tumour lysate
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BMJ Open ◽  
2018 ◽  
Vol 8 (8) ◽  
pp. e021701 ◽  
Author(s):  
Laura Ridolfi ◽  
Francesco de Rosa ◽  
Laura Fiammenghi ◽  
Massimiliano Petrini ◽  
Anna Maria Granato ◽  
...  

IntroductionSurgery is one of the treatments of choice for patients with a single metastasis from melanoma but is rarely curative. Such patients could potentially benefit from consolidation immunotherapy. Vaccination with dendritic cells (DCs) loaded with tumour antigens elicits a tumour-specific immune response. In our experience, patients who developed delayed type hypersensitivity (DTH) after DC vaccination showed a median overall survival (OS) of 22.9 monthsvs4.8 months for DTH-negative cases. A phase II randomised trial showed an advantage OS of a DC vaccine over a tumour cell-based vaccine (2-year OS 72% vs31%, respectively). Given that there is no standard therapy after surgical resection of single metastases, we planned a study to compare vaccination with DCs pulsed with autologous tumour lysate versus follow-up.Methods and analysisThis is a randomised phase II trial in patients with resected stage III/IV melanoma. Assuming a median relapse-free survival (RFS) of 7.0 months for the standard group and 11.7 months for the experimental arm (HR 0.60), with a two-sided tailed alpha of 0.10, 60 patients per arm must be recruited. An interim futility analysis will be performed at 18 months. The DC vaccine, produced in accordance with Good Manufacturing Practice guidelines, consists of autologous DCs loaded with autologous tumour lysate and injected intradermally near lymph nodes. Vaccine doses will be administered every 4 weeks for six vaccinations and will be followed by 3 million unit /day of interleukin-2 for 5 days. Tumour restaging, blood sampling for immunological biomarkers and DTH testing will be performed every 12 weeks.Ethics and disseminationThe protocol, informed consent and accompanying material given to patients were submitted by the investigator to the Ethics Committee for review. The local Ethics Committee and the Italian Medicines Agency approved the protocol (EudraCT code no.2014-005123-27). Results will be published in a peer-reviewed international scientific journal.Trial registration number2014-005123-27.


PLoS ONE ◽  
2016 ◽  
Vol 11 (3) ◽  
pp. e0151008 ◽  
Author(s):  
Veronica Rainone ◽  
Cristina Martelli ◽  
Luisa Ottobrini ◽  
Mara Biasin ◽  
Gemma Texido ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (1) ◽  
pp. e0146622 ◽  
Author(s):  
Veronica Rainone ◽  
Cristina Martelli ◽  
Luisa Ottobrini ◽  
Mara Biasin ◽  
Manuela Borelli ◽  
...  

2014 ◽  
Vol 16 (suppl 2) ◽  
pp. ii33-ii33
Author(s):  
G. Stragliotto ◽  
S. Holm ◽  
L. Adamson ◽  
G. Giraud ◽  
J. I. Henter

2012 ◽  
Vol 14 (4) ◽  
pp. 271-279 ◽  
Author(s):  
Nourredine Himoudi ◽  
Rebecca Wallace ◽  
Kathryn L. Parsley ◽  
Kimberly Gilmour ◽  
Alpha-Umaru Barrie ◽  
...  

2011 ◽  
Vol 106 (1) ◽  
pp. 92-98 ◽  
Author(s):  
S J Win ◽  
D G G McMillan ◽  
F Errington-Mais ◽  
V K Ward ◽  
S L Young ◽  
...  

2009 ◽  
Vol 59 (5) ◽  
pp. 687-695 ◽  
Author(s):  
Matthias May ◽  
Sabine Brookman-May ◽  
Bernd Hoschke ◽  
Christian Gilfrich ◽  
Friederike Kendel ◽  
...  

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