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Panitumumab maintenance phase (3 months) 9mg/kg BW every 3 weeks

Volker Heinemann, Prof. Dr. med.

Clemens Gießen, Dr. med.

Clemens Giessen, Dr. med.

Up to 50% of patients with colorectal cancer (CRC) develop liver metastasis during the course of their disease. In 30-40% of patients metastasis is confined to the liver. In these patients R0-resection of metastases may contribute to marked improvement of overall survival. Primary resection of liver metastasis is possible in about 15-20% of patients (Scheele 2005, Petrelli 2005). Recent studies indicate that perioperative chemotherapy may improve survival after resection of liver metastases (Portier 2007, Nordlinger 2007). Nevertheless, there is evidence that 70-80% of patients have recurrent disease after resection of liver metastasis. Stratification for the risk of recurrence may be performed using the FONG-score (Fong 1999).

This study is designed to investigate the efficacy of postoperative chemotherapy combined with an anti-EGFR treatment using panitumumab.

The majority of patients present to the surgeon after chemotherapeutic pretreatment with various not necessarily standardized regimens. Also postoperative therapy after resection of liver metastasis is not a clearly defined standard of care in Germany.

Based on the study by Nordlinger et al. an oxaliplatin-based regimen is chosen for postoperative therapy (Nordlinger 2008). For reasons of practicability mFOLFOX6 was selected as the chemotherapy backbone for additive treatment (Allegra 2010).

Also, there is evidence that the combination of FOLFOX with panitumumab is associated with enhanced antitumor activity (Douillard et al. ESMO 2009). The experimental treatment arm will therefore evaluate the combination of FOLFOX plus panitumumab. Since in colorectal cancer monoclonal antibodies directed against the EGFR are not active in KRAS mutant patients, the experimental arm including panitumumab will only be performed in KRAS wild-type patients (Amado 2008).

The planned study aims to assess the efficacy of postoperative therapy with FOLFOX plus panitumumab followed by maintenance with panitumumab for 3 months in KRAS wild-type patients, compared to the historical data for standard FOLFOX chemotherapy alone, which are verified by a randomised control group without the antibody. (Figure 1: Study Design).

The study will allow preoperative treatment with regimens such as FOLFIRI, XELIRI, FOLFOX or XELOX +/-bevacizumab or +/- cetuximab. However, only those patients will be considered eligible who did not progress during preoperative therapy.

After surgery, a treatment-free interval of at least 4 weeks, but no longer than 8 weeks will be granted.

KRAS-wild-type patients (60% of all pts) will then be randomized in a 2:1 ratio to an experimental arm with FOLFOX + panitumumab or to a reference arm with FOLFOX alone. Combination treatment will be performed for a duration of 3 months, after which patients in the experimental arm will receive maintenance therapy with panitumumab for further 3 months. In the reference arm, treatment will, however, be ended after 3 months.

Panitumumab After Resection of Liver Metastases From Colorectal Cancer in KRAS Wild-type Patients

Amgen

PD Dr. med. Volker Heinemann

Sponsor Delegatated Person

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization	Link
Panitumumab After Resection of Liver Metastases From Colorectal Cancer in KRAS Wild-type Patients	NCT01384994	Colorectal Canc... KRAS Wildtype After Resection...	Folic Acid 5-FU 5-FU Oxaliplatin Panitumumab Panitumumab Folic Acid 5-FU 5-FU Oxaliplatin	18 Years -	Ludwig-Maximilians - University of Munich
Panitumumab After Resection of Liver Metastases From Colorectal Cancer in KRAS Wild-type Patients	NCT01384994	Colorectal Canc... KRAS Wildtype After Resection...	Folic Acid 5-FU 5-FU Oxaliplatin Panitumumab Panitumumab Folic Acid 5-FU 5-FU Oxaliplatin	18 Years -	Ludwig-Maximilians - University of Munich

Spots Global Cancer Trial Database for after resection of liver metastases