Radiobiology Flashcards

1
Q

Influence of fraction size and overall treatment time

A

Fraction size mainly influences late effects, overall treatment time has little influence
But, fraction size and overall treatment time both determine the response of acutely responding tissue

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2
Q

What is kick in time?

A

Repopulation is accelerated at about 28 days (kick-in time). They need to finish treatment in prescribed time period. Better to delay the initiation of treatment than to introduce delays during treatment

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3
Q

Different fractionation schedules

A
  1. Standard fractionation 1.8 - 2Gy.
  2. Hyperfractionation-Radiation treatment in which the total dose of radiation is divided into small doses (less than 1.8Gy) and treatments are given more than once a day.
  3. Hypofractionation- A treatment schedule in which the total dose of radiation is divided into large doses and treatments are given once a day or less often
  4. Accelerated fractionation -a conventional number of dose fractions is delivered in a significantly shortened overall treatment time (by-daily
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4
Q

Why do multiple fractions per day?

A

Spare early reaction and allow adequate reoxygenation in tumours

Overall treatment time reduction: if overall treatment time is too long, it could decrease acute reactions without sparing late injury and allows the surviving tumour cells to proliferate

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5
Q

Why use hyperfractionation schedule?

A
  • Increased opportunity for tumour cell redistribution and reoxygenation between dose fractions
    • A possibly lower OER with small incremental doses
  • Different sparing of late reacting normal tissue with small dose fractions
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6
Q

Why use Hypofractionation?

A
  • A treatment schedule in which the total dose of radiation is divided into large doses and treatments are given once a day or less often
    have equal efficacy and toxicity, as well as noninferiority, compared with standard radiation treatment.
    Concern - higher rates of acute and late toxicities
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7
Q

Why are unscheduled interruptions bad?

A

reduction of local control of 1-1.4%. Treatment should not exceed 42 days

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8
Q

Major causes of unscheduled disruptions:

A
  1. Machine and staff availability -Adequate staff,
  2. Public holidays -Ideally all patients should be treated on public holidays, but this may not be practicable.
  3. Transport problems -Efficient communication with local ambulance service
  4. Medical problems -Management of acute side effects
  5. Social circumstances -that lead to a patient’s failure to attend for treatment as scheduled - Psychological and social work support
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9
Q

Which patients get prioritised?

A

Categorise patients from most at risk of loss of tumour control/cure rates from unscheduled interruptions

Category 1: priority for patients with radical intent and have evidence of prolongation effect on their cancer type, SCC of lung, and H+N
Category 2: 2 days prolongment is ok, TCC bladder, SCC Cervix

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10
Q

Managing interruptions that have occurred:

A
  • Accelerated scheduling: treat twice daily on some days remaining between interruptions and end of treatment. BIDs not recommended for fraction sizes larger than 2.2Gy.6 hour difference between two fractions
    • Biological allowance: increase total dose or dose per fraction. Requires radiobiological calculations
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11
Q

Additional considerations for managing interruptions

A
  1. Concurrent Chemotherapy
  2. Previous treatment
  3. SBRT/SRS techniques- very high doses per fraction
  4. Proton Treatments- Limited data • General principles are the same as for photon treatments. • In a proton dept, there should be plans in place to minimize interruptions in treatment.
  5. Brachytherapy- a variety of dose/fractionation schedules are used
  6. Combination treatments – integration of EBRT with other modalities e.g. brachy
  7. Radioprotectors
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12
Q

What are radioprotectors

A

chemicals that reduce the biologic effects of radiation
radioprotectors containing a sulfhydryl
Group exert their effect by scavenging free radicals and by reducing free-radical damage to DNA
Most effective for radiations characterised by LET

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13
Q

Retreatment after RT

A
  • If its after 10 years, it is approved to be treating
    • Use highly conformal techniques
    • Reirradiation is possible in various sites with reduced doses and with a high price in terms of morbidity
      Reirradiation with 50 to 60 Gy within a few years of the initial treatment improves local control and possibly survival, but with severe toxicity and functional sequelae
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14
Q

What is BED

A

Biologic effective dose: measure of true biological effect of dose
ND X (1+d/a/b)

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15
Q

What is EQD

A

Biological effective dose converted to standard dosing
EQD= BED/1+2/A/B

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16
Q

Clinical example of hyperfractionation schedule

A

CHART trial
50Gy in 36 Fractions in 12 days

17
Q

Clinical example of hypofractionation

A

Breast
40Gy in 15#
Prostate
60Gy in 20#