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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01775267
Other study ID # USZ-ZH-VIS-ALPPS
Secondary ID
Status Terminated
Phase Phase 2
First received January 22, 2013
Last updated June 8, 2015
Start date November 2012
Est. completion date November 2015

Study information

Verified date June 2015
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: SwissmedicUnited States: Food and Drug AdministrationArgentina: Ministry of Health
Study type Interventional

Clinical Trial Summary

This randomized phase II trial compares how well associating liver partition with portal vein ligation for staged hepatectomy (ALPPS) or portal vein occlusion (PVO) works in treating patients with liver cancer. Both treatments are types of 2-stage hepatectomies for removing liver cancer. ALPPS may be more effective than PVO in patients whose disease would traditionally be considered inoperable.

- Trial with surgical intervention


Recruitment information / eligibility

Status Terminated
Enrollment 7
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria: •Patient may have primary or secondary hepatic malignancies with a FLR/TLV < 30% or a FLR/BW ratio of < 0.5 for patients with normal liver function (defined as normal transaminases, normal bilirubin, normal factor V, and normal PT/INR). In case of injury due to chemotherapy, known high grade steatosis, or cholestasis > 50 mmol/L, patient may be enrolled into the trial if FLR/TLV is < 40% or FLR/BW ratio < 0.8.

- Patient must have extensive liver tumors that would require portal vein embolization or a two-stage hepatectomy and portal vein embolization or ligation by the judgment of surgeons in the tumor board.

- Patient may have extrahepatic disease as long as it may be addressed after liver surgery and there is a tumor board decision to proceed with liver resection (mostly applicable to CRC metastases).

- Patient may have received previous chemotherapy.

- In cases of cholestasis, preoperative drainage procedures (PTC or ERCP) are left up to judgement of physicians.

- Patient must be = 18 years of age. The patient population over 65 years old needs to be carefully included based on comorbidities.

- Patient may have undergone previous liver resection.

- Patient's location must be such that proper staging and follow-up may be performed.

- Patient's case must be presented at the Multidisciplinary Meeting attended by hepatobiliary surgeons, oncologists, hepatologists, and radiologists, or must be approved directly by Dr. Strasberg or Dr. Chapman.

Exclusion criteria: •Patient must not have any significant concomitant diseases rendering him/her unsuitable for major liver surgery by the judgment of the physicians involved, especially if the patient is > 65 years old.

- Patient must not have enrolled into a clinical trial within 4 weeks of study entry.

- Patient must not have peritoneal carcinomatosis or other extensive extrahepatic disease.

- Patient must not have advanced stages of carcinoma of the gallbladder (T3/T4)

- Patient must not have issues such as drug and/or alcohol abuse.

- Patient must not need major extrahepatic surgery (e.g. pancreas resection, gastric resection, rectal surgery) within 3 months of study entry.

- Patient must not be a candidate for liver transplantation in case of HCC.

- Patient must not be pregnant or breastfeeding. If a female of childbearing potential, patient must have a negative pregnancy test within 14 days of enrollment.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Associating liver partition and portal vein ligation for staged hepatectomy

Portal vein embolization or ligation


Locations

Country Name City State
Argentina Italian Hospital, Department of Surgery, Division of HPB surgery and Liver Transplatn Unit Buenos Aires
Switzerland University Hospital Zurich, Division of Visceral and Transplant Surgery Zurich ZH
United States Washington University St. Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Countries where clinical trial is conducted

United States,  Argentina,  Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Liver free of tumors [ Time Frame: At 3 months ] [ Designated as safety issue: No ] 2012 to 2015 No
Secondary rate of hypertrophy over time 2012 to 2015 No
Secondary Complications of treatment 2012-2015 Yes
Secondary Progression of disease Progression free survival 2012-2015 No
Secondary Postoperative liver and renal function 2012 to 2015 Yes