scholarly journals Isolated limb perfusion with melphalan activates interferon-stimulated genes to induce tumor regression in patients with melanoma in-transit metastasis

2019 ◽  
Vol 9 (1) ◽  
pp. 1684126 ◽  
Author(s):  
Junko Johansson ◽  
Roberta Kiffin ◽  
Ebru Aydin ◽  
Malin S. Nilsson ◽  
Kristoffer Hellstrand ◽  
...  
Author(s):  
Flavia Brunstein ◽  
Dirk J. Grünhagen ◽  
Timo ten Hagen ◽  
Alexander M. M. Eggermont

2016 ◽  
Vol 23 (7) ◽  
pp. 2330-2335 ◽  
Author(s):  
Lesly A. Dossett ◽  
Ilan Ben-Shabat ◽  
Roger Olofsson Bagge ◽  
Jonathan S. Zager

2008 ◽  
Vol 15 (8) ◽  
pp. 2195-2205 ◽  
Author(s):  
Georgia M. Beasley ◽  
Rebecca P. Petersen ◽  
Jin Yoo ◽  
Nicole McMahon ◽  
Thomas Aloia ◽  
...  

2008 ◽  
Vol 15 (4) ◽  
pp. 1218-1223 ◽  
Author(s):  
Carlo Riccardo Rossi ◽  
Francesco Russano ◽  
Simone Mocellin ◽  
Vanna Chiarion-Sileni ◽  
Mirto Foletto ◽  
...  

2010 ◽  
Vol 28 (1) ◽  
pp. 114-118 ◽  
Author(s):  
H. Richard Alexander ◽  
Douglas L. Fraker ◽  
David L. Bartlett ◽  
Steven K. Libutti ◽  
Seth M. Steinberg ◽  
...  

Purpose In-transit disease afflicts approximately 10% of patients with extremity melanoma; no single treatment approach has been uniformly accepted as the most effective. We report long-term outcomes in patients with in-transit extremity melanoma who underwent isolated limb perfusion (ILP) in an era of increasingly accurate staging, uniform operative and treatment conditions, and regular long-term follow-up. Patients and Methods Between May 1992 and February 2005, 91 patients (median age, 57 years; 50 women, 41 men) underwent a 90-minute hyperthermic ILP (melphalan, 10 to 13 mg/L limb volume, tumor necrosis factor [TNF; n = 44], or interferon [n = 38]) using uniform operative technique and intraoperative leak monitoring. Patients were prospectively followed for response, in-field progression-free survival (PFS), and overall survival (OS). Parameters associated with in-field PFS and OS were analyzed by standard statistical methods. Results There was one operative death (1.1%). There were 62 complete responses (69%) and 23 partial responses (26%) in 90 assessable patients. At a median potential follow-up of 11 years, median in-field PFS was 12.4 months and median OS was 47.4 months; 5 and 10-year actuarial OS probabilities were 43% and 34%, respectively. Female sex and low tumor burden (≤ 20 lesions) were associated with prolonged in-field PFS (male:female hazard ratio [HR], 2.07; 95% CI, 1.27 to 3.38; 21+ v ≤ 20 tumors HR, 2.29; 95% CI, 1.21 to 4.34; P < .011 for both). Female sex was associated with improved OS (P = .027; male:female HR, 1.82; 95% CI, 1.07 to 3.09). Conclusion In appropriately selected patients, ILP has clinical benefit. The use of TNF was not associated with improved in-field PFS, while female sex was associated with better survival.


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