staging and grading cancer

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    STAGING

    AND

    GRADING CANCERPATHOLOGY DEPARTMENT,

    FACULTY OF MEDICINE,

    GADJAH MADA UNIVERSITY

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    The stageof cancer is a measure how much the cancer

    has grown and spreadThe gradingof cancer is determined by looking at certain

    features of the cancer cells under the microssope

    The aim: help to predict how a cancer might behave, howadvanced it is, how well it may respond to treatment.

    THE EARLY THE STAGE AND THE

    LOWER THE GRADE OF CANCER, THEBETTER THE OUTLOOK (PROGNOSIS)

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    GROWING AND SPREADING OF CANCER

    A cancer if untreated1. Growing from one celldivides and multiplies

    primary tumorinvade surrounding tissue

    2. Some cancer cellsget into local lymph channel

    lymph node(s)entrappedmultiplyenlargementof lymph node

    3. Some cancer cellsget into local small blood vesselinto bloodstreamspread to other areasmultiplysecondary tumor may then grow and invadenearby tissuespread again

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    GROWING AND SPREADING OF CANCER

    Each type of cancer differs in the speed ofgrowing and spreading

    Some cancer may spread easily and quickly,other may grow slowly and remain in the

    primary site for a long times

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    CANCER STAGING

    A way of describing how much a cancer has grown and

    spread the stage is based on 3 factors

    Primary tumor size and whether or not the tumor has growninto other nearby areas

    Whether or not the cancer has spread to the nearby lymphnodes

    Whether or not the cancer has spread to distant areas of thebody

    Leukemia, and other some cancer of the blood are notformally stagedthey are assumed to be in all parts ofthe body

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    CANCER STAGING

    TYPE OF STAGING

    1. Clinical staging, based on1. Phisical exam

    2. Imaging test (x-rays, CT scan, etc.)

    3. Sometimes biopsies

    4. Blood test (for certain cancers)2. Pathologic staging (only on patient who have had

    surgery to remove or explore the extent of the cancer)1. Combines: clinical staging + results from the surgery

    2. The pathology stage may be different from the clinicalstaging

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    CANCER STAGING

    STAGING SYSTEMS

    There were many different systems.

    Sometimes different systems were used to stage

    the same type of cancer.

    Although some of the better ones are still

    used, many of these systems did not give doctorsvery useful information

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    T(tumor)N(nodule)M(metastasis)

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    CANCER STAGING

    STAGING SYSTEMS

    TNM system1. Developed by AJCC (the American Joint Commitee on Cancer)

    2. Replaced many of the older systems

    TheT category describes the primary tumor

    1. Tx: tumor cant be measured2. T0: there is no evidence of primary tumor

    3. T1s: the cancer is in situ (has not started growing into the surroundingstructures)

    4. T1T4: describes the size and/or level of invasion. The higher the Tnumber, the larger the size and/or the further it have may grown into thenearby structures

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    CANCER STAGING

    STAGING SYSTEMS

    TNM system

    The N category describes whether or not the cancer has reached nearby lymphnodes

    Nx: the nearby lymph nodes cant be measured or found

    N0: nearby lymph nodes do not contain cancer

    N1N3: the size, location, and/or the number of lymph nodes involved.The higher N number, the more involved the lymph nodes are

    The M category tells whether there are distant metastasis

    Mx: metastasis cant be measured or found

    M0: there are no known distant metastasis M1: distant metastasis are present

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    CANCER STAGING

    STAGING SYSTEMS

    TNM system

    Note:

    Each cancer type has its own classification system.

    Letters and numbers do not always mean the same thing for everykind of cancer

    For example:

    Some cancer may have subcategories, s.a. T3a and T3b, while othermay not have an N3 category

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    CANCER STAGING

    STAGING SYSTEM

    STAGE GROUPING

    T, N, M are combinedoverall stageI, II, III, IV

    Sometimes stages are subdivided s.a. IIIA, IIIB

    For example, for breast cancer

    T1, N0, M0: primary tumor 2cm -

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    BREAST CANCER

    Stage I

    T1a: T 0.5 cm

    T1b: 0.5 cm < T 1 cm

    T1c: 1 cm < T 2 cm

    T1 N0 M0

    T 2 cm

    T1

    N0 = no regional lymph node metastasis

    M0 = no distant metastasis

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    BREAST CANCER

    Stage IIA

    T2 N0 M0

    N1 = metastasis to movable ipsilateral axillary lymph node(s)

    M0 = no distant metastasis

    2 cm < T < 5 cm

    No evidenceof tumor

    T0

    T0

    T1N1 M0}

    T2

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    BREAST CANCER

    Stage IIB

    T3 N0 M0

    N1 = metastasis to movable ipsilateral axillary lymph node(s) (p) N1a, N1b

    M0 = no distant metastasis

    T > 5 cm

    T2 N1 M0

    T3

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    BREAST CANCER

    Stage IIIAT0

    T1T2

    T3

    Metastasis to ipsilateral axillary lymph node(s)

    N1 = movable

    N2 = fixed to one another or to other structures

    M0 = no distant metastasis

    T3 N1 M0N2 M0

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    BREAST CANCER

    Stage IIIB

    Any T N3 M0

    N3 = metastasis to ipsilateral internal mammary lymph node(s)M0 = no distant metastasis

    Tumor of any size

    with direct extensionto chest wall or skin

    T4d = inflammatorycarcinoma

    T4 any N M0

    T4

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    BREAST CANCER

    Stage IV

    M1 = distant metastasis (including metastases to ipsilateral supraclavicular,

    cervical, or contralateral internal mammary lymph nodes)

    Any T any N M1

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    CANCER STAGING

    STAGING SYSTEM

    Other Staging System1. Duke system (for colorectal cancer)

    Stage A: the cancer is just in the bowel wall

    Stage B: the cancer has grown to the outer surface of

    the bowel wall Stage C: the cancer has spread to the lymph nodes

    near to the bowel

    Stage D: the cancer has spread to other parts of the

    body (metastases, or secondary tumors hanedeveloped)

    2. Other than TNM system used for lymphoma, some

    childhood cancers, cancer in some female reproductive

    organs

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    Modified DukeAThe tumor penetrates into the mucosa of the bowel wall but no further.Modified Duke B

    B1: tumor penetrates into, but not through the muscularis propria (themuscular layer) of the bowel wall.

    B2: tumor penetrates into and through the muscularis propria of the bowel wall.

    Modified Duke CC1: tumor penetrates into, but not through the muscularis propria of the bowelwall; there is pathologic evidence of colon cancer in the lymph nodes.

    C2: tumor penetrates into and through the muscularis propria of the bowel wall;there is pathologic evidence of colon cancer in the lymph nodes.

    Modified Duke DThe tumor, which has spread beyond the confines of the lymph nodes

    (to organs such as the liver, lung or bone).

    Modified Duke Staging

    System

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    Staging system for

    renal cancer Stage I:

    in the kidney only, < 7.0 cm FYS > 90%

    Stage II:

    in the kidney only, >7.0 cm

    FYS > 75%

    Stage III:

    in the kidney, may be any

    size, does not extend beyondGerota's fascia.

    Additionally, cancer hasspread to the renal vein, tothe inferior vena cava, or tothe adjacent adrenal gland

    FYS >65 % depending oninvolved sites

    Stage IV:

    extends beyond Gerota'sfascia, and/orhas spread to> 1 lnn. near the kidney

    spread to other organs in thebody: lungs, liver, brain,bones, intestines or pancreas

    FYS

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    GRADING CANCER

    TUMOR GRADE

    Degree of abnormality of cancer cells

    compared with the normal counterpart cell

    Estimate how quickly the tumor is likely to grow

    and spread (degree of malignancy andaggresiveness)

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    GRADING CANCER

    Benign or

    malignant

    Tumor grade

    Degree of cell differentiation

    Tissue (biopsy)

    Pathologist

    DETERMINING THE TUMOR GRADE

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    GRADING CANCER

    THE SIGNIFICANCY OF CANCER GRADE

    Cancer grade is determined based on microscopicappearances of:

    1. Degree of resemblance to the normal tissue (degreeof differentiation)

    2. Mitotic activity

    3. Nuclear size and pleomorphisme

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    GRADING CANCER

    THE SIGNIFICANCY OF CANCER GRADE

    Cancer grade recommended by AJCC (the AmericanJoint Commission on Cancer)

    GX: grade can not be assed (undetermined grade)

    G1: well differentiated (low grade)

    G2: moderately differentiated (intermediate grade)

    G3: poorly differentiated (high grade)G4: undifferentiated (high grade)

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    GRADING CANCER

    THE SIGNIFICANCY OF CANCER GRADE

    Grade 1: tumor cells resemble normal cells, tend to growand multiply slowlygenerally considered the least

    aggressive in behavior

    Grade 2 : tumor cells appears between 1 and 3

    Grade 34: tumor cells do not look like normal cells,tend to grow rapidly and spread faster than tumor

    with a lower grade

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    Well grade

    squamous cell carcinoma

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    Keratin pearl

    Keratin pearl

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    Moderate to poorly grade

    Squamous Cell Carcinoma

    Individual keratine

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    Well differentiated adenocarcinoma

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    Tubular/ glandular pattern

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    Poorly grade adenocarcinoma

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    Anaplastic tumor

    Pleomorphic Rhabdomyosarcoma

    Bizzare cell

    Multinucleated giant cell

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    Cancer grade + other factors (s.a., cancer stage)

    treatment plan and to predict the prognosis.

    Generally: a lower grade -- a better prognosis

    (the likely outcome or course of a disease; the chance ofrecovery or recurrence)

    Tumor grade is very important for certain types ofcancers:

    soft tissue sarcoma

    primary brain tumors

    Lymphomas

    breast cancer

    and prostate cancer

    http://www.cancer.gov/dictionary/db_alpha.aspx?expand=phttp://www.cancer.gov/dictionary/db_alpha.aspx?expand=rhttp://www.cancer.gov/dictionary/db_alpha.aspx?expand=shttp://www.cancer.gov/dictionary/db_alpha.aspx?expand=lhttp://www.cancer.gov/dictionary/db_alpha.aspx?expand=lhttp://www.cancer.gov/dictionary/db_alpha.aspx?expand=shttp://www.cancer.gov/dictionary/db_alpha.aspx?expand=rhttp://www.cancer.gov/dictionary/db_alpha.aspx?expand=p
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    GRADING CANCER

    APPLYING THE GRADING SYSTEM

    Grading systems are different for each

    type of cancer, for example:

    1. Gleason system for prostate cancer

    2. Bloom-Richardson (Nottingham)system for breast cancer

    3. Furhman system for kidney cancer

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    Breast cancer

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    DIAGNOSIS LABORATORIK

    MORFOLOGIK :

    - biopsi - IHC

    - Frozen Section - Flowytometry- AJH

    BIOKIMIAWI : Tumor marker

    MOLEKULAR : DNA microanalysis

    TUMOR MARKER / PETANDA TUMOR

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    MARKER TUMOR

    Hormon

    HCG (Human Chorionic Gonadotropin)

    Kalsitonin

    Katekolamin dan metabolit

    Hormon ektopik

    Antigen onkofetal

    Alfa-fetoprotein

    CEA (carcinoma embryonicantigen)

    Isoenzim

    Prostatic Acid Phosphatase

    Neuron specific enolase (NSE)

    Protein spesifikImunoglobulin

    PSA

    Musin & glikoprotein lain

    CA-125

    CA-19-9CA-15-3

    Tumor trofoblastik dan testis non-seminoma

    Ca medular tiroid

    Feokromositoma dan tumor yang berhubungan

    Paraneoplastic syndrome

    HCC, tumor testis sel benih non seminomatosa

    Ca kolon, pankreas paru, gaster, mama

    Ca prostat

    Ca sel kecil paru, neuroblastoma

    Mieloma multipel dan gamopati lain

    Ca prostat

    Ca ovarium

    Ca kolon, pankreasCa mama

    TUMOR MARKER / PETANDA TUMOR

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