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General Principles and Practical Points
in Target Delineation: Esophageal Ca
Yong Chan Ahn, MD, PhD
Dept of Radiation Oncology
Samsung Medical Center
Sungkyunkwan University School of Medicine
Anatomy & Basics
Histology
Sq cell ca Adenoca
Etiology Tobacco/alcohol Barrett’s esophagus
GERD, smoking,
high body mass
Incidence Decreasing in US Increasing in US
Location Upper to mid
thoracic
GE junction
Prognosis Better prognosis
AJCC 7th edition
AJCC 6th AJCC 7th
T1 Subdivided into T1a and T1b
T4 Subdivided into T4a and T4b
N stage – N1 N1~3 based on number of nodes (+)
M1a
M1b
M1a  regional LN
Regional LN Cervical to celiac nodes
Overall stage Incorporation of tumor grade,
location and histology (AD vs SQ)
AJCC 6th vs 7th
NCCN Guidelines
Variability in Target Delineation
• Median Jaccard conformity index was 0.69, with
28% (14 of 50 investigators) achieving JCI≥0.7.
• Median geographical miss index was 0.09.
• Mean discordance index was 0.27.
• CI was highest in middle section of volume,
where tumor was bulky and more easily
definable.
• GTV delineation by 6 radiation oncologists on
10 patients using CT alone and PET-CT.
Inter-personal (6 observers)
Intra-personal
• GTV delineation by 3 radiation oncologists on
28 patients using CT alone and PET-CT.
• PET-CT modified tumor
delineation in 61% (17/28) in
cranial and/or caudal
direction.
• Mean concordance indexes
for CT- and PET-CT-based
CTV/PTV were 72%/77%,
vs. 72%/76%.
• PET and CT may improve
target volume definition with
less geographic misses, but
without significant effects on
inter-observer variability.
• PET was able to identify most primary tumors, with a
sensitivity and specificity for the detection of metastatic
lymph nodes of 30~93% and 79~100%.
• PET-CT resulted in target volume changes.
• Evidence on validity of PET-CT is very limited.
– 3 studies  significant positive correlation between PET-based
tumor lengths and pathological findings.
– 2 studies  inter- and intra-observer variability (results were
not same).
– No study demonstrated improved locoregional control or
survival by PET-CT.
LR CC AP
Mean 3.5 8.3 4.0
SD 1.8 3.8 2.6
Importance of Target Delineation
From Classic to Conformal
• Fundamental tenet of RT is delivery of high dose
to tumor while limiting dose to normal tissues.
• OAR’s and normal tissue tolerance have limited
dose to tumor.
• Conformal RT:
– Dose escalation to tumor while limiting dose to
normal tissues
– Better local control, enhancing quality of life, and
reducing Tx-associated morbidity
– Need to improve accuracy of every step!
RT Process
Steps in RT that can be represented by links in a chain.
Tx accuracy will be limited by the weakest link in the chain
Can IGRT Be Solution?
If you can’t see it, you can’t hit it.
And if you can’t hit it, you can’t cure it.
(by Harold Johns)
• IGRT:
– The latest imaging techniques to monitor target
volume.
– As good as accuracy only when target is known!
– Improved accuracy by IGRT is limited by target
delineation accuracy.
Target delineation: The problem!
• Current practice in RT uses ICRU definition of
target volume
– Gross tumor volume (GTV)
– Clinical target volume (CTV)
– Planning target volume (PTV)
GTV
• GTV is part of tumor that is visible with 3D
imaging.
• Actual GTV delineated is dependent on imaging
modality utilized and data acquisition process.
• Uncertain & variable!
GTV to CTV
• Margins!
– Based on assumptions from clinical or pathological
experience.
– Subject to high degrees of uncertainty.
– Making target delineation highly imprecise.
• Uncertain & variable!
CTV to PTV
• Margins!
– Based on clinical experience
– +/- suggested theoretical margins based on observed
variations.
• PTV frequently includes large amount of normal
healthy tissue within high dose volume 
limiting total dose to PTV.
• Uncertain & variable!
Importance of Target Delineation
• Target contouring errors generate systematic errors
which no level of image guidance will eliminate.
• Target delineation accuracy cannot be overemphasized!
Guideline (Protocol)
• Lack of continuous education and training --
cause of variability in tumor delineation.
• Guidelines for tumor delineation increases
agreement between observers (prostate, lung, and
nasopharynx):
– Average variation of GTV was reduced from 20% to
13% with protocol.
– Protocol included level and window settings, and
tumor identification by diagnostic radiologist.
Collaboration with Diagnosticians
• Development of closer links between radiologists
and oncologists to optimize interpretation of
imaging and target volume definition.
• Radiologists -- to read and interpret films
• Oncologists -- to treat cancer
Conclusion
• Tumor delineation:
– Is the weakest link in RT accuracy,
– Will continue to have significant impact,
– Improvement is necessary.
• Possibility of converging and making tumor
identification and definition less subjective and
less observer-dependent with advancement of
computer programming and imaging technology
(MRI, PET).
Classic RT Target Volumes
• Large T: bilat SCN + whole mediast + Lt gastric –
’97 Mei
• Middle T: bilat SCN + mediast – ’91 Teniere
• Small T: bilat lower neck + SCN + upper mediast
– ’89 Nishimura
• Tumor bed only – ’93 Fok
• Tumor bed + vertical 5~8 cm + horizontal 2 cm +
no bilat SCN – ’01 Bedard
Target Delineation Tips:
Definitive RT Setting
(Japanese Style?)
Initial Findings of Primary Tumor
• Circumferential location
• Tumor size
• Tumor type
• Depth of tumor invasion
Metastatic Lesions
• Lymph node metastasis:
– Naming, number and extent of LN’s
– LN groups
– Degree of LN (N)
• NX: LN metastasis cannot be assessed
• N0: No lymph node metastasis
• N1: Metastasis to Group 1 LN
• N2: Metastasis to Group 2 LN
• N3: Metastasis to Group 3 LN
• N4: Metastasis to Group 4 LN
Target Delineation Tips:
Definitive RT Setting
(Chinese Style?)
• Feb 2003~Dec 2008, Shandon Cancer Hospital
• 1,077 thoracic ESCC patients who underwent
surgery
• Feb 2003~Sep 2011, Shandon Cancer Hospital
• 1,893 thoracic ESCC patients who underwent
surgery
JTO, ’13
Feb/’03~Dec/’08 (N=1,077) Feb/’03~Sep/’11 (N=1,893)
• 45 observational studies with a total of 18,415
patients were included in meta-analysis.
2010 (N=1,077) 2013 (N=1,893)
Target Delineation Tips:
Salvage RT Setting
• July 2005~January 2009, 140 patients with
recurrent or metastatic thoracic esophageal SqCC
were treated with surgery alone.
• Surgical LND: 2 filed in 119; 3 field in 21
• Pathologic surgical margins were negative.
• None received CTx or RT before and after surgery.
• 350 recurrence or metastasis in 140 patients.
• Median time to progression = 18.3 (15.4~21.1) mo
How Do I Do?
(Gangnam Style?)
Case: M/58 Cervical~Upper Thoracic
• Squamous cell ca, cT3N1
Case: M/58 Cervical~Upper Thoracic
• Definitive RT (66~70 Gy/6.5~7
weeks) concurrent with FP chemo #2
Case: M/60 Low Thoracic
• Squamous cell ca, cT3N2
Case: M/60 Low Thoracic
• Preop RT (44 Gy/4.5 weeks)
concurrent with FP chemo #2
Case: M/70 Local Recurrence
• 2Y 3M ago: s/p I-L Op, pT2N0
• A-site recurrence, rT4N1
Case: M/70 Local Recurrence
• Salvage RT (66~70 Gy/6.5~7 weeks)
concurrent with FP chemo #2
# of Esophageal Ca Pt at SMC
(~Nov 2012)
4
14
27
14
27
43
28
54
40
50
64
47
36
55
60
92
67
83
97
0
20
40
60
80
100
120
Total 902 pts
Aim of RT
Total 902 pts
Overall Survival vs RT Setting
Whenever Possible!
• Gather any small piece of important information:
– Clinical – P/E, EGD, EUS, CT, PET…
• Evaluate operability & resectability (anatomic &
physiologic staging).
• Consider aggressive & multi-modal approach.
• Optimize RT target volume to achieve Tx goal.
• Monitor and adapt to changes during RT course.
Whenever Possible!
• To go, or not to go?
– 길이 아니면 가지 말라.
– 질 것이 뻔한 싸움은 덤비지 말라.
• Stay optimistic & affirmative if not definitely negative!
– Down-staging if equivocal.
– 보이는 gross tumor를 control 못하면서, 안 보이는
subclinical metastasis를 너무 걱정할 필요가 없다.
• If I have to go, go well!
– 최악의 부작용은 local failure!
– Acute & reversible side effect는 차라리 즐겨라.
– Life-long complication은 무조건 피하도록.
Whenever Possible!
• 어떤 경우에도 환자는 길고, 고통스러우며, 비
싼 방사선치료를 받고자 하지 않는다.
• In every case,
– As effective as possible.
– As less toxic as possible.
– As simple as possible.
– As short as possible.
– As economic as possible.
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Esophageal cancer practical target delineation 2013 may

  • 1. General Principles and Practical Points in Target Delineation: Esophageal Ca Yong Chan Ahn, MD, PhD Dept of Radiation Oncology Samsung Medical Center Sungkyunkwan University School of Medicine
  • 3. Histology Sq cell ca Adenoca Etiology Tobacco/alcohol Barrett’s esophagus GERD, smoking, high body mass Incidence Decreasing in US Increasing in US Location Upper to mid thoracic GE junction Prognosis Better prognosis
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  • 9. AJCC 7th edition AJCC 6th AJCC 7th T1 Subdivided into T1a and T1b T4 Subdivided into T4a and T4b N stage – N1 N1~3 based on number of nodes (+) M1a M1b M1a  regional LN Regional LN Cervical to celiac nodes Overall stage Incorporation of tumor grade, location and histology (AD vs SQ)
  • 10. AJCC 6th vs 7th
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  • 20. Variability in Target Delineation
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  • 22. • Median Jaccard conformity index was 0.69, with 28% (14 of 50 investigators) achieving JCI≥0.7. • Median geographical miss index was 0.09. • Mean discordance index was 0.27. • CI was highest in middle section of volume, where tumor was bulky and more easily definable.
  • 23. • GTV delineation by 6 radiation oncologists on 10 patients using CT alone and PET-CT.
  • 25.
  • 26. • GTV delineation by 3 radiation oncologists on 28 patients using CT alone and PET-CT.
  • 27.
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  • 29. • PET-CT modified tumor delineation in 61% (17/28) in cranial and/or caudal direction. • Mean concordance indexes for CT- and PET-CT-based CTV/PTV were 72%/77%, vs. 72%/76%. • PET and CT may improve target volume definition with less geographic misses, but without significant effects on inter-observer variability.
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  • 37. • PET was able to identify most primary tumors, with a sensitivity and specificity for the detection of metastatic lymph nodes of 30~93% and 79~100%. • PET-CT resulted in target volume changes. • Evidence on validity of PET-CT is very limited. – 3 studies  significant positive correlation between PET-based tumor lengths and pathological findings. – 2 studies  inter- and intra-observer variability (results were not same). – No study demonstrated improved locoregional control or survival by PET-CT.
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  • 40. LR CC AP Mean 3.5 8.3 4.0 SD 1.8 3.8 2.6
  • 41. Importance of Target Delineation
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  • 43. From Classic to Conformal • Fundamental tenet of RT is delivery of high dose to tumor while limiting dose to normal tissues. • OAR’s and normal tissue tolerance have limited dose to tumor. • Conformal RT: – Dose escalation to tumor while limiting dose to normal tissues – Better local control, enhancing quality of life, and reducing Tx-associated morbidity – Need to improve accuracy of every step!
  • 44. RT Process Steps in RT that can be represented by links in a chain. Tx accuracy will be limited by the weakest link in the chain
  • 45. Can IGRT Be Solution? If you can’t see it, you can’t hit it. And if you can’t hit it, you can’t cure it. (by Harold Johns) • IGRT: – The latest imaging techniques to monitor target volume. – As good as accuracy only when target is known! – Improved accuracy by IGRT is limited by target delineation accuracy.
  • 46. Target delineation: The problem! • Current practice in RT uses ICRU definition of target volume – Gross tumor volume (GTV) – Clinical target volume (CTV) – Planning target volume (PTV)
  • 47. GTV • GTV is part of tumor that is visible with 3D imaging. • Actual GTV delineated is dependent on imaging modality utilized and data acquisition process. • Uncertain & variable!
  • 48. GTV to CTV • Margins! – Based on assumptions from clinical or pathological experience. – Subject to high degrees of uncertainty. – Making target delineation highly imprecise. • Uncertain & variable!
  • 49. CTV to PTV • Margins! – Based on clinical experience – +/- suggested theoretical margins based on observed variations. • PTV frequently includes large amount of normal healthy tissue within high dose volume  limiting total dose to PTV. • Uncertain & variable!
  • 50. Importance of Target Delineation • Target contouring errors generate systematic errors which no level of image guidance will eliminate. • Target delineation accuracy cannot be overemphasized!
  • 51. Guideline (Protocol) • Lack of continuous education and training -- cause of variability in tumor delineation. • Guidelines for tumor delineation increases agreement between observers (prostate, lung, and nasopharynx): – Average variation of GTV was reduced from 20% to 13% with protocol. – Protocol included level and window settings, and tumor identification by diagnostic radiologist.
  • 52. Collaboration with Diagnosticians • Development of closer links between radiologists and oncologists to optimize interpretation of imaging and target volume definition. • Radiologists -- to read and interpret films • Oncologists -- to treat cancer
  • 53. Conclusion • Tumor delineation: – Is the weakest link in RT accuracy, – Will continue to have significant impact, – Improvement is necessary. • Possibility of converging and making tumor identification and definition less subjective and less observer-dependent with advancement of computer programming and imaging technology (MRI, PET).
  • 54. Classic RT Target Volumes • Large T: bilat SCN + whole mediast + Lt gastric – ’97 Mei • Middle T: bilat SCN + mediast – ’91 Teniere • Small T: bilat lower neck + SCN + upper mediast – ’89 Nishimura • Tumor bed only – ’93 Fok • Tumor bed + vertical 5~8 cm + horizontal 2 cm + no bilat SCN – ’01 Bedard
  • 55. Target Delineation Tips: Definitive RT Setting (Japanese Style?)
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  • 57. Initial Findings of Primary Tumor • Circumferential location • Tumor size • Tumor type • Depth of tumor invasion
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  • 62. Metastatic Lesions • Lymph node metastasis: – Naming, number and extent of LN’s – LN groups – Degree of LN (N) • NX: LN metastasis cannot be assessed • N0: No lymph node metastasis • N1: Metastasis to Group 1 LN • N2: Metastasis to Group 2 LN • N3: Metastasis to Group 3 LN • N4: Metastasis to Group 4 LN
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  • 73. Target Delineation Tips: Definitive RT Setting (Chinese Style?)
  • 74. • Feb 2003~Dec 2008, Shandon Cancer Hospital • 1,077 thoracic ESCC patients who underwent surgery
  • 75.
  • 76. • Feb 2003~Sep 2011, Shandon Cancer Hospital • 1,893 thoracic ESCC patients who underwent surgery JTO, ’13
  • 77.
  • 79. • 45 observational studies with a total of 18,415 patients were included in meta-analysis.
  • 80.
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  • 82. 2010 (N=1,077) 2013 (N=1,893)
  • 83.
  • 85. • July 2005~January 2009, 140 patients with recurrent or metastatic thoracic esophageal SqCC were treated with surgery alone.
  • 86. • Surgical LND: 2 filed in 119; 3 field in 21 • Pathologic surgical margins were negative. • None received CTx or RT before and after surgery.
  • 87. • 350 recurrence or metastasis in 140 patients. • Median time to progression = 18.3 (15.4~21.1) mo
  • 88. How Do I Do? (Gangnam Style?)
  • 89. Case: M/58 Cervical~Upper Thoracic • Squamous cell ca, cT3N1
  • 90. Case: M/58 Cervical~Upper Thoracic • Definitive RT (66~70 Gy/6.5~7 weeks) concurrent with FP chemo #2
  • 91. Case: M/60 Low Thoracic • Squamous cell ca, cT3N2
  • 92. Case: M/60 Low Thoracic • Preop RT (44 Gy/4.5 weeks) concurrent with FP chemo #2
  • 93. Case: M/70 Local Recurrence • 2Y 3M ago: s/p I-L Op, pT2N0 • A-site recurrence, rT4N1
  • 94. Case: M/70 Local Recurrence • Salvage RT (66~70 Gy/6.5~7 weeks) concurrent with FP chemo #2
  • 95. # of Esophageal Ca Pt at SMC (~Nov 2012) 4 14 27 14 27 43 28 54 40 50 64 47 36 55 60 92 67 83 97 0 20 40 60 80 100 120 Total 902 pts
  • 96. Aim of RT Total 902 pts
  • 97. Overall Survival vs RT Setting
  • 98. Whenever Possible! • Gather any small piece of important information: – Clinical – P/E, EGD, EUS, CT, PET… • Evaluate operability & resectability (anatomic & physiologic staging). • Consider aggressive & multi-modal approach. • Optimize RT target volume to achieve Tx goal. • Monitor and adapt to changes during RT course.
  • 99. Whenever Possible! • To go, or not to go? – 길이 아니면 가지 말라. – 질 것이 뻔한 싸움은 덤비지 말라. • Stay optimistic & affirmative if not definitely negative! – Down-staging if equivocal. – 보이는 gross tumor를 control 못하면서, 안 보이는 subclinical metastasis를 너무 걱정할 필요가 없다. • If I have to go, go well! – 최악의 부작용은 local failure! – Acute & reversible side effect는 차라리 즐겨라. – Life-long complication은 무조건 피하도록.
  • 100. Whenever Possible! • 어떤 경우에도 환자는 길고, 고통스러우며, 비 싼 방사선치료를 받고자 하지 않는다. • In every case, – As effective as possible. – As less toxic as possible. – As simple as possible. – As short as possible. – As economic as possible.