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EKUSILENI CLINICAL LABORATORY

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Class 1: Antigens unique to a neoplasm not shared by other tumours ... yolk sac tumour. Immature tetratoma /- 4. Mixed germ cell tumour /- 5. Choreocarcinoma ... – PowerPoint PPT presentation

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Title: EKUSILENI CLINICAL LABORATORY


1
EKUSILENI CLINICAL LABORATORY
  • PSA AND CEA AS SURROGATE MARKERS FOR CANCER
    DIAGNOSIS
  • TALENTS MURAHWA
  • (BIOMEDICAL SCIENTIST)

2
LAB CANCER MANAGEMENTWhat are tumor markers
  • Definition -
  • A tumour marker is a biochemical indicator
    selectively produced by the neoplastic tissue and
    released into blood and detected in blood or in
    other body fluids.
  • It may be used to -
  • Detect the presence of a tumour
  • Monitor the progress of disease
  • Monitor the response to treatment

3
Tumour Markers - Classification
  • Class 1 Antigens unique to a neoplasm not
    shared by other tumours of same histological type
    .
  • Class 2 Antigens expressed by many or most
    tumours of a specific histological type and of
    other histological type,
  • But not expressed by normal adult tissue.
  • Class 3 Antigens expressed by both cancer and
    normal adult tissue.

4
NATURE OF TUMOUR MARKERS
  • 1.Oncofetal antigens
  • Alpha Feto Protein
  • CEA
  • Pancreatic Oncofoetal Antigen
  • 2.Proteins
  • Casein By breast carcinoma
  • Ferritin- Leukaemia
  • 3.Enzymes
  • Creatinekinase Prostate tumour
  • Alkaline Phosphatase Lungs tumour
  • Acid Phosphatase Prostate tumour

5
  • Receptors
  • Oestrogen, Progesterone, Androgen
  • Polyamines
  • Spermine, Spermidine, Putridine leukemia,
    lymphoma, colorectal CA
  • Cell Markers
  • T cell marker, B cell marker-lymphoma
  • Ectopic Hormones
  • HCG, GH, Erythropoetin, Renin

6
  • LOCAL LABORATORY TESTS ON OFFER
  • 1.Alfa Feto Protein
  • 2.CEA
  • 3.PSA
  • ALPHA AMYLASE
  • LDH

7
Alfa Feto Protein-
  • Measurement of maternal serum and amniotic fluid
    levels play an important role in the screening
    for
  • Foetal neural tube defects
  • Chromosomal abnormalities including Downs
    Syndrome.
  • Most measurements are done at 16 weeks of
    gestation.
  • Raised maternal serum AFP levels are not specific
    for neural tube defects.
  • Must be used in combination with other modalities
    such as USG, amniotic fluid AFP and acetylcholine
    esterase.

8
Alfa Feto Protein-
  • Many fetal conditions are associated with
    abnormal maternal serum AFP levels.
  • Elevated
  • NTD, GI obstruction, Liver necrosis, Abdominal
    wall defects (Omphalocele, Gastroschisis),
    Sacrococcygeal tumour, Cystic hygroma, IUGR,
    multiple pregnancies, renal anmalies.
  • Low
  • Chromosomal trisomies (Downs syndrome),
    Gestational trophoblastic diseae, IUD, placental
    defects, GA underestimated, Foetal distress,
    Hydrops Foetalis, TOF, Cyclopia.

9
Alfa Feto Protein-
  • After birth AFP usually falls, within 8 to 12
    months of delivery to a very low conc.of 10mcg/ml
    and persists at this low level throughout life.
  • Unexplained and persistent elevation of AFP in
    nonpregnant state should be screened, as it may
    be due to-
  • Hepatocellular Ca, germ cell tumour, hereditary
    persistence of AFP, viral hepatitis and cirrhosis
    .
  • In addition to its role in prenatal diagnosis, it
    is also widely used in the diagnosis, therapeutic
    monitoring and follow up of patients in germ cell
    tumours.

10
Germ Cell Tumours Producing AFP
  • AFP
  • Dysgerminoma --
  • Endodermal Sinus tumour /
  • yolk sac tumour
  • Immature tetratoma /-
  • 4. Mixed germ cell tumour /-
  • 5. Choreocarcinoma --
  • 6. Embryonal CA --

11
CEA-
  • It is a glycoprotein of mol.wt 200kda.
  • Though it is a tumour marker for GI cancers, it
    is also expressed by
  • malignant mucinous tumor (100),
  • 100 cases of atypical hyperplasia of
    endometrium,
  • 60 cases of endometrial Ca,
  • 50-80 cases of squamous cell of Cx,
  • 75-100 cases of adenocarcinoma of Cx.
  • It is also produced in pneumonia, hypothyroidism
    and pancreatic tumours.

12
PSA
  • Prostate-Specific Antigen (PSA)
  • A prostate-specific antigen (PSA) test measures
    the amount of prostate-specific antigen in the
    blood. PSA is released into a man's blood by his
    prostate gland.

13
  • Healthy men have low amounts of PSA in the blood.
    The amount of PSA in the blood normally increases
    as a man's prostate enlarges with age. PSA may
    increase as a result of an injury, a digital
    rectal exam, sexual activity (ejaculation),
    inflammation of the prostate gland (
    prostatitis), or prostate cancer

14
PSA Why is it done?
  • Why It Is Done
  • The prostate-specific antigen (PSA) test is done
    to
  • Monitor prostate cancer and how it responds to
    treatment. If PSA levels increase, the cancer may
    be growing or spreading. PSA is usually not
    present in a man who has had his prostate gland
    removed. A PSA level that rises after prostate
    removal may mean the cancer has returned or has
    spread.

15
PSA
  • Prostate cancer often grows very slowly, without
    causing major problems. Detecting prostate cancer
    early and treating it may prevent some health
    problems and reduce the risk of dying from the
    cancer. However, some treatments for prostate
    cancer can cause other problems, such as

16
PSA
  • Determine if cancer may be present when other
    tests, such as a digital rectal exam, are not
    normal. A PSA test does not diagnose cancer, but
    it can be used along with other tests to
    determine if cancer is present.

17
PSA
  • Check men for prostate cancer. Experts disagree
    on the usefulness of PSA testing as a screening
    tool for prostate cancer. If a PSA test is used
    for screening, it is usually done for men older
    than age 50 or for those at high risk for
    prostate cancer, such as men with a family
    history of prostate cancer, or for
    African-American men who have a higher chance of
    developing cancer than other men. Since other
    common medical conditions, such as prostatitis,
    can cause high PSA levels, a prostate biopsy is
    needed to confirm a diagnosis of cancer.

18
CONCLUSIONTM cannot be
NECESSARILY constructed as primary modalities for
diagnosis of tumours THANK YOU
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