TNF-Based Isolated Limb Perfusion Followed by Consolidation Biotherapy with Systemic Low-dose Interferon Alpha 2b in Patients with In-transit Melanoma Metastases: A Pilot Trial

• Published in: Annals of surgical oncology 2008-04, Vol.15 (4), p.1218-1223
• Main Authors: Rossi, Carlo Riccardo, Russano, Francesco, Mocellin, Simone, Chiarion-Sileni, Vanna, Foletto, Mirto, Pilati, Pierluigi, Campana, Luca G., Zanon, Antonio, Picchi, Gian Franco, Lise, Mario, Nitti, Donato
• Format: Article
• Language: English
• Subjects: Adult; Aged; Antineoplastic Agents - administration & dosage; Chemotherapy, Cancer, Regional Perfusion; Female; Humans; Injections, Subcutaneous; Interferon-alpha - administration & dosage; Male; Medicine; Medicine & Public Health; Melanoma - drug therapy; Melanoma - secondary; Melanomas; Melphalan - administration & dosage; Middle Aged; Oncology; Pilot Projects; Recombinant Proteins; Skin Neoplasms - drug therapy; Skin Neoplasms - pathology; Surgery; Surgical Oncology; Tumor Necrosis Factor-alpha - administration & dosage
• ISSN: 1068-9265; 1534-4681
• DOI: 10.1245/s10434-007-9791-z

Background Tumor necrosis factor (TNF)-based isolated limb perfusion (ILP) yields high tumor response rates in patients with in-transit melanoma metastases. However, most patients will ultimately experience disease recurrence. The aim of this pilot study was to test the hypothesis that systemic low-dose interferon α-2b (LDI) might consolidate the therapeutic effect of ILP. Methods A total of 12 patients with in-transit melanoma metastases not amenable to surgical excision were given LDI subcutaneously (3 million IU/day, 7 days/week for 12 months) after TNF-based ILP (TNF 1 mg + melphalan (L-PAM) 10 mg/L) (group A). The clinical outcome of these patients was historically compared with that of 19 patients with similar anthropometric and disease characteristics who underwent TNF-based ILP alone (group B). Results In group A, LDI was well tolerated, only grade 2 systemic toxicity being recorded in 50% of patients. The progression-free survival analysis showed a statistically significant advantage for group A patients as compared with group B (median time to progression: 26 and 17 months, respectively; log-rank test P -value: 0.037). This survival benefit was confirmed at multivariate analysis, where treatment was the only prognostic factor retained by the prediction model. The analysis of the risk of disease progression over time suggested that this survival benefit appears to vanish after LDI discontinuation, which further strengthens the hypothesis that LDI might consolidate the therapeutic effect of TNF-based ILP. Conclusions These preliminary findings support the conduction of larger trials to formally assess the ability of LDI to improve the clinical outcome of melanoma patients with in-transit metastases undergoing TNF-based ILP.