Antitumor activity in melanoma and anti-self responses in a phase I trial with the anti-cytotoxic T lymphocyte-associated antigen 4 monoclonal antibody CP-675,206

被引:444
作者
Ribas, A
Camacho, LH
Lopez-Berestein, G
Pavlov, D
Bulanhagui, CA
Millham, R
Comin-Anduix, B
Reuben, JM
Seja, E
Parker, CA
Sharma, A
Glaspy, JA
Gomez-Navarro, J
机构
[1] Univ Calif Los Angeles, Dept Med, Div Hematol Oncol Surg, Div Surg Oncol, Los Angeles, CA USA
[2] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Exptl Therapeut Melanoma Med Oncol & Hematop, Houston, TX USA
[4] Pfizer Global Res & Dev, New London, CT USA
关键词
D O I
10.1200/JCO.2005.01.109
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Cytotoxic T lymphocyte-associated antigen 4 (CTLA4) blockade with CP-675,206, a fully human anti-CTLA4 monoclonal antibody, may break peripheral immunologic tolerance leading to effective immune responses to cancer in humans. A phase I trial was conducted to test the safety of CIP-675,206. Patients and Methods Thirty-nine patients with solid malignancies (melanoma, n = 34; renal cell, n = 4; colon, n = 1) received an intravenous (IV) infusion of CP-675,206 at seven dose levels. The primary objective was to determine the maximum-tolerated dose and the recommended phase 11 dose. Results Dose-limiting toxicities and autoimmune phenomena included diarrhea, dermatitis, vitiligo, panhypopituitarism and hyperthyroidism. Two patients experienced complete responses (maintained for 34+ and 25+ months), and there were two partial responses (26+ and 25+ months) among 29 patients with measurable melanoma. There have been no relapses thus far after objective response to therapy. Four other patients had stable disease at end of study evaluation (16, 7, 7, and 4 months). Additionally, five patients had extended periods without disease progression (36+, 35+, 26+, 24+, and 23+ months) after local treatment of progressive metastases. Longer systemic exposure to CP-675,206 achieved in higher dose cohorts predicted for a higher probability of response. Conclusion CP-675,206 can be administered safely to humans as a single IV dose up to 15 mg/kg, resulting in breaking of peripheral immune tolerance to self-tissues and antitumor activity in melanoma.
引用
收藏
页码:8968 / 8977
页数:10
相关论文
共 33 条
[11]   Biologic activity of cytotoxic T lymphocyte-associated antigen 4 antibody blockade in previously vaccinated metastatic melanoma and ovarian carcinoma patients [J].
Hodi, FS ;
Mihm, MC ;
Soiffer, RJ ;
Haluska, FG ;
Butler, M ;
Seiden, MV ;
Davis, T ;
Henry-Spires, R ;
MacRae, S ;
Willman, A ;
Padera, R ;
Jaklitsch, MT ;
Shankar, S ;
Chen, TC ;
Korman, A ;
Allison, JP ;
Dranoff, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (08) :4712-4717
[12]   Activity and safety of CTLA-4 blockade combined with vaccines in cynomolgus macaques [J].
Keler, T ;
Halk, E ;
Vitale, L ;
O'Neill, T ;
Blanset, D ;
Lee, S ;
Srinivasan, M ;
Graziano, RF ;
Davis, T ;
Lonberg, N ;
Korman, A .
JOURNAL OF IMMUNOLOGY, 2003, 171 (11) :6251-6259
[13]   Enhancement of antitumor immunity by CTLA-4 blockade [J].
Leach, DR ;
Krummel, MF ;
Allison, JP .
SCIENCE, 1996, 271 (5256) :1734-1736
[14]   Association of asthma severity and bronchial hyperresponsiveness with a polymorphism in the cytotoxic T-lymphocyte antigen-4 gene [J].
Lee, SY ;
Lee, YH ;
Shin, C ;
Shim, JJ ;
Kang, KH ;
Yoo, SH ;
In, KH .
CHEST, 2002, 122 (01) :171-176
[15]  
*MATHS, 2000, SPLUS 2000 GUID STAT, V1, P301
[16]   Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) can regulate dendritic cell-induced activation and cytotoxicity CD8+ T cells independently of CD4+ T cell help [J].
McCoy, KD ;
Hermans, IF ;
Fraser, JH ;
Le Gros, G ;
Ronchese, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (07) :1157-1162
[17]   Specific subsets of murine dendritic cells acquire potent T cell regulatory functions following CTLA4-mediated induction of indoleamine 2,3 dioxygenase [J].
Mellor, AL ;
Chandler, P ;
Baban, B ;
Hansen, AM ;
Marshall, B ;
Pihkala, J ;
Waldmann, H ;
Cobbold, S ;
Adams, E ;
Munn, DH .
INTERNATIONAL IMMUNOLOGY, 2004, 16 (10) :1391-1401
[18]   Randomized phase III study of temozolomide versus dacarbazine in the treatment of patients with advanced metastatic malignant melanoma [J].
Middleton, MR ;
Grob, JJ ;
Aaronson, N ;
Fierlbeck, G ;
Tilgen, W ;
Seiter, S ;
Gore, M ;
Aamdal, S ;
Cebon, J ;
Coates, A ;
Dreno, B ;
Henz, M ;
Schadendorf, D ;
Kapp, A ;
Weiss, J ;
Fraass, U ;
Statkevich, P ;
Muller, M ;
Thatcher, N .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (01) :158-166
[19]  
MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO
[20]  
2-6