Anal Cancer Flashcards

1
Q

Epidemiology - What is the incidence, sex predominance, and median age?

A

2% of all GI cancers; more females, median age of diagnosis is 62

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2
Q

List 5 General Risk Factors

A

HIV (can impact mgmt, but not at BCCA), HPV, Immunosuppression, Smoking (4x risk), Chronic perianal irritation

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3
Q

What is the strongest risk factor?

A

HPV - most caused by HPV16/18 (so no history of genital warts necessary); usually in younger patients, and may be a risk factor even if no HPV DNA is detected

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4
Q

What are the proximal and distal borders? Where does rectal Ca begin?

A

Proximal: Where rectum enters puborectalis sling
Distal: Where squamous mucosa blends with perianal skin
Rectal Ca: If epicentre >2cm from dentate line (transition from glandular to squamous mucosa)

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5
Q

List the lymphatic drainage of the: Distal rectum, proximal anal canal, dentate region, and distal anal canal (beyond dentate)

A

Distal rectum: perirectal –> presacral
Prox anal: hemmoroidal –> perirectal –> obturator –> internal iliac –> common iliac
Dentate: Hypogastric, obturator & presacral
Distal anal canal: Inguinal LNs –> femoral LNs –> external iliacs

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6
Q

What is the blood supply of the anal canal?

A

Upper 2/3s of the anal canal –> portal system (aorta to IMA to SRA, as well as aorta to CI to II to middle rectal
Lower 1/3 enters the systemic system (aorta to CI to II to internal pudendal to inferior rectal

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7
Q

List local, regional and distant patterns of spread

A

Local: Commonly see invasion into sphincter muscles and perianal connective tissue (50% sphincter invasion at presentation). Also, see vaginal invasion in women and rarely prostatic in men (fistula <5% of the time)
Regional: Lymphatic spread ++ common and happens early, depending on location will vary which chains are involved (25% LN+ at presentation, 10% with inguinal)
Distant: Rarer at presentation (~10%); common sites liver, lung, extra-pelvic LN

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8
Q

List some benign and pre-malignant lesions to have on the ddx

A

Benign: hemorrhoid, anal fissure (less common AVM, peri-rectal abscess, condyloma, fistula, rectal prolapse, skin tag, lipoma, trauma)
Pre-malignant: anal intraepithelial neoplasia (AIN) - similar to cervix, at transition zone with low and high grade due to HPV

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9
Q

How do we approach AIN

A

If low grade - observation as many will spontaneously regress, but some will progress to high-grade AIN
If high grade - True precursor of anal SCC, refer for ablative procedures

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10
Q

What is the most common malignant pathology? List 10 other, rare, pathologies

A

Most common: Squamous cell (~80%); Keratinizing usually from lower anal canal (aka below dentate) and non-keratinizing above dentate
Others: Adenocarcinoma (from anal glands, usually actually distal rectal with extension, treat like low rectal ca); SCC/BCC (from perianal skin); Bowen’s disease; Paget’s disease; Melanoma; Neuroendocrine; Lymphoma; Sarcoma; Kaposi’s sarcoma; Mets

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11
Q

What is the roll of CT, MR, and PET in workup?

A

CT - Usually inferior to PE for evaluating primary, useful to look for distant dz and regional LNs
MR - no evidence this is superior to CT, so not SOC
PET - useful to evaluate dz extent (primary, regional, and distant), so standardly done for staging and 3 mos post tx to evaluate response

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12
Q

List 5 common clinical presentations

A

Rectal bleeding (most common), anorectal pain, sensation of anal/rectal mass, change in bowel habits, inguinal LAD if advanced

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13
Q

Is there a role for screening?

A

No RCT evidence & no tumour marker
In general population - too rare, so no
Screening controversial in HIV+ or those with HPV genital dz (done in Vancouver but not universal)

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14
Q

List 6 demonstrated prognostic factors

A
  1. Primary tumour size
  2. LN status (survival with LN+ about half that if LN- for same T stage)
  3. HgB<100
  4. Poor ECOG
  5. HIV+ with CD4<200 (higher recurrence rate)
  6. Poorly differentiated tumour
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15
Q

Does addition of chemo reduce rate of distant mets?

A

It seems no - addition of chemo had not decreased number of patients who develop mets post tx
Overall rare, only 10-20% will have distant relapse after curative local treatment
only ~10% with mets at presentation

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16
Q

List the TNM staging

A

T: TX, not assessed; T0, no evidence of primary; Tis, high grade AIN; T1, less than 2cm; T2, more than 2cm but less than 5cm; T3, greater than 5cm; T4, any size with invasion of adjacent organs
N: Nx, cannot be assessed; N0, no nodal mets; N1 any local nodal mets; N1a, gets in inginal, mesorectal, or II LNs; N1b, mets in EI LNs; N1c both N1b and N1a
Note - any LNs beyond EI is technically considered metastatic dz

17
Q

What is the work-up of a suspected lesion

A

Hx + P/E (including DRE +/- gyne!!!!)
Consider anoscopy or sigmoidoscopy
Biopsy -> must have bx of primary and ideally sus LNs
BW -> CBC, lytes, renal fxn, LFTs, Alk Phos; consider HIV and CD4 count
Imaging: CT or MR pelvis (both bad at detecting LNs as 50% <5mm), can consider transanal U/S; for distant dz - CXR, CT chest, or PET for evaluation (20-25% upstaged w/ PET)
Consider pregnancy test in woman and sperm banking in men

18
Q

List acute RT S/E

A

Fatigue
Proctitis (tenesmus, flatus, mucous in stool, small stool pellets)
Enteritis (abdo cramps, watery brown stool ~7-10 days after tx start)
Cystitis
Alopecia (likely permanent)
Skin rxn - typically severe moist desquamation to perianal skin and surrounding region (sitz baths, pat dry, cortisone cream for comfort until moist desquam, then flamazine)

19
Q

List late RT S/E

A

Bowel - altered vasculatre; Malabsorption (terminal ileum); altered bowel habits (freq, diarrhea), rectal bleeding, small risk stricture, perf, SBO
Impaired anal sphincter fxn & incontinence -> risk seems to be related to pre-rx fxn; colostomy rate for tx toxicity 2-10% (30% overall with salvage)
Skin - telangiectasia, hyper- and hypo-pigmentation
Sexual - Vaginal dryness, stenosis, fibrosis, decreased drive, dysparenuia, ED
Reproductive - Menopause, sterility
Hip #
Second malignancy

20
Q

What are the consequences of treatment breaks?

A

Increased colostomy rate! IF necessary try to do before second chemo cycle to facilitate scheduling