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Fig. 37.6 Transanal Minimally Invasive Surgery (TAMIS). Instead of a platform containing a rigid procto­scope, a small GelPort (Applied Medical. Rancho Santa Margarita, CA) is inserted into the anus
alization. Instead of a platform containing a rigid proctoscope, a small GelPort (Applied Medical) is inserted into the anus (Fig.37.6), 3 5mm ports are placed through the gel port in a triangular manor and insufation attached to one of the ports to distend the rectum. Newer technology is available to provide balanced insufation (Air Seal) and smoke evacuation. When working in small spaces even minimal amount of suctioning can deate the lumen and obscure visualization. The ability to pro­vide balanced insufation and smoke evacu­ation while performing TAMIS has been a signicant advance over the use of standard laparoscopic insufators. A 5 or 10mm 30° laparoscope is inserted through one of the ports and held by an assistant. Laparoscopic instruments are placed through the other two working ports for dissection. Similar to TEM, the location of the mass determines patient positioning with TAMIS.The patient should be positioned so that the mass in the inferior location. However, unlike TEM, the laparo­scope is not xed and can be moved freely. It is therefore, technically possible, although potentially more difcult, to resect a mass in any location with the TAMIS platform while keeping the patient in the lithotomy position. This may be advantageous for patients whose body habitus prohibits prone or lithotomy positioning. The steps of TAMIS are similar
D. M. Lisle and D. R. Sands
to TEM and involve full thickness excision of
the tumor with a 1cm margin similar to that
method described above.
Anatomical Considerations inSelecting Method ofLocal Excision (Refer toTable 37.2)
I. Transanal excision is limited to distal rectal
cancers as proximal and mid rectal cancers
are difcult to visualize through an open
transanal technique even with an anal retrac-
tor device. Some surgeons argue that even
distal rectal cancers are difcult to visualize
and perform sound oncologic local resection
on especially in patients with difcult body
habitus. Several studies have shown higher
recurrence rates with transanal excision com-
pared to radical resection (12.5% vs 6.9%).
However, 5 year overall survival is similar
(77.4% vs 81.7%).
J. TEM is the preferred modality for cancers that
are larger and those above the rst rectal
valve. The TEM platform is able to reach the
more proximal rectum and distal sigmoid
compared to the TAMIS platform due to the
availability of both a 12 and 20cm procto-
scope. The benet of the rigid proctoscope is
not only in proximal reach, it also serves as a
retractor of the rst and second rectal valves
which can hinder visualization when using a
soft platform. This feature can prove invalu-
able in the excision of proximal lesions and
perhaps more importantly, obtaining adequate
closure of the defect in cases of peritoneal
entry. In addition it has the advantage of being
single operator if there is no assistant avail-
able to hold the camera which is necessary for
TAMIS. A Meta analysis comparing TEM to
radical excision for T1N0 rectal cancers
showed equivalent 5year overall survival.
K. TEM or TAMIS is often the preferred plat-
form for small early rectal cancers below the
rst rectal valve. The TEM platform has the
option of a straight edge proctoscope rather
than the beveled edge which can interfere
with the seal at the level of the anus in low
37 Rectal Cancer: Local Therapy
295
lesions. The TAMIS platform is more exi­ble, allowing access to lesions which may be located in intermediate locations on the rectal wall, but may overlap the most distal rectal lesions potentially covering them and obscur­ing their view. In this case, the dissection may be initiated with traditional transanal approach and eversion of the anus. Once the distal tumor has been mobilized enough to allow placement of the TAMIS or straight edge TEM proctoscope advanced endoscopic assistance can be utilized for the more proxi­mal dissection.

Suggested Reading

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cancer. Curr Colorectal Cancer Rep. 2016;12:162–9.
Brodsky JT, Richard GK, Cohen AM, Minsky
BD. Variables correlated with the risk of lymph node metastasis in early rectal cancer. Cancer. 1992;69(2):322–6.
Garcia-Aguilar J, Renfro LA, Chow OS, Shi Q, Carrero
XW, Lynn PB, Thomas CR Jr, Chan E, Cataldo PA, Marcet JE, Medich DS, Johnson CS, Oommen SC, Wolff BG, Pigazzi A, McNevin SM, Pons RK, Bleday R.Organ preservation for clinical T2N0 distal rectal cancer using neoadjuvant chemoradiotherapy and local excision (ACOSOG Z6041): results of an open­label, single-arm, multi-institutional, phase 2 trial. Lancet Oncol. 2015;16(15):1537–46.
Glasgow SC, Bleier JI, Burgart LJ, Finne CO, Lowry
AC. Meta-analysis of histopathological features of primary colorectal cancers that predict lymph node metastases. J Gastrointest Surg. 2012;16(5):1019–28.
Kidane B, Chadi SA, Kanters S, Colquhoun PH, Ott
MC.Local resection compared with radical resection in the treatment of T1N0M0 rectal adenocarcinoma: a systematic review and meta-analysis. Dis Colon Rectum. 2015;58(1):122–40.
Luna-Pérez P, Rodríguez-Ramírez S, Vega J, Sandoval
E, Labastida S. Morbidity and mortality following abdominoperineal resection for low rectal adenocarci­noma. Rev Investig Clin. 2001;53(5):388–95.
Miles WE. A method of performing abdominoperineal
excision for carcinoma of the rectum and terminal por­tion of the pelvic colon. Lancet. 1908;2:1812–3.
Minsky BD, Rich T, Recht A, Harvey W, Mies
C.Selection criteria for local excision with or without adjuvant radiation therapy for rectal cancer. Cancer. 1989;63(7):1421–9.
Rosen L, Veidenheimer MC, Coller JA, Corman
ML. Mortality and morbidity, and patterns of recur­rence after abdominal perineal resection for cancer of the rectum. Dis Colon Rectum. 1982;25(3):202–8.
Saraste D, Gunnarsson U, Janson M. Predicting lymph
node metastases in early rectal cancer. Eur J Cancer. 2013;49(5):1104–8.
Williams NS, Durdey P, Johnston D. The outcome fol-
lowing sphincter-saving resection and abdomino­perineal resection for low rectal cancer. Br J Surg. 1985;72(8):595–8.
You YN, Baxter NN, Stewart A, Nelson H.Is the increas-
ing rate of local excision for stage I rectal cancer in the United States justied? A nationwide cohort study from the National Cancer Database. Ann Surg. 2007;245(5):726–33.

Rectal Conditions: Rectal Cancer—Proctectomy

AaronS.Rickles andFergalJ.Fleming
38
Refer toAlgorithm inFig. 38.1
A. In the current climate of evolving oncologic
therapies, increasing evidence has shown that a multidisciplinary approach, with surgical resection at the forefront of curative treat­ment, improves oncologic, clinical decision­making, and functional outcomes for patients with rectal cancer. For this chapter, we will be focusing on the surgical therapy for resect­able rectal cancer and reserve discussion of treatment for unresectable disease and dis­ease amenable to local therapies for else­where in this text. Quality oncologic resection requires experience and a deep understand­ing of the pelvic anatomy in order to yield the best probability of good oncologic and func­tional outcomes.
B. In order to determine the most appropriate
treatment options for the patient, a preopera­tive evaluation must include not only staging of the cancer according to the TNM classi­cation, but also evaluation of the location of the tumor relative to the sphincter complex, involvement of any adjacent structures, and
A. S. Rickles Rochester Colon and Rectal Surgeons, P.C. Rochester, New York, NY, USA e-mail: arickles@rochestercolon.com
F. J. Fleming (*) Department ofSurgery, University ofRochester Medical Center, Rochester, NY, USA e-mail: Fergal_Fleming@URMC.Rochester.edu
proximity or involvement of the circumfer­ential resection margin (CRM).
• Thorough physical examination including detailed digital rectal examination can help determine location of the tumor and proximity to anal sphincters, rmness, ulceration, and xation.
• Carcinoembryonic Antigen (CEA).
• Colonoscopy, if not already performed, to exclude proximal synchronous tumor(s), to obtain histology, and location of tumor including distance from anal verge or den­tate line, as well as circumferential location as it relates to surrounding structures. A rigid proctoscope is often preferred in this setting to more accurately assess tumor dis­tance from the verge and distinguish among upper, mid, and lower rectal locations.
• Endorectal Ultrasound (ERUS) or Magnetic Resonance Imaging (MRI) for local- regional staging. ERUS may have advantage in evaluating depth of involve­ment for early stage tumors, whereas MRI is the only modality that can assess cir­cumferential margin and is the most com­monly used method presently. MRI is the accepted standard by the Commission on Cancer (CoC). National Accreditation Program for Rectal Cancer (NAPRC).
• Computed Tomography (CT) of the chest, abdomen, and pelvis to evaluate for dis­tant metastasis.
© Springer Nature Switzerland AG 2020 S. R. Steele etal. (eds.), Clinical Decision Making in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-65942-8_38
297
298
A. S. Rickles and F. J. Fleming
Fig. 38.1 Algorithm for treatment of rectal cancer– proctectomy. IMA inferior mesenteric artery, IMV inferior mesenteric vein, APR abdominal perineal resection, AR
C. Neoadjuvant chemoradiotherapy for locally
advanced rectal cancer (cT3-4, cN0 or any cT, cN1-2) reduces the risk for local recur­rence when compared to surgery alone in several landmark studies. Chemoradiation delivered in the neoadjuvant setting is asso­ciated with a lower rate of recurrence and higher treatment completion rates compared to adjuvant chemoradiation. Short-course radiation can also be delivered in neoadju­vant setting and shown to signicantly reduce local recurrence. Neoadjuvant chemoradiotherapy may also be considered for those patients with low rectal tumors where sphincter- preserving surgery would not yield adequate results without reduction of the tumor burden. Upper rectal lesions (above the peritoneal reection) are more controversial, and in many cases do not require neoadjuvant therapy and can be resected primarily.
D. The anatomy of the rectum can be quite vari-
able from patient-to-patient and requires experience and reliance on key anatomical constants when operating in a radiated and occasional difcult anatomical of the pelvis. The location of the rectal tumor is often mea­sured as the distance from the anal verge or
anterior resection, LAR low anterior resection, TME total mesorectal excision, taTME transanal total mesorectal excision
the dentate line, and the height of the rectum varies between 12 and 15cm by rigid proc­toscopy, depending on the type of measure­ment and size of the patient. Some surgeons will use the relationship of the tumor to the rectal valves as a reference point for height of the tumor (low, middle, and upper rectum).
The superior aspect of the rectum is iden-
tied as the colon passes over the sacral promontory into the pelvis and the taeniae coalesce to form a complete layer of longitu­dinal muscle. The anatomy which comprises the mesorectal excision can be separated similarly to how they are encountered surgi­cally, the anterior, posterior, and deep anat­omy. From superior to inferior the anterior excision is comprised of:
• The intraperitoneal anterior wall of the rectum.
• The peritoneal reection.
• Denonvilliers’ fascia behind the seminal vesicles and fusing with the fascia on the back of the prostate in males.
Posteriorly the mesorectum is largely comprised of a bilobed lipomatous like structure that lies anterior to the sacrum and enveloped by the investing visceral fas­cia of the hindgut. Waldeyer’s fascia invests
38 Rectal Conditions: Rectal Cancer—Proctectomy
299
the front of the sacrum and provides some protection from the venous plexus and autonomic nervous plexus of the pelvis. Between the investing fascia of the meso­rectum and the investing fascia of the sacrum posteriorly is an avascular plane of dissection that guides the surgeon to a com­plete mesorectal excision, the so-called “Holy Plane” of dissection. Distally the mesorectum narrows or tapers into a “waist” as the lipomatous lymphatic and vascular supply tapers and the muscular wall of the rectum becomes the internal anal sphincter as it inserts into the pelvic oor.
Essential to functional outcomes fol­lowing a TME is an understanding and awareness of the sympathetic and parasym­pathetic bers that supply the rectum and genitourinary tract. The sympathetic or superior hypogastric plexus arises from T12-L2 and passes anteriorly over the aor­tic bifurcation and sacral promontory as it divides laterally into the right and left hypogastric nerves. Damage to these nerves can result in urinary incontinence and ret­rograde ejaculation. As the superior hypo­gastric plexus travels inferior and lateral in the pelvis, posterior to the mesorectum it joins the pelvic splanchnic nerves, or nervi erigentes, to form the inferior hypogastric plexus. Injury to the parasympathetic nerves when dissecting out the mesorectum can lead to erectile dysfunction and bladder dysfunction.
As the TME dissection commences, the avascular presacral plane will act as a guide for the rest of the abdominal approach to the dissection. The plane can reliably be found by retracting the rectum up and out of the pelvis and scoring the peritoneum over the sacral promontory from the right side of the patient. Care should be taken to avoid the sympathetic trunks at this loca­tion. Once entered, this plane can be fol­lowed both distally and laterally to completely encompass the visceral fascia of the mesorectum.
E. Consistent with oncologic principles of sur-
gery, the mesentery of the colon and rectum should be taken en bloc with the specimen. For rectal cancer, ligation proximal to the superior rectal artery (low tie) has similar survival outcomes to ligation of the IMA proximal to the left colic artery (high tie). However, a high ligation is often necessary in order to provide adequate length for a tension- free anastomosis and should be per­formed when patients have suspicious lymph node involvement proximal to the superior rectal artery. Additionally, a high ligation of the inferior mesenteric vein is advocated both for lymph node yield and adequate mobilization for tension-free anastomosis. Routine high ligation of the vessels and com­plete splenic exure mobilization are can be essential maneuvers to ensuring a tension­free anastomosis. In those patients with a redundant and oppy colon who are under­going a more proximal anastomosis or an abdominal perineal resection (APR), a splenic exure mobilization may not be required.
F. The location of rectal tumors is often
described in reference to the upper (11– 15 cm from anal verge), middle (7–11 cm from anal verge), or lower third (anorectal ring to 7cm from anal verge) of the rectum. The anatomical association to this reference is that the upper third of the rectum is intra­peritoneal and covered by peritoneum anteri­orly and laterally. The middle rectum is anteriorly covered by peritoneum while the lower third is devoid of peritoneum and is entirely extraperitoneal.
G. Tumors of the middle and lower third of the
rectum should undergo a complete TME including anterior dissection through Denonvilliers’ fascia. This will allow for complete excision of lymphatic drainage and minimize risk of local recurrence.
H. Secondary to several anatomic constraints,
tumors of the lower rectum often present the greatest challenge to successful outcomes. Proximity to the pelvic oor and sphincter complex may make satisfactory functional
300
A. S. Rickles and F. J. Fleming
outcomes unobtainable and complete excision of the tumor may require an abdominal­perineal resection (APR) for adequate onco­logic and functional outcomes. Additionally, the natural mesorectal plane narrows deep in the pelvis making the circumferential margin at higher risk of being threatened. Extra-organ involvement is also more likely with tumors in this location given the proximity of the semi­nal vesicles, prostate, and vagina.
I. Much controversy exists over the most
appropriate distal margin of resection. Distal lymphatic or intramural spread of the tumor presents the potential for a positive distal margin despite a clear gross margin intralu­minally. However, a distal mesorectal margin of 5 cm for an anterior resection has been accepted for rectal cancer of the upper third of the rectum, but should be weighed against other clinical and pathologic features of the tumor. A complete posterior and lateral dis­section should be performed during this operation while maintaining the lateral stalks prior to determining where to divide the dis­tal margin.
J. While concern over technical difculties and
risks for morbidity following increased rates of anastomotic leaks and pelvic sepsis are present, middle rectal tumors should undergo a low anterior resection with total mesorec­tal excision with a stapled or hand-sewn anastomosis.
K. When possible, a sphincter-sparing operation
should be the operation of choice for rectal cancer, including low rectal tumors where sphincter preservation and reasonable func­tional outcomes are possible without increas­ing the risk of unfavorable oncologic outcomes. Whereas 5cm of distal margin is ideally accepted for more proximal tumors, various studies have found that margins of 2 cm or less have resulted in similar onco­logic outcomes. When compared to the dif­ference in quality of life between an APR and a sphincter-sparing operation, a low colorec­tal or even coloanal anastomosis is often pre­ferred for patients with good preoperative sphincter function.
Once the oncologic concerns of proper resection margins have been met and anal sphincter function accounted for, the greatest concern in the postoperative period is the risk of anastomotic leak and pelvic sepsis. The risk of anastomotic leak in a low pelvic anas­tomosis can be up to 3–32% depending on multiple risk factors including tumor height, receipt of neoadjuvant therapy, and comorbid conditions. Technical factors increasing the risk of anastomotic leak include relative isch­emia and tension on the anastomosis. Several meta-analyses have been published evaluat­ing the role of diverting ileostomy for low anterior resections (LAR) and confer that a diverting stoma reduces the risk of both anas­tomotic leak and the need for reoperation by approximately 60–70%. For this reason the authors advocate routine diverting loop ileos­tomy for low and ultra-low anterior resec­tions in addition to leak testing all colorectal and coloanal anastomoses.
L. Reconstructive options following low and
ultra-low anterior resection include a straight anastomosis, colonic J-pouch, coloplasty, or a Baker-type side-to-end anastomosis. Several factors should be taken into account when deciding on restorative technique for optimizing function of the postoperative neo- rectum. With the loss of the rectum as a reservoir, and disturbance of the anorectal reex with low pelvic dissections patients can experience frequency, urgency, soiling, and incomplete evacuation, a constellation of symptoms known as the LAR syndrome. The risk of these symptoms are increased with lower anastomoses and with decreased reservoir compliance. Large systematic reviews have shown that for the rst 1–2 postoperative years the functional outcomes for patients are improved following colonic J-pouch reconstruction compared to straight coloanal or colorectal anastomosis. For this reason, when colonic length is adequate, and the pelvic volume can accommodate a larger reconstructed reservoir, the authors prefer where feasible, a colonic J-pouch recon­struction or side-to-end as opposed to a
38 Rectal Conditions: Rectal Cancer—Proctectomy
301
straight anastomosis for low and ultra-low sphincter- sparing operations. Prior to advancing the circular stapler or performing an anastomosis, rectal washout with a tumoricidal agent may reduce any theoreti­cal risk of exfoliating intraluminal tumor cells, although data has not consistently shown benet to this maneuver.
M. Minimally invasive techniques in colorectal
surgery have repeatedly shown benets in outcomes of early postoperative recovery; however, studies comparing laparoscopic to open surgery have less consistency and yield conicting results for short- and long-term oncologic outcomes. In the MRC CLASICC trial, 794 patients in the UK were random­ized 2:1 to laparoscopic or open resection for rectal cancer. The laparoscopic group had a higher rate of positive CRM; however this did not translate into long-term differences in outcomes, with the laparoscopic group have equivalent overall survival, disease-free sur­vival, and local recurrence rates. The COLOR II Trial was another randomized controlled trial comparing the oncologic outcomes of 1044 patients who underwent laparoscopic or open resection for rectal cancer. In this large European study, there was no differ­ence in the 3-year locoregional recurrence rate, disease free survival, or overall survival between the laparoscopic and open groups. The ACOSOG Z6051 Trial was a multicenter randomized controlled trial in the U.S. and Canada involving 486 patients with Stage II or III rectal cancer who underwent neoadju­vant therapy. In this study laparoscopic approach was compared to open approach in a non-inferiority analysis for pathologic out­comes clear distal and circumferential mar­gins and well as the completeness of the mesorectal excision. For the authors, the pre­ferred technique remains to be a minimally invasive approach. Challenges still exist for treating low rectal tumors, particularly when operating in a narrow pelvis or on patients with increased visceral adiposity. Newer techniques that have growing popularity are the use of robotic surgery and combined
transanal and transabdominal approach. Advocates for robotic surgery suggest that articulating instruments and improved visu­alization aid in improved dissection in the difcult pelvis and low-lying tumors. Proponents of transanal total mesorectal excision also advocate that this technique adds benet to improved oncologic speci­mens primarily for low and ultra-low tumors, possibly increasing the feasibility of sphinc­ter sparing operations for patients with ultra­low cancers, although data on the long-term value of these techniques are still being formulated.
N. Sphincter preservation is not advisable for
those patients with poor sphincter control or who have low tumors invading the levators or anal sphincters following neoadjuvant treat­ment. These patients should undergo en bloc resection of the anus, rectum, and sigmoid colon with permanent descending colostomy possibly as an extralevator APR.
O. While APR has long been the gold standard
operation for patients with low rectal cancer, recent evidence has shown that the improved oncologic outcomes associated with TME and neoadjuvant chemoradiation have not been routinely replicated in patients under­going APR. Keeping in mind that these tumors have a higher propensity for local spread and invasion into adjacent tissues given the lack of a mesorectum, studies have shown positive circumferential resection margin (CRM) rates in the 30% range for APR compared to 11% for LAR.Additionally, APR has a higher rate of incomplete dissec­tion and a perforation rate nearly 14% com­pared to 2.5% for LAR.Some surgeons have advocated for extralevator APR to combat the high risk for positive margins or incom­plete resections. In this approach the perineal dissection is started with a wide cylindrical incision and carried through the ischiorectal fat and the levator ani divided at the attach­ment to the sidewall, therefore eliminating the “waist” associated with the standard APR specimen and decreasing the risk of a posi­tive CRM.The downside to this technique,
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A. S. Rickles and F. J. Fleming
however, is the resultant large perineal defect which often requires a ap for closure and has a higher rate of wound complications.

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Bonjer HJ, Deijen CL, Abis GA, etal. A randomized trial
of laparoscopic versus open surgery for rectal cancer. N Engl J Med. 2015;372:1324–32.
Brown CJ, Fenech DS, McLeod RS.Reconstructive tech-
niques after rectal resection for rectal cancer. Cochrane Database Syst Rev. 2008;(2):CD006040.
Dietz DW, Consortium for Optimizing Surgical Treatment
of Rectal Cancer (OSTRiCh). Multidisciplinary man­agement of rectal cancer: the OSTRICH.J Gastrointest Surg. 2013;17:1863–8.
Fleshman J, Branda M, Sargent DJ, et al. Effect of
laparoscopic- assisted resection vs open resection of stage II or III rectal cancer on pathologic outcomes: the ACOSOG Z6051 randomized clinical trial. JAMA. 2015;314:1346–55.
Heald RJ. The ‘Holy Plane’ of rectal surgery. J R Soc
Med. 1988;81:503–8.
Jayne DG, Guillou PJ, Thorpe H, etal. Randomized trial
of laparoscopic-assisted resection of colorectal carci-
noma: 3-year results of the UK MRC CLASICC Trial Group. J Clin Oncol. 2007;25:3061–8.
Nagtegaal ID, van de Velde CJ, Marijnen CA, et al.
Low rectal cancer: a call for a change of approach in abdominoperineal resection. J Clin Oncol.
2005;23:9257–64.
https://www.facs.org/quality-programs/cancer/naprc.
Peeters KC, Marijnen CA, Nagtegaal ID, etal. The TME
trial after a median follow-up of 6 years: increased
local control but no survival benet in irradiated
patients with resectable rectal carcinoma. Ann Surg.
2007;246:693–701. Pollett WG, Nicholls RJ. The relationship between the
extent of distal clearance and survival and local recur-
rence rates after curative anterior resection for carci-
noma of the rectum. Ann Surg. 1983;198:159–63. Tan WS, Tang CL, Shi L, Eu KW. Meta-analysis of
defunctioning stomas in low anterior resection for rec-
tal cancer. Br J Surg. 2009;96:462–72. Taylor FG, Quirke P, Heald RJ, et al. Preoperative high-
resolution magnetic resonance imaging can identify
good prognosis stage I, II, and III rectal cancer best
managed by surgery alone: a prospective, multicenter,
European study. Ann Surg. 2011;253:711–9. Wexner SD, Berho ME. The rationale for and reality
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https://doi.org/10.1097/DCR.0000000000000840.

Rectal Conditions: Rectal Cancer—Adjuvant and Neoadjuvant Therapy

TerryZwiep, JulieAnnVan Koughnett, andPatrickH.D.Colquhoun
39

Refer to Algorithm in Fig. 39.1

A. Introduction
The American Cancer Society predicted an incidence of rectal cancer of approximately 43,340 patients in United States alone in 2020. Surgical resection remains the mainstay of curative therapy for rectal cancer in most patients; however, the treatment algorithms for rectal cancer are complex when the roles of neoadjuvant and adjuvant treatments are con­sidered. The appropriate use of neoadjuvant and adjuvant therapies requires proper workup and staging. A multidisciplinary approach is critical to account for these treatment nuances and ensure optimal patient outcomes.
B. Staging
Staging of rectal cancer is multifactorial and utilizes a combination of magnetic resonance imaging (MRI), endorectal ultrasound (ERUS), computed tomography (CT), colo­noscopy, and serum carcinoembryonic anti­gen (CEA) level. The AJCC staging system is standardly accepted for colorectal cancer and is shown in Table 39.1. T and N stage are determined by clinical impression on digital rectal examination (DRE), endoscopy, and
T. Zwiep · J. A. Van Koughnett P. H. D. Colquhoun (*) Department ofSurgery, London Health Sciences Center University Hospital, London, ON, Canada e-mail: Patrick.Colquhoun@lhsc.on.ca
MRI or ERUS.DRE has been shown by the MERCURY group to be fairly accurate in locally staging a rectal mass in experienced hands, but is not adequate as the sole modal­ity to determine local stage; rather, it can be helpful to provide a clinical impression and guide further staging. There was debate in the past about the best form of local staging with MRI or ERUS. MRI has been denitively established as the superior method for local staging in most situations. MRI provides both T stage and N stage, and even more impor­tantly visualizes the proximity of the tumour and involved lymph nodes to the mesorectal fascia (circumferential radial margin— CRM). It also offers better visualization of potential invasion of surrounding structures in the case of locally advanced disease, such as the pelvic side wall and sphincters. MRI is thus preferred for routine staging of rectal cancer in order to best determine CRM status and mesorectal and extramesorectal pelvic lymph nodes. In addition, experienced radi­ologists and improved MRI techniques have now allowed for the detection of extramural vascular invasion, tumor budding, and extrar­ectal tumor deposits, all of which may more accurately guide the recommendation for the role of neoadjuvant chemoradiotherapy. The use of ERUS without MRI for rectal cancer should be limited to early T stage tumors or very advanced adenomas, where it may pro­vide better resolution. It must be noted that
© Springer Nature Switzerland AG 2020 S. R. Steele etal. (eds.), Clinical Decision Making in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-65942-8_39
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T. Zwiep et al.
Fig. 39.1 Algorithm for management of a complete clinical response after neoadjuvant treatment. TME total mesolec- tal excision
the accuracy and utility of both MRI and ERUS staging are highly dependent on the expertise of the interpreter, and one must account for local expertise when choosing the staging modality and considering their results. A CT of the thorax, abdomen, and pelvis is recommended for assessment of any metastatic disease. Extramesorectal disease may be surgically resectable and should involve input from a multidisciplinary tumor board in choosing the sequence of potential treatments. The concepts of resectable and curable metastatic rectal cancer have resulted in major shifts in treatment paradigms and heavily utilize both neoadjuvant and adjuvant treatment. This issue will be discussed in fur­ther detail later in the chapter.
C. Neoadjuvant Chemoradiotherapy
Following staging, a decision must be made about the need for neoadjuvant chemoradio-
therapy. According to the National Comprehensive Cancer Network (NCCN) guidelines for the treatment of rectal cancer, all patients who are locally staged as T3 N0, or Tany N1-2, or T4 should undergo neoadjuvant therapy. However, the benet of radiation in patients with a clear CRM and no suspicious lymph nodes on staging MRI is limited. As mentioned earlier, MRI has been demonstrated to be highly accurate in the interpretation of the CRM status. Radiation is not benign or without potential morbidity. Complications of radiation include diarrhea, radiation enteritis, radiation proctitis, perianal skin irritation, anastomotic leak, and secondary malignan­cies. Neoadjuvant therapy can also alter nal pathology and make the role for adjuvant ther­apy questionable in those who have seemingly been downstaged on nal surgical pathology, when compared to pre-operative MRI stage of