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| Name | Class |
|---|---|
| Hoffmann-La Roche | INDUSTRY |
| Sanofi | INDUSTRY |
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The percentage of patients with defined unresectable metastatic disease who will benefit from a first-line treatment enabling secondary complete metastasectomy is unknown but limited. Definition of optimized treatment algorithms is difficult due to very inhomogeneous patient populations.
This open label, multicentre Phase II study primarily aims to assess the resection rate achievable in a selected patient population with initially unresectable metastatic disease limited to the liver only in order to evaluate feasibility, safety and efficacy with regards to secondary resection of hepatic lesions in these patients.
The trial aims to enrol only patients meeting defined criteria of unresectability with regards to their hepatic lesions and will exclude patients with extrahepatic lesions in order to examine the most appropriate, highly active treatment regimen for this group of unresectable patients with the highest probability of a successful secondary metastasectomy with curative intent. The trial will be conducted in highly specialized centres with a track record of successful interdisciplinary treatment approaches in the field of metastatic colorectal cancer to allow the precise assessment of the peri-operative safety parameters as well as an evaluation of the surgical treatment approaches.
The IXO regimen selected for this study has shown in a phase I/II study promising efficacy and a favourable safety profile. Bevacizumab has demonstrated a significant survival benefit in combination with chemotherapy in metastatic colorectal cancer. Therefore the study will allow evaluation of its potential benefit in combination with the two most active current chemotherapy regimens in the first-line and post-operative treatment setting.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| IXO+A | Experimental | IXO regimen with Avastin |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| irinotecan, capecitabine, oxaliplatin (IXO) and bevacizumab | Drug | IXO plus bevacizumab regimen is given every 3 weeks (Q3W), in the following order: Bevacizumab (A): 7.5 mg/kg via IV infusion, day 1 Oxaliplatin (O): 100 mg/m2 via 2-hour IV infusion, day 1 Irinotecan (I): 160 mg/m2 via 1-hour IV infusion, day 1 Capecitabine (X): 950 mg/m2 twice daily PO, days 2 - 15 |
| Measure | Description | Time Frame |
|---|---|---|
| conversion to resectability during downsizing therapy with IXO+A patients with initially unresectable liver-only metastases associated with colorectal cancer | after 8 IXO+A cycles |
| Measure | Description | Time Frame |
|---|---|---|
| Recurrence-free survival (RFS) | Every 2 cycles | |
| Progression-free survival (PFS) | Every 2 cycles | |
| Time to response (TTR) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jean Maroun, MD | The Ottawa Hospital Cancer Centre | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Ottawa Hospital Cancer Center | Ottawa | Ontario | K1H 8L6 | Canada | ||
| Sunnybrook Health Sciences Centre |
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| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| ID | Term |
|---|---|
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
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| ID | Term |
|---|---|
| D000077146 | Irinotecan |
| D000069287 | Capecitabine |
| D000077150 | Oxaliplatin |
| D000068258 | Bevacizumab |
| ID | Term |
|---|---|
| D002166 | Camptothecin |
| D000470 | Alkaloids |
| D006571 | Heterocyclic Compounds |
| D003841 | Deoxycytidine |
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|
| Every 2 cycles |
| Overall survival (OS) | Every 2 cycles |
| Pathological complete response (pCR) rate | assessed post-operatory |
| Overall response rate (ORR) | Every 2 cycles |
| Number of participants with Adverse Events as a measure of Safety and Tolerability | Every 3 weeks |
| Surgical safety (frequency of surgical complications) | assessed post-operatory |
| Pathological changes in the non-tumoural liver following therapy with IXO+A | assessed post-operatory |
| R0, R1, R2 resection rate after up to 8 cycles of downsizing therapy with IXO+A | assessed post-operatory |
| Toronto |
| Ontario |
| M4N 3M5 |
| Canada |
| University Health Network | Toronto | Ontario | M5T 2S8 | Canada |
| McGill University Health Centre | Montreal | Quebec | H3A 1A1 | Canada |
| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D012002 | Rectal Diseases |
| D003562 |
| Cytidine |
| D011741 | Pyrimidine Nucleosides |
| D011743 | Pyrimidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D005472 | Fluorouracil |
| D014498 | Uracil |
| D011744 | Pyrimidinones |
| D003853 | Deoxyribonucleosides |
| D009705 | Nucleosides |
| D009706 | Nucleic Acids, Nucleotides, and Nucleosides |
| D056831 | Coordination Complexes |
| D009930 | Organic Chemicals |
| D061067 | Antibodies, Monoclonal, Humanized |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
| D007162 | Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |