Retreatment with ipilimumab has been shown to re-establish disease control in some patients with disease progression. Here, we report the efficacy and safety of retreatment with ipilimumab 3 mg kg(-1) among patients participating in an expanded access programme in Italy.Patients who achieved disease control during induction therapy were retreated with ipilimumab upon progression (3 mg kg(-1) every 3 weeks for up to four doses), providing they had not experienced toxicity that precluded further dosing. Tumour assessments were conducted after retreatment, and patients were monitored throughout for adverse events.Of 855 patients treated with ipilimumab, 51 were retreated upon disease progression. Of these, 28 (55\%) regained disease control upon retreatment and 42\% were alive 2 years after the first induction dose of ipilimumab; median overall survival was 21 months. Eleven patients (22\%) had a treatment-related adverse event of any grade during retreatment. These were generally mild-to-moderate and resolved within a median of 4 days. No new types of toxicity were reported.For patients who meet predefined criteria, retreatment with ipilimumab is generally well tolerated and can translate into clinical benefit. This strategy should be compared with other therapeutic options in randomised controlled trials.

Ipilimumab retreatment in patients with pretreated advanced melanoma: the expanded access programme in Italy / V., Chiarion Sileni; J., Pigozzo; P. A., Ascierto; E., Simeone; M., Maio; L., Calabrò; Marchetti, Paolo; F. D., Galitiis; A., Testori; P. F., Ferrucci; P., Queirolo; F., Spagnolo; P., Quaglino; F. C., Schianca; M., Mandalà; L. D., Guardo; M. D., Vecchio. - In: BRITISH JOURNAL OF CANCER. - ISSN 0007-0920. - ELETTRONICO. - 110:(2014), pp. 1721-1726. [10.1038/bjc.2014.126]

Ipilimumab retreatment in patients with pretreated advanced melanoma: the expanded access programme in Italy.

MARCHETTI, PAOLO;
2014

Abstract

Retreatment with ipilimumab has been shown to re-establish disease control in some patients with disease progression. Here, we report the efficacy and safety of retreatment with ipilimumab 3 mg kg(-1) among patients participating in an expanded access programme in Italy.Patients who achieved disease control during induction therapy were retreated with ipilimumab upon progression (3 mg kg(-1) every 3 weeks for up to four doses), providing they had not experienced toxicity that precluded further dosing. Tumour assessments were conducted after retreatment, and patients were monitored throughout for adverse events.Of 855 patients treated with ipilimumab, 51 were retreated upon disease progression. Of these, 28 (55\%) regained disease control upon retreatment and 42\% were alive 2 years after the first induction dose of ipilimumab; median overall survival was 21 months. Eleven patients (22\%) had a treatment-related adverse event of any grade during retreatment. These were generally mild-to-moderate and resolved within a median of 4 days. No new types of toxicity were reported.For patients who meet predefined criteria, retreatment with ipilimumab is generally well tolerated and can translate into clinical benefit. This strategy should be compared with other therapeutic options in randomised controlled trials.
2014
Adult, Aged, Aged; 80 and over, Antibodies; Monoclonal; therapeutic use, Disease Progression, Female, Health Plan Implementation, Health Services Accessibility, Humans, Immunotherapy; methods, Italy, Male, Melanoma; mortality/pathology/therapy, Middle Aged, Program Development, Remission Induction, Retreatment, Skin Neoplasms; mortality/pathology/therapy, Survival Analysis, Young Adult
01 Pubblicazione su rivista::01a Articolo in rivista
Ipilimumab retreatment in patients with pretreated advanced melanoma: the expanded access programme in Italy / V., Chiarion Sileni; J., Pigozzo; P. A., Ascierto; E., Simeone; M., Maio; L., Calabrò; Marchetti, Paolo; F. D., Galitiis; A., Testori; P. F., Ferrucci; P., Queirolo; F., Spagnolo; P., Quaglino; F. C., Schianca; M., Mandalà; L. D., Guardo; M. D., Vecchio. - In: BRITISH JOURNAL OF CANCER. - ISSN 0007-0920. - ELETTRONICO. - 110:(2014), pp. 1721-1726. [10.1038/bjc.2014.126]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/760633
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