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D. Yang and M. H. Whiteford
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23 Management ofMalignant Polyps
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Colorectal Cancer: Preoperative Evaluation andStaging
AmandaV.Hayman andCarol-AnnVasilevsky
24
Key Concepts
• The method chosen to screen a patient for colorectal can­cer (CRC) should be individualized based on patient comorbidities and life expectancy, access, cost, baseline risk, compliance, and tolerance for invasive procedures due to differing costs, sensitivities, and cadences of the various options.
• Dening the anatomic location where the sigmoid colon transitions to the rectum is increasingly determined by cross-sectional imaging due to its reproducibility and is less dependent on endoscopic localization alone, as body habitus and gender can inuence the location of the peri­toneal reection.
• Proper tumor localization and staging is essential to establishing treatment recommendations; understanding the pitfalls of each staging modality is important to avoid under- or overtreatment.
• Magnetic resonance imaging (MRI) using a rectal cancer protocol is now standard of care for locally advanced rec­tal tumors. Endorectal ultrasound (ERUS) is being used less commonly as it is more operator dependent, less reproducible, and invasive for the patient; however, ERUS remains an important staging modality for early stage rec­tal tumors when determining eligibility for local excision.
• A combination of histologic and radiographic factors should be used to risk stratify CRC; higher-risk tumors should be considered for more aggressive neoadjuvant treatments; however, patient frailty or comorbidities
A. V. Hayman (*) Division of Gastrointestinal & Minimally Invasive Surgery, TheOregon Clinic, Portland, OR, USA e-mail: ahayman@orclinic.com
C.-A. Vasilevsky Department of Surgery, Jewish General Hospital, Montreal, QC, Canada
may limit these treatment options and should be individualized.
• Preoperative optimization and preparation of the colorec­tal cancer patient is essential to maximizing postoperative and oncologic outcomes; a variety of tools, including guidelines and checklists, are available to assist the surgi­cal team in this endeavor.
Diagnosis ofColorectal Cancer
A diagnostic workup for colorectal cancer may follow a pos­itive result from one of the various screening tests available or follow investigation of symptoms, which may be acute or subacute. A positive noninvasive screening test or unex­plained iron-deciency anemia typically prompts colonos­copy, which then detects malignancy. Alternatively, a patient may present with abdominal pain or distension and seek emergent care. Cross-sectional imaging may then demon­strate an intraluminal lesion in the colon or rectum, resulting in further workup.
Screening andDiagnostic Modalities
The ideal screening test for any disease should be easily available, inexpensive, and noninvasive, with high sensitivity and specicity. Because CRC is often asymptomatic, screen­ing tests are universally recommended for patients starting at either age 45 [1] or 50 [2] and ending between ages 75 and 86, based on the patient’s life expectancy and health status (see Chap. 22). Once symptoms occur, the disease is typi­cally in an advanced state with poorer survival rates.
There are a myriad of options for CRC screening; the
choice for a specic patient should be individualized based on a constellation of factors, including personal and family history of CRC or polyps, family history of inherited CRC
© Springer Nature Switzerland AG 2022 S. R. Steele etal. (eds.), The ASCRS Textbook of Colon and Rectal Surgery, https://doi.org/10.1007/978-3-030-66049-9_24
429
430
Table 24.1 Summary of the pros and cons of the most commonly used CRC screening modalities
Pros Cons
FOBT(fecal occult blood testing)
FIT Inexpensive
DNA-FIT Every 3years
Colonoscopy Can differentiate between polyps and cancer
Inexpensive Noninvasive Reduces CRC mortality by 15–33% Convenient Widely available
Noninvasive No dietary/medication modication required Higher specicity than FOBT (less chance of false positive for UGIB) Comparable sensitivity to colonoscopy Recommended by USPSTF
Covered by Medicare 92% sensitive for all CRC (less sensitive for stage IV)
Preventative (removes adenomas before they progress to cancer) Diagnostic and therapeutic Highest specicity/sensitivity Longer time interval between tests (up to 10years)
Low specicity and sensitivity Requires annual testing Requires dietary/medication restrictions Inaccurate in setting of benign GI bleeding (peptic ulcers, hemorrhoids, diverticulosis) Requires daily testing for 3days Cannot differentiate between polyp and cancer Positive test requires colonoscopy
Requires annual testing Cannot differentiate between polyp and cancer Positive test requires colonoscopy
Expensive, insurance may not cover Minimal long-term data Positive test requires colonoscopy Higher false-positive rates Less sensitivity for adenomas
Requires bowel preparation Invasive with risk of serious complication Typically requires sedation Variable based on endoscopist skill May not be widely available Expensive
A. V. Hayman and C.-A. Vasilevsky
syndromes, personal history of inammatory bowel disease (IBD), medical comorbidities, age/life expectancy, tolerance for risk, anxiety, access to healthcare resources, compliance with follow-up, and insurance coverage/cost.
It can be a confusing discussion for the physician to choose the appropriate screening modality for his or her patients. Understanding the benets and drawbacks is essen­tial for the patient and physician to make the correct choice. Table 24.1 may assist the healthcare team involved in this decision-making. We cover the available diagnostic and screening modalities for CRC below.
Fecal Sampling
The least invasive and most widely available screening test for asymptomatic, average-risk persons is fecal sampling for occult blood or tumor DNA.This method may be palatable for some patients as it avoids mechanical bowel preparation and is more practical in geographic areas with poor access to endoscopy. These tests do not replace endoscopy, and it should be noted that any positive test usually prompts colo­noscopy. However, this initial triage test can conserve colo­noscopy for a smaller population. The three fecal-based tests available are discussed below:
FOBT (fecal occult blood test): a guaiac-based test detects
presence of heme (nonprotein portion of hemoglobin) and
detects blood for all sources (including animal). Patients are instructed to put a smear of their stool on a different stool card 3 days in a row and then mail the cards in. Testing is recommended on an annual basis. This is the oldest stool-based test available and is quite inexpensive. It requires dietary and medication modication for sev­eral days prior to the test, including avoiding red meat, raw produce, antacids, vitamin C, nonsteroidal anti­inammatory agents, loperamide, and iron supplements. Menstruation is a relative contraindication. Relatively low specicity and pretest dietary and medication restric­tions have made it less attractive than newer stool tests [3]
FIT (fecal immunochemical test): a.k.a. “safety- chemical” method detects antibodies to the human protein globin portion of hemoglobin found in red blood cells. This results in less cross-reactivity to nonhuman blood and improved specicity over FOBT [3]. It also requires only a single card and thus better compliance. However, it is still a test that is recommended to be performed annually.
Multitarget stool DNA-FIT (Cologuard®) test: combines the FIT test with an additional test that detects genetic mutations found in cancer cells ((KRAS, NDRG4, BMP3, β-actin). It has a 13% false-positive and 8% false-negative rate. It is recommended to be performed every 3years. It was approved for use in 2014. However, it is relatively expensive ($649 out-of-pocket) compared to other stool assays and may not be covered by insurance. Further, it
24 Colorectal Cancer: Preoperative Evaluation andStaging
431
cannot differentiate between advanced polyps and adeno­carcinoma [4, 5]
Flexible Sigmoidoscopy
Flexible sigmoidoscopy can examine the distal portion of the colon and can be performed in an ofce setting with minimal preparation and without sedation. Flexible sigmoidoscopy is typically more easily tolerated than rigid proctoscopy and can extend beyond 25cm. It has been suggested as a screen­ing tool in younger adults since there is a higher incidence ofleft-sided cancers in this population and was used histori­cally in conjunction with barium enema. It is, however, insufcient in older individuals due to a shift of polyps and cancers to the more proximal colon. As such, it has been combined with FIT or FOBT which theoretically enhances detection.
Computed Tomography (CT) Colonography
CT colonography (CTC or “virtual colonoscopy”) is another option available for screening. The technique involves obtaining multiple thin-slice CTimages after carbon dioxide insufation of the colon via a rectal tube, typically in two positions (supine and lateral). The images are reconstructed to give both two and three dimensional views of the colon mucosa. The advantage of CTC is that it avoids the need for sedation and may be preferable for patients with comorbidi­ties who cannot undergo optical colonoscopy or who have a tortuous colon. It does, however, require a full cathartic bowel preparation prior to the procedure, and any suspicious ndings usually prompt subsequent optical colonoscopy. Patients are exposed to radiation and may have a risk of con­trast nephropathy. It has comparable sensitivity to colonos­copy for polyps greater than 1cm but is less effective for detecting smaller lesions as they are difcult to differentiate from stool [4]. Since it involves the instillation of air or car­bon dioxide into the rectum, it may be associated with abdominal cramping and may rarely result in perforation. It may also identify incidental abdominal ndings that may require subsequent additional investigation. Lastly, this test is typically not covered by Medicare. It can be difcult to obtain insurance approval, despite receiving an “A” grade from the US Preventive Services Task Force.
CTC is the procedure of choice in the setting of incom­plete colonoscopy due to technical limitations, or an obstruct­ing lesion, and provides better imaging resolution than more traditional uoroscopic tests (i.e., contrast enema). However, in the setting of a known malignancy, the costs and risks of CTC should be considered in light of how treatment deci­sions would be altered by CTC ndings. If a patient has been
diagnosed with CRC and has an endoscopically obstructing tumor of the proximal colon that does not allow for comple­tion colonoscopy, it is unlikely that a CTC will provide any ndings that would drastically change management, as the colon proximal to the tumor will likely be resected. For patients with endoscopically obstructing tumors of the distal colon, CTC may be helpful to rule out synchronous tumors preoperatively. However, it is also reasonable to forgo CTC, as these patients will receive staging via CT scan which, although not as sensitive as CT colonography, should at least be able to detect any synchronous large lesions. Furthermore, even if CTC does detect a small proximal lesion, it cannot be biopsied in the setting of a distal untraversable lesion. Therefore, in these settings, the patient’s clinical situation needs to be carefully considered regarding the benet of any further assessment for synchronous lesions. If the patient is to undergo any neoadjuvant treatment, this will hopefully allow completion colonoscopy after tumor shrinkage and prior to surgical resection.
Colonoscopy
Colonoscopy is the most sensitive and specic test for colorectal cancer and polyps, being both diagnostic (i.e., detects polyps and cancers), therapeutic (can remove pol­yps), and preventive (can prevent polyp progression to can­cer). It can also detect other abnormalities, such as inammatory bowel disease or diverticulosis. However, it is the most invasive option, requiring full bowel preparation, which is associated with nausea, vomiting, abdominal pain, and dehydration, and is generally distasteful. It also carries periprocedural risks, including colonic perforation (0.1%), gastrointestinal bleeding (especially after biopsy or polypec­tomy), missing a lesion (false negative), or incomplete pro­cedure (either knowingly or unknowingly, which occurs about 5–10% of the time) [5]. Also, the quality of the proce­dure varies based on the performing physician’s technical expertise, which can lead to false negatives. Lastly, most rural areas have lower volume providers and less access to endoscopy overall, often resulting in unacceptably long travel times for patients.
If during colonoscopy a neoplasm is encountered, the endoscopist should then consider the potential benets of biopsy and tumor localization. For patients with obvious adenomatous neoplasms of the intraperitoneal colon which will clearly require colectomy, it could be argued that biopsy results will be unlikely to change subsequent management and may incur unnecessary cost to the patient, can exacer­bate bleeding, carries a risk of perforation, and can have false-negative results that only serve to confuse the patient. However, biopsy may be helpful in detecting Lynch syn­drome preoperatively (which may alter treatment decisions)
432
anal canal
Anal canal Anodem Anal verge
and help guide chemotherapeutic choices if the patient is found to have incurable distant metastatic disease on preop­erative staging and is to be treated nonoperatively. Moreover, insurance companies may refuse to cover the cost of staging tests without a histologic cancer diagnosis. If the etiology of the lesion is in question, i.e., possible lymphoma or ischemic ulcer, then biopsy is warranted. If the tumor is small and unlikely to be appreciated from the serosal side intraopera­tively, the distal extent of the tumor should be marked with tattoo to assist with intraoperative localization (see Chaps.
23 and 25).
If a rectal tumor is encountered, biopsy should be per­formed routinely, and molecular testing including immuno­histochemistry for mismatch repair proteins (IHC for MMR) should be performed. Rectal cancer patients are often treated with neoadjuvant radiotherapy and chemotherapy, which may alter the tumor so that molecular analysis is not possible postoperatively. In addition, some medical and radiation oncologists will be reluctant to initiate neoadjuvant therapy in a patient without histologic conrmation of adenocarci­noma. The distal extent of the tumor should be marked with tattoo to ensure complete resection following neoadjuvant therapy.
A. V. Hayman and C.-A. Vasilevsky

Delineating Colon Versus Rectum

Where the colon ends and the rectum begins is hotly debated. The various potential modalities used to make this distinc­tion include intraoperative visualization, endoscopy, and cross-sectional imaging. A reproducible denition is impor­tant for numerous reasons, including eligibility for clinical trials, localization for serial surveillance of rectal cancer, determining treatment plans (i.e., upfront surgery versus neoadjuvant chemoradiation), and for prognostic estimates. The clinical implications are also critical, since rectal tumors demonstrate clinical features that differ from colon tumors, such as risk of peritoneal disease, lymphatic drainage, threat­ened radial and/or distal margins, consideration of sphincter preservation, and need for protecting ileostomy.
According to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology, the rectum is dened as beginning at a virtual line drawn from the sacral promontory and symphysis pubis on mag­netic resonance imaging (MRI) of the pelvis, ending at the upper border of the anorectal ring [6, 7]. The rectum is arbi­trarily divided into three parts, based on measurement on rigid proctoscopy: low (0–6cm from the anal verge); mid (7–11cm), and high (12–15cm) (Fig.24.1) [8].
Superior
rectal valve
Middle
rectal valve
Anorectal line
Pectinate
(dentate) line
Deep external
sphincter muscle
Internal
sphincter
muscle
Surgical
Anatomical
anal canal
Fig. 24.1 Delineation of the low, mid, and upper rectum with relevant landmarks
Inferior rectal valve
Levator ani muscle
Rectum
Anal transition zone
Non-keratinized squamous mucosa
Keratinized squamous mucosa
8-9 cm
5-6 cm
4-5 cm
2.5-3 cm
0.5-1 cm
24 Colorectal Cancer: Preoperative Evaluation andStaging
433
Table 24.2 Commonly used criteria for delineating colon from rectum
Intraoperative/ Surgical Criteria
- where the teniae splay
- where the epiploica terminate at the peritoneal reection (varies by gender)
the sacral promontory
Cross-sectional imaging (CT/MRI) Endoscopic
- a delineating line between the sacral promontory and the pubic symphysis
- the sigmoid “takeoff” from the rectum (i.e., end of the mesorectum), seen as an acute angulation
- distance from the anal verge on rigid proctoscopy (typically 12 or 15cm)
- beyond the third rectal valve
Initial National Cancer Institute consensus guidelines [7] used 12cm via rigid proctoscopy in the left lateral decubitus position as the commonly accepted cutoff for the rectosig­moid junction. However, an international Delphi consensus concluded that the “sigmoid takeoff” should be utilized, as seen on cross-sectional imaging, marking a shift from a sin­gle clinician’s physical evaluation to a radiographic one [9]. One of the drivers behind this transition is the growing use of MRI in staging newly diagnosed rectal cancers, buoyed by the growth of programs such as the National Accreditation Program for Rectal Cancer (NAPRC) [10], newer staging guidelines, and criteria for clinical trial eligibility, all of which favor, or even require, MRI for initial staging. The purported benet of using MRI versus endoscopic evaluation for staging is that imaging is more reproducible and thus more easily interpreted and comparable over time in multi­disciplinary discussions such as tumor boards. However, there is still clear variation in all these denitions and a wide variety of clinical implications for each modality, which will be discussed later on in the chapter. In Table24.2, we com­pile the most commonly used criteria for delineating the colon from the rectum.
Adding to this complexity is a newer algorithm for treat­ing locally advanced colon cancer with upfront chemother­apy, as seen in the recently published FOxTROT trial [11]. This is also an option for bulky upper rectal cancers and is in line with NCCN guidelines [7]. Although in daily practice it can be challenging to denitiviely differentiate a colon from a rectal location of the tumor, every attempt should be made to do so as the clinical behavior and treatment recommenda­tions differ.
Staging andWorkup ofColon andRectal Cancer
Once the diagnosis of colorectal cancer has been established, the extent of locoregional and distant spread should be deter­mined. Many of the staging examinations are similar for
colon and rectal cancers. However, the locoregional staging of rectal cancer does involve additional evaluation. Appropriate staging is especially important for rectal cancer as it drives treatment decisions in order to minimize under­or overtreating the tumor, both of which have future implica­tions with respect to prognosis and quality of life (see Table24.3).
TNM Staging
Both colon and rectal cancers are staged according to the American Joint Committee on Cancer (AJCC) TNM staging system, eighth edition [12], which is based on the depth of invasion of the tumor (T stage), the extent of lymph node involvement (N stage), and the presence of distant metasta­ses (M stage) (see Table 24.4). For rectal cancer, staging requires consideration of both the initial clinical stage upon which treatment decisions are made and the nal pathologic stage which may be the most important prognosticator (Table 24.5) [13]. The prex “c” for clinical is added to denote an estimate of stage based typically upon radio­graphic imaging, and “p” is added to denote histologic stag­ing postoperatively, while the prex “yp” is used to denote histologic staging following neoadjuvant treatment [12].
History
Initial workup should include a complete tumor-specic his­tory, such as duration of symptoms, abdominal or pelvic pain, rectal bleeding and its characterization whether mixed in with stool, bright red or maroon in color, tenesmus, incon­tinence, change in bowel habits (new onset constipation, diarrhea, frequent thin stools), and weight loss. Patients may also present with fatigue, shortness of breath, and reduced endurance during exertion due to iron-deciency anemia. Urinary problems, baseline fecal continence, and sexual function should also be ascertained with regard to rectal can­cers. In addition, family history should be elicited to rule out the possibility of a hereditary or familial syndrome which
Table 24.3 Diagnostic workup of primary rectal cancer
Parameter Method of choice Location (distance from anal
verge) Visualization of colon Colonoscopy
Morphological verication Biopsy cT stage -Early ERUS, MRI -Intermediate/advanced MRI, preferred over ERUS -Sphincter inltration MRI, DRE, ERUS cN stage MRIpreferred, CT, ERUS M stage CT chest and abdomen, PET/CT if
Digital rectal exam (DRE) Rigid sigmoidoscopy
Virtual colonography
extensive EMVI for other sites
434
Table 24.4 American Joint Committee on Cancer (AJCC) TNM Staging Classication for Colorectal Cancer 8th ed, 2017
T-PRIMARY TUMOR Tx Primary tumor cannot be assessed T0 No evidence of primary tumor Tis Carcinoma in situ invasion of lamina propria T1 Tumor invades submucosa T2 Tumor invades muscularis propria T3 Tumor invades subserosa or into non-peritonealized pericolic or perirectal tissue T4 Tumor directly invades other organs or structure and/or perforates visceral peritoneum T4a Tumor perforates visceral peritoneum T4b Tumor directly invades other organs or structures N -REGIONAL NODES Nx Regional nodes cannot be assessed N0 No regional lymph nodes identied N1
N1a Metastasis in one regional node N1b Metastasis in two to three regional lymph nodes N1c No regional lymph nodes are positive, but there are tumor deposits, i.e., satellites in the subserosa or in
N2 Metastasis in four or more regional lymph nodes N2a Metastasis in four to six regional lymph nodes N2b Metastasis in seven or more regional lymph nodes M -DISTANT METASTASIS M0 No distant metastasis M1 Distant metastasis M1a Metastasis conned to one organ-liver, lung, ovary, non-regional lymph nodes without peritoneal metastasis M1b Metastasis in more than one organ M1c Metastasis to the peritoneum with or without other organ involvement
T categories
Although these categories have not changed, and T4 was divided into T4a and T4b in the previous edition, further clarication that tumors with perforation in which tumor cells are continuous with the serosal surface through inammation are considered to be T4a. In the lower rectum, in the absence of peritoneal covering, tumors that invade or directly adhere to adjacent organs or structures are considered T4b.
N categories
There is a discussion regarding isolated tumor cells in lymph nodes and micrometastases. Isolated cells consist of up to 20 cells within subcapsular or marginal sinus of a lymph node should be designated N0 (or NOi+), but their presence does not change the state to stage III.Micrometastases are clusters of 20 or more cells or metastases measuring >0.2mm and <2mm in diameter. Lymph nodes with micrometastases are considered positive and designated N1. Outcomes in tumors with nodal micrometastases ranging from 0.2 to 2mm are similar to those with metastases >2mm; thus the designation of N1mi is unnecessary. The interpretation of discrete tumor nodules found within the lymph drainage area of the primary rectal carcinoma is claried. Nodules that contain no identiable lymph tissue or vascular/neural structures should be considered tumor deposits and designated N1c. Tumor deposits within a vessel wall should be considered lymphovascular invasion with the site-specic designations of L+ for lymphatic or small vein invasion and V+ for deposits in endothelial cell-lined spaces with associated red blood cells or smooth muscle cells. If tumor nodules are found around neural structures, they are classied as perineural invasion. N1c changes the disease to stage III even in the absence of nodal metastases. The number of deposits has no inuence on the designation and is not added to the number of positive nodes.
M categories
M1c which denotes peritoneal metastases has been added
Key changes to AJCC staging of colorectal cancer [12]
Metastasis in one to three lymph nodes (tumor in lymph nodes measuring 0.2mm) or any number of tumor deposits are present, and all identiable lymph nodes are negative
non-peritonealized pericolic or perirectal soft tissue without lymph node metastasis
A. V. Hayman and C.-A. Vasilevsky
would prompt genetic counseling and testing. Comorbidities must be ascertained in order to establish suitability for surgi­cal procedures or chemotherapy. The patient may warrant a cardiology or pulmonary assessment, nutritional consult, and, if appropriate, a geriatric evaluation including frailty screening [14] prior to recommendation of treatment. Past surgical history should also be queried since this may affect choice of future surgical approach.
Physical Examination
On physical examination, the abdomen should be assessed for previous scars, as well as palpable masses, hepatomegaly, or abdominal distention, especially in the presence of suspected obstruction. If the patient has a thin body habitus and a large intra-abdominal luminal mass, it may be possible to palpate the mass on abdominal exam. In the presence of a high-grade obstruction, the patient may present with abdom-
24 Colorectal Cancer: Preoperative Evaluation andStaging
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Table 24.5 American Joint Committee on Cancer (AJCC)
Stage 0 T1s N0 M0 Stage 1 T1,T2 N0 M0 Stage II T3, T4 N0 M0 Stage IIA T3 N0 M0 Stage IIB T4a N0 M0 Stage IIC T4b N0 M0 Stage III Any T N1,N2 M0 Stage IIIA T1, T2 N1 M0
T1 N2a M0
Stage IIIB T1, T2 N2b M0
T2, T3 N2a M0 T3, T4a N1 M0 T4a N2a M0
T4b N1, N2 M0 Stage IV Any T Any N M1 Stage IVA Any T Any N M1a Stage IVB Any T Any N M1b Stage IVC Any T Any N M1c
TNM Staging System for Colorectal Cancer 8th ed., 2017
inal distention and pain. For distal rectal tumors, perhaps the most important diagnostic test is a thorough digital rectal exam (DRE). If the lesion is palpable, the surgeon should determine and document: percentage of luminal circumfer­ence involved; quadrant(s) involved; distance between the distal margin of the tumor and the superior aspect of the ano­rectal ring; tactile characteristics (rm versus soft, mobile versus tethered versus xed, etc.), and involvement of other structures (anal sphincter muscles, posterior vaginal wall, levator muscles, prostate). In addition, DRE allows the eval­uation of sphincter bulk and tone, which is important should restorative proctectomy be considered. DRE is limited in that it can only be used to assess distal tumors that are within range of the examining nger and may be also limited by patient body habitus.
Proctoscopy
Proctoscopy should be performed by the operating surgeon to determine the exact location of any tumor reported to be in the rectosigmoid by the endoscopist at index colonoscopy, prior to initiation of treatment. This examination is critical, as determination of tumor location at index colonoscopy is often inaccurate [15]. This is especially true for tumors described as being in the “sigmoid” or “rectosigmoid” which are subsequently found to be in the mid or distal rectum [15]. For rectal cancers, it is important to clearly delineate tumor location relative to anatomic landmarks in order to determine if sphincter-sparing surgery would be an option and to mark the distal extent of the tumor with tattoo (see above). It is also useful as a surveillance tool to assess tumor response to neoadjuvant therapy. Proctoscopy can be performed in clinic without sedation, with only an enema preparation in most patients. Rigid proctoscopy requires less equipment, but one
cannot see beyond 25cm, and it can be challenging to see lateral lesions. Furthermore, it can be quite uncomfortable for some patients and technically difcult in patients with a larger body habitus. Video exible proctosigmoidoscopy is better tolerated by the patient and allows for photo documen­tation of tumor morphology and location; however, it is still subject to the vagaries of exact delineation of distance as pre­viously mentioned .
Colonoscopy
Colonoscopy is required to fully evaluate the colon after the diagnosis of a colorectal malignancy or unresectable polyp has been made to exclude synchronous cancers which may occur in 3–5% of patients with primary rectal cancer as well as synchronous polyps which occur in as many as 30% [16]. In general, sufcient biopsies of the tumor should be obtained to conrm both the diagnosis of cancer, as well as to obtain tissue for immunohistochemistry to ascertain biomarkers which may guide chemotherapeutic options and prognosis.
Occasionally, there are conditions that may preclude a complete examination of the colon preoperatively, such as the presence of an obstructing lesion or perforation. In some cases, a water-soluble contrast enema could be considered in patients who present with acutely obstructing tumors of the left colon or rectum, in order to rule out distal synchronous large lesions and help prep the distal colon should intraop­erative colonoscopy be required. CT with rectal contrast is generally preferred over water-soluble enema due to three­dimensional perspective, but typically the patient has already received a CT in the emergency room, so the risks of a repeated scan must be weighed against the benets. Evaluation of the proximal colon may occasionally be obtained via CT colonography in cases of partial obstruction or deferred until the postoperative period or after reversal of a diverting ileostomy. If a patient presents with a completely obstructing colon or rectal cancer and either diverting loop colostomy or Hartmann’s resection are performed, comple­tion colonoscopy can be performed prior to resection or Hartmann reversal via both limbs of the stoma or via the colostomy and rectal stump to ensure that a synchronous tumor or polyp will not be ignored at the time of reanastomo­sis. Another feasible option in the face of an obstructing lesion is the placement of an endoscopic stent, which allows the opportunity for biopsy and can serve as a bridge to sur­gery following resolution of the obstruction, as well as facili­tate pre-treatment colonoscopy (See Chap. 25).
Tumor Localization
Endoscopic tattooing is recommended for all colonic lesions for surgical localization. Endoscopic measurements either via landmarks or centimeters from the anal verge are notori­ously inaccurate. With the exception of the cecum, which has distinct, reproducible anatomic landmarks (ileocecal valve,
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appendiceal orice), the standard recommendation is sub­mucosal tattooing with India ink distal to the tumor in at least two quadrants.
However, because referring endoscopists may differ in their routine practice, it is imperative that the surgeon com­municate with the endoscopist regarding if and how a tumor was marked with tattoo. This is especially important in the setting of a malignant polyp that has been completely removed endoscopically and is later found to have invasive carcinoma, typically to the endoscopist’s surprise. In this situation, the endoscopist should repeat the colonoscopy as soon as possible in order to detect the polypectomy scar and tattoo just distal to that site. This can be quite challenging in the setting of multiple polypectomies and may require mul­tiple tattoos, which poses treatment dilemmas for the opera­tive surgeon [17, 18]. It is always favored to have the index endoscopist perform the repeat colonoscopy for tattooing as that individual will have the greatest chance of accurately localizing the polypectomy site in question. These cases are often best managed by a multidisciplinary discussion with the surgeon and the endoscopist. Fortunately, even when the polypectomy site may not be visible to the naked eye on endoscopy, once the surgical resection specimen has been xed, it can often be detected pathologically, conrming resection of the appropriate segment.
As noted above, rectal tumors must be accurately local­ized prior to initiation of neoadjuvant treatment since assessment of distal resection margins after treatment is often difcult due to downstaging of the tumor. A few cave­ats should be mentioned. Tattooing with India ink for rectal cancer has been found by some investigators to be inaccu­rate with error rates ranging from 2% to 21% [19]. It should be remembered that submucosal tattoos that are placed pre­operatively are often difcult to visualize from the abdo­men because of the thick mesorectum. Some authors have suggested that submucosal rectal wall tattoos be placed in the operating room at the time of resection to accurately mark the distal resection margin [20], although this may not be possible in the setting of complete clinical response, which is why placement of tattoo at the time of diagnosis is favored. Unlike for intraperitoneal colon cancers, tattoo of extraperitoneal rectal cancers will primarily be visible dur­ing intraoperative endoscopy, and a exible colonoscope/ sigmoidoscope or rigid proctoscope should be available for localization during resection. Several case reports have also raised the issue of potential tumor implantation by improper endoscopic tattooing directly through the tumor, which obviously should be avoided [21]. In addition, tattooing may induce altered appearance of the rectal wall on MR or reactive lymphadenopathy, with possible resultant over­staging on MRI [22]. Thus, if a rectal tumor was not tat­tooed at diagnosis, it is optimal to obtain staging MRI and CT prior to marking the tumor endoscopically with ink. If
tattoo is placed transmurally, it can render resection more difcult because the dye can obscure normal anatomic planes [23]. As such, preoperative clipping has been sug­gested as a feasible alternative; however, clips carry the risk of falling off [19].
Blood Work
Blood work including complete blood count, basic chemis­try, and carcinoembryonic antigen (CEA) should be obtained. CEA is used as a prognosticator whereby levels <5ng/ml have been found to have better prognoses stage for stage as opposed to CEA 5ng/ml [24]. Moreover, normalization of previously elevated CEA levels in patients who were treated with neoadjuvant treatment has been associated with com­plete pathologic response [25]. CEA levels that fail to nor­malize post-resection should raise the suspicion of metastatic or residual disease. CEA should be routinely measured dur­ing surveillance of patients posttreatment since elevation of previously normal levels may signal the development of recurrent or metastatic disease. Routine testing for transami­nases, bilirubin, and/or alkaline phosphatase, unless indi­cated for other reasons, is not necessary preoperatively as they have been found to be neither sensitive nor specic for the diagnosis of liver metastases and are no longer routinely recommended by NCCN for staging or surveillance [6], although their use is still advocated by the European Society of Medical Oncology [26].
Imaging
Computed Tomography (CT) Scan
Initial staging includes CT scan of chest, abdomen, and pel­vis in order to detect the presence of synchronous metastatic disease which may be present in 30% of patients at presenta­tion. CT scan of the chest is used to determine the presence of lung metastases and to set a baseline for any preexisting suspected benign lesions [7]. Its overall accuracy in detect­ing lung metastases is 84% with a sensitivity and specicity of 73% and 74%, respectively [27]. CT will also detect inde­terminate pulmonary lesions in 4–42% of patients; however, upon further evaluation, only 1% are eventually conrmed as metastases [28]. Abdominal CT will indicate the presence of liver metastases, which may occur in 20–34% of patients [7]. CT is the most common imaging modality used to stage met­astatic disease with an estimated sensitivity of 85%, positive predictive value of 96%, and false-positive rate of 4% [29]. For liver lesions measuring <10mm, MRI outperforms CT because of enhanced soft tissue resolution [30]. CT may also demonstrate tumor-related complications such as perfora­tion, obstruction, and invasion of adjacent organs and should be done with both oral and IV contrast whenever possible. If a patient has an iodine allergy, they can be prepped with ste­roids and diphenhydramine. In the case of renal insuf-