FOLFOX Plus SIR-SPHERES MICROSPHERES Versus FOLFOX Alone in Patients With Liver Mets From Primary Colorectal Cancer
Status: | Completed |
---|---|
Conditions: | Colorectal Cancer, Liver Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/28/2019 |
Start Date: | August 2006 |
End Date: | May 2015 |
Randomised Comparative Study Of Folfox6m Plus Sir-Spheres® Microspheres Versus Folfox6m Alone As First Line Treatment In Patients With Nonresectable Liver Metastases From Primary Colorectal Carcinoma
This study is a randomized multi-center trial that will assess the effect of adding Selective
Internal Radiation Therapy (SIRT), using SIR-Spheres microspheres®, to a standard
chemotherapy regimen of FOLFOX as first line therapy in patients with non-resectable liver
metastases from primary colorectal adenocarcinoma.
Treatment with the biologic agent bevacizumab, if part of the standard of care at
participating institutions, is allowed within this study at the discretion of the treating
Investigator.
Internal Radiation Therapy (SIRT), using SIR-Spheres microspheres®, to a standard
chemotherapy regimen of FOLFOX as first line therapy in patients with non-resectable liver
metastases from primary colorectal adenocarcinoma.
Treatment with the biologic agent bevacizumab, if part of the standard of care at
participating institutions, is allowed within this study at the discretion of the treating
Investigator.
Inclusion Criteria:
- Unequivocal and measurable CT evidence of liver metastases which are not treatable by
surgical resection or local ablation.
- Limited extra-hepatic metastases in the lung and/or lymph nodes are permitted (Lung: 5
lesions total, < 1 cm, or 1 single lesion of up to 1.7 cm; Lymph nodules in one single
anatomic area (pelvis, abdomen or chest): any number, < 2 cm).
- Suitable for either treatment regimen.
- Prior chemotherapy for metastatic colorectal cancer is not allowed.
- WHO performance status 0-1.
- Adequate hematological, renal and hepatic function.
- Age 18 years or older.
- Willing and able to provide written informed consent.
- Life expectancy of at least 3 months without any active treatment.
Exclusion Criteria
- Evidence of ascites, cirrhosis, portal hypertension, main portal or venous tumor
involvement or thrombosis as determined by clinical or radiologic assessment.
- Previous radiotherapy delivered to the upper abdomen.
- Non-malignant disease that would render the patient unsuitable for treatment according
to the protocol.
- Peripheral neuropathy > grade 1 (NCI-CTC).
- Dose limiting toxicity with previous adjuvant 5-FU or oxaliplatin chemotherapy.
- Prior non-adjuvant chemotherapy for any malignancy. Adjuvant chemotherapy for
colorectal cancer is not an exclusion criteria provided that it was completed more
than 6 months before entry into the study.
- Pregnant or breast-feeding.
- Other active malignancy.
We found this trial at
22
sites
100 NW 170th St # 410
North Miami Beach, Florida 33169
North Miami Beach, Florida 33169
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University of Pittsburgh Medical Center UPMC is one of the leading nonprofit health systems in...
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