IXO+A in mCRC With Liver-only Metastases

Ottawa Hospital Research Institute

Status and phase

Withdrawn

Phase 2

Conditions

Metastatic Colorectal Cancer

Treatments

Drug: irinotecan, capecitabine, oxaliplatin (IXO) and bevacizumab

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01293942

OTT 10-01

Details and patient eligibility

About

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.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Primary colorectal cancer with unresectable metastatic lesion(s)
At least one measurable lesion, confirmed by CT scan
Male and female patients, aged ≥ 18 years
ECOG performance score of 0 or 1 (within 1 week of study treatment start)
Written informed consent
Adequate general condition, cardiopulmonary functions and performance status
Liver metastases no initially foreseen R0 resection of all hepatic lesions, but deemed potentially resectable after response to downsizing therapy

Exclusion criteria

Extrahepatic metastatic disease
Prior systemic or local treatment for metastatic disease, prior therapy with a biologic agent, prior adjuvant or neo-adjuvant chemotherapy, prior radiotherapy to the liver, other concurrent chemotherapy
Inadequate bone marrow, liver, renal function, uncontrolled hypertension
Pregnancy or lactation