The purpose of this study is to determine the effect of short-duration pre-operative FOLFOX based therapy on postoperative problems after liver surgery for patients with metastatic colorectal cancer.
Although early stage, localized colon and rectal cancers are associated with 5 year survival rates of nearly 90%, only a minority of patients present with localized disease. Unfortunately, at the time of their initial presentation, approximately 35% of patients with colon or rectal cancer have metastatic disease. Nearly two thirds of these patients with stage IV disease have evidence of extrahepatic spread and have a median overall survival rate of 8-10 months in the absence of further treatment. Even with the most intensive chemotherapeutic regimens, the median overall survival for these patients ranges from 12 months to 20 months. However, a small subset of patients with stage IV disease has isolated hepatic metastatic disease and can undergo resection. The patients with completely resected liver metastases enjoy a significantly higher overall five-year survival, which is as high as 58% in carefully selected patients. Ten-year overall survival has been reported in 22% of patients. Despite this improvement, the five-year disease-free survival for these patients is at best 35%, with hepatic recurrences occurring in 46%. The fact that adjuvant chemotherapy improves the three-year survival rate for stage II disease and five-year survival rates for stage III disease implies that it can treat micrometastatic disease in some fraction of patients. Because micrometastatic disease is likely the cause of the high recurrence rate in patients who undergo liver resection, there is a clear biologic rationale for using postoperative adjuvant chemotherapy after liver resection. Although this strategy is a common practice in many centers, no convincing data that this improves survival have been reported. A large randomized phase III trial (EORTC 40983) examining this question is currently ongoing and effect on survival has not yet been reported. Given that systemic chemotherapy after liver resection remains of unproven benefit at the present time, many have wondered if preoperative treatment might have more promise in improving recurrence rates.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
9
Washington University School of Medicine
St Louis, Missouri, United States
Postoperative Complication Rate
Fraction of patients with any grade of complication I-V
Time frame: 30 days following surgery
Major Postoperative Complication Rate
Fraction of patients with any complication grades IV and V
Time frame: 30 days following surgery
All-cause Mortality
Time frame: 30 days following surgery
Postoperative Recurrence Patterns
Liver only vs distant disease
Time frame: Up to 5 years
Histologic Hepatic Toxicity at Surgery
Time frame: Time of surgery (approximately 11-16 weeks)
Nonalcoholic Steatohepatitis Score (0-3)
* NASH Scoring * Steatosis \*\*\<5% = 0 \*\*5-33%=1 \*\*\>33-66%=2 \*\*\>66%=3 * Lobular inflammation \*\*No foci=0 \*\*\<2 foci per x 200 field=1 \*\*2-4 foci per x 200 field=2 \*\*\>4 foci per x 200 field=3 * Hepatocellular ballooning \*\*None=0 \*\*Few balloon cells = 1 \*\*Many cells/prominent ballooning=2
Time frame: Time of surgery (approximately 11-16 weeks)
Liver Injury Scale Score (0-27)
Time frame: Time of surgery (approximately 11-16 weeks)
Effect of Preoperative Chemotherapy on Tumor Size
Number of participants whose tumor size decreased from baseline to completion of preoperative chemotherapy.
Time frame: Upon completion of neoadjuvant chemotherapy (approximately 2 months)
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Change in Tumor Size From Pretreatment to Preoperative CT Scan
-Compare total longest diameter from baseline to preoperative CT scan.
Time frame: Completion of neoadjuvant therapy (approximately 8 weeks)