dr. iain tan -...
TRANSCRIPT
![Page 1: Dr. Iain Tan - oncologypro.esmo.orgoncologypro.esmo.org/content/download/125640/2375309/file/2017... · Dr. Iain Tan Senior Consultant GI ... 2011; 8. Van Cutsem. J Clin Oncol. 2011;](https://reader030.vdocument.in/reader030/viewer/2022021509/5aa044ae7f8b9a89178dcf9e/html5/thumbnails/1.jpg)
ESMO-ASIA 2017 Preceptorship (GI cancers)
Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
Dr. Iain Tan
Senior Consultant GI Medical Oncologist
National Cancer Centre Singapore
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1. The case for aggressive therapy in borderline resectable / unresectable liver limited metastases
2. Components Multidisciplinary / Multi-modality management
3. Chemotherapy & Targeted Therapy prior to surgery
4. Chemotherapy & Targeted Therapy after surgery
5. The left and right issue
6. How I choose systemic therapy in borderline resectable/unresectable
ESMO-ASIA 2017 Preceptorship (GI cancers)Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
OUTLINE
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Overall survival for patients with mCRC treated at MD Anderson and Mayo clinics, by year of diagnosis
Over the past decade, OS has improved substantially in patients with mCRC
• 2470 patients from two highly specialized centers were included
0 60483624120
20
40
60
80
100
Time (months)
OS
(%)
1990–19911992–19941995–19971998–20002001–20032004–2006
Kopetz S, et al. J Clin Oncol 2009;27:3677–3683
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Multiple active systemic agents in mCRC
Overall Survival (months)
5-FU/LV bolus
5-FU/LV infusion
IFL
LVFU2/irinotecan
FOLFOX
IFL + bevacizumab
FOLFOX/FOLFIRI
XELOX/FOLFOX + bevacizumab
FOLFOX + cetuximab
FOLFIRI + cetuximab
FOLFOX + panitumumab
FOLFIRI + cetuximab
FOLFOXIRI + bevacizumab
*KRAS wildtype tumors.Note: Informal comparison as these are not head-to-head clinical trials.
1. Saltz. N Engl J Med. 2000; 2. Douilliard. Lancet. 2000; 3. Goldberg. J Clin Oncol. 2004; 4. Hurwitz. N Engl J Med. 2004; 5. Saltz. J Clin Oncol. 2008; 6. Falcone. J Clin Oncol. 2007; 7. Bokemeyer. Ann Oncol. 2011; 8. Van Cutsem. J Clin Oncol. 2011; 9. Douilliard. ASCO; 2011. Abstract 3510. 10.
Heinemann. ASCO 2013. Abstract LBA3506. 11. Falcone. ASCO 2013. Abstract 3505.
Treatment Approaches to First-Line mCRC
2000
2013
2011
2011
2008
2007
2004
2004
2000
2000
2000
2011
2013
2013
FOLFIRI + bevacizumab
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ORR PFS PFS
HR
OS OS
HR
AVF2107g IFL 35% 6.4 15.6
+ Bevacizumab 45% 10.6 0.54 20.3 0.66
PRIME FOLFOX 7.9 20.2
+ panitumumab 10.1 0.72 26 0.72
CRYSTAL FOLFIRI 8.4 20.2
+ Cetuximab 11.4 0.56 28.4 0.69
TRIBE FOLFIRI/Bev 53% 9.7 25.8
FOLFOXIRI/Bev 65% 12.1 0.75 31 0.79
FIRE3 FOLFIRI/Bev 56% 10.2 25
FOLFIRI/Cet 71% 10.4 0.93 33.1 0.7
CALGB Chemo + Bev 57% 11.3 31.2
Chemo + Cet 69% 11.4 1.1 32 0.9
Landmark 1st line CRC studies
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CORRECT
(3rd line) Regorafenib Placebo
HR
[n=760] p-value
Median PFS 1.9 mo 1.7 mo 0.49 <0.000001
Median OS 6.4 mo 5.0 mo 0.77 0.0052
VELOUR
(2nd line)
Placebo +
FOLFIRI
(n = 614)
Aflibercept +
FOLFIRI
(n = 612)
Hazard
ratio p-value
Median OS 12.1 mo 13.5 mo 0.82 0.0032
Median PFS 4.7 mo 6.9 mo 0.76 0.00007
Overall response 11.1% 19.8% — 0.0001
RECOURSE
(3rd line)
TAS-102
(n=534)
Placebo
(n=266) HR p-value
Median PFS 2.0 mo 1.7 0.48 <0.0001
Median OS 7.1 mo 5.3 mo 0.68 <0.0001
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Low disease burden, generally with a single solitary site of spread
Stage 4 Colorectal Cancer is a Continuum of disease
Less extensive More extensive
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Low disease burden, generally with a single solitary
site of spread
Less extensive More extensive
Chemotherapy & Surgical removal of the site of metastasis with the intention of achieving cure
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Less extensive More extensive
Chemotherapy to reduce size of metastases with the intention of to convert to a situation where surgery becomes feasible
intermediate disease burden,
generally not operable upfront but with limited disease
spread
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Less extensive More extensive
Chemotherapy to control tumor, improve symptoms, maintain quality of life and prolong life
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Liver resection improves long-term survival
• 12-month landmark analysis evaluated the impact of liver resection on OS
70% of population included
Patient
status
Median
OS (mo)
5-year
OS rate
Resected 65.3 55%
Non
resected26.7 19.5%
HR 0.35
Liver resection dramatically improves long-term survival and offers a real chance for cure
Time (months)
012 24 36 48 60 72
20
40
60
80
100
Ove
rall
surv
ival
(%
)
Lan
dm
ark
No liver resection
Liver resection
0
Kopetz S, et al. J Clin Oncol 2009;27:3677–3683
Error bars represent 95% CIs
Simmonds PC, et al. Br J Cancer. 2006;94:982–99
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Kanas GP, et al. Clin Epidemiol 2012;4:283–301;
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Adam R. 2009
New definition of resectability
• All liver metastases that can be completely removed while leaving at least 30% of remnant liver...
• Even in cases with extrahepatic tumors, if these are also resectable…
‘Practical’ rather than ‘dogmatic’
• Easily resectable: – Complete resection with good margins
• Marginally resectable: – No margins, small liver remnant– Concomitant extrahepatic (resectable)
• Definitely non-resectable: – Widespread hepatic disease– Non-resectable extrahepatic– Multiple metastatic sites
In practice: 3 categories of patients
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Strategies Liver metastases
resectable
neo CT +Liver resection
non optimal resectable
> 4 Metastases
synchronous CRCLM
Primary LN-positive
bilobar CRCLM
technically problematic:
Close to 3 hepatic veins
Close to portal bifurcation
Neoadjuvant Chemotherapy→ Operation
Primaryunresectable
PalliativeChemotherapy
possible
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1. The case for aggressive therapy in borderline resectable / unresectable liver limited metastases
2. Components Multidisciplinary / Multi-modality management
3. Chemotherapy & Targeted Therapy prior to surgery
4. Chemotherapy & Targeted Therapy after surgery
5. The left and right issue
6. How to choose systemic therapy
ESMO-ASIA 2017 Preceptorship (GI cancers)Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
OUTLINE
![Page 17: Dr. Iain Tan - oncologypro.esmo.orgoncologypro.esmo.org/content/download/125640/2375309/file/2017... · Dr. Iain Tan Senior Consultant GI ... 2011; 8. Van Cutsem. J Clin Oncol. 2011;](https://reader030.vdocument.in/reader030/viewer/2022021509/5aa044ae7f8b9a89178dcf9e/html5/thumbnails/17.jpg)
Components of Multidisciplinary / Multi-modality management
• Neoadjuvant systemic therapy
• Staged hepatectomy
• Portal vein embolization (PVE)
• Portal vein ligation (PVL)
• Radioembolization
• Locoregional ablative therapies
• Advanced imaging
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The impact of a multidiscplinary team approach
in the treatment of colorectal cancer withliver metastases:
Liver-limited metastatic colorectal cancer as a curable disease
The multidisciplinary team
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1. The case for aggressive therapy in borderline resectable / unresectable liver limited metastases
2. Components Multidisciplinary / Multi-modality management
3. Chemotherapy & Targeted Therapy prior to surgery
4. Chemotherapy & Targeted Therapy after surgery
5. The left and right issue
6. How I choose systemic therapy in borderline resectable/unresectable
ESMO-ASIA 2017 Preceptorship (GI cancers)Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
OUTLINE
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General principles of systemic chemotherapy in borderline / unresectable liver-limited mCRC
• Give the most active regimen• Goal of treatment
– Achieve R0 resection; maximum tumor shrinkage– Early management of unseen micrometastases
• Consider surgery once it is resectable– Achieve resectability rather than a CR
• If convertible to surgery, – Sequencing of the different procedures– Management of the primary – role of post-operative chemotherapy
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Resection rate of metastases and tumor response
Studies including non-selected patients with mCRC (solid line) (r=0.74; p<0.001)
Studies including selected patients(liver metastases only, no extrahepatic disease)(r=0.96; p=0.002)
Phase III studies including non-selected patients with mCRC (dashed line)(r=0.67; p=0.024)
Folprecht G, et al. Ann Oncol 2005;16:1311–1319
Response rate
0.90.80.70.60.50.40.3
Re
sect
ion
rat
e
0.6
0.5
0.4
0.3
0.2
0.1
0
Jones R et al. Eur J Cancer, 2014
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When to send for surgery?
• Achieve resectability rather than a CR
• 83% of lesions that disappear whilst on chemotherapy are still active
• Need to resect before metastases completely disappear
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Chemotherapy:The use of triplets
PFS 10 m vs 7 m
OS 23 m vs 17 m
+ Greek Study (R0 resectn)
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Chemotherapy:The use of triplets
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ORR PFS PFS
HR
OS OS
HR
AVF2107g IFL 35% 6.4 15.6
+ Bevacizumab 45% 10.6 0.54 20.3 0.66
Targeted Therapy:The use of anti-VEGF
Modest, if any impact on ORRIssues of surgical safety/timing
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Targeted Therapy:The use of anti-EGFR
Response and R0 resection rates:CRYSTAL and OPUS (KRAS exon2 wt)
n RR (%)R0 resections
(%)
CRYSTAL
FOLFIRI + Cetuximab
FOLFIRI
316
350
57
40p<0.001
5.1
2.0p=0.03
OPUS
FOLFOX + Cetuximab
FOLFOX
82
97
57
34p<0.003
7.3
3.1p=0.22
FOLFIRI + Cetuximab
FOLFIRI
68
72
71
44p=0.002
13.2
5.6p=0.15
FOLFOX + Cetuximab
FOLFOX
25
23
76
39p=0.018
16.0
4.3p=0.35
Left vs Right & extended Ras not considered
All
pat
ien
tsLi
ver
limit
ed
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PRIME study post-hoc analysis
Mean (95% CI) percentage change in tumour load
(sum of all target lesions)† (WT RAS)
Douillard JY, et al. Eur J Cancer 2015;51:1231−42.
*Tumour shrinkage at nadir versus baseline tumour load
(sum of the longest diameters of all target lesions).
Mean c
hange fro
m b
aselin
e (
%)
−40
−20
0
−60
Week number of measurement
−80
0 8 16 24 32 40 48 56
Panitumumab + FOLFOX4 (n = 236)
FOLFOX4 (n = 224)
−100
Median DpR*, % (Q1, Q3)
46 (23, 66)
54 (31, 72) P = 0.0149
245
242
219
221
195
183
157
147
116
110
96
71
71
39
55
25
Patients at risk:
Panitumumab + FOLFOX4
FOLFOX4
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PRIME study post-hoc analysis
Resection rates (WT RAS and LLD)
Douillard JY, et al. Eur J Cancer 2015;51:1231−42. *Descriptive P-value (Fisher exact test).
Patients
(%
)
∆ = 6.5%
P = 0.644*
Any resection0
10
20
30
Panitumumab + FOLFOX4 (n = 48)
35
25
15
5
Complete resection
FOLFOX4 (n = 41)
Updated analysis
33%
27%
31%
17%
∆ = 14.2%
P = 0.145*
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Events,n
Median OS, months
Panitumumab + FOLFOX4 (n = 35)
16 57.4
FOLFOX4 (n = 29) 15 54.5
PRIME study post-hoc analysis
OS in patients with any resection
(WT RAS, LLD and non-LLD)
Douillard JY, et al. Eur J Cancer 2015;51:1231−42.
Censor indicated by vertical bar.
WT RAS = WT KRAS and NRAS exons 2/3/4.
RFS, relapse-free survival.
• Median RFS after resection (n = 38) was 22.0 vs 12.4 months with panitumumab +
FOLFOX4 vs FOLFOX4, respectively (HR = 0.66; P = 0.3419)
Ka
pla
n−
Me
ier
estim
ate
100
80
60
40
20
0
0 4 8 12 16 20 24 28
Months
32 36 40 44 48 52 56 60 64 68
HR = 0.66 (95% CI, 0.32–1.35)
P = 0.2534
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Four RCTs involving 484 WT KRAS patients were included:PRIME (Douillard et al. 2010)COIN (Maughan et al. 2011)CRYSTAL (Van Cutsem et al. 2011)OPUS (Bokemeyer et al. 2011)WT KRAS = WT KRAS exon 2 (codons 12 and 13) for PRIME, CRYSTAL and OPUS plus WT KRAS exon 3 (codon 61) for COIN
Targeted Therapy:The use of anti-EGFR
Left vs Right & extended Ras not considered
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Targeted Therapy:The use of anti-EGFR
Left vs Right & extended Ras not considered
liver-confined metastases deemed nonresectable by a
local multidisciplinary team, which included > three liver surgeons and one radiologist.
Ye et al. JCO 2013
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CELIM: Study design
Randomization
Primary endpoint: Response rate
Patients with technically unresectable/ ≥5 liver metastases of CRC without extrahepatic metastases
BiopsyEGFR screening
FOLFOX6 + cetuximab FOLFIRI + cetuximab
Therapy: 8 cycles (~4 months)
Evaluation of resectability
Technically resectableTechnically unresectable
4 further treatment cycles Resection
Therapy continuation for 6 cycles (~3 months)
Blinded surgicalreview
Folprecht G, et al. Lancet Oncol 2010;11:38–47
liver-confined metastases deemed nonresectable
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CELIM :Objective Response and Resection Rates
Objective
Response
Rate
KRAS
wild-type
(n=67)
CR/PR, % 70
95% CI, % 58–81Responses confirmed by 2nd CT scan according to RECIST or by resection
Folprecht G, et al. Lancet Oncol 2010;11:38–47 ; Van Cutsem ASCO-GI 2011
FOLFOX6 +
cetuximab
(n=53) (%)
FOLFIRI
+cetuximab
(n=53) (%)
All
patients
(n=106) (%)
R0 resections 38 30 34
R1-resect / Resect + RFA 2 8 5
RFA 9 6 8
R0/R1 resect / RFA 49 43 46
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Folprecht. Lancet Oncol 2010;Alberts. JCO 2005
Time to intervention
0
10
20
30
40
50
60
0 2 4 6 8 10 12 14 16
Pro
bab
ility
, %
CELIM: Time to intervention
44 patients were resected, 5 patients had exploratory laparotomyMedian time to intervention (resection/laparotomy): 5.1 monthsMedian number of cycles prior to intervention: 8
Time of chemotherapy 1 month shorter than with FOLFOX alone
Time (months)
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CELIM: Prolonged survival after R0 resection
Folprecht G, et al. EMCC 2011 (Abstract No 6009)
— R0 resected— Not R0 resected
HR=2.34 (1.37-4.01)
p=0.002
— R0 resected— Not R0 resected
OSPFS
HR=2.07 (1.35-3.16)p=0.001
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Depth of Response and Early Tumour Shrinkage
Chemo + / - Anti-EGFR Median DpR% w ETS >
20%(>20% vs <20%)
:PFS HR OS HR % w ETS > 30%(>30% vs <30%):
PFS HR OS HR
Study n +EGFR-ab chemo +EGFR-ab chemo +EGFR-ab chemo +EGFR-ab chemo +EGFR-ab chemo +EGFR-ab chemo +EGFR-ab chemo
PRIME (updated RAS analysis) 440 54% 46% 72% 57% 0.62 0.67 0.47 0.50 59% 38% 0.56 0.62 0.52 0.46
CRYSTAL WT KRAS 631 62% 39% 0.32 0.58 0.53 0.71
OPUS WT KRAS 168 69% 54% 0.22 0.89 0.43 0.89
20060314: 1 arm Pan/FOLFIRI 65 59% 74%13.3 vs
5.9 49% 14.3 vs 7.8
Chemo + / - Biologic Median DpR % ETS > 20%PFS HR (ETS
>20% vs< 20%)OS HR (ETS
>20% vs< 20%) % ETS > 30%PFS HR (ETS
>30% vs<30%)OS HR (ETS
>30% vs<30%)
Study n +EGFR-ab +VEGF-ab +EGFR-ab +VEGF-ab +EGFR-ab +VEGF-ab +EGFR-ab +VEGF-ab+EGFR-
ab+VEGF-
ab +EGFR-ab+VEGF-
ab +EGFR-ab +VEGF-ab
PEAK WT-RAS (final analysis) 154 65% 46% 75% 62%13.1 vs
9.811.3 vs
9.543.4 vs
21.232.5 vs
21.8 64% 45%13.0 vs
11.611.1 vs
9.743.8 vs
34.235.1 vs
23.9
FIRE3 WT-RAS (wk 6) 330 49% 32% 68% 49% 0.59 0.71 0.52 0.49CALGB 1137 ORR: 69% ORR: 54%
Triplet chemo: (combined analysisTRIP/MACBETH/TRIBE (wt RAS/RAF)
153 49% 38% 70% 62%
VEGF + 2 vs 3 chemo n + Ox Bev/5FU-iri + Ox Bev/5FU-iri
TRIBE (no RAS analysis) 441 44% 38% 63% 52%
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1. The case for aggressive therapy in borderline resectable / unresectable liver limited metastases
2. Components Multidisciplinary / Multi-modality management
3. Chemotherapy & Targeted Therapy prior to surgery
4. Chemotherapy & Targeted Therapy after surgery
5. The left and right issue
6. How I choose systemic therapy in borderline resectable/unresectable
ESMO-ASIA 2017 Preceptorship (GI cancers)Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
OUTLINE
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Adjuvant Chemo post resection of colorectal liver mets
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% absolute
difference
in 3-year PFS
Hazard
Ratio
P-value
All patients
(n=182 per
arm)
+7.2% (28.1% to 35.4%)
0.79 P=0.058
All eligible
Patients
(n=171 per
arm)
+8.1% (28.1% to 36.2%)
0.77 P=0.041
All resected
Patients
(n=151 per
arm)
+9.2%(33.2% to 42.4%)
0.73 P=0.025
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The NEW EPOC StudyA randomised clinical trial of chemotherapy compared to chemotherapy in
combination with cetuximab in KRAS wild-type patients with operable metastases from colorectal cancer
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ChemotherapyResults
HR 1.49 95%CI (1.04, 2.12); p=0.030
0.0
00.2
50.5
00.7
51.0
0
Pro
port
ion p
rogre
ssio
n fre
e
117 87 54 24 15 5 3 2 1 0 0Arm B116 89 65 38 23 12 5 2 1 1 0Arm A
Number at risk
0 6 12 18 24 30 36 42 48 54 60
Time to progression or death (months)
Arm A Arm B
HR 1.48 95%CI (0.85, 2.58); p=0.163
0.0
00.2
50.5
00.7
51.0
0
Pro
port
ion e
ve
nt fr
ee
127 99 81 55 38 22 7 2 1 0 0Arm B127 113 90 61 40 29 12 4 2 1 0Arm A
Number at risk
0 6 12 18 24 30 36 42 48 54 60
Time to death (months)
Arm A Arm B
ORR PFS PFS
HR
OS OS
HR
Chemo 42% 20.5 NR
+ Cetuximab 50% 14.1 1.49 39.1 1.48
The NEW EPOC StudyA randomised clinical trial of chemotherapy compared to chemotherapy in
combination with cetuximab in KRAS wild-type patients with operable metastases from colorectal cancer
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1. The case for aggressive therapy in borderline resectable / unresectable liver limited metastases
2. Components Multidisciplinary / Multi-modality management
3. Chemotherapy & Targeted Therapy prior to surgery
4. Chemotherapy & Targeted Therapy after surgery
5. The left and right issue
6. How I choose systemic therapy in borderline resectable/unresectable
ESMO-ASIA 2017 Preceptorship (GI cancers)Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
OUTLINE
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Primary CRC tumor localization (left vs right)
Iacopetti, B. Int J Cancer 2002;101:403–408;
Brule SY, et al. ASCO 2013 (Abstract No. 3528);
Adams R, et al. ASCO 2012 (Abstract No. 3516)
Right-sided tumors ~40% (increasing)*
● Associated with:
● Older, female patients
● Mucinous, signet-ring histology
● Microsatellite instability
● Poorly differentiated
● KRAS and BRAF mutations
● EGFR expression
Left-sided tumors ~60%*
● Associated with:
● Chromosomal instability
● p53 mutation
● COX2 expression
● Aneuploidy
● High EGFR ligand expression (COIN
study)
*High-incidence CRC populations
Transverse colon
Right colon
(ascending)Left colon
(descending)
Rectum
Anus
Small
intestine
Sigmoid
(colon)
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Right versus left: RAS WTData from retrospective analysis
• 1st line– PRIME– CRYSTAL– FIRE-3– CALGB– PEAK
• 2nd line– 181
• ? 3rd line and beyond– CO-17
Left sided primary mCRC, anti-EGFR leads to better clinical
outcome compared to chemotherapy or chemotherapy
plus bevacizumab
Right sided primary results suggest little survival benefit for anti-EGFR 1st line +/- 2nd line, but
small numbers does impact on interpretation
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Holch et al, EJC 2017 (70) 87-98
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Arnold et al, Annals of Oncology 28: 1713–1729, 2017
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Targeted Therapy: Head-to-head ORR (1st line)
FIRE3PEAK
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1. The case for aggressive therapy in borderline resectable / unresectable liver limited metastases
2. Components Multidisciplinary / Multi-modality management
3. Chemotherapy & Targeted Therapy prior to surgery
4. Chemotherapy & Targeted Therapy after surgery
5. The left and right issue
6. How I choose systemic therapy in borderline resectable/unresectable
ESMO-ASIA 2017 Preceptorship (GI cancers)Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
OUTLINE
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RIGHT LEFT
RAS wildtype FOLFOXIRI Anti-EGFR/FOLFOX or FOLFOXIRI
RAS mutant FOLFOXIRI FOLFOXIRI
All FOLFOXIRI (+/- Bev)
ESMO-ASIA 2017 Preceptorship (GI cancers)Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
How I choose systemic therapy in borderline resectable/unresectable
Colorectal Liver Metastasis :
A Continuum of
disease
Low disease burden, generally with a single solitary site
of spread
Less extensive More extensive
intermediate disease burden, generally not operable upfront but potentially
“convertible” to an operable state
Chemotherapy to control tumor, improve symptoms, maintain quality
of life and prolong life
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1. The case for aggressive therapy in borderline resectable / unresectable liver limited metastases
2. Components Multidisciplinary / Multi-modality management
3. Chemotherapy & Targeted Therapy prior to surgery
4. Chemotherapy & Targeted Therapy after surgery
5. The left and right issue
6. How I choose systemic therapy in borderline resectable/unresectable
ESMO-ASIA 2017 Preceptorship (GI cancers)Session: Metastatic colorectal cancer, liver limited metastases
Topic: Unresectable or borderline resectable : chemotherapy +/- targeted agents
CONCLUSION
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58