Status:
COMPLETED
Efficacy Study of Intra-hepatic Administration of Therasphere® in Association With Intravenous Chemotherapy to Treat Cholangiocarcinoma
Lead Sponsor:
Center Eugene Marquis
Conditions:
Cholangiocarcinoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to assess efficacy and tolerance of intra-hepatic administration of Yttrium 90-labelled microsphere (Theraspheres®, Nordion) in association with intravenous chemotherapy w...
Eligibility Criteria
Inclusion
- Histologically confirmed intra-hepatic cholangiocarcinoma.
- Measurable target of at least 2 cm diameter.
- Healthy liver or cirrhosis CHILD \< B8.
- WHO-PS: 0-1.
- Age ≥ 18 years.
- Non-Metastatic disease in extra-hepatic (are permitted: local lymph nodes \< 3 cm, less than 5 lung nodes \< 11 mm).
- Creatinine clearance (calculated with Cockcroft and Gault formula) ≥ 55 ml/min, polymorphonuclear neutrophils ≥ 1500 G/L, platelets ≥ 80 G/L, prothrombin ≥ 40% (INR ≤ 2.3), serum albumin ≥ 28 g/l, serum bilirubin ≤ 3 x LSN.
- Pregnancy test: negative for women of childbearing potential.
- Reliable contraception for a childbearing couple, men and woman must have an reliable contraception during the treatment and until 6 months following the end of the treatment by chemotherapy
- Signed informed consent form.
- Patient with national health insurance.
Exclusion
- Pancreas cancer or duodenum cancer invading the bile duct or ampullary cancer. Cholangiocarcinoma of the bile ducts: hilar, main duct, gallbladder.
- Extra-hepatic metastasis (including local lymph nodes measuring \> 30 mm).
- Primary sclerosing cholangitis.
- History of chemoembolization or radioembolization.
- Cirrhose CHILD \> B7
- Portal vein trunk tumoral thrombosis
- History of hepato-biliary neo adjuvant or palliative chemotherapy and/or radiotherapy.
- Contra indication of Gemcitabine and/or Cisplatin.
- Other invasive active cancer, excepting in situ cervical cancer and basocellular or spino cellular skin cancer treated adequately. Any history of cancer not considered as completely cured for at least one year.
- Technical failure of the diagnostic arteriography.
- Extra hepatic uptake on the pre-therapeutic scintigraphy not manageable with an arteriography.
- Dosimetry study predicting lung exposure \> 30 Gy.
- Any unstable medical history (diabetes, hypertension …).
- History of organ transplant.
- Symptomatic grade 1 angina pectoris or grade ≥ 2 angina pectoris.
- An evolutive neuropathy.
- Patient who already has been involved in a clinical trial with drug intake, whether this drug was experimental or not, within 30 days before.
- Pregnant patient or patient with breastfeeding.
- Patient under administrative supervision.
- Regular follow-up impossible for various reasons (psychological, familial, economical, and social).
Key Trial Info
Start Date :
September 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2017
Estimated Enrollment :
41 Patients enrolled
Trial Details
Trial ID
NCT01912053
Start Date
September 1 2013
End Date
November 1 2017
Last Update
May 11 2018
Active Locations (7)
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1
Hôpital Beaujon - Service de Chirurgie
Clichy, France, 92118
2
Hôpital Henri Mondor
Créteil, France, 94010
3
Hôpital saint-Eloi
Montpellier, France, 34295
4
CHU Nancy - Hôpital Brabois
Nancy, France, 54000