High and low dose regions to normal tissues in IMRT -...
Transcript of High and low dose regions to normal tissues in IMRT -...
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High and low dose regionsto normal tissues
in IMRT
Rick Haas NKI/AvL
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IMRT and dose
• IMRT is focused to– Increase the target dose and/or– Decrease the normal tissue dose
• This involves multiple directions of radiation and potentially more low dose volume
• IMRT is, generally, not aiming atreducing secondary cancers
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•Clark et al R&O 2004
IMRT and doseCRT IMRT
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IMRT and doseMore low dose volume
•Clark et al R&O 2004
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IMRT and dose Lung cancer dose escalation
Belderbos et al 2006
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IMRT and dose lung dose and pneumonitis
Mean Lung Dose
Seppenwoolde 2003
V 13 Gy (cm3)
Grade II pneumonitis
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IMRT and dose FFS Prostate 68 vs 78 Gy
Peeters et al 2006
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ProstateAcute GI toxicity
Conformal SIB IMRT P-value
Grade ≥ 2 61 % 20 %0.001
Grade ≥ 3 13 % 0 %
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ProstateLate GI toxicity (grade ≥ 2)
Time from start radiotherapy (years)
6543210
Cum
ulat
ive
inci
denc
e
1.0
.9
.8
.7
.6
.5
.4
.3
.2
.1
0.0
Conformal
SIB IMRT
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IMRT and dose
�Using IMRT for both lung and prostate cancer allows for dose escalation
�IMRT for head and neck cancer decreases side effects and increases coverage
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� Increase in monitor units:� Larger total-body radiation dose (photon and neutron
component for higher energy)� but no wedges, or physical compensators etc.
� Related to delivery units (IMRT, TOMO, etc)
� Larger volume of normal tissue exposed to lower radiation: the effects related to dose-response curve for radiation induced carcinogenesis or nonmalignant toxicities
� Clinically relevant in pediatric oncology
Impact of IMRTIMRT vs CRT: differences in dose distribution
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Long Latencylate side effects and secondary cancers
Courtesy Hans Langendijk
0%
5%
10%
15%
20%
25%
30%
35%
40%
45%
0 4 8 12 16 20 24
Jaren na behandeling
Ris
ico
Recidief
Tweede primaire tumor
Cardiale complicaties
Years after treatment
Ris
k
Recurrence 2nd primarycardiac
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IMRT and dose
• Mu et al 2005• Pediatric case spinal cord irradiation• RT comparison with photon, electron
and proton techniques
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IMRT and dose
Mu et al 2005
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Fotonen versus protonen: Vergelijkende planning
Courtesy Hans Langendijk
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Estimation of secondary lethal cancers pediatric case
Oesophagus 0.20 0.20 0.20 0.20 0.13
Thyroid 0.15 0.15 0.18 0.16 0.00
Lung 0.17 0.37 0.21 0.12 0.02
Mammary glands 0.05 0.12 0.03 0.00 0.00
Liver 0.11 0.15 0.09 0.05 0.00
Stomach 0.24 0.44 0.27 0.15 0.01
Abdominal cavity 0.23 0.34 0.24 0.19 0.02
Patient outline 0.02 0.03 0.02 0.01 0.01
Effective dose 1.761 2.696 1.863 1.326 0.306
Total risk of SLC 0.198 0.303 0.210 0.149 0.034
Photon IMRT Electr IMET IMPT
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(IM)RT and dose
=> Late toxicity
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Myocard infarction after mediastinal RT
Aleman 2007
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Late toxicity
3-7 fold increased risk for sec. cancer after 30 Gy for testicular cancer predominantly inside the field
Leeuwen et al 1993
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(IM)RT and late toxicity
• Increased breast cancer after Hodgkin disease– <5 Gy no increased risk– >5 Gy Relative Risk 2.7 fold– Protective effect of chemotherapy due to
early menopause
Hill et al 2005
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(IM)RT, dose and volume
• Does reduction of fields reduce secondary cancer risk?
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(IM)RT, dose, volume and age applied
• 1122 female patients treated with RT for Hodgkin disease
• <51 years • Incidence of breast cancer
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Breast cancer after RT for HD
0 5 10 15 20 25 30 35
Time since diagnosis (years)
0.0
0.1
0.2
0.3
0.4
Cu
mu
lativ
e in
cid
en
ce
<=20 years at first treatment
21-30 years at first treatment
31-40 years at first treatment
41-50 years at first treatment
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Breast cancer after RT for HD
Time since diagnosis (years)
0.0
0.1
0.2
0.3
0.4
Cu
mu
lativ
e in
cid
en
ce
Mantlefield, no pelvic RT
Mediastinal RT, no pelvic RT
Mantlefield + pelvic RT
Nr at riskMantlefieldMediastinumMantle&pelvic RT
637 582 448 293 151 64 11109 99 42 20 11 10 5107 87 69 51 33 19 1
Population-expected risk
5 10 15 20 25 30 35
De Bruin et al submitted
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Particle therapy?
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Fotonen versus protonen: Vergelijkende planning of in silico studie
Courtesy Hans Langendijk
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Gemiddelde dosis
Kan
s op
com
licat
ies
(%)
In silico studiesVertaling naar klinisch voordeel m.b.v. NTCP-model
Courtesy Hans Langendijk
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Conclusions
• Toxicity is more than your gantry can cause• Integral dose is largely dependent on machine and
technique not on IMRT or not• Patient data on IMRT sec. cancers are not mature
yet• Risk for sec. cancers is higher for younger patients• A difference in radiation field can translate in less
cancer (BC in HD disease)
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