respectively.
Phased-array surface coil MRI may prove to be the option of choice for staging of more advanced rectal cancers. The technique has been useful in predicting the likelihood of a tumor-free resection margin by visualizing tumor involvement of the mesorectal fascia.
32
Preparation of the Rectal Cancer Patient for Surgery
After the diagnosis and staging of a rectal cancer, a decision needs to be made regarding optimal method of treatment. The surgical approach is dependent on the location of the tumor, its depth of invasion, and whether, in the preoperative evalua­tion, metastases have been discovered. Whether the patient is a candidate for a local excision or for a radical resection, the patient needs to be prepared for the procedure and the anes­thetic so as to minimize perioperative and postoperative com­plications. Particular attention needs to be given to the patient’s medical comorbidities. Unique to colon and rectal surgery is the need for a bowel preparation.
Bowel Preparation
Before the use of mechanical preparations and perioperative antibiotics, infection rates after colorectal surgery ranged as high as 60%. mechanically cleanse the large intestine. These include a diet of clear liquids 1–3 days before surgery combined with one of the following: laxatives, enemas, wholegut irrigation with saline via a nasogastric tube, mannitol solutions, polyethylene glycol (PEG) electrolyte lavage solutions, or PEG-based tablets. In a survey of colon and rectal surgeons in 1990, almost two-thirds preferred the PEG solutions for their patients because of the reliability of the cleansing results. Many surgeons today continue to use these PEG solutions as a bowel preparation. There have been two recent metaanaly­ses that have concluded that mechanical bowel cleansing before colorectal surgery has no significant impact on periop­erative infection rates. would still recommend that some type of colonic cleansing occur before surgery because it is easier to manipulate the bowel if it is not filled with stool. It should be emphasized that one should not force a preparation on a patient because the benefits may be minimal. Furthermore, the choice of prepara­tion should be selected depending on the individual. For instance, large-volume lavage solutions should not be used in patients with gastric emptying problems such as gastroparesis caused by diabetes. Saline laxatives are often phosphate- or magnesium-based and should not be used in patients with renal failure.
33,34
Currently, there are several methods used to
36,37
Despite these recent studies, we
35
416 R. Bleday and J. Garcia-Aguilar
Antibiotic Prophylaxis
After mechanical cleansing of the large intestine, antibiotic prophylaxis is used to decrease the incidence of postoperative septic complications, because mechanical cleansing decreases the total volume of stool in the colon but does not affect the concentration of bacteria per milliliter of effluent.
38
Traditional prophylaxis uses an oral regimen known as the Nichols/Condon preparation. This regimen consists of neomycin 1 g and eryth­romycin base 1 g by mouth at 1:00
PM, 2:00 PM, and 11:00 PM
on the day before surgery.39Many surgeons have substituted metronidazole 500 mg for the erythromycin base because it is bacteriocidal against a greater percentage of gut anaerobes.
Most surgeons use perioperative systemic antibiotics instead of oral antibiotics for antibiotic prophylaxis. Regimens need to include coverage for both aerobic and anaerobic gut bacteria. For long procedures, redosing should be considered depending on the serum half-life of the antibiotics used. Some have argued that double prophylaxis with both oral and intra­venous antibiotics is of benefit in immunocompromised patients or in patients in whom the dissection is below the peritoneal reflection.
Other Perioperative Issues
Besides the mechanical and antibiotic preparation of the bowel, all patients are prepared in the usual manner for major surgery. Blood loss is usually quite minimal for most elective colorectal surgery and typically patients are not asked to donate autologous blood. Cardiac, pulmonary, and nutritional evaluations are performed when necessary. Perioperative sys­temic antibiotic coverage is expanded in patients with high­risk cardiac lesions such as prosthetic heart valves, a history of endocarditis, or a surgically constructed systemic-pulmonary shunt, and with intermediate-risk cardiac lesions such as mitral valve prolapse, valvular heart disease, or idiopathic hyper­trophic subaortic stenosis.
38
Intravenous ampicillin 2 g and gentamicin 1.5 mg/kg are given 1/2–1 hour before the proce­dure and for at least one postoperative dose. Oral anticoagula­tion is stopped, and patients are placed on intravenous anticoagulation or on Lovenox approximately 5 days before surgery. The heparin or Lovenox is then stopped at the appro­priate time before surgery (8 or 12 hours, respectively). Depending on the individual risk of the patient and the extent of the operative dissection, anticoagulation is restarted as early as 8 hours postoperatively, but without a bolus. Careful moni­toring of the patient’s hematocrit and partial thromboplastin time are necessary if early reheparinization is instituted.
Anatomic and Biologic Issues
Surgical Anatomy
The type of operation that can be offered to a patient with rec­tal cancer depends not only on tumor stage, but also on the location of the tumor in relation to the surgical anatomy.
Surgical anatomy refers to the anatomic landmarks that deter­mine resectability and sphincter preservation. The NCI con­sensus on rectal cancer recommended localizing the tumor relative to the anal verge which is defined as starting at the intersphincteric groove. Another important landmark defining the upper limit of the anal canal is the anorectal ring. From the surgeon’s perspective, the top of the anorectal ring is the lower limit of a distal resection margin. A large, full-thickness cancer needs to be located high enough above the top of the anorectal ring to allow for an adequate distal margin if sphinc­ter preservation is contemplated. If the dissection is to be car­ried lower toward the dentate line, then the tumor must be confined to the mucosa, submucosa, and superficial layer of the internal sphincter.
Biologic Issues
It is important to understand the clinical biology of rectal can­cer. “Clinical” biology, means the typical pattern of growth and natural history of the spread of the disease. Studies have shown that colon cancer frequently arises in adenomatous polyps of the colon or rectum. Also, there is a 13%–62% inci­dence of polyps in patients with carcinoma of the colon or rectum. isting adenomas with carcinoma of the colon or rectum depends in part on the method of study. used to study the issue, one can clearly say that the vast majority of carcinomas arise in preexisting adenomas. preparing a patient for surgery, the surgeon should have the colon completely evaluated preoperatively so as to be able to operatively treat any synchronous disease that cannot be removed endoscopically.
cancer is important to note and is somewhat different from that of other solid tumors such as breast cancer. Gabriel et al. have “skip” metastases. Rectal cancers usually proceeded in an orderly march from the adjacent mesorectal nodes up the lymphatic chain to the upper extent of the mesentery along the inferior mesenteric artery (IMA) and vein systems. From the surgeon’s perspective, this means that early intervention along with proper locoregional resection will cure most can­cers. As part of a multimodality team that now treats most solid tumors, it must be emphasized to our medical col­leagues that a rectal cancer is not a systemic disease from the first abnormal cell division. Aggressive local therapy in the form of an adequate resection is still the “anchor” to any therapy.
with certain polyposis syndromes or in cancers associated with inflammatory bowel disease. With both of these condi­tions, a total proctocolectomy needs to be performed. Sphincter preservation can be considered in certain patients but one needs to recognize that any mucosa left intact is at an increased risk of developing cancer. The anal transitional zone needs to be biopsied to identify dysplasia. If dysplasia is
40–43
The variation observed in the incidence of coex-
1,2
Whatever method
44–46
In
The biology of lymph node metastases with invasive rectal
47
reported in 1935 that colorectal cancers tend not to
Surgical therapy may need to be customized in patients
30. Surgical Treatment of Rectal Cancer 417
present, then a proctocolectomy with end ileostomy needs to be performed.
Surgical Procedures: Principles
Resection of the bowel with primary anastomosis was not a common phenomenon until the late 1940s. Before that time, surgery of the colon and rectum usually meant a permanent
48
stoma. techniques for rectal cancer. The result is that primary resec­tion and anastomosis without a colostomy or ileostomy is now the rule rather than the exception.
tive resection is not possible. If the patient is a reasonable operative risk and the extent of metastatic disease is minimal, then complete but palliative resection of the primary tumor leads to a better quality of life and prevents many of the dis­tressing symptoms of an advanced primary lesion such as obstruction, bleeding, and pain. If the primary lesion is not resectable, then diversion of the fecal stream can signifi­cantly improve the patient’s immediate status. Nonoperative therapy should be considered when there is significant metastatic disease and the primary tumor is relatively small and uncomplicated. In this situation, it is likely that the patient will die of metastatic disease before a complication from the primary tumor.
Variability in Outcome Based on Surgeon and Hospital Volume
The cancer resection margin in the extraperitoneal rectum is limited by the bony confines of the pelvis as well as by the proximity of adjacent anterior organs. In some cases, locoregional recurrence may be inevitable. However, locoregional failure may also result from incomplete sur­gery. There is accumulating evidence of variability among surgeons in local recurrence rates for stage-matched rectal cancers. McArdle and Hole patients undergoing colorectal cancer resection at the Royal Infirmary in Glasgow. They observed significant variability in patients’ postoperative morbidity, mortality, and ultimate survival, depending on the surgeon. The proportion of patients undergoing a curative resection varied from 40% to 76%, operative mortality from 8% to 30%, local recurrence from 0% to 21%, and anastomotic leak rates from 0% to 25%.
rates, postoperative mortality, and overall survival as shown in a series of 7257 patients diagnosed with Stage I–III rectal cancer between 1994 and 1997. highest quartile of volume (more than 20 procedures annu­ally) were compared with those with volumes in the lowest quartile (fewer than seven procedures annually), there were
Recent advances have been made in the surgical
Palliation should be the goal in a patient for whom cura-
49
presented a review of 645
Hospital volume can also have an impact on colostomy
50
When hospitals with the
statistically significant differences in colostomy rates (29.5% versus 36.6%), 30-day postoperative mortality (1.6% versus 4.8%), and in overall 2-year survival (83.7% versus 76.6%).
The ability to perform sphincter-sparing surgery is also affected by hospital volume. In the United States Intergroup 0114 trial of 1330 patients with Stage II or III rectal cancer participating in an adjuvant treatment trial, APR rates were significantly higher in low-volume hospitals (46% versus 32% at lowest and highest volume hospitals, respec-
51
tively).
Low hospital surgical volume was only an impor­tant predictor of inferior overall or recurrence-free survival in patients who did not complete their planned adjuvant chemoradiotherapy.
Total Mesorectal Excision
Total mesorectal excision in conjunction with an LAR or an abdominal perineal resection involves precise sharp dissec­tion and removal of the entire rectal mesentery, including that distal to the tumor, as an intact unit. tional blunt dissection, the rectal mesentery is removed sharply under direct visualization emphasizing autonomic nerve preservation, complete hemostasis, and avoidance of violation of the mesorectal envelope. Its rationale is under­scored by the hypothesis that the field of rectal cancer spread is limited to this envelope and its total removal encompasses virtually every tumor satellite. The reduction of positive radial margins can be reduced from 25% in conventional surgery to 7% in cases resected by TME. Furthermore, Adam et al.
53
showed that patients with posi­tive radial margins were 3 times more likely to die and 12 times more likely to have local recurrence than patients without radial margin involvement.
Conventional surgery violates the circumference of the mesorectum during the blunt dissection along undefined planes. This leaves residual mesorectum in the pelvis. The higher rate of pelvic recurrence in conventional surgery is a reflection of inadequate resection and residual viable tumor burden within the pelvis. Several surgical teams using the TME technique have reported local failure rates ranging from 5% to 7% for Stage II and Stage III cancers. the North Central Cancer Treatment Group, NCCTG, control arm consisting of surgery plus radiotherapy had a local failure rate of 25% and the addition of chemotherapy only decreased the local failure rate to half that value.
Of greater importance is the fact that improved local con­trol seems to be translatable into improved overall survival. Survival ranges from 68% to 78% are observed among large published series when this technique is applied.
The meticulous dissection, however, is not without conse­quence. Prolonged operative time and increased anastomotic leak rates are noted. Anastomoses 3–6 cm from the anal verge have led up to 17% leak rates. Some centers are now routinely fashioning a protective diverting ostomy.
52
52–56
57
Unlike conven-
By contrast,
418 R. Bleday and J. Garcia-Aguilar
Conventional rectal surgery is associated with a significant incidence of sexual and urinary dysfunction. Presumably, this is related to damage to the pelvic autonomic parasympathetic and sympathetic nerves by blunt dissective forces. Postoperative impotence and retrograde ejaculation or both have been observed in 25%–75% of cases particularly if lat­eral wall lymphadenectomy and splanchnic nerve resection are performed. By contrast, after TME with its careful nerve­sparing dissection, impotence has been reported in only 10%–29% of cases. A recent prospective study confirms that autonomic nerve preservation yields good results in terms of morbidity and functional outcome.
59
There are well-recognized points during the rectal dissec­tion where nerve injury can occur. The most proximal is the sympathetic nerve plexus surrounding the aorta. These sym­pathetic nerve trunks are also prone to injury near the pelvic brim as the bifurcate to each side of the pelvis. Intact nerves should look like a “wishbone” near the sacral promontory after a proper dissection. The clinical consequence of an iso­lated sympathetic nerve injury is retrograde ejaculation. If one proceeds with a dissection beneath the presacral or pelvic fascia from the sacral promontory around to the lat­eral pelvic sidewall, then one can injure both parasympa­thetic and sympathetic nerves which can result in impotence and bladder dysfunction. In the lower part of the mid rectum, the hypogastric plexus and nervi erigentes can be injured in the anterolateral pelvis. A radial dissection well outside the lymphovascular bundle which lies adjacent to the nerve and nerve plexus can also lead to a mixed parasympathetic and sympathetic injury. This bundle and
the nerve structure are typically located just lateral to the seminal vesicles in a man or the cardinal ligaments in a woman. Finally, a dissection anterior to both layers of
58
Denonvillier’s fascia in a man can also put at risk the nerve and nerve plexus.
To date, all data are from prospectively gathered series and comparisons with historical controls. There are no random­ized control data clearly showing benefits in terms of disease­specific and overall survival in patients undergoing TME as opposed to more conventional resection.
Adjuvant therapy has recently been shown to improve the results of TME surgery. In a two-arm, randomized study com­paring TME with or without preoperative radiotherapy for resectable rectal cancer, patients receiving the combined ther­apy had a lower rate of local recurrence at 2 years. Subset analysis showed the most significant benefit in node-positive cancers. with prognosis.
60
The “completeness” of the TME also correlated
61
Adjuvant therapy should therefore be con­sidered in patients undergoing TME surgery with Stage II and Stage III disease.
Figure 30-1 demonstrates schematically how the dissection should proceed. Figure 30-2 shows a cross-section of the rec­tum, the mesorectal fat, and the associated fascia.
Distal Margins and Radial Margins
The extent of resection margins in rectal cancer remains con­troversial. Although the first line of rectal cancer spread is upward along the lymphatic course, tumors below the peritoneal reflection also spread distally by intramural or
FIGURE 30-1. Schematic representation of the correct TME dissection versus an incorrect dissection. The dissection should proceed between the mesorectal fascia and the pelvic wall fascia to ensure a “complete” TME.
30. Surgical Treatment of Rectal Cancer 419
ence in local recurrence rates whether distal margins of <2 cm, 2–5 cm, or >5 cm were achieved. Finally, in two early studies from the British literature, surgical pathology of rectal and rec­tosigmoid cancer demonstrated the clinical biology of extra-
67
mural lymphatic spread. In the series by Goligher et al.
from 1951, only 6.5% of patients had metastatic glands below the primary tumor, whereas 93.5% had no retrograde spread. Approximately two-thirds of patients with retrograde spread had metastasis limited to within 6 mm of the distal tumor edge, and only 2% had metastasis beyond 2 cm. Dukes
68
published similar results in a study of more than 1500 patients with abdominoperineal cancer.
Further data from a randomized, prospective trial con­ducted by the National Surgical Adjuvant Breast and Bowel Project demonstrated no significant differences in survival or local recurrence when comparing distal rectal margins of <2 cm, 2–2.9 cm, and >3 cm.
69
As a result, a 2-cm distal margin
has become acceptable for resection of rectal carcinoma,
70
although a 5-cm proximal margin is still recommended.
The
radial margin is more critical for local control.
It seems reasonable to conclude that a 2-cm distal margin is justified over a 5-cm distal margin. Even smaller distal margins may be acceptable in certain patients for whom there is no other option for sphincter preservation. In these cases, a frozen section analysis of the distal margin must be performed to confirm a cancer-free margin.
The discussion concerning the distal margin should not be
FIGURE 30-2. Transverse diagram of the structures of the mid rectum. The proper dissection proceeds just outside the mesorectal fat and fas­cia but with sparing of the neurovascular bundle and hypogastric plexus that is located anterolaterally along the pelvic sidewall. One or both layers of Denonvillier’s fascia should be included in males and the equivalent fascial dissection along the back of the vagina in females.
confused with the issues regarding a TME and the radial mar­gin. It is now clear that the status of the radial margin is per­haps the most critical in determining prognosis. Quirke et al. in 1986 demonstrated tumor spread to the radial margins of 14 of 52 rectal cancers on whole mount specimens (27%). Twelve of these 14 patients subsequently developed local recurrence suggesting that local recurrence is largely a result of radial
55
also documented that tumor involve­extramural lymphatic and vascular routes. When distal intra­mural spread occurs, it is usually within 2.0 cm of the tumor, unless the lesion is poorly differentiated or widely metasta-
62–64
tic.
Williams et al,65in 1983 reported distal intramural spread in 12 of 50 resected rectal cancer surgical patients. It was observed that 10 of the 12 had Stage III lesions. Only 6% had distal intramural spread greater than 2 cm. They con­cluded a “wet” margin of 2.5 cm was adequate in 94% of the patients. They noted that only five patients (10%) had tumor beyond a 1.5-cm margin, and all five of these had poorly dif­ferentiated, node-positive cancers. Also, the mortality in this group of patients was attributable to distant metastases, not local recurrence. All these patients had undergone an APR and had distal margins of greater than 5 cm. Grinnell
62
reported
five cases of extramural retrograde lymphatic spread within
1.5 cm in 93 rectal cancers. He also reviewed 28 patients with atypical retrograde lymphatic dissemination. All these patients died within 5 years. He concluded retrograde lymphatic spread was a poor prognostic sign and more radical operations were not advantageous. Pollett and Nicholls
66
observed no differ-
spread. Cawthorn et al. ment of the lateral resection margin correlated with poor prog­nosis; however, it seemed to correlate more with distant spread and it was not a useful indicator of local recurrence.
Selection of Appropriate Therapy for Rectal Cancer
The management of rectal cancer has become increasingly complex. Presently, a surgeon has three major curative options: local excision, sphincter-saving abdominal surgery, and APR. Ideal candidates for local therapy that preserves anal sphincter anatomy and function include small T1 lesions (invasion only into the submucosa) and T2 lesions (invasion into the muscularis propria). As will be discussed, patients with T2 lesions probably should not have surgery alone. Recurrence is high. Preoperative or postoperative adjuvant chemoradiation is of benefit. At present, patients with T3 lesions (invasion into the perirectal fat) are not suitable candi­dates for local therapy and should be treated with an appropri­ate major resection as well as adjuvant therapy in most cases.
71