Hepatic Arterial Chemotherapy With Raltitrexed and Oxaliplatin Versus Standard Chemotherapy in Unresectable Liver Metastases From Colorectal Cancer After Conventional Chemotherapy Failure

Colorectal Cancer Clinical Trial

— HEARTO  

Official title:

Phase II Randomized Study Comparing the Association of Intraarterial Perfusion of Raltitrexed and Oxaliplatin Versus Standard Chemotherapy Using Intravenous Perfusion for Colorectal Cancer Patient With Metastases Localized to Liver After Failure of Conventional Treatments.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01348412
• Other study ID #: 0329-1ghfr09
• Status: Completed
• Phase: Phase 2
• Start date: December 15, 2010
• Est. completion date: April 18, 2018

Study information

• Verified date: July 2018
• Source: Centre Georges Francois Leclerc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Standard treatment of metastatic colorectal cancers relies on fluoropyrimidines, irinotecan alone or in association with fluoropyrimidines, oxaliplatin in association with fluoropyrimidines, bevacizumab and anti EGFR antibodies. After failure of classical regimen the national reference frame on the basis of phase II study proposes an association of fluoropyrimidine and mitomycin. These treatments give response rates of 10-20% with progression free survivals from 2 to 3 months. Hepatic intra-arterial chemotherapy is logical in the case of isolated hepatic metastases nonaccessible to curative resection: 1) hepatic metastases are vascularized by hepatic arterial system in contrast to nontumoral hepatic parenchyma; 2) arterial perfusion of oxaliplatin leads to a strong extraction by the liver during the first passage, a high intra-tumoral concentration and a low systemic concentration. So oxaliplatin is a drug of choice for arterial treatment but combination with fluoropyrimidines is impossible because of need for prolonged perfusion. Floxuridin is not available in France. Raltitrexed, a definitive inhibitor of the thymidylate synthase, does not require a prolonged perfusion and could be a good substitute.In a previous pilot study we demonstrated the feasibility, safety and efficacy of combination of raltitrexed and oxaliplatin arterial perfusion. Now we propose a phase II randomized clinical trial to evaluate the efficacy of hepatic arterial infusion of raltitrexed and oxaliplatin association versus standard chemotherapy for patients with metastases of colorectal origin restricted to the liver after failure of conventional chemotherapy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: April 18, 2018
• Est. primary completion date: December 15, 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Informed consent signature by the patient-

• Cover by an health insurance

• Age between 18 and 75 years

• Age between 76 et 80 years if patient WHO Status 0

• WHO status of 0 or 1

• Estimated Life expectancy > 3 months

• Hepatic metastases of colorectal cancer confirmed on CT Scan without extra-hepatic metastasis (the presence of asymptomatic primary tumor is tolerated)

• TEP-Scan without fixation outside the liver and the primary tumor

• Histological proven colorectal cancer obtained from primary tumor or the hepatic metastases

• Metastases not accessible to curative hepatectomy (impossible R0 surgery or leaving less than 30 % of residual liver), or requiring a complex, very wide hepatectomy (5 segments or more) and\or risky procedure (RPC Class II)- - Presence of hepatic lesion > 10 mm on CTScan or hepatic MRI

• Failure or arrest of a previous chemotherapy because of intolerance to oxaliplatin, irinotecan, a fluoropyrimidine and/or target therapies (bevacizumab, cetuximab or panitumumab given for tumor expressing wild type Ki-Ras)

• Bilirubinemia< 1,5 times the superior limit of the normal ( N ),

• ASAT and ALAT < 5 N,

• Creatinemia < 1.5 N and creatinine clearance > 65ml/mn,

• Neutrophils > 1,5 x 109/L, platelets 100 x 109/L, hemoglobin > 9 g/dL (patients includables even after red blood cell transfusion)-Reference CTScan +/-MRI performed in 21 days preceding the first cycle of treatment

Exclusion Criteria:

• extra-hepatic metastases (presence of 1 to 3 pulmonary nodules, of a maximal diameter of 5 mm with non specific aspect on CTScan and with no fixation on TEP Scan does not constitute a criterion of exclusion)

• Symptomatic primary colorectal tumor in place

• Contraindication for allergy of rank 3-4 for one of the compounds of chemotherapy- Peripheral neuropathy > 2 (Levy Scale)

• Current participation or in the 30 days preceding the inclusion in the study in another therapeutic trial with an experimental molecule

• Concomitant systemic treatment by immunotherapy, chemotherapy or hormonotherapy- Unbalanced serious illness, unchecked active infection or the other underlying serious disorder susceptible to prevent the patient from receiving the treatment

• Pregnancy (pregnancy test compulsory for the inclusion), breast-feeding

• Intestinal occlusion or sub-occlusion or history of inflammatory intestinal disease

• Other cancer during the 5 years preceding entry in the trial or concomitant (except in situ cancer of the cervix or skin basal cell carcinoma)Patient in custody or under guardianship, Impossibility to adhere to the medical follow-up for geographical, social or psychiatric reason

Related Conditions & MeSH terms

• Colorectal Cancer
• Colorectal Neoplasms
• Liver Metastases
• Liver Neoplasms
• Neoplasm Metastasis
• Neoplasms, Second Primary

Intervention

Drug:
• oxaliplatin
130 mg/m²Every 21 days
• raltitrexed
3 mg/m² with a maximum of 6 mg every 21 days
• other intravenous chemotherapy drugs

Locations

Country	Name	City	State
France	Centre Georges François Leclerc	Dijon

Sponsors (3)

Lead Sponsor	Collaborator
Centre Georges Francois Leclerc	Hospira, now a wholly owned subsidiary of Pfizer, National Cancer Institute, France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	progression-free survival		for each patient after the 6 months of treatment
Secondary	Estimate the parameters of tumor perfusion using arterial CT Scan data		for each patient of experimental arm every 9 weeks after the six months of treatment or until progression
Secondary	Estimate the rate of objective response according to the criteria of CHOI and RECIST		for each patient every 9 weeks during the 6 months of treatment or until progression
Secondary	Estimate the overall survival which will be compared with the median of overall survival in other studies published in the literature		after all data completion after the end of all patient follow-up (december 2013-anticipated)
Secondary	Estimate the rate of secondary resectable hepatic metastases		after all data completion after the end of all patient follow-up (december 2013-anticipated)
Secondary	Estimate the tolerance of the treatment (NCI-CTCAE version 4.0)		For each patient every 21 days during the six months of treatment and for one year of follow up or until progression
Secondary	Estimate the quality of life (QLQ C30) and the fatigue MFI20		after all data completion after the end of all patient follow-up (december 2013-anticipated)