Literature DB >> 22699779

Chemosaturation with percutaneous hepatic perfusion for unresectable isolated hepatic metastases from sarcoma.

Jeremiah L Deneve1, Junsung Choi, Ricardo J Gonzalez, Anthony P Conley, Steven Stewart, Dale Han, Philip Werner, Tariq A Chaudhry, Jonathan S Zager.   

Abstract

PURPOSE: Treatment of patients with unresectable liver metastases is challenging. Regional therapies to the liver have been developed that maximize treatment of the localized disease process without systemic toxic adverse effects. We discuss the procedural aspects of liver chemosaturation with percutaneous hepatic perfusion (CS-PHP).
METHODS: We present as an illustration of this technique a case report of the treatment of unresectable metastatic leiomyosarcoma of the liver.
RESULTS: A randomized phase III trial for unresectable liver metastases from melanoma was recently completed comparing CS-PHP with melphalan vs. best alternative care (BAC). When compared with BAC, CS-PHP was associated with a significant improvement in hepatic progression-free survival (8.0 months CS-PHP vs. 1.6 months BAC, p < 0.0001) and overall progression-free survival (6.7 months CS-PHP vs. 1.6 months BAC, p < 0.0001), respectively. On the basis of these results, and given our experience as one of the treating institutions for this phase III trial, we appealed for compassionate use of CS-PHP in a patient with isolated bilobar unresectable hepatic metastases from leiomyosarcoma. Four target lesions were identified and monitored to assess treatment response. A total of 4 CS-PHP procedures were performed, with a 25 % reduction in size of the largest lesion observed and 16 month hepatic progression-free survival. Toxicity was mild (neutropenia) and manageable on an outpatient basis.
CONCLUSION: CS-PHP offers several advantages for unresectable hepatic sarcoma metastases. CS-PHP is minimally invasive and repeatable, and it has a predictable and manageable systemic toxicity profile. For appropriately selected patients, CS-PHP can delay tumor progression and could potentially improve survival.

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Year:  2012        PMID: 22699779     DOI: 10.1007/s00270-012-0425-x

Source DB:  PubMed          Journal:  Cardiovasc Intervent Radiol        ISSN: 0174-1551            Impact factor:   2.740


  5 in total

1.  Percutaneous Hepatic Perfusion (PHP) with Melphalan as a Treatment for Unresectable Metastases Confined to the Liver.

Authors:  Eleonora M de Leede; Mark C Burgmans; Christian H Martini; Fred G J Tijl; Arian R van Erkel; Jaap Vuyk; Ellen Kapiteijn; Cornelis Verhoef; Cornelis J H van de Velde; Alexander L Vahrmeijer
Journal:  J Vis Exp       Date:  2016-07-31       Impact factor: 1.355

2.  Endovascular Ion Exchange Chemofiltration Device Reduces Off-Target Doxorubicin Exposure in a Hepatic Intra-arterial Chemotherapy Model.

Authors:  Colin Yee; David McCoy; Jay Yu; Aaron Losey; Caroline Jordan; Terilyn Moore; Carol Stillson; Hee Jeung Oh; Bridget Kilbride; Shuvo Roy; Anand Patel; Mark W Wilson; Steven W Hetts
Journal:  Radiol Imaging Cancer       Date:  2019-09-27

3.  Chemosaturation with percutaneous hepatic perfusion for unresectable metastatic melanoma or sarcoma to the liver: a single institution experience.

Authors:  Meghan R Forster; Omar M Rashid; Matthew C Perez; Junsung Choi; Tariq Chaudhry; Jonathan S Zager
Journal:  J Surg Oncol       Date:  2013-11-19       Impact factor: 3.454

Review 4.  Chemosaturation Percutaneous Hepatic Perfusion: A Systematic Review.

Authors:  Arndt Vogel; Sanjay Gupta; Martin Zeile; Rebecca von Haken; Roland Brüning; Gösta Lotz; Alexander Vahrmeijer; Thomas Vogl; Frank Wacker
Journal:  Adv Ther       Date:  2016-10-31       Impact factor: 3.845

Review 5.  Intra-arterial perfusion-based therapies for regionally metastatic cutaneous and uveal melanoma.

Authors:  Kristy K Broman; Jonathan S Zager
Journal:  Melanoma Manag       Date:  2019-09-02
  5 in total

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