Lecture 22: Histopathology case studies / Neoplastic phenotype 2 Flashcards

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1
Q

What is meant by prognosis?

A
  1. Prediction of probable outcome of a disease based on:
    a. individuals condition
    b. Usual course of disease in similair situations
  2. Important neoplastic diseases:
    a. Benign neoplasms: usually good prognosis
    b. Malignant neoplasms: prognosis variable
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2
Q

What does the prognosis depend on in neoplastic disease?

A
  1. Type of neoplasm
    a. Grade
    b. Stage
    c. Functional characteristics
    d. Complications of the neoplasm or its therapy
  2. Effectiveness of treatment available
  3. Co-morbidity (other, co-existing diseases)
    a. Chronic heart, lung, kidney disease, etc
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3
Q

What is meant by grade and stage of neoplasms?

A
  1. Grade (Differentiation of a neoplasm)
    a. “How similar or different from equivalent normal
    cells/architecture”
    b. Usually 2-3 grades, somtimes 4
  2. Stage (how advanced the neoplasm is)
    a. Size
    b. Extent of local invasion
    c. Presence and extent of metastases (lymph node/distant sites)
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4
Q

Are benign neoplasms graded?

A

No, only malignant

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5
Q

What does determining the stage of a neoplasm determine?

A
  1. Extent or severity of malignant neoplasm
  2. This helps:
    a. Plan treatment (taking account of patients wishes and co-
    morbidity)
    b. Estimate the prognosis
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6
Q

What is the TNM Staging System?

A
  1. Local extent of ‘primary Tumour’ (T)
  2. Have cancer cells spread to nearby ‘lymph Nodes’ (N)
  3. Is there ‘distant Metastasis’ (M)
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7
Q

Explain the grading and staging of bladder cancer as an eg

A
  1. Most bladder cancer shows urothelial differentiation (urothelial
    carcinoma)
  2. Often shows blood in urine, also may result in frequent, urgent,
    uncomfortable urination
  3. Two grades of carcinoma:
    a. low-grade
    b. high-grade
  4. Tumour stages:
    a. Tis
    b. Ta
    c. T1
    d. T2
    e. T3
    f. T4
  5. Lymph node stages:
    a. N0
    b. N1
    c. N2
    d. N3
  6. Distant metastasis stages:
    a. M0
    b. M1
  7. Different groups
    a. Stage group 1, 2, 3, 4
  8. Survival rates in men:
    a. 5-year net survival (56.1% 2013-2017) (58.6% 2012-2016)
    b. a decrease in survival rates can be seen
    c. why? maybe shortage of Bacille Calmette-Guerin (BCG)
    d. Used to treat higher-risk bladder cancer patients
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8
Q

What are tumour markers?

A
  1. Aids diagnosis: increasingly important to histopathologists and
    haematologists
  2. Prognostic factors: may help define therapy
  3. Targets for therapy: adds specificity to therapy
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9
Q

What are examples of tumour markers?

A
  1. Oestrogen receptor (ER) in breast cancer
  2. Epidermal growth factor receptor (HER2) in breast cancer
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10
Q

Explain histopathological diagnosis of neoplasms

A

Why might this be challenging?
1. Poor differentiation of the tumour
2. Tumour necrosis
3. Tumour mimicry - malignant melanoma
4. Rare tumours
5. Unusual site of origin
6. Primary v. metastatic tumour

  1. Benign tumours can mimic neoplasms:
    a. inflammatory / reparative conditions
    b. Drug effects
    c. Radiotherapy
    d. Hyperplasias
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11
Q

What dies therapy look like?

A

Based on:
1. Tumour types
2. Grade & stage
3. Tumour markers

Takes into account co-morbidity and life expectancy

Patients wishes important

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12
Q

What is the multidisciplinary team (MDT)?

A
  1. Surgeon
  2. Radiologist
  3. Pathologist
  4. Medical oncologist / radiation oncologist
  5. Cancer care nurse
  6. Supportive and palliative care specialist
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13
Q

How can we improve cancer therapies?

A
  1. Prevention - public education
  2. Earlier diagnosis - public education, better healthcare access, GP
    training
  3. Continue to improve diagnostic methods
  4. Continue to improve therapies
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