Prognosis_Lecture_Flashcards

(73 cards)

1
Q

What does ‘prognosis’ mean in medicine?

A

The predicted outcome or course of a disease, including chances of recovery, recurrence, or death.

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2
Q

What are the main purposes of determining prognosis?

A

To guide treatment decisions, inform patients, predict survival, and help plan follow-up care.

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3
Q

What are prognostic factors?

A

Disease or patient characteristics that influence outcome independent of treatment.

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4
Q

How are prognostic factors different from predictive factors?

A

Prognostic = overall outcome; Predictive = response to specific treatment.

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5
Q

What are the three main categories of prognostic factors?

A

1) Disease/tumour-related 2) Patient-related 3) Treatment-related.

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6
Q

What is the most important prognostic factor in early breast cancer?

A

Axillary lymph node status.

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7
Q

Why is axillary lymph node status important?

A

Shows regional spread and predicts recurrence and survival.

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8
Q

How does tumour size affect prognosis?

A

Larger tumours have higher recurrence risk and poorer survival.

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9
Q

What does histologic type mean in breast cancer?

A

Microscopic tumour subtype (ductal, lobular, tubular, etc.) influencing aggressiveness.

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10
Q

Which breast cancer subtypes have better prognosis?

A

Tubular, mucinous, and cribriform carcinomas.

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11
Q

What is histologic grade?

A

Degree of differentiation (1–3). High grade = more aggressive, worse prognosis.

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12
Q

What does lymphatic or vascular invasion indicate?

A

Cancer cells have entered lymph/blood vessels → higher metastasis risk.

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13
Q

How does metastasis affect prognosis?

A

Presence of distant metastases = incurable disease, poor survival.

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14
Q

What are proliferation markers?

A

Markers like Ki-67 indicating cell division rate; high = poor prognosis.

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15
Q

What is ER/PR status and why is it important?

A

ER+/PR+ tumours grow slower and respond to hormone therapy (better prognosis).

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16
Q

What does HER2 positivity mean?

A

HER2+ tumours are aggressive but respond well to trastuzumab (Herceptin).

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17
Q

How does age affect breast cancer prognosis?

A

Younger women have fewer cases but more aggressive tumours.

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18
Q

Which age group has the highest breast cancer incidence?

A

Ages 50–70.

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19
Q

How does ethnicity influence prognosis?

A

Black women have lower incidence but higher mortality (triple-negative, healthcare barriers).

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20
Q

What are modifiable patient-related prognostic factors?

A

Diet, weight, exercise, alcohol, smoking.

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21
Q

What are semi-modifiable factors?

A

Socioeconomic status and comorbidities.

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22
Q

What are non-modifiable factors?

A

Age, genetics, ethnicity.

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23
Q

What are treatment-related prognostic factors?

A

Factors related to treatment type, quality, and timing affecting outcome.

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24
Q

How does treatment modality affect prognosis?

A

Combination of surgery, chemo, and radiation improves survival.

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25
What is the main difference between mastectomy and lumpectomy?
Mastectomy removes entire breast; lumpectomy removes tumour only (requires radiation).
26
How does radiation treatment volume affect prognosis?
Larger field = better control but more toxicity.
27
What does 'dose and fractionation' mean in radiation therapy?
Total dose and how it’s divided over time.
28
What is the purpose of a 'boost' in breast radiation therapy?
Extra dose to tumour bed to reduce recurrence, especially in young patients.
29
Why is treatment time important in prognosis?
Delays allow tumour regrowth → worse outcomes.
30
What is Oncotype DX used for?
Genomic test predicting recurrence risk and chemo benefit (ER+, HER2−).
31
What does a low recurrence score (<18) in Oncotype DX mean?
Low recurrence risk → hormone therapy only, no chemo.
32
How can local tumour growth cause death?
By compressing or invading vital organs (e.g., brain, airway, liver).
33
What is lymphovascular spread?
Spread through lymph/blood to nodes/organs, worsening prognosis.
34
What is distant metastasis?
Spread to distant organs (lungs, liver, bone, brain) — main cause of death.
35
How can infection cause death in cancer patients?
Due to immunosuppression and neutropenia → sepsis.
36
What are common metabolic disturbances in advanced cancer?
Hypercalcemia, hyponatremia, liver/kidney failure, cachexia.
37
Why are cancer patients hypercoagulable?
Tumour cells activate clotting → DVT, PE, or DIC.
38
What are the six stages of cancer treatment decision-making?
1. Diagnosis 2. Prognostic/predictive review 3. Define goals 4. Review options 5. Assess side effects 6. Choose plan.
39
What are the main goals of cancer treatment?
Cure, control, or palliation.
40
What factors influence treatment choice?
Stage, performance status, tumour biology, patient preference.
41
What does shared decision-making mean?
Clinician and patient collaborate based on evidence and values.
42
What is the therapeutic ratio?
Balance between tumour control and normal tissue complications.
43
What do the two curves on a therapeutic ratio graph represent?
Tumour Control Probability (TCP) and Normal Tissue Complication Probability (NTCP).
44
What does the gap between TCP and NTCP curves show?
The therapeutic window — effective but safe dose range.
45
How can we increase the therapeutic ratio?
Precision targeting, fractionation, radiosensitizers, radioprotectors, and fewer delays.
46
What is performance status (PS)?
Measure of patient’s ability to perform daily activities and tolerate treatment.
47
What are the two main performance status scales?
Karnofsky (0–100) and ECOG (0–5).
48
What does ECOG 0 mean?
Fully active, no restrictions.
49
What does ECOG 3 mean?
Confined to bed/chair >50% of day; limited self-care.
50
What is the treatment threshold for curative therapy?
ECOG ≤2 or Karnofsky ≥70.
51
What are the four main roles of therapeutic intervention?
Neoadjuvant, Radical (Curative), Adjuvant, and Palliative.
52
What is neoadjuvant therapy?
Treatment before main therapy to shrink tumour.
53
What is adjuvant therapy?
Treatment after surgery to kill microscopic disease.
54
What is radical therapy?
Curative-intent treatment to eliminate cancer.
55
What is palliative therapy?
Relieves symptoms and improves quality of life, not curative.
56
Why is radiation therapy fractionated?
To allow normal tissue repair while continuing to kill tumour cells.
57
What does the α/β ratio tell us?
How sensitive a tissue is to fractionation (low = more sensitive).
58
Which tissues are late-responding and more sensitive to large fraction sizes?
Normal tissues with low α/β ratio (spinal cord, kidney).
59
What happens if radiation treatment is delayed or interrupted?
Tumour repopulation → reduced control, poor prognosis.
60
What are the 5 R’s of Radiotherapy?
Repair, Reoxygenation, Redistribution, Repopulation, Radiosensitivity.
61
What does Repair refer to?
Normal tissues repair sublethal DNA damage between fractions.
62
What is Reoxygenation?
Hypoxic tumour cells become oxygenated and more radiosensitive.
63
What is Redistribution?
Cells move into radiosensitive phases (G₂/M).
64
What is Repopulation?
Cell regrowth during therapy — delays worsen prognosis.
65
What is Radiosensitivity?
Inherent cell response to radiation (varies by tumour type).
66
Which tumours are most radiosensitive?
Lymphomas, leukemias, germ cell tumours.
67
Which tumours are radioresistant?
Melanoma, sarcoma, renal cell carcinoma.
68
What is the clinical goal of the 5 R’s?
Maximize tumour kill, minimize normal tissue injury.
69
Which R explains why normal tissue tolerates fractionation?
Repair.
70
Which R explains why hypoxic cells become radiosensitive over time?
Reoxygenation.
71
Which R explains why we use multiple fractions?
Redistribution and Repair.
72
Which R explains why treatment delays are dangerous?
Repopulation.
73
Which R explains tumour-specific differences in radiation response?
Radiosensitivity.