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Hyperthermic Isolated Limb Perfusion With Low-Dose Tumor Necrosis Factor-α and Melphalan for Bulky In-Transit Melanoma Metastases.

Authors :
Rossi, Carlo
Foletto, Mirto
Mocellin, Simone
Pilati, Pierluigi
Lise, Mario
Source :
Annals of Surgical Oncology: An Oncology Journal for Surgeons; Feb2004, Vol. 11 Issue 2, p173-177, 5p
Publication Year :
2004

Abstract

Background: Melphalan (L-PAM) hyperthermic isolated limb perfusion (HILP) is currently considered the standard treatment for patients with in-transit metastases from cutaneous melanoma. We here report on the results of L-PAM and low-dose tumor necrosis factor (TNF)α HILP in patients with bulky disease. Methods: Twenty patients underwent TNFα (1 mg) and L-PAM (10 mg/L) HILP. Perfusion was performed for 90 minutes, and systemic leakage was strictly monitored. Locoregional toxicity was evaluated according to Wieberdink’s criteria, whereas tumor response was evaluated with physical examination and ultrasound scan with or without fine-needle aspiration of any suspected recurrence. Results: In all cases, systemic leakage was <5%. No postoperative deaths occurred, and locoregional toxicity was mild (grade 1 or 2) in 95% of patients. A complete tumor response was obtained in 14 patients (70%), and partial responses were obtained in 5 patients (25%). After a median follow-up of 18 months, six patients are alive and disease free, seven are alive with local or distant recurrence or both, and seven have died of disease. Conclusions: Low-dose TNFα HILP can achieve tumor responses comparable with those reported with higher doses of cytokine. Moreover, this drug regimen is associated with acceptable local toxicity, carries a smaller risk of systemic toxicity, and incurs lower costs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10689265
Volume :
11
Issue :
2
Database :
Complementary Index
Journal :
Annals of Surgical Oncology: An Oncology Journal for Surgeons
Publication Type :
Academic Journal
Accession number :
49874498
Full Text :
https://doi.org/10.1245/ASO.2004.03.019