Perioperative Treatment of Resectable Liver Metastases (PERIMAX)
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|ClinicalTrials.gov Identifier: NCT01540435|
Recruitment Status : Withdrawn (insufficient recruitment)
First Posted : February 28, 2012
Last Update Posted : May 29, 2013
|Condition or disease||Intervention/treatment||Phase|
|Colon Cancer Liver Metastasis||Drug: Bevacizumab||Phase 2|
Recurrence rates after R0-resection of colorectal liver metastases are still very high (about 60-70 %). Therefore, multidisciplinary treatment of these patients is frequently used in order to achieve a beneficial impact regarding progression-free and overall survival. The point in time of treatment, pre- and/or postoperative, is still a matter of debate. In the EORTC 40983 trial, perioperative chemotherapy with 5-Fluorouracil and oxaliplatin (FOLFOX-Regimen) displayed a non-significant benefit in 3 year disease free survival in the intent to treat population (HR 0.79, 95% CI 0.62 to 1.02) (Nordlinger, Sorbye et al. 2008). The combined analysis of two adjuvant trials, with a (non-contemporary) 5-FU Bolus regimen, showed a non-significant prolongation of median disease free survival (DFS) from 18.8 to 27.9 months (p=0.058) and OS from 47.3 to 62.2 months (p=0.095) (Mitry, Fields et al. 2008). However, postoperative treatment with 6 months of FOLFOX is often used in daily practise. Thus, further investigation is urgently warranted.
This phase II trial evaluates two strategies with intensified perioperative or postoperative treatment regimens. Current studies established the role of the FOLFOXIRI regimen in the metastatic setting (Falcone, Ricci et al. 2007). A further intensification of a three drug regimen with bevacizumab seem to be feasible yielding response rates up to 84% and a disease control rate up to 100% (Falcone 2008; Bruera, Santomaggio et al. 2010; Masi, Loupakis et al. 2010). Regarding the efficacy, evaluation of FOLFOXIRI and bevacizumab in preoperative treatment for resectable CLM seems to be promising. Postoperative treatment with FOLFOX for 6 months was chosen for arm A.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Perioperative FOLFOXIRI and Bevacizumab Compared With Postoperative FOLFOX in Patients With Resectable Liver Metastases From Colorectal Cancer (PERIMAX). A Randomized, Multidisciplinary DGAV(CAO-V/CALGP)/AIO Phase II Trial|
|Study Start Date :||September 2012|
|Actual Primary Completion Date :||May 2013|
|Actual Study Completion Date :||May 2013|
No Intervention: Postoperative Arm (Arm A)
Oxaliplatin at a dose of 85 mg/m2 iv over two hours (day 1) I-LV at a dose of 200 mg/m2 iv over two hours (day 1) 5-FU at a dose of 3200 mg/m2 iv over 48 hours (day 1-3)
Duration of treatment:
Treatment will be administered for 12 cycles (6 months) postoperatively starting 6 weeks after surgery.
Experimental: Perioperative Arm (Arm B)
Therapy will be administered in a biweekly schedule. First preoperative cycle will be administered with 75% of dosage for FOLFOXIRI, if no diarrhea ≥ grade 3 occurs, following cycles should be administered in full dosage.
FOLFOXIRI + bevacizumab:
bevacizumab at a dose of 5 mg/kg iv over 30 to 90 min (day 1) irinotecan at a dose of 165 mg/m2 iv over two hours (day 1) oxaliplatin at a dose of 85 mg/m2 iv over two hours (day 1) I-LV at a dose of 200 mg/m2 iv over two hours (day 1) 5-FU at a dose of 3200 mg/m2 iv over 48 hours (day 1-3)
Duration of treatment:
Treatment will be administered for 6 cycles (3 months) preoperatively (last cycle without bevacizumab), after 6 weeks followed by liver surgery, after further 6 weeks followed by 6 cycles (3 months) postoperatively.
Bevacizumab at a dose of 5 mg/kg iv over 30 to 90 min (day 1) + FOLFOXIRI in a biweekly schedule, 6 cycles preoperatively, 6 cycles postoperatively
Other Name: VEGF antibody
- Failure-free survival (FFS@18) [ Time Frame: 18 months ]Failure will be defined as no R0 resection, local or distant recurrence or death from any cause.
- Disease Free Survival (DFS) [ Time Frame: 5 years ]
- Overall survival (OS) [ Time Frame: 5 years ]
- Perioperative morbidity [ Time Frame: 30 days (hospital stay) ]
- Quality of life [ Time Frame: 12 months ]
- Achievability of R0 resection [ Time Frame: intraoperative ]
- Overall response rate (Arm B) [ Time Frame: 3 months ]
- Pathologic response rate [ Time Frame: 18 weeks ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01540435
|Study Chair:||Hans J. Schlitt, Prof. MD||Department of Surgery, University Medical Center Regensburg|
|Study Director:||Hans-Joachim Schmoll, Prof. MD||Department of Internal Medicine IV, University Hospital Halle|