Overview of Advances in Treatment of Gastrointestinal ......9) If a patient is not candidate for...
Transcript of Overview of Advances in Treatment of Gastrointestinal ......9) If a patient is not candidate for...
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Overview of Advances in Treatment of Gastrointestinal Malignancies
Dre Eve St-Hilaire, Hematologist-oncologist October 24th 2014
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Support de recherche / Research support
Aucun / None
Employé /
Employee
Aucun / None
Consultant Aucun / None
Porteur d’action /
Major stock holder
Aucun / None
Honoraires /
Honoraria
Roche, Novartis, Bristol-Myers Squibb, Celgene, Pfizer
Comité consultatif scientifique /
Scientific advisory board
Novartis, Pfizer, Lundbeck, Celgene, Janssen, Sanofi, Alexion, Roche
Utilisation de médicaments hors indication / Off label use of medications
Aucun / None
Possible Conflicts of Interest
(
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Plan
Rectal cancer, adjuvant
Colorectal cancer follow up after adjuvant treatments
Metastatic colorectal cancer
Extended RAS mutation analysis
First line treatments
Chemotherapy breaks
Metastatic pancreatic cancer
First line treatments
Second line treatments
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Rectal cancer adjuvant
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Staging with EUS or MRI
Stage 1 (T1-T2, N0) Stage 2 (T3-T4, N0) Stage 3 ( any T, N+)
Resection
Pathological stage
Stage 1 Stage 2-3
No adjuvant tx Adjuvant tx
Chemotx x 2 months Chemoradiation Chemotx x 2 months
Neoadjuvant chemoradiation (infusional 5FU or Capecitabine
Resection
4 months adjuvant chemotx
FOLFOX-4 or 5FU ⁄ cape ??
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AIO-94
OS DFS
NEJM 351;17 october 21, 2004
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AIO-94
Local recurrence Distance recurrence
NEJM 351;17 october 21, 2004
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What do we know from previous trials ?
Infusional 5FU and Capecitabine are equal During radiation treatment
As adjuvant chemotherapy
There is some evidence that, compare to bolus 5FU, the infusion during radiation increases the chances of pCR. It as also been demonstrated to be superior in adjuvant chemoradiation
The addition of oxaliplatin during radiation does not lead to better rate of pCR Should not be considered as a standard
Even if there is still uncertainty about the use of adjuvant chemotherapy after neoadjuvant treatment, it is considered a standard in North America (even for patients with pCR)
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Problematic for adjuvant chemotherapy ?
Use of FOLFOX-4 in rectal cancer was based on extrapolation of data from colon cancer (MOSAIC trial)
3 randomised trials presented at ASCO 2014 about oxaliplatin use in rectal cancer
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ADORE trial
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PETACC-6 trial
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Trials AIO-04 (phase 3 N=1265)
ADORE (phase 2 N= 321)
PETACC 6 (phase 3 N= 1094)
Staging* Clinical Pathological Clinical
Investigational arm treatment
mFOLFOX-6 FOLFOX-4 CAPEOX
Control arm treatment
Bolus 5FU Bolus 5FU Capecitabine
3y DFS 75,9 vs 71,2% (HR 0,79; p=0,030)
71,6 vs 62,9% (HR 0,63; p=0,032)
74,5 vs 73,9 % (NS)
M follow up 50 months 38,2 onths 31 months
Stage 3 74% 63,8% 71%
Benefit for stage 2 (vs 3)
HR 0,56 (vs 0,91) HR 0,74 NS (vs 0,60 significant)
1,04 (vs 0,99) NS
Received all adjuvant cycles
79% 96,6% 57%
*Clinical = before neoadjuvant Pathological= after neoadjuvant
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Conclusion (1)
FOLFOX as an adjuvant treatment (4 months) for rectal cancer improves 3 years DFS
CAPEOX showed no difference compare to Capecitabine
Imbalance between arms
More toxicities, fewer patients completed treatments
Before ASCO 2014
FOLFOX-4 for stage 3 only
Should we now give FOLFOX to stage 2 ?
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Conclusion (2)
Majority of patients in the 3 trials were stage 3
Subgroup analysis for stage 2 (not significant in some trials)
ADORE trial is a phase 2, are these results definitive ?
What about older patients ??
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Conclusion (2)
My approach
FOLFOX-4 if
clinical or pathological stage 3
young patients with stage 2 ?
Minimal downstaging after neoadjuvant treatments
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Follow up of colorectal cancer after adjuvant therapy :ASCO Guidelines Update
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1) Surveillance should be guided by presume risk of recurrence and functional status of patient where early detection of disease would lead to aggressive treatments including surgery
2) Medical history, physical exam and CEA q 3-6 months x 5 years
Frequency of visits should be driven by the fact that 80% of the recurrence are in the first 2,5 years
3)Abdominal and chest imaging for 3 years
For higher risk patients, q 6-12 months
JCO 2013;31(35):4465
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4) For patients with rectal cancer, a pelvic CT is also recommended (annually for 3-5 years, depending on risk)
If no radiation, rectosigmoidoscopy q 6 months x 2-5 years
5) A surveillance colonoscopy should be performed approximately 1 year after initial surgery and then
q 5 years if normal
If colonoscopy incomplete before surgery, should be done as soon as adjuvant treatment completed (not wait the 1 year time point)
6) A new, persistent or worsening symptoms warrant the consideration of a recurrence
JCO 2013;31(35):4465
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7) Despite the lack of high-quality evidence, it is reasonable to counsel patients on maintening a healthy body weight, being physically active and eating a healthy diet
8) A treatment plan from the specialist should be sent to the patient’s other providers
9) If a patient is not candidate for systemic therapy because of comorbidities, no surveillance should be done
JCO 2013;31(35):4465
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Metastatic colorectal cancer: KRAS analysis
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KRAS in colorectal cancer
www.pathologyoutlines.com
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RAS mutations as exclusion for anti EGFR therapy in metastatic CRC<br /><br />
Presented By Sabine Tejpar at 2014 ASCO Annual Meeting
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Metastatic colorectal cancer: first line treatment
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<br />CALGB/SWOG 80405: Phase III trial of FOLFIRI or FOLFOX with Bevacizumab or Cetuximab for patients w/ KRAS wild type untreated metastatic adenocarcinoma of the colon
or rectum <br />
Presented By Alan Venook at 2014 ASCO Annual Meeting
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CALGB/SWOG 80405: <br /> FINAL DESIGN
Presented By Alan Venook at 2014 ASCO Annual Meeting
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Slide 11
Presented By Alan Venook at 2014 ASCO Annual Meeting
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CALGB/SWOG 80405: Overall Survival <br />
Presented By Alan Venook at 2014 ASCO Annual Meeting
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CALGB/SWOG 80405: Progression-Free Survival<br />(Investigator Determined)
Presented By Alan Venook at 2014 ASCO Annual Meeting
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Slide 23
Presented By Alan Venook at 2014 ASCO Annual Meeting
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CALGB/SWOG 80405: Conclusions
Presented By Alan Venook at 2014 ASCO Annual Meeting
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Conclusion (1)
The results will have to be presented with the extended RAS analysis to confirm which combination is superior
EGFR inhibitors in Canada
Mainly used as a 3rd line option
Final recommendation of pCODR January 2014: Cetuximab not recommended for first line
Decision might change with the recent results
First line use not currently funded by provinces, under consideration by some
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Metastatic colorectal cancer: Continuation of chemo vs chemo breaks ??
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Background
In United States ( and some Canadian provinces), the first line treatment choice for mCRC is FOLFOX and Bevacizumab
For responders, prolong treatments = peripheral neuropathy
Different strategies studied to decrease or control this problem
OPTIMOX 1 and 2 trials were done before the use of Bevacizumab (chemo alone)
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No difference in OS or PFS
Tx with FOLOFX 7 = 3 months
No difference in OS PFS 8,6 vs 6,6 months
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No difference in OS or PFS
Tx with FOLOFX 7 = 3 months
No difference in OS PFS 8,6 vs 6,6 months
Based on Optimox 2, many oncologists give oxaliplatin breaks,
but tend to continue FL and bevacizumab
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mCRC with response or stability after chemotherapy
Continuation Chemotherapy break
Toxicities Hospital visit Cost for patient Cost for the hospital Effect on survival ?
Better quality of life Effect on survival ?
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<br />Maintenance treatment with capecitabine + bevacizumab versus observation after induction treatment with chemotherapy + bevacizumab in <br />metastatic colorectal
cancer <br /><br />Final results and subgroup analyses of the<br />phase 3 CAIRO3 study <br />of the Dutch Colorectal Cancer Group (DCCG)
Presented By Miriam Koopman at 2014 ASCO Annual Meeting
No overall survival benefit
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Maintenance strategy with fluoropyrimidines (FP) plus bevacizumab (Bev), Bev alone, or no treatment, following a standard combination of FP, oxaliplatin (Ox), and Bev as first-line
treatment for patients with metastatic colorectal cancer (mCRC): <br />A non-inferiority phase III trial: AIO 0207
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
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AIO 0207: Treatment algorithms
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
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AIO 0207: Treatment algorithms
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
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AIO 0207: Treatment algorithms
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
Hypothesis:
No treatment OR bevacizumab alone would be
NON-INFERIOR compare to FL and bevacizumab
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TFS: All arms
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
Difference between Bev and no therapy is 12 days
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Non-inferiority, vs. FP/Bev
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
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End of maintenance: Main reasons
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
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OS from start of maintenance
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
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Summary
Presented By Dirk Arnold at 2014 ASCO Annual Meeting
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How to interpret these results ?
Compare to chemotherapy breaks, maintenance failed to show
OS benefit
Meaningful TFS for patients
Maintenance increase
Cost (for patients and institutions)
Potential of side effects
Data would have been more convincing if superiority design used
Decision as to be individualised
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Pancreatic cancer
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Background
Only 15-20% resectable at presentation
Close to 90% of diagnosed patients will die from their disease
NEJM 371:11 september 11 2014
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Background
For metastatic pancreatic cancer, gemcitabine was the most frequently use chemo for metastatic patients until…
1) FOLFIRINOX
2) Gemcitabine+ nab-paclitaxel
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FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer
Inclusion criteria
18-75 yo
ECOG 0-1
Measurable disease
Bilirubin less then 1,5 x N
Primary endpoint = OS
NEJM 2011;364:1817
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NEJM 2011; 364:1817
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NEJM 2011; 364:1817
Median OS: FOLFIRINOX 11,1 months Gemcitabine 6,8 months
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NEJM 2011; 364:1817
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NEJM 2011; 364:1817
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Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine
Inclusion criteria
18 yo or more
Karnofsky 70 or more
Measurable disease
Bilirubin at or below upper range of N
Primary endpoint = OS
NEJM 2013;369:1691
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NEJM 2013; 369:1691
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NEJM 2013;369:1691
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NEJM 2013;369:1691
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NEJM 2013;369:1691
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Conclusion (1)
FOLFIRINOX
central KT require (not with gem-nab paclitaxel)
46 hours of 5fu infusion
More nausea, more risk of febrile neutropenia BUT
Seems to be more active
QoL analysis
At 6 months, degradation in QoL in 31% with FOLFIRINOX (vs 66%)
Gemcitabine+ nab-paclitaxel
More patients able to tolerate it
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Conclusion (2)
My approach
3 categories for metastatic patients
Young and fit (good performance status)= FOLFIRINOX
Unfit = gemcitabine alone or palliative care
Somewhere in the middle = gemcitabine- nab paclitaxel
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Metastatic pancreatic cancer: second line therapy
PANCREOX (poster from Dr Charlene Gill, ASCO 2014)
CONKO-3 trial showed a OS benefit for OFF (oxaliplatin based regimen) after gemcitabine treatment
Trial to confirm if the same population would benefit from mFOLFOX-6
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PANCREOX trial
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PANCREOX trial
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PANCREOX trial
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Questions ?