CA Colon. Mzux

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    Click to edit Master subtitle style

    4/13/12

    COLON CANCER

    Presenter: Dr. Harrison R. Chuwa, M.Med ClinicalOncology Resident

    Special thanks to Dr. Maunda, Consultant Oncologist

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    Key Issues/Lay-out

    Introduction

    Anatomy

    Epidemiology Natural history

    Pathology

    Mode of Spread

    Clinical Presentation

    Diagnostic Work-up

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    Introduction

    Is the 2nd leading

    cause of cancer

    death in thewestern world.

    Develops over

    a number of years

    & normally begins

    as a polyp.

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    Anatomy

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    Arterial Supply

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    Venous Supply

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    Lymphatic Drainage

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    Cross-section of Colon

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    Epidemiology

    Approximately 6% of individuals inthe US will develop a cancer of thecolon or rectum within their lifetime

    Male: female = 1.37:1

    The incidence in developingcountries is increasing

    At ORCI, 60 cases (0.55%) were Rx-ed for colon ca from 2008 to 2010.70% male

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    Etiology & Risk Factors

    Aging

    Hereditary Risk Factor

    Environmental Life style and Dietary Factor

    Inflammatory Bowel Diseases

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    Genetic SusceptibilitySyndromes

    Familial Adenomatous Polyposis(FAP)- APC

    Hereditary Nonpolyposis ColorectalCancer (HNPCC)- hMLH1/hMSH2

    Turcot syndrome

    Peutz-Jeghers syndrome-STK11 MUTYH-associated polyposis

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    Colon Cancer

    Sporadic(averagerisk)(65%85%)

    Fami

    lyhistory(10%30%)

    Ra

    resyndromes(

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    Pathogenesis of ColonCancer

    i. Tumour suppressor genemutations

    APC gene defect DCC

    p53

    ii. Proto-oncogene amplification

    K-ras : Proto-oncogene

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    Natural History of

    Colon Cancer

    Normalepithel

    ium

    Hyper-prolifera

    tive

    epithelium

    Earlyadeno

    ma

    Inter-mediat

    e

    adenoma

    Lateadeno

    ma

    Carcinoma

    Metastasis

    Loss ofAPC

    Activation

    ofK-ras

    Deletion of

    18q

    Lossof

    P53

    Otheralteratio

    ns

    Adapted from Fearon ER. Cell 61:759,1990

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    Pathology

    Macroscopically

    ulcerative, polypoid, annular, orinfiltrative

    Microscopically

    Adenocarcinoma >95% Carcinoid tumours

    Gastrointestinal stromal tumours (GITS)

    Lymphomas

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    Distribution of Cancer alongthe Colon

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    Mode of Spread

    Direct extension

    Peritoneal seeding

    Lymphatic drainage Hematogeneous

    Note: skip metastasis (retrograde

    spread) occurs in 1-3% of nodepositive pts

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    Clinical Presentation

    Early sign

    A change in bowel habits

    fatigue Late sign

    Colon obstruction

    Ribbon-like stool

    Hematochezia

    Cachexia (wasting syndrome)

    Di ti W k

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    Diagnostic Work-up H&P

    Colonoscopy or sigmoidoscopy

    Bx

    Imaging

    - Ba enema

    - CXR

    - US

    - CT scan

    - MRI

    - PET scan

    Blood testing

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    Staging

    1. Dukes classification for staging in colorectalcancer:

    Stage A: Tumour confined w/in bowelwall

    -Prevalence at Dx: 10%

    - 5yr survival rate: > 90% Stage B: Extension through bowel

    wall

    Prevalence at Dx: 35%

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    TNM Staging

    Stage O(in situ)Thetumor issmallandlimited toThemucosa

    Stage I

    The tumorhasspread tothemuscularis,but not to

    theouter wall

    Stage II

    The tumorhasspread totheouter wall ofthe colon,butnot to

    Stage III

    The tumorhasspread intonearbylymphnodes, but

    notto other

    Stage IVThe tumorhasspread tootherorgans suchasthe liver,

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    Management

    Surgery

    Chemotherapy

    Targeted therapySometimes used in combination with

    standard chemotherapy

    Radiation

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    Treatment by Stage

    Stage O:

    Local surgery (polypectomy or removalof larger tumors)

    Stage I:

    Surgery followed by observation

    Stage II: Surgery followed by chemotherapy or

    observation

    Stage III:

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    Surgery

    Polypectomy

    Laser or diathermy therapy

    Radical surgery Total colectomy

    Transverse colectomy

    Rt hemicolectomy

    Lt hemicolectomy

    Lymphadenectomy

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    chemotherapy

    Neoadjuvant down staging

    1st line

    Adjuvant micro remnants 1st line

    Palliative metastatic disease

    2nd line + targeted therapy

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    Chemotherapy cont...

    1st line regimen

    5-FU +LV

    5-FU + LV + OX (FOLFOX 4/6) 5-FU + LV + Irinotecan (FOLFIRI)

    Irinotecan + 5-FU + LV (IFL)

    Capecitabine 2nd line regimen

    5-FU + LV+ OX + Irinotecan (FOLFOXIRI)

    FOLFOX + bevacizumab cetuximab

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    Radiation

    No clear evidence of survival benefitwith RT

    Mainly for stage 4 tumours fixed toabdominal lining

    Adjuvant EBR +/- chemo i.e.Adjuvant chemoradiation

    Brachytherapy has no role in colonca

    XRT also has a role for metastatic

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    XRT Techniques

    Field should include margin aroundtumor bed, LNs and residual diseasebased on pre-op imaging and/or

    surgical clips. 3D simulation to define the tumour

    volume

    Bladder distension & prone position

    Dose 50.4Gy/1.8Gy/28# OR46Gy/2Gy/23#

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    Follow-up

    Follow-up visits

    Serial (CEA) measurements arerecommended

    Colonoscopy one year after removalof colon cancer

    Surveillance colonoscopy every threeto five years to identify new polypsand/or cancers

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    Prognostic factors

    - Stage and grade of disease.

    - Pre op CEA Level.

    - Presence of microsatellite instability& loss of DCC gene.

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    Screening

    FOBT

    Colonoscopy

    Sigmoidoscopy Ba enema

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