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A randomized two arm phase III study in patients post radical resection of liver metastases of colorectal cancer to investigate bevacizumab in combination with capecitabine plus oxaliplatin (CAPOX) vs CAPOX alone as adjuvant treatment
BMC Cancervolume 10, Article number: 545 (2010)
About 50% of patients with colorectal cancer are destined to develop hepatic metastases. Radical resection is the most effective treatment for patients with colorectal liver metastases offering five year survival rates between 36-60%. Unfortunately only 20% of patients are resectable at time of presentation. Radiofrequency ablation is an alternative treatment option for irresectable colorectal liver metastases with reported 5 year survival rates of 18-30%. Most patients will develop local or distant recurrences after surgery, possibly due to the outgrowth of micrometastases present at the time of liver surgery. This study aims to achieve an improved disease free survival for patients after resection or resection combined with RFA of colorectal liver metastases by adding the angiogenesis inhibitor bevacizumab to an adjuvant regimen of CAPOX.
The Hepatica study is a two-arm, multicenter, randomized, comparative efficacy and safety study. Patients are assessed no more than 8 weeks before surgery with CEA measurement and CT scanning of the chest and abdomen. Patients will be randomized after resection or resection combined with RFA to receive CAPOX and Bevacizumab or CAPOX alone. Adjuvant treatment will be initiated between 4 and 8 weeks after metastasectomy or resection in combination with RFA. In both arms patients will be assessed for recurrence/new occurrence of colorectal cancer by chest CT, abdominal CT and CEA measurement. Patients will be assessed after surgery but before randomization, thereafter every three months after surgery in the first two years and every 6 months until 5 years after surgery. In case of a confirmed recurrence/appearance of new colorectal cancer, patients can be treated with surgery or any subsequent line of chemotherapy and will be followed for survival until the end of study follow up period as well. The primary endpoint is disease free survival. Secondary endpoints are overall survival, safety and quality of life.
The HEPATICA study is designed to demonstrate a disease free survival benefit by adding bevacizumab to an adjuvant regime of CAPOX in patients with colorectal liver metastases undergoing a radical resection or resection in combination with RFA.
ClinicalTrials.gov Identifier NCT00394992
Colorectal cancer (CRC) is the second leading cause of cancer-related-deaths in the western world. The incidence of CRC is still increasing [1–3]. About 50% of patients with progressed colorectal cancer develop liver metastasis . The pathway from colon to liver metastases is via the portal vein and liver metastases are usually the first metastases to appear, often without signs of systemic dissemination meaning possibility of cure for these patients . The median survival of patients with colorectal liver metastases is 6-12 months if untreated [6, 7]. Complete surgical resection is the only treatment modality that offers hope for cure, resulting in 5 year survival for 36-60% [8–11]. Improved imaging, and surgical techniques as well as neoadjuvant therapy have increased the number of patients receiving R0 resection for colorectal liver metastasis. R0 resection is defined as a resection with tumor free margins as confirmed by the pathologist. Liver resection is a relatively safe procedure with mortality rates less that 5% [12, 13]. Unfortunately only approximately 25% of patients are resectable at time of presentation. Radiofrequency ablation (RFA) is an alternative treatment option with promising five year survival rates for patients with small (< 4 cm) colorectal liver metastases. There are few studies reporting long term survival after RFA ranging from 18-30% [14–19]. The success rate of RFA greatly depends on size and open approach of the tumors treated as shown in a large meta-analysis examining 5224 treated tumors . In all abovementioned studies, treated tumors had a mean diameter of less than 5 cm and patients did not have more than 3 tumors per patient on average. Surgical resection or RFA of CRLM alone is obviously not sufficient as 40%-70% of patients will develop local or distant recurrences after surgery of colorectal liver metastasis.
Different clinical studies comparing surgery and systemic adjuvant therapy with surgery and observation demonstrate a benefit in disease free survival (DFS) for the treatment arm [21–24]. Adding chemotherapy after resection might prevent the outgrowth of micrometastases present in the liver at the time of resection . Portier and colleagues published the results of the first randomized controlled phase III study comparing surgery with observation with surgery and adjuvant chemotherapy with 5 FU/LV, demonstrating a disease free survival benefit for the systemic chemotherapy arm . Chemotherapy regimens for advanced colorectal cancer have improved. FOLFOX and CAPOX have proven to be most effective regimens in the treatment of advanced colorectal cancer. In the CAPOX regimen infusional 5 FU is replaced with the oral derivate capecitabine 
After resection or RFA, regeneration of the liver takes place until the liver has reached its original volume. This takes about 6 months till a year [27–29]. Directly after liver resection, growth factors such as vascular endothelial growth factor (VEGF), hepatocellular growth factor (HGF), transforming growth factor (TGF), epidermal growth factor (EGF), macrophage inflammatory protein (MIP) en interleukine-6 (IL-6) are upregulated. Most of these growth factors that play a role in liver regeneration also are pro-angiogenic and involved with migration of tumor cells and tumor growth. Because of this production of many pro-angiogenic factors, the liver is a perfect environment for angiogenesis and tumor growth. Because small metastases (< 5 mm) are not detectable on CT scanning, there is a chance that micrometastases are present in the liver at the time of resection. Oxygen and other nutrients reach the tumor cells by diffusion, however to exceed beyond 2 mm, a tumor needs its own blood supply . Pre-clinical studies demonstrate an excessive increase in the growth of intra-hepatic and extra-hepatic tumors after hepatectomy compared with sham operated mice [25, 31, 32]. Adding an anti-angiogenic target, such as bevacizumab, seems a logical next step in the attempt to further improve disease free survival (DFS) for patients with resected colorectal liver metastases. Bevacizumab is a monoclonal antibody against VEGF and has proven to be effective in patients with metastatic colon cancer .
The effect of adjuvant therapy can not yet be measured or predicted. In order to investigate the underlying mechanisms of recurrence and to predict which patient is most likely to benefit from adjuvant therapy, blood and tissue will be collected during and after therapy.
To demonstrate a disease free survival benefit by adding bevacizumab to an adjuvant regimen of CAPOX chemotherapy in patients with colorectal liver metastases undergoing radical resection or radical resection in combination with RFA.
The disease free survival is defined as the interval between randomization and recurrence of disease or death, whatever occurs first.
Secondary objectives are to compare survival, toxicity and quality of life. Survival is defined as the interval between randomization and death of any cause. The grade of toxicity will be assessed using the NCI-CTC criteria version 3.0. Quality of life will be studied by means of the EORTC QLC C30.
The Hepatica study is a two-arm, international, multicenter, randomized, comparative efficacy and safety study comparing adjuvant CAPOX vs CAPOX and bevacizumab in patients with resected or resected in combination with ablated colorectal liver metastases. Randomization is stratified according to clinical prognostication and treatment site.
Treatment assignment will be stratified, based on
(i) number (< 4 or ≥ 4) of liver metastases;
(ii) metachronous or synchronous liver metastases;
(iii) prior adjuvant chemotherapy or no prior adjuvant chemotherapy;
(iv) blood transfusion or no blood transfusion post liver surgery;
(v) treatment site;
(vi) neoadjuvant treatment with 3 cycles of CAPOX;
(vii) use of RFA in combination with resection
Criteria for RFA:
largest liver tumor </= 4 cm
number of liver tumors </= 3.
Patients will be enrolled in 28 Dutch hospitals and 3 Swedish centers.
Inclusion Criteria: In order to be eligible for the trial, patients have to fulfil the following criteria:
1. Signed written informed consent obtained prior to any study-specific procedure;
2. Age ≥ 18 years;
3. Liver metastases radically resected (R0 resection) or liver metastases radically resected in combination with RFA
Criteria for RFA:
largest liver tumor </= 4 cm
number of liver tumors </= 3;
4. Study medication started ≥ 4 and ≤ 8 weeks post liver surgery;
5. Histologically confirmed liver metastasis of colorectal cancer after surgery;
6. ECOG performance status 0 or 1 (Appendix 1);
7. Adequate hematology: neutrophils ≥ 1.5 × 109/L, platelets ≥100 × 109/L, Hb ≥ 5.5 mmol/L, INR ≤ 1.5, APTT < 1.5 × UNL;
8. Adequate biochemistry: total bilirubin ≤1.5 UNL, ASAT and ALAT ≤ 2.5 × UNL, alkaline phosphatase ≤ 2.5 × UNL, serum creatinin ≤ 1.5 UNL.
9. Urine dipstick < 2+ for protein.
Exclusion Criteria: Patients presenting with any of the following criteria are not eligible for the study:
1 Extra-hepatic metastatic disease;
2 Adjuvant chemotherapy given < 6 months prior to detection of the liver metastases.
3 Chemotherapy for metastatic disease with the exception of max 3× CAPOX given as neoadjuvant therapy max 6 weeks before resection of the colorectal liver metastases;
4 Prior non colorectal malignancies, except adequately treated basalioma of the skin or carcinoma in situ of the cervix;
5 Bleeding diathesis or coagulation disorders or the need for full-dose anticoagulation;
6. Major surgical procedure < 4 weeks prior to start of study treatment;
7. Radiofrequency ablation without resection;
8. Females with a positive pregnancy test (within 14 days before treatment start);
9. Lactating women;
10. Fertile women (< 2 years after last menstruation) and women of childbearing potential not willing to use effective means of contraception;
11. History of psychiatric disability judged by the investigator to be clinically significant, precluding informed consent or interfering with compliance for oral drug intake;
12. Clinically significant (i.e. active) cardiovascular disease e.g. cerebrovascular accidents (≤ 6 months prior to randomization), myocardial infarction (≤ 1 year prior to randomization), uncontrolled hypertension while receiving chronic medication, unstable angina, New York Heart Association (NYHA) Grade II or greater congestive heart failure, or serious cardiac arrhythmia requiring medication;
13. Lack of physical integrity of the upper gastro-intestinal tract, malabsorption syndrome, or inability to take oral medication;
14. Known peripheral neuropathy, including oxaliplatin-induced neuropathy > grade 1. Absence of deep tendon reflexes as the sole neurological abnormality does not render the patient ineligible;
15. Organ allografts requiring immunosuppressive therapy;
16. Serious, non-healing wound, ulcer, or bone fracture;
17. Chronic treatment with corticosteroids (dose of ≥ 10 mg/day methylprednisolone equivalent excluding inhaled steroids);
18. Serious intercurrent infections (uncontrolled or requiring treatment);
19. Current or recent (within the 28 days prior to randomization) treatment with another investigational drug or participation in another investigational study;
20. Patients with known allergy to Chinese hamster Ovary cell proteins or other recombinant human or humanized antibodies or to any excipients of bevacizumab formulation, platinum compounds or to any other component of the study drugs.
After having properly checked all eligibility criteria, stratification parameters and having obtained patient's written informed consent, patients will be randomized by fax at the Trial Office IKO Nijmegen (fax 024-3619080). Randomized treatment will be confirmed by fax or email within one (1) working day. Randomization takes place wit TENALEA, this program uses a minimization procedure.
This study is to be conducted according to globally accepted standards of Good Clinical Practice, and in agreement with the latest revision of the Declaration of Helsinki (2000, including the notes of clarification 2002 and 2004) and local regulations.
This protocol has been submitted and approved by the Ethical Committee (EC) of the University Medical Centre Utrecht http://www.umcutrecht.nl/MeTC and the Central Committee on Research Involving Human Subjects http://www.ccmo.nl in accordance with Dutch legal requirements. The independent medical ethics committees of all participating hospitals have approved the study protocol
Administrative changes to the protocol are minor corrections and/or clarifications that have no impact on the study conduct. The EC may be notified of administrative changes at the discretion of the investigator. Oral and written informed consent in form is obtained from all patients prior to randomization.
All serious adverse events during the study period, whether or not considered by the Investigator to be related to study treatment, must be reported by fax to the central data management office (Trial Office IKO, 024-361 90 80) within 24 hours using the completed SAE report. The principal investigators are responsible for the management of the safety reporting requirements according to the local regulations and guidelines. Copies of all report submissions by the principal investigators to regulatory authorities and to the ethical committee that has approved the study will be provided to the pharmacovigilance department of the license holders of the study drugs. If necessary, additional information and clarifications on cases will be forwarded to the license holders by the principal investigator.
An independent monitoring committee will discuss all reported (serious) adverse events.
A data and safety monitoring board will monitor the recruitment, the reported serious adverse events and the data quality at least every 2 months. Relevant information will be included in regular study reports, and will be made available to an Independent Data Monitoring Committee (IDMC), which will be independent of the trial organizers.
The IDMC will review the data and safety data on a regular basis and report their findings to the principal investigator. The principal investigator will submit these reports to the ethics committee.
Data quality assurance
Data forms will be entered in the database of the NKI-AVL Data centre by a double data entry procedure. Computerized and visual consistency checks will be performed on newly entered forms; queries will be issued in case of inconsistencies.
On-site quality control
The sponsor will perform on-site monitoring. The monitoring visits will be scheduled at a frequency of about 1 visits per site every 6 months which may be adapted according to the site accrual.
The aim of on-site visits will be:
- To evaluate the local facilities available to the responsible investigator for performing clinical trials and to comply to all requirements of the present protocol;
- To assess the consistency of the data reported on the CRF with the source data (source data verification);
- To check that all SAE's have been properly reported;
- To resolve all previous unanswered queries.
An interim analysis will be conducted 12 months after all participating hospitals have started the inclusion of patients or 18 months after inclusion of the first patient. An independent data monitoring committee (IDMC) will assess:
Safety, especially any unexpectedly high frequency of serious adverse events;
Data compared with previous experience which are the basis of the current the trial;
Any safety or efficacy data that do not justify the continuation of the trial as planned, including statistically significant differences between treatments.
The IDMC will decide on the impact of any findings for the continuation of the trial.
All statistical analyses will be done according to the intention-to-treat principle, i.e. all eligible patients will be included in the analysis in the arm to which they were randomized independently of whether they received the assigned treatment or not. The final analysis will be performed when 191 events (recurrences or deaths) will be observed. It is estimated that this will be possible approximately 1 year after the last patient is randomized in the study. In the final analysis tables presenting the distribution of the stratification and other important factors of all cases entered by treatment arm will be included.
Disease free survival and survival curves will be constructed by means of the Kaplan Meier technique. Curves by treatment arm will be compared using the log rank test. To adjust for possible confounding factors, the treatment effect will also be estimated by adjusting Cox's proportional hazard regression model.
Clinical and laboratory toxicity graded according NCI-CTC (version 3.0) will be collected for all patients. Comparisons by treatment of the continuous variables will be done by means of Student's t-test. Comparisons of categorical date (e.g. grades of toxicity) will be done by the chi-square test.
Quality of life will be measured using the QLC-C30 questionnaire will be completed by the patients between surgery and the start of adjuvant treatment and every 6 months thereafter, until 2 years after surgery. Quality of life assessment is discontinued when adjuvant treatment is discontinued (i.e. in case of progression in arm A or B or when off-study for any reason).
Changes over time in quality of life items will be evaluated with a repeated measurement ANOVA using a mixed effect modeling procedure (SAS Proc Mixed). This model allows retaining in the analysis patients who drop out during follow-up. F-tests are used for testing main effects of group and time and an interaction effect of group and time
The primary endpoint of the study is the DFS measured from randomization. Patients will be randomized just after R0 resection (+/- RFA). Patients receiving 3 courses of CAPOX before resection will also be included in the study. It is expected that about 1/4 of the patients will have been treated by resection and RFA. The median DFS is estimated to be 9 months for RFA treated patients and 20 months in resection treated patients. The median of the whole mixed group is estimated to be 17 months.
Based on the results in previous recent series, it is hypothesized that the addition of bevacizumab to CAPOX would result in a decrease of at least 1/3 of the hazard of progression (HR = 0.67) [34–36]. The total number of events that is necessary to provide 80% power to detect such a decrease, if truly present, with a 2 tailed logrank test at 5% significance is 191. Assuming an accrual rate of 100 patients per year, a total of 300 patients would be randomized (150 receiving Bevacizumab and 150 not) in 3 years. If all patients are followed for about 1 year further after accrual is completed, 191 events would be observed and the study will have the required power.
The total duration of the study would then be 4 years and patients would have been followed for 1 to 4 years, depending on whether they were included at beginning or by the end of the accrual in the study.
Assessments during Study Treatment Phase
- Adverse events will be collected continuously during the Study Treatment Phase and followed until the event is either resolved or adequately explained, even after the patient has completed his/her study treatment.
- Concomitant diseases/treatment and compliance to study drugs will be monitored continuously during the Study Treatment Phase.
- History, vital signs, weight, ECOG Performance Status, urinalysis (dipstick) will be performed at each visit. Toxicity assessment, hematology, serum chemistry will be performed at each visit until cycle 8. If dipstick analysis shows ≥2+ protein, 24-hours urine needs to be collected for accurate measurement of renal protein excretion.
- ECG and chest X-ray will be performed as clinically indicated.
- Assessment for recurrence (abdominal CT, CEA measurements AND chest CT) will be done after surgery but before randomization (before cycle 1). Thereafter every 3 months in the first two years. If the patient shows signs of a recurrence/new colorectal cancer (e.g. clinical status OR rising CEA), possible re-operation or/and further cancer therapy will be recorded.
- Nature and duration of any hospitalization, treatment of any adverse event and nature and duration of any outpatient care will be recorded during the Study Treatment Phase.
Assessment during Follow up Phase
- CEA determinations will be done every 3 months after surgery for the first two years and thereafter every 6 months until a confirmed recurrence/new CRC and at end of follow-up after 5 years.
- Assessment for recurrence (abdominal CT AND chest CT) will be done every 3 months for the first two years after cycle 8 of chemotherapy and every 6 months thereafter until a confirmed recurrence/new CRC and at the end of follow-up after 5 years, or if the patient shows signs of a recurrence/new colorectal cancer (e.g. clinical status OR rising CEA). Possible re-operation or/and further cancer therapy will be recorded.
- Extended follow-up of hypertension, proteinuria and wound healing complication until resolution.
- Additional cancer therapy to be recorded as it occurs.
Capecitabine is an oral fluoropyrimidine carbamate rationally designed to generate 5-FU preferentially in tumor tissue through exploitation of high intratumoral concentrations of thymidine phosphorylase (TP), an enzyme present at significantly increased concentrations in a wide range of tumor types, including colorectal, breast and gastric cancers, compared with normal tissue .
Human pharmacokinetic studies have shown that after oral administration, capecitabine is readily and almost completely absorbed through the gastro-intestinal wall, thus avoiding direct intestinal exposure to 5-FU. Capecitabine is metabolized to 5-FU via a three-step enzymatic cascade, with the final stage of this conversion mediated by TP .
Oxaliplatin is a platinum derivative in which the platinum atom is complexed with a 1,2 diaminocyclohexane (DACH) and with an oxolate ligand. It was synthesized with the goal of trying to overcome resistance to first- and second generation platinum compounds (Sanofi-Synthelabo, 2001). The mechanism of action of oxaliplatin is similar to that of cisplatin as well as other platinum (Pt) compounds. Studies conducted to date indicated that the types and percentages of Pt-DNA adducts formed by oxaliplatin were qualitatively similar to those formed by cisplatin, but preclinical data suggested several unique attributes of the cytotoxic/antitumor activity of oxaliplatin. Oxaliplatin demonstrated a broad spectrum of in vitro cytotoxicity and in vivo antitumor activity that differed from that of either cisplatin or carboplatin. Oxaliplatin was active against several cisplatin-resistant cell lines, colon carcinoma and other solid tumors that were not responsive to cisplatin. In addition, oxaliplatin in combination with 5-FU led to synergistic antiproliferative activity in several in vivo models .
Bevacizumab is a humanized monoclonal antibody targeting vascular endothelial growth factor (VEGF or VEGF-A) which is a ligand with a central role in signaling pathways controlling tumor blood vessel development and survival [40–43]. VEGF binding to cell surface receptors stimulates the process of angiogenesis, the formation of blood vessels. These receptors, VEGF receptors 1 and 2, are found on vascular endothelial cells. VEGF binding stimulates endothelial cell proliferation, migration and survival [41, 44, 45].
The mode of action of bevacizumab can be summarized as follows:
- Prevents the formation of new blood vessels, thereby inhibiting the growth of existing tumors and preventing metastases from developing blood supply.
- Normalizes existing tumor blood vessels. The subsequent effects include reduction of the tortuousness of tumor blood vessels and normalization of vessel permeability. The latter effect is important because tumors usually exhibit high interstitial pressure which can prevent chemotherapeutic agents penetrating tumors and accessing tumor cells, where they exert their effects. Normalization of permeability, and therefore intratumoral pressure gradients, thus, promotes chemotherapy access .
- Produces blood vessel breakdown, probably through inhibition of the anti-apoptotic effects of VEGF on immature endothelial cells. VEGF also has activities beyond angiogenesis, affecting immune function via inhibition of dendritic cell maturation, formation of lymph vessels and lymphatic metastasis. All of these actions indicate that VEGF may be an important target for anticancer drug development. Bevacizumab has proven to be clinically effective in fase III studies with solid tumors.
Arm A (CAPOX+Bevacizumab) consists of 8 cycles of CAPOX (either all cycles postoperatively or 3 cycles preoperatively followed by 5 cycles postoperatively).
Postoperatively patients will be treated with: bevacizumab at 7.5 mg/kg, administered as an intravenous infusion over 20-30 minutes for a maximum of 48 weeks. CAPOX will be given as follows: oxaliplatin administered as a 130 mg/m2 intravenous infusion over 2 hours (day 1, every 3 weeks) in combination with capecitabine, which will be administered orally at a dose of 1000 mg/m2 twice-daily (equivalent to a total daily dose of 2000 mg/m2), with first dose the evening of day 1 and the last dose the morning of day 15, given as intermittent treatment (3-week cycles consisting of 2 weeks of treatment followed by 1 week. without treatment). After completion of the 8 CAPOX cycles, bevacizumab will be continued as single agent (7.5 mg/kg q3w) treatment. Bevacizumab will be stopped after 48 weeks
Arm B (CAPOX) consists of 8 cycles of CAPOX (either all cycles postoperatively or 3 cycles preoperatively followed by 5 cycles postoperatively). CAPOX will be given as follows: Oxaliplatin administered as a 130 mg/m2 intravenous infusion over 2 hours (day 1, every 3 weeks) in combination with capecitabine, which will be administered orally at a dose of 1000 mg/m2 twice daily (equivalent to a total daily dose of 2000 mg/m2), with first dose the evening of day 1 and the last dose the morning of day 15, given as intermittent treatment (3-week cycles consisting of 2 weeks of treatment followed by 1 week without treatment).
Patients undergoing radical resection or radical resection in combination with RFA for their colorectal liver metastases can be included in this randomized controlled phase III trial where they will receive adjuvant treatment with CAPOX or CAPOX and bevacizumab. There has been much debate during the development of the study whether or not to include a surgery only arm. There were no results of randomized trials that compared surgery with surgery and adjuvant treatment for patients with resectable colorectal liver metastases until November 2006. However, worldwide patients were commonly treated with adjuvant chemotherapy even in the absence of positive studies. Portier et al. demonstrated, in a phase III randomized controlled trial a disease free survival benefit for surgery and adjuvant chemotherapy with 5 FU and Leucovorin compared to surgery alone in patients with resectable colorectal liver metastases . Nordlinger and colleagues presented the results of a RCT comparing surgery with surgery and peri-operative chemotherapy . With this publication, the debate has shifted towards whether or not to treat this specific patient group with peri-operative chemotherapy instead of adjuvant chemotherapy. The intention to treat analysis of Nordlinger's study unfortunately demonstrated only a trend in disease free survival benefit towards the treatment arm. From the results of this study and previous adjuvant studies it cannot be concluded that peri-operative chemotherapy is better than adjuvant chemotherapy. We have amended the protocol in December 2009 to allow 3 cycles CAPOX to be administered to bridge time to surgery. However, the steering committee of the study does feel that adjuvant treatment unless proven to be inferior of peri-operative chemotherapy in a randomized trial, is preferred. Since this amendment, we also allow patients in the study that undergo resection in combination with RFA. RFA is a frequently used in addition to resection in patients where the liver volume is insufficient to resect all tumor tissue. Since local recurrence is a frequent phenomenon after RFA in larger tumors we only allow patients with tumors smaller than 4 cm . Also RFA alone or RFA for more than 3 tumors is not allowed in the study.
Administering pre-operative chemotherapy to patients with resectable colorectal liver metastases and thereby postponing a possible curative treatment seems undesirable since there are many disadvantages associated with neoadjuvant treatment. Neoadjuvant chemotherapy induces liver toxicity, such as steatosis, steatohepatitis and sinusoidal changes. Patients receiving pre-operative chemotherapy increase their chance of post-operative complications significantly (25% vs 16%)  Some patients undergoing neoadjuvant treatment demonstrate complete radiologic response. This only translates to complete pathologic response in 3-4% of the cases . Remarkably complete pathologic response is sometimes seen in patients demonstrating incomplete radiologic response. It is therefore well established that all initial metastases should be resected. Moreover, due to chemotherapeutic alterations in the liver parenchyma, the original lesions are difficult to identify. Patients who progress during chemotherapy might result in inoperable patients due to this delay. There is also the danger of operating on benign lesions. Since there is no demonstrated benefit of peri-operative chemotherapy compared to adjuvant treatment, there is no justification to jeopardize resectability. Immediate surgery is preferred and results in direct control of the hepatic tumor without additional toxicity and should therefore not be postponed when possible. Response to preoperative chemotherapy could serve as a biological marker for good prognosis. Nonetheless patients with poor response still reach 5 year survival. Adjuvant chemotherapy can overcome many of the disadvantages mentioned above with equal benefit of increasing DFS. Neoadjuvant treatment should be preserved for irresectable patients in order to reduce tumor mass and transfer a substantial number of patients to resectable. However for resectable patients, there is no trial comparing a peri-operative regimen with adjuvant chemotherapy in terms of DFS. Until the result of such a study demonstrates a benefit for either arm it seems unjustifiable to postpone a possible curative treatment.
Because pro-angiogenic factors are upregulated during liver regeneration it is conceivable that liver regeneration will be inhibited if angiogenesis is inhibited. Clinical studies show that patients receiving bevacizumab undergoing surgery have more wound healing complications than patients not receiving bevacizumab (13% vs 3,4%) . This difference might be explained by the relative long half life of bevacizumab compared to the compound (PTK/ZK) used in the animal model. Fortunately a five week interval between bevacizumab treatment and resection had shown to be sufficient to diminish the effect on wound heeling and liverregeneration . Unfortunately oxaliplatin has a negative impact on the liver parenchyma demonstrating in sinusoidal obstruction syndrome in 20% of all patients . Ribero et al show in a retrospective study the pathological response and dilation of sinusoids in the liver of patients who have been treated with neoadjuvant Folfox in comparison with patients who where treated with bevacizumab and FOLFOX . Forty-three patients received FOLFOX and 62 patients received folfox and bevacizumab. The bevacizumab group showed a significant tumor regression in comparison with the FOLFOX group. Remarkably the incidence and severity of sinusoidal dilatation reduced in the bevacizumab. This phenomenon might be due to the fact that oxaliplatin treated sinusoid cells release MMP-2 and MMP-9 which induce the destruction of extracellular matrix and degeneration of endothelial cells. VEGFG induces the expression of MMP-9. By inhibiting VEGF, MMP-9 will also be inhibited.
The HEPATICA study is designed to demonstrate that adjuvant treatment with the combination of bevacizumab and CAPOX is superior to CAPOX alone as adjuvant chemotherapy in terms of disease free survival in patients with colorectal liver metastases.
Key staff at coordinating centre
Richard van Hillegersberg, MD, PhD, surgeon (principal investigator)
Emile E. Voest, MD, PhD, medical oncologist (principal investigator),
Nikol Snoeren, Msc (trial coordinator)
Sonja Verkleij/Roelien Kronemeijer (trial research nurse medical oncology)
Prof. R. Adam, Surgeon, Hospital Paul Brousse Paris, France
Prof. Dr. E. van Cutsem, Medical Oncologist, Katholieke Universiteit Leuven, Belgium
Prof. Dr. T. Wiggers, Surgeon, University Medical Centre Groninging, the Netherlands
Prof. Dr. D.J. Richel, Medical Oncologist, Academical Medical Centre Amsterdam
Ir. H. van Tinteren, Statistician, Antonie van Leeuwenhoek Hospital Amsterdam, the Netherlands
The principal investigators of the local hospitals are mentioned below. Investigators are of the department of Surgery (S), Oncology (O) or Gastroenterology (G).
Academic Medical Centre Amsterdam: ORC Busch (S), DJ Richel (O); Amphia Hospital Breda: A Rijken (S), OJL Loosveld (O); Atrium Medical Centre Heerlen: J Wals (O); Deventer Hospital: M Liem (S), ALT Imholz (O); Diakonessenhuis Utrecht: CI Perre (S), D ten Bokkel Huinink (O); Gelre Hospital Apeldoorn EJ Hesselink (S), JM Smit (O); Jeroen Bosch Hospital Den Bosch: K Bosscha (S), JFM Pruijt (O); Leiden University Medical Centre: R Tollenaar (S), AJ Gelderblom (O); Maastricht University Medical Centre: CHC Dejong (S) RLH Jansen (O); Maxima Medical Centre Veldhoven: R Roumen (S), G Vreugdenhil (O); Meander Medical Centre Amersfoort: B van Ooijen (S), C Rodenburg (O); Medical Centre Alkmaar: CH Smorenburg; Medical Centre The Hague: JRM van der Sijp (S), HM Oosterkamp (O); Medical Centre Leeuwarden JPEN Pierie (S), MB Polée (O); Medical Spectrum Twente Enschede: JM Klaase (S), MCJC Legdeur (O); Onze Lieve Vrouwe Gasthuis Amsterdam: PJ Borgstein (S), B de Valk (O); Saint Elisabeth Hospital Tilburg: JMGH van Riel (O); Slingeland Hospital Doetinchem: EW Muller (O); Antoni van Leeuwenhoek Hospital; F van Coevorden (S) A Cats (G); Tergooiziekenhuizen Blaricum/Hilversum HP van den Berg; University Medical Centre Groningen: RJ Porte (S) KP de Jong (S), GA Hospert (O); University Medical Centre Utrecht: R van Hillegersberg (S), EE Voest (O); VieCuri Venlo: AJ van der Wouw (O); VU Medical Centre Amsterdam: MP van den Tol (S) E Boven (O) Westfriesgasthuis Hoorn: JWD de Waard (O); Haga Hospital The Hague: JEA Portielje (O); Röpcke-Zweers Ziekenhuis - Saxenburg Groep Hardenberg: EA Runhaar (O); Gelderse Vallei Apeldoorn: C Sietses (S), E Balk (O)
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The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/10/545/prepub
We like to thank all other participating investigators and referral centres for their efforts.
The authors declare that they have no competing interests.
NS, EV, RH drafted the manuscript
AB wrote the original protocol for the study
All authors participated in the design of the study
OD performed the statistical analysis.
All authors read and approved the final manuscript.