Efficacy and safety of ipilimumab in elderly patients with pretreated advanced melanoma treated at Italian centres through the expanded access programme

被引:90
作者
Sileni, Vanna Chiarion [1 ]
Pigozzo, Jacopo [1 ]
Ascierto, Paolo Antonio [2 ]
Grimaldi, Antonio Maria [2 ]
Maio, Michele [3 ]
Di Guardo, Lorenza [4 ]
Marchetti, Paolo [5 ,6 ]
de Rosa, Francesco [7 ]
Nuzzo, Carmen [8 ]
Testori, Alessandro [9 ]
Cocorocchio, Emilia [10 ]
Bernengo, Maria Grazia [11 ]
Guida, Michele [12 ]
Marconcini, Riccardo [13 ]
Merelli, Barbara [14 ]
Parmiani, Giorgio [15 ]
Rinaldi, Gaetana [16 ]
Aglietta, Massimo [17 ,18 ]
Grosso, Marco [19 ]
Queirolo, Paola [19 ]
机构
[1] Oncol Inst Veneto IRCCS, Melanoma Canc Unit, I-35128 Padua, Italy
[2] Ist Nazl Tumori Fdn G Pascale, Unit Melanoma Canc Immunotherapy & Innovat Thera, Naples, Italy
[3] Univ Hosp, Ist Toscano Tumori, Med Oncol & Immunotherapy Div, Siena, Italy
[4] Natl Canc Inst, I-20133 Milan, Italy
[5] IRCCS, Dermopath Inst Immaculate IDI, Rome, Italy
[6] Univ Sapienza, St Andreas Hosp, Rome, Italy
[7] Romagna Natl Canc Inst, Immunotherapy Unit, Meldola, Italy
[8] Regina Elena Inst Canc Res, Dept Med Oncol A, Rome, Italy
[9] Ist Europeo Oncol, Div Melanoma & Sarcomi Muscolo Cutanei, Milan, Italy
[10] Ist Europeo Oncol, Melanoma Med Oncol Div, Milan, Italy
[11] Univ Hosp St John Baptist, Turin, Italy
[12] Natl Canc Res Ctr Giovanni Paolo II, Dept Med Oncol, Bari, Italy
[13] Univ Hosp Pisa, Gathered Hosp Santa Chiara, Pisa, Italy
[14] Papa Giovanni XXIII Hosp, Dept Haematol & Oncol, Unit Clin & Translat Res, Bergamo, Italy
[15] Hosp San Raffaele, Unit Immunobiotherapy Melanoma, I-20132 Milan, Italy
[16] Paolo Giaccone Polyclin Univ Hosp, Palermo, Italy
[17] Piedmont Oncol Fdn, Inst Canc Res & Treatment, Candiolo, Italy
[18] Univ Turin, Turin, Italy
[19] Natl Inst Canc Res, Genoa, Italy
关键词
Melanoma; Ipilimumab; Expanded access; Elderly patients; Treatment outcome; Safety; ADVERSE EVENTS; IMMUNE; AGE;
D O I
10.1186/1756-9966-33-30
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Elderly patients with metastatic melanoma have different disease characteristics and a poorer prognosis than younger patients. Data from clinical trials and expanded access programmes (EAPs) suggest ipilimumab confers a consistent survival benefit and has a similar safety profile across different age groups of patients with metastatic melanoma. Here we report the efficacy and safety of ipilimumab 3 mg/kg in elderly patients enrolled in an EAP in Italy. Methods: Patients aged > 70 years with pretreated melanoma received ipilimumab 3 mg/kg every 3 weeks for four doses through an EAP. Tumour response was evaluated at baseline and after completion of induction therapy using immune-related response criteria and patients were monitored throughout the treatment period for adverse events (AEs), including immune-related AEs. Results: The immune-related disease control rate among 188 evaluable patients was 38%, including four patients with an immune-related complete response, 24 with an immune-related partial response and 44 with immune-related stable disease. Median progression-free survival (PFS) was 4.0 months and the 1-and 2-year PFS rates were 21% and 12%, respectively. Median overall survival (OS) was 8.9 months; 1- and 2-year OS rates were 38% and 22%, respectively. The safety profile of ipilimumab was consistent with that observed in the general population of the Italian EAP and treatment-related AEs generally resolved within a median of 2 weeks with treatment as per protocol-specific guidelines. Conclusions: These results suggest ipilimumab is a feasible treatment option in elderly patients with metastatic melanoma. Ipilimumab treatment was generally well tolerated and resulted in clinical benefit and extended survival in elderly patients treated at centres in Italy.
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页数:7
相关论文
共 34 条
[1]   Never too old?: Age should not be a barrier to enrollment in cancer clinical trials [J].
Aapro, MS ;
Köhne, CH ;
Cohen, HJ ;
Extermann, M .
ONCOLOGIST, 2005, 10 (03) :198-204
[2]  
[Anonymous], MEDSCAPE MULTISPECIA
[3]  
[Anonymous], SEER CANC STAT REV 1
[4]  
[Anonymous], ANN ONCOL S9
[5]  
[Anonymous], TREATMENT PATIENTS P
[6]  
[Anonymous], ANN ONCOL S8
[7]  
[Anonymous], J CLIN ONCOL S
[8]  
[Anonymous], ANN ONCOL S9
[9]  
[Anonymous], J CLIN ONCOL S
[10]  
[Anonymous], J CLIN ONCOL S