2019 Management of rectal cancer Masterclass · consider adjuvant ChT in rectal cancer patients...
Transcript of 2019 Management of rectal cancer Masterclass · consider adjuvant ChT in rectal cancer patients...
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D Papamichael MD FRCP
Clinical Session – Gastrointestinal Tumours
6th ESO-ESMO Eastern Europe and Balkan Region
Masterclass in Medical Oncology
12.04.2019 - 17.04.2019
Sibenik (Split area), Croatia
Management of rectal cancer
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Disclosures
• None
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Outline
• Background / historical perspective
• Staging / TME
• Pre-operative RT (and CRT)
• Adjuvant chemotherapy
• Ongoing/future clinical trials
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My best hopes from this lecture
• You will understand better short course(SCPRT)/ chemoradiation(CRT) for rectal cancer
• You will be able to select patients suitable for short course/long course chemoradiation or surgery alone
• You will rationally decide regarding adjuvant chemotherapy after SCPRT or CRT
• You will be able to tailor the treatment to the individual patient
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Outline
• Background / historical perspective
• Staging / TME
• Pre-operative RT (and CRT)
• Adjuvant chemotherapy
• Ongoing/future clinical trials
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Targets of therapeutic Management
• Reduction of local recurrence rates
• Increase in overall and disease free survival
• Preservation of anal sphincter
• Preservation of quality of life and sexual function
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SS
204 patients
Bolus 5-FUSemustine
RR
Postoperative radiochemotherapy
Krook JE et al, N Engl J Med, 1991Krook JE et al, N Engl J Med, 1991
• After a median follow up of 7 years Local recurrence reduction by 46% (p < 0.03)
Distant recurrence reduction by 37% (p < 0.01)ESO-ESMO E
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Postoperative radiochemotherapy
Disease-free survival
Overall survival
Krook JE et al, N Engl J Med, 1991
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Postoperative radiochemotherapy
Disease-free survival
Overall survival
Krook JE et al, N Engl J Med, 1991
HISTORICAL
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Outline
• Background / historical perspective
• Staging / TME
• Pre-operative RT (and CRT)
• Adjuvant chemotherapy
• Ongoing/future clinical trials
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Recommended staging procedures
• TRUS for early T1 cancers – for anatomical detail
• MRI for all cancers (CRM, EMVI, levator assessment, cT substage and cN nodal status)
• CT scan – to image distant spread
• PET/CT for extensive EMVI
• Colonoscopy to rule out synchronous tumours in the colon
• EUA
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Relevant factors that need to be imaged
• CRM status
• Extramural Vascular Invasion (EMVI)
• Involvement of levators
• cT substage (cT3c and cT3d)
• cN status
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High Quality MRI
• Gives the surgeon a road map for surgery
• Determines need for neoadjuvant chemoradiotherapy or SCPRT
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• Extensive vascular invasion can destroy the vessel wall leaving little evidence of normal venous cellular architecture,
• 10% -50% - underreporting widespread by pathologists
• Poor interobserver agreement for EMVI by pathologists
• Human Pathology, 2012
EMVI -not just T3 tumor
Gross nodular expansion of mesorectal veins
EXTRAMURAL VASCULAR INVASION (EMVI)
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clinicaloptions.com/oncologyCCO Independent Coverage of the 2015 Gastrointestinal Cancers Symposium
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What are we trying to stage? Most malignant nodes 3-5mm
Malignant2mm focus
MalignantFully replaced
ReplacedExtracapsularbreach
MalignantMicroscopicfocus
7mmbenign With thanks to Gina Brown
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Outline
• Background / historical perspective
• Staging / TME
• Pre-operative RT (and CRT)
• Adjuvant chemotherapy
• Ongoing/future clinical trials
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Preoperative radiotherapy
9.6%
3.6%
Dutch study: Peeters et al., Ann Surg 2007
Local Recurrence Rates: median 6y FU
10.9%
5.6%
P<0.001
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Advantages of pre-operative RT
• Decreased risk for local recurrence
• Decreased risk for early and late toxicity
• Improved therapeutic effect due to increased tumor oxygenation
• Downstaging – Increased rates for sphincter preserving surgeryESO-E
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Pre- versus post- operative radiochemotherapy
TMETME
TMETME
RR
Sauer et al. N Eng J Med 2004
823 patients
Primary endpoint: overall survival
(4 cycles)
(4 cycles)
Local recurrence rate
5-FU
5-FU
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EORTC trial
Bosset et al. N Eng J Med 2006
SS
SS
RR
(4 cycles)
(4 cycles)
1011 patients
SS
SS
TME in 37%
5-FU
5-FU
5-FU
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SCPRT versus CRT : Equivalence in overall survival
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Benefits and harms of preoperative RT addressed by radiation oncologists in decision consultations
Kunneman M et al Br J Cancer 2015;112:39-43ESO-E
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Rectal cancer therapy<br />(in Sweden) 2016
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local failure
vs.
distant mets.
vs.
5y OS
vs.
FFCD JCO 2006
RT vs. RChT 16% 8% 36% 38% 66% 67%
EORTC NEJM 2006
RT vs. RChT 17% 9% 32% 35% 65% 65%
AIO/CAO/ARO NEJM 2004
Pre vs. post 13% 6% 36% 38% 74% 76%*
Marijnen ASCO GI 2005
5x5 11% 6% n.a. 63% 64%
Preoperative RT trials: Patterns of failurePreoperative RT trials: Patterns of failure
Despite significant reduction of local relapse, no influence on distant mets. and survival observed
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Outline
• Background / historical perspective
• Staging / TME
• Pre-operative RT (and CRT)
• Adjuvant chemotherapy
• Ongoing/future clinical trials
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Chemotherapy for (non-metastatic) rectal cancer
Post-op – after surgery
In the context of CRT/pre-op
Adjuvant chemotherapy / following resection
– To eradicate micro-metastatic disease and prevent distant recurrences
– When is it indicated
(what is the benchmark: pre-op staging, post-op histopathology report or both)ESO-E
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clinicaloptions.com/oncologyCCO Independent Coverage of the 2015 Gastrointestinal Cancers Symposium
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clinicaloptions.com/oncologyCCO Independent Coverage of the 2015 Gastrointestinal Cancers Symposium
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‘Summarising, it is reasonable to consider adjuvant ChT in rectal cancer patients after preoperative CRT/RT with yp stage III (and ‘high-risk’ yp stage II). The level of scientific evidence for sufficient benefit is much lower than in colon cancer and is probably limited to DFS rather than toOS [II, C]. Hence, the decision on postoperative ChT (fluoropyrimidine alone or combined with oxaliplatin) should be risk-balanced, taking into account both the predicted toxicity for a particular patient and the risk of relapse, and should be made jointly by the individual and the clinician.’
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Adjuvant chemotherapy
Cochrane report 2012, CD004078
– 9221 patients from 21 trials
– Trials run through multiple decades, great heterogeneity (stage, treatment, setting)
– HR for OS 0.88 (0.76-0.91), for DFS 0.75 (0.68-0.83), small but statistically significant gain
“Modern” trials
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Adjuvant chemotherapy
Cochrane report 2012, CD004078
– 9221 patients from 21 trials
– Trials run through multiple decades, great heterogeneity (stage, treatment, setting)
– HR for OS 0.88 (0.76-0.91), for DFS 0.75 (0.68-0.83), small but statistically significant gain
“Modern” trials
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Adjuvant chemotherapy
Cochrane report 2012, CD004078
– 9221 patients from 21 trials
– Trials run through multiple decades, great heterogeneity (stage, treatment, setting)
– HR for OS 0.88 (0.76-0.91), for DFS 0.75 (0.68-0.83), small but statistically significant gain
“Modern” trials
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“modern” adjuvant rectal trials
EORTC 22921 – (Bosset Lancet Oncol 2014)
Italian – (Cionini Radiother Oncol 2014)
Chronicle – (Glynne-Jones Ann Oncol 2014)
Dutch - (Breugom Ann Oncol 2015)
Meta-analysis
Breugom (Lancet Oncol 2015)
None of the above are positive
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EORTC 22921
With a 10.4 year median follow-up (Bosset et al Lancet Oncol 2014) no
difference in:
Study designed and powered to show an absolute 10% OS benefit
OS
PFS
Cumulative incidence of distant spread
But
Chemotherapy arms showed lower LR
Benefit of adj. chemo seen in first analysis for ypT0-2 disappeared
Chemotherapy given as a bolus regimen in the Mayo Clinic schedule but with a dose reduction
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Chronicle
Patients who received CRT were then randomly assigned:
CapeOx vs observation
Poor accrual; 113 patients randomised
Observation group had higher number of node+ve patients, but no suggestion of benefit for the chemotherapy arm
Results are difficult to interpret due to small numbers
R Glynne-Jones et al Ann Oncol 2014ESO-ESMO E
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What about adding oxaliplatin?
CRT +/- oxaliplatin
– ACCORD 12/0405 PRODIGE 2
– STAR – 01
– German CAO/ARO/AI0-04
– PETACC 6
ADORE
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Slide 5
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Slide 18
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Slide 22
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ADORE (Adjuvant Oxaliplatin in Rectal Cancer)
5FU/LV vs FOLFOX for 4 months
Primary end-point: DFS
ITT: 3 yr DFS 71.6% v 62.9 p=.047, 3yr OS 95% v 85.7% p=0.036
When benefit evaluated by post-CRT pathologic stage only yp stage III patients had DFS benefit
No observational arm
Randomised phase II study with 80% power
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So what have these trials shown us?
● All Oxaliplatain trials used low dose oxaliplatin as a radiosensitizer with CRT
● 2 trials mandated oxaliplatin also as postoperative adjuvant (so if benefit which component?)
● Some of these trials did not mandate TME
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Why these negative results ?
Impact of adjuvant chemotherapy may be over-estimated in the “modern” era due to stage migration, better surgery and other mitigating factors
Difference between “clinical” stage II-III may be too broad; therefore looking for a 10% difference may be an error. Some patients at least will have stage II disease.
Timing of adjuvant chemotherapy:
CRT 6 weeks
Surgery wait 6-8 weeks
Recovery from surgery 4-6 weeks
Total: 16-20 weeks
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Adjuvant chemotherapy in rectal cancer
After SCRT (and immediate surgery) – should treat as colon cancer according to histology (hardly evidence –based !)
After CRT
- if pCR, perhaps no benefit
- if PR, then chemo indicated, but uncertain benefit?
- if no response, then clearly indicated, but benefit unlikely.
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Adjuvant chemotherapy in rectal cancer
After SCRT (and immediate surgery) – should treat as colon cancer according to histology
After CRT
- if pCR, perhaps no benefit
- if PR, then chemo indicated, but uncertain benefit?
- if no response, then clearly indicated, but benefit unlikely.
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Conclusions
• Adjuvant chemotherapy should not be standard of care for all fullly resected localised rectal cancer patients
• Should be considered for patients at risk, who did not receive neo-adjuvant therapy for whatever reason
• Should be considered for yp stage III disease after neo-adjuvant therapy
• Joint decision between patient and clinician balancing risks and benefits
• (and I have not even started to consider the elderly ! )
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Outline
• Background / historical perspective
• Staging / TME
• Pre-operative RT (and CRT)
• Adjuvant chemotherapy
• Ongoing/future clinical trials
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Organ Preservation in Rectal Cancer After Neoadjuvant Therapy With CR: ResultsKaplan-Meier estimates at 4 yrs
Rectal preservation: 72%
Local tumor regrowth: 26%
– Pelvic recurrence after salvage: 1.5%
Smith JJ, et al. ASCO GI 2015. Abstract 509.
Rectum Preservation1.0
0.8
0.6
0.4
0.2
0.0
Pro
po
rtio
n W
ith
ou
t L
oca
l R
egro
wth
0 1 2 3 4 5 6 7
72% sustainedcCR at 4 yrs
Yrs From End of Neoadjuvant Treatment
pCRNOM
7273
6653
5635
4823
3012
128
26ESO-E
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Organ Preservation in Rectal Cancer After Neoadjuvant Therapy With CR: Survival
Smith JJ, et al. ASCO GI 2015. Abstract 509.
Disease-Specific Survival OS
1.0
0.8
0.6
0.4
0.2
0
Dis
ease
-Sp
ecif
ic S
urv
ival
0 1 2 3 4 5 6 7Yrs From End of Neoadjuvant Treatment
pCRNOM
7273
6661
5647
4831
3017
1211
27
pCRNOM
P = .2374
1.0
0.8
0.6
0.4
0.2
0O
S0 1 2 3 4 5 6 7
Yrs From End of Neoadjuvant Treatment
pCRNOM
7273
6661
5647
4831
3017
1211
27
pCRNOM
P = .4713
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Current Wisdom
• Pre-operative CRT better than post-op
• Improves Local recurrence but not OS
• If CRM threatened on MRI needs response so CRT – if still CRM +ve, consider further systemic chemo pre-op
• Low rectal cancers (below the levators) always have threat to CRM
• T1/T2N0 mid/upper rectum don’t usually need RT or CRT unless if you want to avoid radical surgery
• CRT helps preserve sphincters
• Adjuvant chemo: uncertainty possibly due to “inaccurate” initial staging. Ongoing trials to establish value of “total” tx up front
• Greatest advances: surgery/TME, staging/MRI
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Thank youESO-E
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