RECTAL CANCER Flashcards

1
Q

ANATOMY

A

Begins at the rectosigmoid junction, at level of third sacral vertebra
o Ends at the anorectal junction, 2-3 cm in front of and a little below the coccyx

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2
Q

Divided into 3 parts:

A

Upper third, Middle third, Lower third

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3
Q

3 distinct intraluminal curves

A

(Valves of Houston)

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4
Q

Peritoneal Relations

A

Superior 1/3rd of the rectum: Covered by peritoneum on the
anterior and lateral surfaces
§ Middle 1/3rd of the rectum: Covered by peritoneum on the
anterior surface
§ Inferior 1/3rd of the rectum: Devoid of peritoneum, Close
proximity to adjacent structure including boney pelvis

NOTE: Distal rectal tumors have no serosal barrier to invasion of adjacent structures and are more difficult to resect given the close confines of
the deep pelvis.

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5
Q

BLOOD SUPPLY

A

Arterial supply
¨ Superior rectal A – fr. IMA; supplies upper and middle rectum
¨ Middle rectal A- fr. Internal iliac A. (supplies lower rectum)
¨ Inferior rectal A- fr. Internal pudendal A.
§ Venous drainage
¨ Superior rectal V- upper & middle third rectum
¨ Middle rectal V- lower rectum and upper anal canal
¨ Inferior rectal vein- lower anal canal
§ Innervations
¨ Sympathetic: L1-L3, Hypogastric nerve
¨ ParaSympathetic: S2-S4
§ Lymphatic drainage
¨ Upper and middle rectum
- Pararectal lymph nodes, located directly on the muscle layer of the rectum
- Inferior mesenteric lymph nodes, via the nodes along the superior rectal vessels
¨ Lower rectum: Sacral group of lymph nodes or Internal iliac lymph nodes
¨ Below the dentate line: Inguinal nodes and external iliac chain

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6
Q

EPIDEMIOLOGY

A

Colorectal cancer is the third most frequently diagnosed cancer in the US men and women.
o It represents 38% of colorectal cancers
o Median age- 7th decade but can occur any time in adulthood. Same incidence male vs. female

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7
Q

TNM

A

TX Primary tumor cannot be assessed
T0 No evidence of primary tumor
Tis Carcinoma in situ: intraepithelial or invasion of lamina propria
T1 Tumor invades submucosa
T2 Tumor invades muscularis propria
T3 Tumor invades through the muscularis propria into pericolorectal tissues
T4a Tumor penetrates to the surface of the visceral peritoneum
T4b Tumor directly invades or is adherent to other organs or structures

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8
Q

DUKES CLASSIFICATION

A

Dukes A: Invasion into but not through
the bowel wall.
§ Dukes B: Invasion through the bowel
wall but not involving lymph nodes.
§ Dukes C: Involvement of lymph nodes
§ Dukes D: Widespread metastases

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9
Q

o Modified astler coller classification-

A

Stage B1: Extending into muscularis
propria but not penetrating through it;
nodes not involved.
§ Stage B2: Penetrating through
muscularis propria; nodes not involved
§ Stage C1: Extending into muscularis
propria but not penetrating through it.
Nodes involved
§ Stage C2: Penetrating through
muscularis propria. Nodes involved
§ Stage D: Distant metastatic spread

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10
Q

RISK FACTORS

A

Etiological agents
§ Environmental & dietary factors
§ Chemical carcinogenesis.
o Associated risk factors
§ Male sex
§ Family history of colorectal cancer
§ Personal history of colorectal cancer, ovary, endometrial, breast
§ Excessive BMI
§ Processed meat intake
§ Excessive alcohol intake
§ Low folate consumption
§ Neoplastic polyps
o Hereditary Conditions (FAP, HNPCC)

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11
Q

PROGNOSTIC FACTORS

A

Good prognostic factors
§ Old age
§ Gender(F>M)
§ Asymptomatic pts
§ Polypoidal lesions
§ Diploid
o Poor prognostic factors
§ Obstruction
§ Perforation
§ Ulcerative lesion
§ Adjacent structures involvement
§ Positive margins
§ LVSI
§ Signet cell carcinoma
§ High CEA
§ Tethered and fixed cancer

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12
Q

CLINICS

A

Symptoms
§ Asymptomatic
§ Change in bowel habit (diarrhoea, constipation, narrow stool, incomplete evacuation, tenesmus).
§ Blood PR.
§ Abdominal discomfort (pain, fullness, cramps, bloating, vomiting).
§ Weight loss, tiredness.

o Acute Presentations
§ Intestinal obstruction
§ Perforation
§ Massive bleeding

o Signs
§ Pallor
§ Abdominal mass
§ PR mass
§ Jaundice
§ Nodular liver
§ Ascites

o Rectal metastasis travel along portal drainage to liver via superior rectal vein as well as systemic drainage to lung via middle inferior rectal veins.

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13
Q

DIAGNOSIS

A

History—including family history of colorectal cancer or polyps
o Physical examinations including
§ DRE
§ Complete pelvic examination in women: size, location, ulceration, mobile vs. tethered vs. fixed, distance from anal verge and sphincter
functions.
o Laboratory exams
§ CEA: High CEA levels associated with poorer survival
§ Routine investigation: Complete blood count, KFT, LFT + Chest X-ray
o Proctoscopy—including assessment of mobility, minimum diameter of the lumen, and distance from the anal verge
o Biopsy of the primary tumor
o Transrectal ultrasound –EUS
§ use for clinical staging.
§ 80-95% accurate in tumor staging
§ 70-75% accurate in mesorectal lymph node staging
§ Very good at demonstrating layers of rectal wall
§ Use is limited to lesion < 14 cm from anus, not applicable for upper rectum, for stenosing tumor
§ Very useful in determining extension of disease into anal canal (clinical important for planning sphincter preserving surgery)
o CT scan
§ Part of routine workup of patients
§ Useful in identifying enlarged pelvic lymph-nodes and metastasis outside the pelvis than the extent or stage of primary tumor
§ Limited utility in small primary cancer
§ Sensitivity 50-80%
§ Specificity 30-80%
§ Ability to detect pelvic and para-aortic lymph nodes is higher than peri-rectal lymph nodes.
§
o Magnetic Resonance Imaging (MRI)
§ Greater accuracy in defining extent of rectal cancer extension and also location & stage of tumor
§ Also helpful in lateral extension of disease, critical in predicting circumferential margin for surgical excision.
§ Different approaches (body coils, endorectal MRI & phased array technique)
§
o PET with FDG
§ Shows promise as the most sensitive study for the detection of metastatic disease in the liver and elsewhere.
§ Sensitivity of 97% and specificity of 76% in evaluating for recurrent colorectal cancer

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14
Q

SURGERY

A

(distal 15 cm of the large intestine). Choice of operation depends on individual case; types of operations:
§ Low anterior resection of rectum (LAR): curative procedure of choice if adequate distal margins; uses technique of total mesorectal
excision.

Tumours located in the distal 3-5 cm of the rectum present the greatest challenge to the surgeon:
¨ Abdominoperineal resection of rectum (APR): if adequate distal margins cannot be obtained; involves the removal of distal
sigmoid colon, rectum, and anus – permanent end colostomy required
¨ Local excision: for select T1 lesions only. Above T2à resection is mendatory.

Palliative procedures involve proximal diversion with an ostomy for obstruction and radiation for bleeding or pain.

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15
Q

ADJUVANT THERAPY

A

Combined neoadjuvant chemoradiation therapy followed by post-operative adjuvant chemotherapy for stages II and III

The retroperitoneal pelvic location being a limitation for surgeons provide an opportunity for treatment by radiation therapy that is
not feasible for colon tumors
§ Pre-operative radiation (usually 4500 to 5040 cGy) with infusional 5-FU–leucovorin, 5-FU alone, or capecitabineà dramatic
downstaging
¨ Can help the surgeon to achieve clear margins without compromising the ANS.
¨ can even result in the disappearance of the tumor, but difficult to predict which patients will benefit from it

The goal is to downgrade the tumor in order to be able to preform LAR and preserve continency

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16
Q

INDICATIONS FOR ADJUVANT THERAPY

A

stage II-III (wall infiltration and/or node positive)
¨ stage II-III which not received preoperative RCHT
¨ patients who did not receive adequate mesorectal resection
¨ circumferential margins involved
¨ high gradig (G3)
¨ Perforation in tumor
¨ maneuvers during the surgical action
¨ not radical surgery
¨ Inadequate lymphadenectomy (<12 lnf)

17
Q

TOXICITY

A

Proctitis
¨ Cystitis
¨ Diarrhea
¨ Skin erythema (intergluteal fold, perineum)

18
Q

PROGNOSIS

A

total mesorectal excision has resulted in a significant increase in 5-year survival rates (50% to 75%), a decrease in local recurrence rates (30% to
5%), and a decrease in the incidence of impotence and bladder dysfunction (85% to <15%).

19
Q

TOTAL MESORECTAL EXCISION

A

a precise dissection of the rectum and all pararectal lymph nodes within an oncologic package: the mesorectal envelope.

A TME is when the surgeon removes some of the fatty tissue around the rectum (mesorectum).

The fatty tissue contains lymph nodes and blood vessels. This means all the lymph nodes near to the tumour are removed, which reduces the risk of the cancer coming back. If possible, the surgeon joins the colon to the top of the anus.

20
Q

1)Total mesorectal excision (TME)

A

Most people with rectal cancer have a TME as part of their surgery. A TME is when the surgeon removes some of the fatty tissue around the rectum (mesorectum).

The fatty tissue contains lymph nodes and blood vessels. This means all the lymph nodes near to the tumour are removed, which reduces the risk of the cancer coming back. If possible, the surgeon joins the colon to the top of the anus.

21
Q

2)Anterior resection

A

Rectal cancers in the upper and middle part of the rectum can be removed by an operation called an anterior resection. The surgeon removes the part of bowel that contains the cancer, then re-joins the two open ends of bowel. The illustrations show the part of the bowel that is removed, and how the two ends are joined together. This operation is also called a low anterior resection (LAR).

You may have a temporary stoma (usually an ileostomy) after this operation. You can usually have a stoma reversal a few months later.

22
Q

3)Colo-anal and J-pouch surgery

A

If the cancer is low in the rectum, the surgeon may use an operation called a colonic J-pouch. This is used to join the bowel to the anus. It is a type of reconstructive surgery. The surgeon makes a pouch, called a J-pouch, from part of the colon, before joining it to the anus. The pouch acts like a new rectum and stores stools (poo) until it is convenient to pass them. The illustration shows a J-pouch.

You may have a temporary stoma (usually an ileostomy) after this operation This allows the bowel to heal. You can usually have a stoma reversal a few months later.

23
Q

4)Abdomino-perineal resection (APR)

A

If the cancer is very close to the anus, you may need an operation called an abdomino-perineal resection. This is when the surgeon needs to remove the rectum and anus, to remove all the cancer. You will have a permanent stoma (usually a colostomy) after this operation.

As well as the wound on your tummy, you will have a wound on your bottom where the anus has been closed. The anus may be closed using muscle, fat and skin from another part of the body. This is called a flap. This operation can be done as either keyhole (laparoscopic) surgery or open surgery, depending on the size of the tumour.

24
Q

RT INDICATIONS

A

To lower local failure rates and improve survival in resectable cancers
¨ to allow surgery in primarly inoperable cancers
¨ to facilitate a sphincter-preserving procedure
¨ to cure patients without surgery: very small cancer or very high surgical risk

25
Q

RT Indications

A

Rectum is not surrounded by a serosa and is near to many pelvic structures, therefore the high risk of invasion is relatively
high
¨ Preoperative treatments in rectal cancer are administered with the aim to reduce the risk of local recurrence and to
perform a more conservative surgery
¨ RT (+/- CHT) is administered in locally advanced rectal cancer: Stage II (T3-4 N0) or Stage III
¨ In contrast adjuvant treatment of colon cancer is more focus on preventing distant metastastes, since this disease is
characterized by a low rate of local recurrence

26
Q

§ Preoperative vs post-operative RT

A

Advantages of preoperative RT are
- Reduce the tumor volume
- Less late toxicities
- Surgery-naïve tissue is more oxygenated, thus is more
sensitive to RT
- Increase the rate of sphincter-sparing procedures
- Less anastomosis complications
¨ Disadvantages of preoperative RT are: Possible overtreatment of
early-stage tumors

27
Q

Preoperative RT can be administered in two main schedules

SHORT COURSE (typically used in Europe and
America):

A

a) RT dose: 25 Gy in 5 daily fractions of 5
Gy (5 Gy x 5).
b) Exclusive preoperative treatment (no
CHT, no boost).
c) Treatment volume: Primitive tumor
(primitive, rectum, mesorectum),
Node: common iliac, internal iliac,
presacral and obturators, Esternal iliac
(if T4)
d) Timing with surgery: 3-5 days
e) No tumor downsizing
f) Do not use if you want to get a
“sphincter saving” surgery

28
Q

LONG COURSE (typically used in North-East
Europe)

A

RT dose: 45-50.4 Gy standard fractionation (1.8-2 Gy). Boost up to 55 Gy on primitive
b) Treatment volume: Primitive tumor (primitive, rectum, mesorectum), Node: common iliac, internal
iliac, presacral and obturators, Esternal iliac (if T4)
c) Associate with chemo!
d) Timing with surgery: 8-10 weeks (not less than 6)
e) Recent evidence shows that deferring surgery (over 10 weeks) would result in an increased rate of
complete pathological response (no evidence of disease at the histological examination).

29
Q

SHORT COURSE

A

No differences in term
of local recurrence
— Shorter treatment time
— Less side effects
— Suggested in case of
emergencies (bowel
obstruction, bleeding) or
in middle/upper rectum
tumors

30
Q

LONG COURSE

A

Longer treatment time
— In lower rectum tumors can
increase the rate of
sphintcher saving surgery, if
associated with CHT
— Deferring surgery ovber 10
weeks can get an higher rate
of complete pathological
response