3 Tumour diagnosis and prognosis - stage and grade Flashcards

1
Q

Describe how tumours are diagnosed

A
  • Symptoms: clinical history
  • Signs: physical examination (lumps and bumps)
  • Imaging (X-ray - look for shadowing, MRI)
  • Tumour markers (overactive - e.g. prostate-specific antigen (PSA) - overexpressed
  • Biopsy: tissue sampling
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2
Q

Describe how tumour markers can help in diagnosis

A
  • Certain tumours liberate products that can be detected in blood/urine/CSF samples, thereby acting as tumour markers
  • These may aid diagnosis but also be used to follow up therapy when blood levels become increased, often before imaging can detect tumour recurrence
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3
Q

give some examples of tumor markers

A
  • HCG - human chorionic gonadotrophin: from tumours with trophoblast elements
  • AFP - alpha fetoprotein: liver cancer, germ cell tumours
  • PSA - prostate-specific antigen from carcinoma of the prostate

High levels may not always mean cancer

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4
Q

Describe how tumour biopsy used in diagnosis

A

Needed to confirm diagnosis - need a biopsy to look at cells involved to make sure that they show characteristics of tumour + check if it is benign or malignant

  • Virtually every site in the body can be biopsied
  • Tissue samples are acquired for examination
  • Techniques used vary according to site and suspected diagnosis
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5
Q

List some biopsy techniques

A
  • Needle biopsy: in the brain, lymph node, eye, thyroid, breast, lung + pleura, liver, kidney, bone, bone marrow, testis, skeletal muscle
  • Endoscopic biopsy: respiratory tract, alimentary tract, urinary tract
  • Transvascular biopsy: kidney, heart
  • Skin
  • Cutterage biopsy - endometrial lining of uterus

Imaging can be used in conjunction with the biopsy technique, to guide the procedure

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6
Q

Describe the handling of biopsy

A
  • Fix in formalin solution for routine histology, special stains and immunohistochemistry
    > (protiens of tissue - HER2 expresssion in breast cancer - Herceptin can be used to target HER2+ patients that have this tumour)
  • FIx in glutaraldehyde for electron microscopy
  • Send fresh for cytogenetics, tumours
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7
Q

Describe diagnostic cytology

A
  • Examination of cells in tissue fluids or exfoliated from surfaces
  • May give a diagnosis of malignancy
  • Useful for screening - the main example is the cervical cytology programme
    > cervical smear - pap smear
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8
Q

Explain how histology of neoplasms allows prediction of behavior

A

Two main assessments are made:

  • analysis of the degree of differentiation and growth pattern of the tumor
  • Evaluation of how far a tumour has spread

Special techinques may be used to obtain further prgnostic information

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9
Q

Define and describe the grade (of a tumour)

[biology]

A

The degree of differentiation of tumour cells relative to normal tissue of origin

  • Variation in size and shape of constituent cells of the tumour [pleomorphism]
  • The proportion of cells containing mitotic figures [mitotic index]
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10
Q

Describe the relatioship between grade and prognosis

A

In general
- LOW-grade tumours are SLOW growing, have a GOOD prognosis

  • HIGH-grade tumours are FAST growing, have a POOR prognosis

These are very general rules that have to be considered with all other clinical aspects

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11
Q

Describe histological grading in breast cancer

A

Assessment of the degree of differentiation of carcinoma from semi-quantitative analysis of its morphological characteristics:

  • Tubule formation
  • Nuclear pleomorphism
  • Mitotic counts

[points given, depending on how much that variable is changed (low 1___3 high)]

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12
Q

Describe the relationship between breast cancer grade and prognosis

A

Patients with low-grade tumours have longer survival than those with high-grade tumours

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13
Q

What else can tumour grade be used for?

[predict ag**]

A

Grade can predict how aggressive cancer can be

- this can help with treatment choice/plans

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14
Q

Describe + define tumour staging

A

[time-dependent factors]

  • The size of primary tumors
  • The degree to which it has locally invaded
  • The extent to which it has spread by distant metastasis
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15
Q

Describe the use of the TNM staging system

A
  • The TNM system is based upon the extent of local tumour spread, regional lymph node involvement and the presence of distant metastases
  • It can be applied to many different types of tumour, although the specific criteria are different for each tumour site
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16
Q

Describe how the TNM staging works

A

The TNM staging system is used to describe most types of cancer:

  • TUMOUR - describes the size of the tumour and any spread of cancer into nearby tissue
  • NODES - describes spread of cancer to nearby lypmh nodes
  • METASTASIS - descirbes metastasis to nearby lypmh nodes

The T, N, and M are given a score

(TX, 0, is, 1, 2, 3 ,4)
(NX, 0, 1, 2, 3)
(MX, 0, 1)
criteria can be found online
e.g. of a TNM staging
- T2N1M0

This TNM staging can be converted to a prognostic TNM stage

17
Q

Describe the relationship between stage and prognosis

A
  • The stage of a tumour is generally the most important indicator of likely prognosis and of approporate tumour
  • Advanced stage tumours (extensive spread) may require aggresive treatments
  • Early stage tumours (locailised) may be treatable by relatively conservative measures
18
Q

Describe tumour therapy

A

Three main nodes of therapy for neoplastic disease

  • Surgery (common 1st line treatment)
  • Radiotherapy (treatment after surgery)
  • Chemotherapy (treatment for [suspected] metastatic disease)

Multimodal therapy is common
- Pathology is pivotal in deciding on appropriate therapy

19
Q

Give an example of a tumour with excellent prognosis

A

Thyroid cancer

20
Q

Give an example of a tumour with a moderate prognosis

A
  • Kidney, prostate, cervix, and breast cancer
21
Q

Give an example of a tumour with a very poor prognosis

A
  • Pancreas, brain, esophagus cancer