Literature DB >> 21892710

Hypoxic liver perfusion with mitomycin-C for treating multifocal metastases and unresectable primary tumours: a single-centre series of 42 patients.

A Bagliani1, A Baggiani, A M Ierardi, B Caspani, F Motta, D Toniolo, P Belloni, E Setola, E Campagnoli, S Tempini, R Crocchiolo, M Bregni, L Belli.   

Abstract

PURPOSE: The purpose of our study was to retrospectively evaluate the feasibility, toxicity and impact on overall (OS) and disease-free (DFS) survival of intra-arterial liver perfusion with mitomycin-C (MMC) [hypoxic liver perfusion with MMC (HLPM)] in patients with multifocal liver metastases or with unresectable primary liver tumours.
MATERIALS AND METHODS: Forty-two patients underwent 56 intra-arterial liver infusions with MMC between June 2001 and May 2009. The patients presented specific characteristics, i.e. they were all refractory to locoregional (LR) and/or systemic treatments. HLPM consists of selective catheterisation of the common hepatic artery, permanent occlusion of the gastroduodenal artery at its origin using metal coils, an inflated balloon catheter placement at the origin of the proper hepatic artery to block blood flow and induce hypoxia for around 10 min, MMC infusion and vascular-bed occlusion through injection of an absorbable haemostatic agent. During the procedure, the patients received anaesthesiological monitoring. Biochemical and morphological responses were evaluated, as were haematological, hepatic and systemic toxicity.
RESULTS: Patients were hospitalised for 10 days on average (range 7-15). Side effects were liver toxicity in all cases, acute pancreatitis in one case and liver failure in one case. Computed tomography performed at 30 days documented a partial response (PR) in 29%, stable disease (SD) in 45% and progressive disease (PD) in 26% of patients. The response lasted 4 months on average (range 3-6). Mean overall survival (OS) was 20 months for all patients, reaching 30 months in those with colorectal carcinoma.
CONCLUSIONS: The procedure is feasible, and treatmentrelated toxicity and mortality rates are acceptable. It may be considered a palliative treatment option in patients with advanced liver disease in centres with adequately experienced medical teams.

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Year:  2011        PMID: 21892710     DOI: 10.1007/s11547-011-0724-3

Source DB:  PubMed          Journal:  Radiol Med        ISSN: 0033-8362            Impact factor:   3.469


  14 in total

Review 1.  Colorectal liver metastases: regional chemotherapy via transarterial chemoembolization (TACE) and hepatic chemoperfusion: an update.

Authors:  Thomas J Vogl; Stephan Zangos; Katrin Eichler; Danny Yakoub; Mohamed Nabil
Journal:  Eur Radiol       Date:  2006-08-30       Impact factor: 5.315

2.  Stop-flow perfusion with mitomycin-C as locoregional approach in the treatment of large-unresectable liver metastases.

Authors:  C Gadaleta; A Catino; V Mattioli
Journal:  In Vivo       Date:  2006 Nov-Dec       Impact factor: 2.155

Review 3.  Surgical resection versus non-surgical treatment for hepatic node positive patients with colorectal liver metastases.

Authors:  Kurinchi Selvan Gurusamy; Rajarajan Ramamoorthy; Charles Imber; Brian R Davidson
Journal:  Cochrane Database Syst Rev       Date:  2010-01-20

4.  [Antiblastic locoregional perfusion with control of the aorto-caval flow: technique of percutaneous access].

Authors:  S Ricci; G Rossi; R Roversi; G Cavallo; M Romanelli; M Roversi; G Fiorentini
Journal:  Radiol Med       Date:  1997-03       Impact factor: 3.469

5.  Toxicity and response criteria of the Eastern Cooperative Oncology Group.

Authors:  M M Oken; R H Creech; D C Tormey; J Horton; T E Davis; E T McFadden; P P Carbone
Journal:  Am J Clin Oncol       Date:  1982-12       Impact factor: 2.339

6.  Hypoxic stop-flow perfusion with mitomycin-C in the treatment of multifocal liver metastases. Usefulness of a vascular arterial stent to prevent iatrogenic lesions of the hepatic arterial wall.

Authors:  C D Gadaleta; A Catino; G Ranieri; F Armenise; G Console; V Mattioli
Journal:  J Exp Clin Cancer Res       Date:  2003-12

7.  Phase III trial of infusional fluorouracil, leucovorin, oxaliplatin, and irinotecan (FOLFOXIRI) compared with infusional fluorouracil, leucovorin, and irinotecan (FOLFIRI) as first-line treatment for metastatic colorectal cancer: the Gruppo Oncologico Nord Ovest.

Authors:  Alfredo Falcone; Sergio Ricci; Isa Brunetti; Elisabetta Pfanner; Giacomo Allegrini; Cecilia Barbara; Lucio Crinò; Giovanni Benedetti; Walter Evangelista; Laura Fanchini; Enrico Cortesi; Vincenzo Picone; Stefano Vitello; Silvana Chiara; Cristina Granetto; Gianfranco Porcile; Luisa Fioretto; Cinzia Orlandini; Michele Andreuccetti; Gianluca Masi
Journal:  J Clin Oncol       Date:  2007-05-01       Impact factor: 44.544

8.  [Antiblastic hypoxic stop-flow perfusion in the treatment of liver metastasis: preliminary results].

Authors:  R Roversi; G Cavallo; S Ricci; G Rossi; M Roversi; G Fiorentini
Journal:  Radiol Med       Date:  1997-04       Impact factor: 3.469

9.  Cancer statistics, 2003.

Authors:  Ahmedin Jemal; Taylor Murray; Alicia Samuels; Asma Ghafoor; Elizabeth Ward; Michael J Thun
Journal:  CA Cancer J Clin       Date:  2003 Jan-Feb       Impact factor: 508.702

10.  Transarterial chemoembolisation (TACE) using irinotecan-loaded beads for the treatment of unresectable metastases to the liver in patients with colorectal cancer: an interim report.

Authors:  Robert Cg Martin; Ken Robbins; Dana Tomalty; Ryan O'Hara; Petar Bosnjakovic; Radek Padr; Miloslav Rocek; Frantisek Slauf; Alexander Scupchenko; Cliff Tatum
Journal:  World J Surg Oncol       Date:  2009-11-03       Impact factor: 2.754

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