Literature DB >> 25296896

Isolated limb perfusion using tumour necrosis factor α and melphalan in patients with advanced aggressive fibromatosis.

D L M van Broekhoven1, J P Deroose, S Bonvalot, A Gronchi, D J Grünhagen, A M M Eggermont, C Verhoef.   

Abstract

BACKGROUND: Aggressive fibromatoses (desmoid tumours) may be locally aggressive, but do not metastasize. Although a conservative approach is advocated for most patients, pain and functional impairment are indications for active treatment. Tumour necrosis factor (TNF) α and melphalan-based isolated limb perfusion (TM-ILP) is a limb-saving treatment modality for soft tissue tumours. This study reports the results of TM-ILP treatment in patients with aggressive fibromatosis.
METHODS: Institutional databases of three European centres were searched. All patients who received TM-ILP treatment for aggressive fibromatosis between 1990 and 2012 were included. Before therapy, the patients were discussed at multidisciplinary tumour board meetings.
RESULTS: Twenty-five patients received 28 TM-ILP treatments. The median age of patients was 28 (i.q.r. 19-34) years and median hospital stay was 8 (7-12) days. Median follow-up was 84 (34-114) months. A complete response was achieved after two TM-ILP treatments, and a partial response after 17 treatments in 16 patients. Stable disease was reported after eight treatments in seven patients, including a patient with stable disease after the first treatment and progression after the second TM-ILP. Toxicity was modest after most treatments; Wieberdink grade IV (extensive epidermolysis, and threatening or manifest compartment syndrome) was seen after two TM-ILP treatments. Systemic leakage was reported after one treatment, but did not lead to systemic toxicity. Functional outcome was good; 16 patients had no physical limitations, and six patients had some limitations but did not need medical aids. Amputation was prevented in all but three patients.
CONCLUSION: TNF-α-based ILP is effective in patients with aggressive fibromatosis.
© 2014 BJS Society Ltd. Published by John Wiley & Sons Ltd.

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Year:  2014        PMID: 25296896     DOI: 10.1002/bjs.9659

Source DB:  PubMed          Journal:  Br J Surg        ISSN: 0007-1323            Impact factor:   6.939


  7 in total

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Authors:  Marco Fiore; Aimee Crago; Rebecca Gladdy; Bernd Kasper
Journal:  Ann Surg Oncol       Date:  2021-01-01       Impact factor: 5.344

2.  A Novel Method to Treat Progressive Desmoid Tumors Involving Neurovascular Bundles: A Retrospective Cohort Study.

Authors:  Jun-Qiang Yin; Yi-Wei Fu; Zhen-Hua Gao; Chang-Ye Zou; Xian-Biao Xie; Bo Wang; Zhi-Hai Zhong; Gang Huang; Jing-Nan Shen
Journal:  Neurosurgery       Date:  2021-05-13       Impact factor: 4.654

3.  Time trends in the incidence and treatment of extra-abdominal and abdominal aggressive fibromatosis: a population-based study.

Authors:  Danique L M van Broekhoven; Dirk J Grünhagen; Michael A den Bakker; Thijs van Dalen; Cornelis Verhoef
Journal:  Ann Surg Oncol       Date:  2015-06-05       Impact factor: 5.344

4.  EXTRA-ABDOMINAL DESMOID TUMOR: ANALYSIS OF 23 CONSECUTIVE CASES IN A SINGLE INSTITUTION.

Authors:  Juan Pablo Zumárraga; Brian Guilherme Monteiro Marta Coimbra; Felipe Gonçalves Dos Santos; André Mathias Baptista; Marcelo Tomio Kohara; Olavo Pires de Camargo
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Review 5.  Management of aggressive fibromatosis.

Authors:  Zhijun Zhang; Jian Shi; Tao Yang; Tongjun Liu; Kai Zhang
Journal:  Oncol Lett       Date:  2020-11-17       Impact factor: 2.967

Review 6.  Desmoid Tumors Characteristics, Clinical Management, Active Surveillance, and Description of Our FAP Case Series.

Authors:  Lupe Sanchez-Mete; Virginia Ferraresi; Mauro Caterino; Aline Martayan; Irene Terrenato; Elena Mannisi; Vittoria Stigliano
Journal:  J Clin Med       Date:  2020-12-11       Impact factor: 4.241

Review 7.  An update on the management of sporadic desmoid-type fibromatosis: a European Consensus Initiative between Sarcoma PAtients EuroNet (SPAEN) and European Organization for Research and Treatment of Cancer (EORTC)/Soft Tissue and Bone Sarcoma Group (STBSG).

Authors:  B Kasper; C Baumgarten; J Garcia; S Bonvalot; R Haas; F Haller; P Hohenberger; N Penel; C Messiou; W T van der Graaf; A Gronchi
Journal:  Ann Oncol       Date:  2017-10-01       Impact factor: 32.976

  7 in total

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