Ignite Creation Date:
2024-05-06 @ 4:10 PM
Last Modification Date:
2024-10-26 @ 2:05 PM
Study NCT ID:
NCT04898504
Status:
RECRUITING
Last Update Posted:
2023-08-31
First Post:
2021-05-10
Brief Title:
HAI-Floxuridine or Liver-Tx Combined With 2nd Line Chemotherapy Versus 2nd Line Chemotherapy Alone for Patients With Colorectal Liver Metastases and Heavy Tumour Burden
Sponsor:
Oslo University Hospital
Organization:
Oslo University Hospital
Study Overview
Official Title:
EXtended CriteriA Treatment for LIver Metastases With Heavy Tumour BURden 1 2
Status:
RECRUITING
Status Verified Date:
2023-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
EXCALIBUR12
Brief Summary:
Patients with colorectal livermetasteses and heavy tumour burden and progression on 1st line chemotherapy have no other available treatment in Norway today other than 2nd line chemotherapy The Investigators will randomize patients to HAI-floxuridine FUDR or liver-Tx in addition to 2nd line chemotherapy versus 2nd line chemotherapy alone Excalibur 1 or systemic chemotherapy with HAIFUDR versus systemic chemotherapy alone Excalibur 2 Primary endpoint is overall survival at 2yrs
Detailed Description:
11 Background - Disease Colorectal cancer CRC is the second most frequent malignant disease in Norway Cancer in Norway 2017 About 50 of the patients will have metastatic disease at time of diagnosis or develop metastatic disease later on Liver metastases are the most frequent site of metastatic disease Liver resection is considered the only curative treatment option in CRC patients with liver metastases however only about 20 of the patients are candidates for liver resection The treatment option for the majority of the patients is palliative chemotherapy with median overall survival from start of chemotherapy of about 2 years and 10-12 months from starting second line chemotherapy
12 Liver resections for Colorectal Liver metastases CRLM While high-quality data randomized trials are lacking it is generally accepted that the only curative treatment for colorectal liver metastases CRLM is surgery Liver resections are generally well tolerated and safe 1 but some patients recur early and probably have limited or no benefit from surgery These are hard to identify upfront Even following three decades of systematic liver surgery for CRLM there is a lack of robust prognostic scoring systems that have sufficient discriminatory power to serve as selectors for surgery or non-operative treatment 2 3 Even among patients with very poor prognostic scores there are some who will survive five years following surgery 4 and even without surgery 5 Over the decades the definition of resectabilityun-resectability has been steadily modified Today any configuration of metastases can be deemed resectable as long as a resection will leave behind a working liver volume of at least 20-30 of the estimated total liver volume with a functioning arterial inflow portal venous inflow draining bile duct and draining hepatic vein
13 The grey zone As resections are generally well tolerated and adequate prognostication is wanting there is a tendency to offer resections to patients who have borderline resectable CRLM or who exhibit other non-favourable traits like large or multiple metastases For patients who have early recurrence of disease such resections represent a net loss of quality-of-life and an unwanted expenditure for society Exploring the optimal treatment modality for patients in this grey zone ie with uncertain benefit from surgery is important to avoid unnecessary resections and providing the optimal treatment for patients in a critical situation
14 Systemic chemotherapy for CRLM Palliative chemotherapy is in general the only treatment option for the vast majority of non-resectable patients The expected median overall survival OS from start of first line chemotherapy is about 2 years and the 5 years OS is about 10 although longer median OS has been obtained in selected patients with good performance status ECOG 0-1 no KRAS or BRAF mutations and left-sided tumors 6-10 OS from start of second line chemotherapy is 10-12 months 11
15 Liver transplant for CRLM Liver transplant LTX has emerged as a possible solution for some patients with unresectable CRLM who otherwise have good prognosis based on available scorings systems 12 13 In patients with non-resectable liver only metastases the investigators have previously shown 5 year OS of 56 compared to 9 in a similar cohort of patients starting first line chemotherapy 6 but due to lack of donor organs this will never become the backbone of any treatment modality for a disease as prevalent as CRLM However LTX is probably the best treatment option in highly selected patients with non-resectable CRLM liver only disease
16 Hepatic artery infusion HAI chemotherapy for CRLM The biological rationale for intra-arterial chemotherapy is that the hepatic artery rather than the portal vein is responsible for most of the blood supply to liver tumors Hepatic Artery Infusion HAI of a cytotoxic drug floxuridine FUDR that has a very high first-pass extraction ca 95 in the liver has shown promising results in selected series for several decades 14-16 It was developed at Memorial Sloan Kettering Cancer Center MSKCC New York USA but is currently unavailable in the European Union because floxuridine is not registered HAI has however not gained foothold as a standard treatment option for CRLM and most publications stem from a very few centres The reasons for this lack of dissemination are unknown but could well be related to the complexity of the treatment algorithm and the lack of modern randomized trials In Europe several centers in The Nederlands have recently started the HAI treatment procedure as adjuvant treatment in CRC patients who have received liver resection Buisman FE et al Ann Surg Oncol 2019 26 4599-4607 Of the 20 patients included in the study in The Nederlands two patients had Clavien-Dindo complication grade III with reoperation due to replacement of a pump with slow flow-rate and a flipped pump The treatment administered both at MSKCC and the two centers in The Nederlands consist of 012 mg FUDRkgday 35000 IE heparin 25 mg dexamethasnone in a total volume of 35ml NaCL administered as a continue infusion for 14 days with dose reduction if liver function is affected Table 2 At day 15 the pump is emtied and refiled with a low dose heparin solution for continuous infusion to avoid coagulation of the catheter A new cycle is started at day 29 The HAI treatment has been combined with both oxaliplatin and irinotecan regimens combined with 5-FU as systemic chemotherapy 141617 HAI has also been combined with systemic gemcitabine-oxaliplatin regimen in patients with non-resectable intrahepatic cholangiocarcinoma18 In the study by DAngelica in non-resectable CRC patients the response rate was 76 median overall survival was 38 months and 23 of 49 patients became resectable and received a liver resection Patients having a liver resection had a 3 year overall survival of 80 In the study by Pak 33 of 64 non-resectable CRC patients received a liver resection with 5 year overall survival of 36 These results are better compared to what has been reported by systemic chemotherapy only with median overall survival of about 24 months in most studies Optimal treatment for patients with CRLM in the grey zone is therefore not yet defined and there is a definte need for further studies
To optimize treatment for patients with a large tumour burden and borderline resectability the investigators will compare three treatment modalities in a randomized controlled trial in patients that have progressive disease on 1st line of chemotherapy treatment
17 Rationale for the Study and Purpose The target population for this study will be patients who based on traditional preoperative criteria have a very dismal prognosis They will - according to the inclusion criteria - have a large tumour burden and have shown progression on 1st line systemic chemotherapy treatment Based on previous trials only 30 of this patient group will be alive after two years These patients have today only one treatment modality available 2nd line systemic chemotherapy Response can however only be expected in a small minority of these patients As of today they are not acceptable for inclusion into any of the liver transplant protocols and hepatic aretery infusion HAI chemotherapy treatment is not offered in Norway or any other European country save the Netherlands as far as the investigators know
With such a dismal outcome for these patients an alternative modality that has the potential to improve survival is highly warranted While transplantation has such a potential the access to donor organs will allways limit the real-life use of such a treatment and the inclusion of a transplant group in this trial is primarily for proof-of-principle reasons to benchmark what the investigators have reason to believe is the optimal treatment
The use of HAI chemotherapy with FUDR has some inherent risks A laparotomy is necessary to apply the catheter and intra hepatic infusion of FUDR has been reported to cause biliary inflammation and necrosis in a small fraction of the patients The risk for the latter is however significantly reduced by concommittant steroid infusion The experiences published from the MSKCC se further does however suggest that the drug has few systemic side effects as the first-pass effect in the liver is close to complete ie there is minimal release of active drug into the systemic circulation
The IMP for use in this protocol does not have a marketing authorization in Europa The institution that has pioneered the HAI treatment in CRC is Memorial Sloan Kettering Hospital MSKCC in New York and the dose is identical to the dose that used in several studies from MSKCC 1416 and The Nederlands17
18 Research hypothesis In patients with large tumour burden andor borderline resectability of colorectal liver metastases and progression on 1st line systemic chemotherapy overall survival following systemic therapy combined with hepatic artery infusion chemotherapy HAI or liver transplantation is better than following conventional systemic chemotherapy alone
12 Liver resections for Colorectal Liver metastases CRLM While high-quality data randomized trials are lacking it is generally accepted that the only curative treatment for colorectal liver metastases CRLM is surgery Liver resections are generally well tolerated and safe 1 but some patients recur early and probably have limited or no benefit from surgery These are hard to identify upfront Even following three decades of systematic liver surgery for CRLM there is a lack of robust prognostic scoring systems that have sufficient discriminatory power to serve as selectors for surgery or non-operative treatment 2 3 Even among patients with very poor prognostic scores there are some who will survive five years following surgery 4 and even without surgery 5 Over the decades the definition of resectabilityun-resectability has been steadily modified Today any configuration of metastases can be deemed resectable as long as a resection will leave behind a working liver volume of at least 20-30 of the estimated total liver volume with a functioning arterial inflow portal venous inflow draining bile duct and draining hepatic vein
13 The grey zone As resections are generally well tolerated and adequate prognostication is wanting there is a tendency to offer resections to patients who have borderline resectable CRLM or who exhibit other non-favourable traits like large or multiple metastases For patients who have early recurrence of disease such resections represent a net loss of quality-of-life and an unwanted expenditure for society Exploring the optimal treatment modality for patients in this grey zone ie with uncertain benefit from surgery is important to avoid unnecessary resections and providing the optimal treatment for patients in a critical situation
14 Systemic chemotherapy for CRLM Palliative chemotherapy is in general the only treatment option for the vast majority of non-resectable patients The expected median overall survival OS from start of first line chemotherapy is about 2 years and the 5 years OS is about 10 although longer median OS has been obtained in selected patients with good performance status ECOG 0-1 no KRAS or BRAF mutations and left-sided tumors 6-10 OS from start of second line chemotherapy is 10-12 months 11
15 Liver transplant for CRLM Liver transplant LTX has emerged as a possible solution for some patients with unresectable CRLM who otherwise have good prognosis based on available scorings systems 12 13 In patients with non-resectable liver only metastases the investigators have previously shown 5 year OS of 56 compared to 9 in a similar cohort of patients starting first line chemotherapy 6 but due to lack of donor organs this will never become the backbone of any treatment modality for a disease as prevalent as CRLM However LTX is probably the best treatment option in highly selected patients with non-resectable CRLM liver only disease
16 Hepatic artery infusion HAI chemotherapy for CRLM The biological rationale for intra-arterial chemotherapy is that the hepatic artery rather than the portal vein is responsible for most of the blood supply to liver tumors Hepatic Artery Infusion HAI of a cytotoxic drug floxuridine FUDR that has a very high first-pass extraction ca 95 in the liver has shown promising results in selected series for several decades 14-16 It was developed at Memorial Sloan Kettering Cancer Center MSKCC New York USA but is currently unavailable in the European Union because floxuridine is not registered HAI has however not gained foothold as a standard treatment option for CRLM and most publications stem from a very few centres The reasons for this lack of dissemination are unknown but could well be related to the complexity of the treatment algorithm and the lack of modern randomized trials In Europe several centers in The Nederlands have recently started the HAI treatment procedure as adjuvant treatment in CRC patients who have received liver resection Buisman FE et al Ann Surg Oncol 2019 26 4599-4607 Of the 20 patients included in the study in The Nederlands two patients had Clavien-Dindo complication grade III with reoperation due to replacement of a pump with slow flow-rate and a flipped pump The treatment administered both at MSKCC and the two centers in The Nederlands consist of 012 mg FUDRkgday 35000 IE heparin 25 mg dexamethasnone in a total volume of 35ml NaCL administered as a continue infusion for 14 days with dose reduction if liver function is affected Table 2 At day 15 the pump is emtied and refiled with a low dose heparin solution for continuous infusion to avoid coagulation of the catheter A new cycle is started at day 29 The HAI treatment has been combined with both oxaliplatin and irinotecan regimens combined with 5-FU as systemic chemotherapy 141617 HAI has also been combined with systemic gemcitabine-oxaliplatin regimen in patients with non-resectable intrahepatic cholangiocarcinoma18 In the study by DAngelica in non-resectable CRC patients the response rate was 76 median overall survival was 38 months and 23 of 49 patients became resectable and received a liver resection Patients having a liver resection had a 3 year overall survival of 80 In the study by Pak 33 of 64 non-resectable CRC patients received a liver resection with 5 year overall survival of 36 These results are better compared to what has been reported by systemic chemotherapy only with median overall survival of about 24 months in most studies Optimal treatment for patients with CRLM in the grey zone is therefore not yet defined and there is a definte need for further studies
To optimize treatment for patients with a large tumour burden and borderline resectability the investigators will compare three treatment modalities in a randomized controlled trial in patients that have progressive disease on 1st line of chemotherapy treatment
17 Rationale for the Study and Purpose The target population for this study will be patients who based on traditional preoperative criteria have a very dismal prognosis They will - according to the inclusion criteria - have a large tumour burden and have shown progression on 1st line systemic chemotherapy treatment Based on previous trials only 30 of this patient group will be alive after two years These patients have today only one treatment modality available 2nd line systemic chemotherapy Response can however only be expected in a small minority of these patients As of today they are not acceptable for inclusion into any of the liver transplant protocols and hepatic aretery infusion HAI chemotherapy treatment is not offered in Norway or any other European country save the Netherlands as far as the investigators know
With such a dismal outcome for these patients an alternative modality that has the potential to improve survival is highly warranted While transplantation has such a potential the access to donor organs will allways limit the real-life use of such a treatment and the inclusion of a transplant group in this trial is primarily for proof-of-principle reasons to benchmark what the investigators have reason to believe is the optimal treatment
The use of HAI chemotherapy with FUDR has some inherent risks A laparotomy is necessary to apply the catheter and intra hepatic infusion of FUDR has been reported to cause biliary inflammation and necrosis in a small fraction of the patients The risk for the latter is however significantly reduced by concommittant steroid infusion The experiences published from the MSKCC se further does however suggest that the drug has few systemic side effects as the first-pass effect in the liver is close to complete ie there is minimal release of active drug into the systemic circulation
The IMP for use in this protocol does not have a marketing authorization in Europa The institution that has pioneered the HAI treatment in CRC is Memorial Sloan Kettering Hospital MSKCC in New York and the dose is identical to the dose that used in several studies from MSKCC 1416 and The Nederlands17
18 Research hypothesis In patients with large tumour burden andor borderline resectability of colorectal liver metastases and progression on 1st line systemic chemotherapy overall survival following systemic therapy combined with hepatic artery infusion chemotherapy HAI or liver transplantation is better than following conventional systemic chemotherapy alone
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None