Exposure-Response Relationships of the Efficacy and Safety of Ipilimumab in Patients with Advanced Melanoma

被引:165
作者
Feng, Yan [1 ]
Roy, Amit [1 ]
Masson, Eric [1 ]
Chen, Tai-Tsang [2 ]
Humphrey, Rachel [1 ]
Weber, Jeffrey S. [3 ]
机构
[1] Bristol Myers Squibb Co, Princeton, NJ USA
[2] Bristol Myers Squibb Co, Wallingford, CT USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
关键词
PHASE-II;
D O I
10.1158/1078-0432.CCR-12-3243
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: This retrospective analysis was conducted to characterize ipilimumab exposure-response relationships for measures of efficacy and safety in patients with advanced melanoma. Experimental Design: Data were pooled from 498 patients who received ipilimumab monotherapy at 0.3, 3, or 10 mg/kg in 1 of 4 completed phase II clinical trials. The relationships between steady-state ipilimumab trough concentration (Cminss), complete or partial tumor response (CR or PR), and safety [immune-related adverse events (irAEs)] were described by logistic regression models. The relationship between exposure and overall survival was characterized using a Cox proportional-hazards model. Results: The steady-state trough concentration of ipilimumab was found to be a significant predictor of a CR or PR (P < 0.001). Model-based estimates indicate that the probabilities of a CR or PR at median Cminss for the 0.3, 3, and 10 mg/kg groups were 0.6%, 4.9%, and 11.6%, respectively. Overall survival at the median Cminss for ipilimumab at 0.3 mg/kg was estimated to be 0.85- and 0.58-fold lower relative to that at the median Cminss for 3 and 10 mg/kg, respectively. Model-based estimates indicate that the probabilities of a grade 3 or more irAE at the median Cminss for the 0.3, 3, and 10 mg/kg doses were 3%, 13%, and 24%, respectively. Conclusions: Higher doses of ipilimumab produce greater Cminss that may be associated with increased tumor responses, longer survival, and higher rates of irAEs. The efficacy and safety of ipilimumab at 3 versus 10 mg/kg in patients with advanced melanoma is being evaluated in an ongoing phase III trial. (C) 2013 AACR.
引用
收藏
页码:3977 / 3986
页数:10
相关论文
共 19 条
[1]
Final Version of 2009 AJCC Melanoma Staging and Classification [J].
Balch, Charles M. ;
Gershenwald, Jeffrey E. ;
Soong, Seng-jaw ;
Thompson, John F. ;
Atkins, Michael B. ;
Byrd, David R. ;
Buzaid, Antonio C. ;
Cochran, Alistair J. ;
Coit, Daniel G. ;
Ding, Shouluan ;
Eggermont, Alexander M. ;
Flaherty, Keith T. ;
Gimotty, Phyllis A. ;
Kirkwood, John M. ;
McMasters, Kelly M. ;
Mihm, Martin C., Jr. ;
Morton, Donald L. ;
Ross, Merrick I. ;
Sober, Arthur J. ;
Sondak, Vernon K. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (36) :6199-6206
[2]
ClinicalTrials.gov, PHAS 3 TRIAL SUBJ ME
[3]
Model-based evaluation of ipilimumab dosage regimen in patients with advanced melanoma [J].
Dai, D. ;
Wu, C. ;
Parker, S. M. ;
Jure-Kunkel, M. N. ;
Pfister, M. ;
Berman, D. ;
Roy, A. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (15)
[4]
A prospective phase II trial exploring the association between tumor microenvironment biomarkers and clinical activity of ipilimumab in advanced melanoma [J].
Hamid, Omid ;
Schmidt, Henrik ;
Nissan, Aviram ;
Ridolfi, Laura ;
Aamdal, Steinar ;
Hansson, Johan ;
Guida, Michele ;
Hyams, David M. ;
Gomez, Henry ;
Bastholt, Lars ;
Chasalow, Scott D. ;
Berman, David .
JOURNAL OF TRANSLATIONAL MEDICINE, 2011, 9
[5]
Improved Survival with Ipilimumab in Patients with Metastatic Melanoma [J].
Hodi, F. Stephen ;
O'Day, Steven J. ;
McDermott, David F. ;
Weber, Robert W. ;
Sosman, Jeffrey A. ;
Haanen, John B. ;
Gonzalez, Rene ;
Robert, Caroline ;
Schadendorf, Dirk ;
Hassel, Jessica C. ;
Akerley, Wallace ;
van den Eertwegh, Alfons J. M. ;
Lutzky, Jose ;
Lorigan, Paul ;
Vaubel, Julia M. ;
Linette, Gerald P. ;
Hogg, David ;
Ottensmeier, Christian H. ;
Lebbe, Celeste ;
Peschel, Christian ;
Quirt, Ian ;
Clark, Joseph I. ;
Wolchok, Jedd D. ;
Weber, Jeffrey S. ;
Tian, Jason ;
Yellin, Michael J. ;
Nichol, Geoffrey M. ;
Hoos, Axel ;
Urba, Walter J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (08) :711-723
[6]
Development of Ipilimumab: Contribution to a New Paradigm for Cancer Immunotherapy [J].
Hoos, Axel ;
Ibrahim, Ramy ;
Korman, Alan ;
Abdallah, Kald ;
Berman, David ;
Shahabi, Vafa ;
Chin, Kevin ;
Canetta, Renzo ;
Humphrey, Rachel .
SEMINARS IN ONCOLOGY, 2010, 37 (05) :533-546
[7]
Meta-analysis of phase II cooperative group trials in metastatic stage IV melanoma to determine progression-free and overall survival benchmarks for future phase II trials [J].
Korn, Edward L. ;
Liu, Ping-Yu ;
Lee, Sandra J. ;
Chapman, Judith-Anne W. ;
Niedzwiecki, Donna ;
Suman, Vera J. ;
Moon, James ;
Sondak, Vernon K. ;
Atkins, Michael B. ;
Eisenhauer, Elizabeth A. ;
Parulekar, Wendy ;
Markovic, Svetomir N. ;
Saxman, Scott ;
Kirkwood, John M. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (04) :527-534
[8]
Immunostimulatory monoclonal antibodies for cancer therapy [J].
Melero, Ignacio ;
Hervas-Stubbs, Sandra ;
Glennie, Martin ;
Pardoll, Drew M. ;
Chen, Lieping .
NATURE REVIEWS CANCER, 2007, 7 (02) :95-106
[9]
Efficacy and safety of ipilimumab monotherapy in patients with pretreated advanced melanoma: a multicenter single-arm phase II study [J].
O'Day, S. J. ;
Maio, M. ;
Chiarion-Sileni, V. ;
Gajewski, T. F. ;
Pehamberger, H. ;
Bondarenko, I. N. ;
Queirolo, P. ;
Lundgren, L. ;
Mikhailov, S. ;
Roman, L. ;
Verschraegen, C. ;
Humphrey, R. ;
Ibrahim, R. ;
de Pril, V. ;
Hoos, A. ;
Wolchok, J. D. .
ANNALS OF ONCOLOGY, 2010, 21 (08) :1712-1717
[10]
Ipilimumab plus Dacarbazine for Previously Untreated Metastatic Melanoma [J].
Robert, Caroline ;
Thomas, Luc ;
Bondarenko, Igor ;
O'Day, Steven ;
Weber, Jeffrey ;
Garbe, Claus ;
Lebbe, Celeste ;
Baurain, Jean-Francois ;
Testori, Alessandro ;
Grob, Jean-Jacques ;
Davidson, Neville ;
Richards, Jon ;
Maio, Michele ;
Hauschild, Axel ;
Miller, Wilson H., Jr. ;
Gascon, Pere ;
Lotem, Michal ;
Harmankaya, Kaan ;
Ibrahim, Ramy ;
Francis, Stephen ;
Chen, Tai-Tsang ;
Humphrey, Rachel ;
Hoos, Axel ;
Wolchok, Jedd D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (26) :2517-2526