Intra-arterial Hepatic Beads Loaded With Irinotecan With Concomitant Chemotherapy With FOLFOX in Patients With Colorectal Cancer With Unresectable Liver Metastases: a Phase II Multicenter Study

Federation Francophone de Cancerologie Digestive

Status and phase

Completed

Phase 2

Conditions

Colorectal Cancer With Non Resectable Hepatic Metastasis

Treatments

Drug: HIA DEBIRI + systemic FOLFOX

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01839877

FFCD 1201 DEBIRI

Details and patient eligibility

About

Treatment of patients with colorectal cancer having liver metastases is currently based on systemic chemotherapy.

Triple therapy with 5FU, oxaliplatin and irinotecan intravenously was effective in terms of response and secondary resectability, however it is particularly toxic.

Hepatic intra-arterial chemotherapy (HIA) has been the subject of several studies. It has shown good efficacy with oxaliplatin and FUDR. However, the procedure is difficult to set up and reserved for experienced centers.

The objective of this protocol is to use a triple therapy based on 5FU and oxaliplatin associated to irinotecan which is administered by hepatic intra-arterial route, loaded onto microbeads (DEBIRI). Furthermore, the procedure for chemo-embolization DEBIRI is limited to 2 sessions, and therefore could be more easily generalized.

Enrollment

58 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Histologically proven colorectal adenocarcinoma,
Liver metastases radiologically or histologically proven
At least one measurable liver lesions by RECIST v1.1
Age ≥ 18 years
WHO Index < or = 2
Life expectancy ≥ 3 months
No extrahepatic disease except lung nodules if number < or = 3 and size < 10 mm each
Healthy liver <60%
Primary tumor resected or still in place
No prior chemotherapy for metastases treatment (except a perioperative chemotherapy, if the last cycle was administered at least 12 months ago)
Adjuvant chemotherapy after resection of the primary authorized if the last cycle was administered at least 12 months ago
Normal hepatic function: total bilirubin ≤ 1.5 N; AST ≤ 5N; ALT ≤ 5N and PAL ≤ 5N
TP ≥ 60%
Adequate hematologic function: ANC ≥ 1500/mm3, platelets ≥ 100 000/mm3, Hb ≥ 9g/dl
Good renal function: creatinine clearance ≥ 60 mL / min
No cardiac dysfunction: no cardiovascular events in the last 6 months or no NYHA ≥ 2

Exclusion criteria

Patient eligible for curative treatment (resection and / or radiofrequency ablation) by a multidisciplinary decision (including the opinion of a liver surgeon)
Pregnant or lactating woman or patients of both sexes and of childbearing age not using adequate contraception
History of cancer, except skin cancer (other than melanoma), carcinoma in situ of the cervix uteri treated curative. Other cancers treated with curative intent are permitted provided they did not relapse over the last 5 years
Peripheral neuropathy
Inflammatory Bowel Diseases
Intestinal obstruction
Chronic liver disease (viral, alcoholic or metabolic)
Immune Deficiency Syndromes (history of transplantation, infection with HIV)
Known to have contraindications to 5FU, oxaliplatin, folinic acid, irinotecan or to contrast products
Patients with known contraindications against hepatic embolization procedures:

Presence of biliary-digestive anastomosis or biliary stent Cruoric or tumor thrombosis of the portal vein

Patient who for psychological, social, family or geographical reasons could not be followed up regularly
Legal disability (persons deprived of liberty or under guardianship)
Patient is not affiliated to a social security scheme
Participation in another concurrent study investigating the effect of treatment and this until 4 weeks after the end of the concurrent study.