Radiotherapy pt.2 Flashcards

1
Q

How much of an increase is expected to be seen in cancer incidence in europe?

A

It has been predicted that in 2035 there will be a 10% increase in the incidence form 2015

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2
Q

What are the pillars of cancer care?

A

Three pillars: Surgery, radiotherapy, and chemotherapy

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3
Q

What accounts for most cancer cases in europe?

A

Breast, colorectal, lung, and prostate cancers account for more than 50% of new cases

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4
Q

What accounts for most cancer deaths in Europe?

A

Breast, colorectal, lung, and pancreatic cancer are the leading causes of deaths

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5
Q

What is the role for the three pillars of cancer therapy?

A

Surgery.
- locally evident disease
Radiotherapy.
- locoregional disease. Another aim is to eradicate microscopic cancer cells that
surround the macroscopic tumour
Chemotherapy.
- systemic disease

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6
Q

What is chemotherapy?

A

Destruction of cancer cells using drugs (anti-cancer drugs)

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7
Q

What does the therapeutic choice in cancer treatment depending on?

A

TNM staging

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8
Q

What is the T criterion in TNM dependent on?

A

The T criterion is established in 2 ways: dimensions or infiltration of the organ wall. The latter is mainly employed for hollow viscera (like the gastrointestinal tract tumour). Breast, prostate and skin for example have their T based on the dimensions of the primary tumour. On the other hand, GIT tube and bladder tumours are graded based on their invasion of the wall layers (mucosa, submucosa ecc.).

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9
Q

What is the N criterion staging dependent on?

A

The N staging can depend on number, dimension and site/laterality of the involved lymph nodes

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10
Q

What can metastasis be divided into?

A

Oligometastatic (usually up to 3 metastasis in the same organ,defined as limited in number and location and are amenable to regional treatment) and plurimetastatic
- Synchronous and metachronous based on the timing of appearance

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11
Q

Synchronous vs metachronous meaning in the setting of metastasis and their implication

A
  • Synchronous means that they are
    found at the time of diagnosis of the primitive tumour while Metachronous ones appear during the follow-up
    visits
  • The timing of appearance
    has pathological implications: multiple synchronous metastasis or
    metachronous metastases after few months from therapy are indicative of an aggressive tumour
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12
Q

What can the different stages of cancer be briefly summarized as?

A
  • Stage I and II (organ limited diseases): early disease, mainly treatable with surgery
  • Stage III: locally advanced, the tumour breaks the organ barrier and/or multiple nodal involvement. 60% of cancer patients undergo radiotherapy at least once
  • Stage IV: advanced and metastatic disease, requires systemic therapies.
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13
Q

Therapy for different stages of cancer

A

Stage I generally requires a monotherapy (surgery OR RT)
- Stage II instead frequently requires adjuvant RT if there’s risk of local recurrence.
- On the other hand, stage III diseases
frequently require neoadjuvant therapies to allow an effective surgical procedure.
- Stage IV tumours mainly require
chemotherapy, and RT can have a role
for palliation or consolidation if patients
respond well.

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14
Q

What are radiotherapy aims?

A
  • Eradicates the MACROscopic TUMOR
  • Eradicates the MICROscopic tumor cells
  • Increases LOCAL CONTROL
  • Decreases LOCAL RECURRENCES
  • Eradication of METASTATIC disease resistant to CT
  • Decreases SYMPTOMS
  • Quanitiy of life
  • Improve overall survival
  • Decreases disease progression
  • Quality of life
  • Decrease symptoms
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15
Q

What does consolidation mean in RT?

A

Consolidation means that Chemo acts
on the majority of cancer cells but as a
consequence, some resistant cells might
remain: consolidation RT aims to target
the population of resistant cancer cells.

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16
Q

Indications advantage and applicability of radical RT

A
  • Early tumors and locally advanced tumors
  • Avoids demolitive surgery
  • Radiosensitive tumors
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17
Q

Indications advantage and applicability of neoadjuvant RT

A
  • Locally advanced
  • To increase resectability and reduce surgical extension
  • Reduces tumor volume and eradicates microscopic Tumor cells
18
Q

Indications advantage and applicability of palliative RT

A
  • Metastatic diseases
  • Decreases pain, haemostatic effect, and spine compression
  • Bone metastases and bleeding tumors
19
Q

Advantages of using RT for benign diseases

A

Avoids surgery and option for disease not responsive to medical treatments

20
Q

What can radiotherapy be divided into based on timing?

A

Exclusive
Combined to surgery Pre-operative (NAD)
Postoperative (ADJ)
Intraoperative (IORT)
Peri-operative (POBT)

Combined to chemotherapy Concomitante
Sequenziale

21
Q

Units used for external beam radiotherapy vs radiology

A
  • Low energies in the order of Kilovoltage in radiology (we don’t want to penetrate tissue)
  • Megavoltages for radiotherapy (we want it to penetrate tissues)
22
Q

Label these

A
23
Q

Tail of X ray radiation

A

The tail of these radiations never reaches zero, so if we have a target in a certain area, all the tissues
deeper that the target will get this “tail” radiations.

24
Q

Name of proton peak

A

Bragg’s peak

25
Q

What do the features of the different sources in brachytherapy depend n?

A
  • Employed radionucleotide
  • Type of radiation emitted (beta radiation in the form of electrons vs gamma radiation/gamma emitters which like x-rays but natural)
  • Halving time
26
Q

What is the halving time for sources used for brachytherapy

A

Most used sources for brachytherapy have t1/2 of around 2-3 months, and are changed every 4 months.

27
Q

What determines the depth reached by gamma rays?

A

Different energies

28
Q

What is brachytherapy a part of?

A

Interventional radiotherapy

29
Q

What can brachytherapy be used in?

A

Brachytherapy can be used in:
- Hollow organs (intracavitary), through specific applicators, such as in the uterine tubes
- Lumens (endoluminal), through endoscopy, such as in bronchi
- Interstitial radiotherapy -Unreachable masses, “aghi gronda” (hollow needles) are used to have the radioactive source reach the target.

30
Q

What depth depend on in brachytherapy?

A

Depth depends on where the applicator is positioned.

31
Q

What can ionizing radiation be divided into?

A

Ionizing radiations can be distingushed between
2 categories:
- With Low Linear Energy Transfer
(LET). photons and electrons, which
cannot directly damage the DNA molecule since before reaching it they meet many targets, like water, which is
split, forming free oxygen radicals (very unstable, these bind DNA and damage it);
- With high Linear Energy Transfer
(HET). protons (high energy particles),
which directly damage the DNA molecule.

32
Q

What is the most used type of radiation?

A

The most used radiations are photons, which act indirectly (through ROS).

33
Q

What type of damage can radiotherapy induce on DNA?

A

Causes 2 kinds of damage:
- Single-strand break (SSB), a light
damage,
- Double-strand break (DSB), a
more severe damage.

34
Q

What does damage to DNA in radiotherapy lead to?

A

Single (SSB) and double-stranded breaks (DSB) in a cell’s DNA prevent that cell from dividing, inhibiting disease growth (mitotic death).
Cells can die also for direct apoptosis, related to not repairable damages.
Generally radiations with low LET are associated with SSB, while the ones with high LET with DSB.

35
Q

What is absorbed dose?

A

Absorbed dose is a measure of the energy deposited in a medium by ionizing radiation.
Its measure unit is the Gray (Gy), corresponding to the energy 1 Joule deposited in 1 Kg of medium.
1 Gy = 1 J / 1 Kg

36
Q

What is the usual absorbed dose administered?

A

A certain dosage is prescribed to be administered at a certain fraction dose. The usual standard fraction dose used is 2 Gy/day.

37
Q

What is dose fractioning?

A

The dose is generally not delivered in one time but fractionated in a period of 6-8 weeks.
Normal cells have higher survival rates thanks to sublethal damage repair, while tumor cells are killed.

38
Q

How is absorbed dose determined

A
  • The number of proliferating
    tumor cells in a mass of 1 cm3 will be 10^9, D_10 is the dose necessary to reduce the exponent of one unit ( 10^9 ⇒ 10^8 cells) which is 7Gy
  • D_10 ≈ 7 Gy 1cm^3 = 10^9 cells
  • E.g. Primary tumor Cells 10^10-12 -> 70-84 Gy
39
Q

Which imaging modality is used in RT for dose calculation and distribution?

A
  • CT scan is the imaging used in RT for DOSE CALCULATION
  • ALGORITHMS for DOSE distribution use electron density of CT scan to calculate the ionizing radiation dose attenuation
40
Q

How much radiation is required for positive nodes?

A

Positive nodes (macroscopic)
Cells 10^8-^10 -> 56-70 Gy

41
Q

How much radition dose is required for subclinical disease?

A

Subclinical disease Cells 10^4-^5 -> 28-35 Gy

42
Q
A