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

被引:52
作者
Chiarion-Sileni, V. [1 ]
Pigozzo, J. [1 ]
Ascierto, P. A. [2 ]
Simeone, E. [2 ]
Maio, M. [3 ]
Calabro, L. [3 ]
Marchetti, P. [4 ,5 ]
De Galitiis, F. [4 ]
Testori, A. [6 ]
Ferrucci, P. F. [7 ]
Queirolo, P. [8 ]
Spagnolo, F. [8 ]
Quaglino, P. [9 ]
Schianca, F. Carnevale [10 ]
Mandala, M. [11 ]
Di Guardo, L. [12 ]
Del Vecchio, M. [12 ]
机构
[1] IRCCS, Veneto Inst Oncol IOV, Melanoma Canc Unit, I-35128 Padua, Italy
[2] Fdn G Pascale, Ist Nazl Tumori, Melanoma Canc Immunotherapy & Innovat Therapy Uni, I-80131 Naples, Italy
[3] Univ Hosp Siena, Ist Toscano Tumori, Med Oncol & Immunotherapy Unit, I-53100 Siena, Italy
[4] IRCCS, Dermopath Inst Immaculate IDI, I-00167 Rome, Italy
[5] Sapienza Univ Rome, St Andrea Hosp, I-00189 Rome, Italy
[6] Ist Europeo Oncol, Div Melanoma, I-20141 Milan, Italy
[7] Ist Europeo Oncol, Oncol Melanoma Unit, I-20141 Milan, Italy
[8] San Martino Hosp, Natl Inst Canc Res, Dept Med Oncol A, I-16132 Genoa, Italy
[9] Univ Turin, Dept Med Sci, Dermatol Clin, I-10126 Turin, Italy
[10] Piedmont Oncol Fdn, IRCC, Inst Canc Res & Treatment, Div Med Oncol, I-10060 Candiolo, Italy
[11] Papa Giovanni XXIII Hosp, Unit Med Oncol, I-24127 Bergamo, Italy
[12] Fdn IRCCS, Ist Nazl Tumori, Dept Med Oncol, I-20133 Milan, Italy
关键词
melanoma; ipilimumab; expanded access; retreatment; treatment outcome; safety; disease control; PHASE-II; CANCER-IMMUNOTHERAPY; METASTATIC MELANOMA; ADVERSE EVENTS; IV MELANOMA; THERAPY; EFFICACY; PROGRESSION; GUIDELINES; MANAGEMENT;
D O I
10.1038/bjc.2014.126
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: 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 3mg kg(-1) among patients participating in an expanded access programme in Italy. Methods: Patients who achieved disease control during induction therapy were retreated with ipilimumab upon progression (3mgkg(-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. Results: 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. Conclusions: 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.
引用
收藏
页码:1721 / 1726
页数:6
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